The currently spreading arbovirus epidemic is having a severe
impact on human health worldwide. The two most common
flaviviruses, dengue virus (DENV) and Zika virus (ZIKV), are
transmitted through the same viral vector, Aedes spp. mosquitoes.
Since the discovery of DENV in 1943, this virus has
been reported to cause around 390 million human infections
per year, approximately 500,000 of which require hospitalization
and over 20,000 of which are lethal. The present
DENV epidemic is primarily concentrated in Southeast Asia.
ZIKV, which was discovered in 1952, is another important
arthropod-borne flavivirus. The neurotropic role of ZIKV
has been reported in infected newborns with microcephaly
and in adults with Guillain-Barre syndrome. Despite DENV
and ZIKV sharing the same viral vector, their complex pathogenic
natures are poorly understood, and the infections they
cause do not have specific treatments or effective vaccines.
Therefore, this review will describe what is currently known
about the clinical characteristics, pathogenesis mechanisms,
and transmission of these two viruses. Better understanding
of the interrelationships between DENV and ZIKV will provide
a useful perspective for developing an effective strategy
for controlling both viruses in the future.
Citations
Citations to this article as recorded by
Cholesterol-Lowering Drugs as Potential Antivirals: A Repurposing Approach against Flavivirus Infections Juan Fidel Osuna-Ramos, Carlos Noe Farfan-Morales, Carlos Daniel Cordero-Rivera, Luis Adrián De Jesús-González, José Manuel Reyes-Ruiz, Arianna M. Hurtado-Monzón, Selvin Noé Palacios-Rápalo, Ricardo Jiménez-Camacho, Marco Antonio Meraz-Ríos, Rosa María De Viruses.2023; 15(7): 1465. CrossRef
Trends in ELISA-Based Flavivirus IgG Serosurveys: A Systematic Review Fatima Ericka S. Vista, Ourlad Alzeus G. Tantengco, Micah D. Dispo, Danna Mae S. Opiso, Christian Luke D. C. Badua, John Patrick Z. Gerardo, Juan Raphael M. Perez, Karol Ann T. Baldo, Day-Yu Chao, Leslie Michelle M. Dalmacio Tropical Medicine and Infectious Disease.2023; 8(4): 224. CrossRef
Dynamic Population Models with Temporal Preferential Sampling to Infer Phenology Michael R. Schwob, Mevin B. Hooten, Travis McDevitt-Galles Journal of Agricultural, Biological and Environmental Statistics.2023; 28(4): 774. CrossRef
New insights into the recombinant proteins and monoclonal antibodies employed to immunodiagnosis and control of Zika virus infection: A review Ilana C.L. Magalhães, Pedro F.N. Souza, Lívia E.C. Marques, Nicolas M. Girão, Fernanda M.C. Araújo, Maria Izabel F. Guedes International Journal of Biological Macromolecules.2022; 200: 139. CrossRef
The Aedes aegypti siRNA pathway mediates broad-spectrum defense against human pathogenic viruses and modulates antibacterial and antifungal defenses Yuemei Dong, Shengzhang Dong, Nahid Borhani Dizaji, Natalie Rutkowski, Tyler Pohlenz, Kevin Myles, George Dimopoulos, Ronald P. Van Rij PLOS Biology.2022; 20(6): e3001668. CrossRef
Interplay between autophagy and Sindbis virus in cells derived from key arbovirus vectors, Aedes albopictus and Aedes aegypti mosquitoes Jialu Qiao, Qingzhen Liu Cellular Signalling.2022; 90: 110204. CrossRef
Cross-reactive antibodies facilitate innate sensing of dengue and Zika viruses Laura K. Aisenberg, Kimberly E. Rousseau, Katherine Cascino, Guido Massaccesi, William H. Aisenberg, Wensheng Luo, Kar Muthumani, David B. Weiner, Stephen S. Whitehead, Michael A. Chattergoon, Anna P. Durbin, Andrea L. Cox JCI Insight.2022;[Epub] CrossRef
Conserved motifs in the flavivirus NS3 RNA helicase enzyme Kelly E. Du Pont, Martin McCullagh, Brian J. Geiss WIREs RNA.2022;[Epub] CrossRef
Surveillance for Common Arboviruses in Whole Blood of Malaria-Free Ill Returned Canadian Travelers to the Americas Ruwandi Kariyawasam, Alireza Eshaghi, Stephen Perusini, Rachel Lau, Samir N. Patel, Jonathan B. Gubbay, Andrea K. Boggild Current Infectious Disease Reports.2021;[Epub] CrossRef
An Integrated Systems Biology Approach Identifies the Proteasome as a Critical Host Machinery for ZIKV and DENV Replication Guang Song, Emily M. Lee, Jianbo Pan, Miao Xu, Hee-Sool Rho, Yichen Cheng, Nadia Whitt, Shu Yang, Jennifer Kouznetsova, Carleen Klumpp-Thomas, Samuel G. Michael, Cedric Moore, Ki-Jun Yoon, Kimberly M. Christian, Anton Simeonov, Wenwei Huang, Menghang Xia, Genomics, Proteomics & Bioinformatics.2021; 19(1): 108. CrossRef
Dengue and Zika virus infection patterns vary among Aedes aegypti field populations from Belo Horizonte, a Brazilian endemic city Raquel Soares Maia Godoy, Luiza dos Santos Felix, Alessandra da Silva Orfanó, Bárbara Aparecida Chaves, Paula Monalisa Nogueira, Breno dos Anjos Costa, Aline Silva Soares, Cinthia Catharina Azevedo Oliveira, Rafael Nacif-Pimenta, Breno Mello Silva, Ana Pa PLOS Neglected Tropical Diseases.2021; 15(11): e0009839. CrossRef
Andrographolide and Its 14-Aryloxy Analogues Inhibit Zika and Dengue Virus Infection Feng Li, Wipaporn Khanom, Xia Sun, Atchara Paemanee, Sittiruk Roytrakul, Decai Wang, Duncan R. Smith, Guo-Chun Zhou Molecules.2020; 25(21): 5037. CrossRef
An antibody panel for highly specific detection and differentiation of Zika virus Md Alamgir Kabir, Ruben Soto-Acosta, Sandhya Sharma, Shelton S. Bradrick, Mariano A. Garcia-Blanco, Massimo Caputi, Waseem Asghar Scientific Reports.2020;[Epub] CrossRef
SARS-CoV-2 and arbovirus infection: a rapid systematic review Keilla Martins Milby, Alvaro Nagib Atallah, César Ramos Rocha-Filho, Ana Carolina Pereira Nunes Pinto, Aline Pereira da Rocha, Felipe Sebastião de Assis Reis, Nelson Carvas Junior, Vinicius Tassoni Civile, Rodolfo Rodrigo Pereira Santos, Laura Jantsch Fer Sao Paulo Medical Journal.2020; 138(6): 498. CrossRef
Clinical relevance of Zika symptoms in the context of a Zika Dengue epidemic Humberto Guanche Garcell, Francisco Gutiérrez García, Manuel Ramirez Nodal, Alfredo Ruiz Lozano, Carlos R. Pérez Díaz, Anaika González Valdés, Luis Gonzalez Alvarez Journal of Infection and Public Health.2020; 13(2): 173. CrossRef
Development of a Cell-Based Immunodetection Assay for Simultaneous Screening of Antiviral Compounds Inhibiting Zika and Dengue Virus Replication Ilaria Vicenti, Filippo Dragoni, Alessia Giannini, Federica Giammarino, Michele Spinicci, Francesco Saladini, Adele Boccuto, Maurizio Zazzi SLAS Discovery.2020; 25(5): 506. CrossRef
7X multiplexed, optofluidic detection of nucleic acids for antibiotic-resistance bacterial screening G. G. Meena, T. A. Wall, M. A. Stott, O. Brown, R. Robison, A. R. Hawkins, H. Schmidt Optics Express.2020; 28(22): 33019. CrossRef
Tryptophan Trimers and Tetramers Inhibit Dengue and Zika Virus Replication by Interfering with Viral Attachment Processes Antonios Fikatas, Peter Vervaeke, Belén Martínez-Gualda, Olaia Martí-Marí, Sam Noppen, Eef Meyen, María-José Camarasa, Ana San-Félix, Christophe Pannecouque, Dominique Schols Antimicrobial Agents and Chemotherapy.2020;[Epub] CrossRef
Wolbachia’s Deleterious Impact on Aedes aegypti Egg Development: The Potential Role of Nutritional Parasitism Megan J. Allman, Johanna E. Fraser, Scott A. Ritchie, D. Albert Joubert, Cameron P. Simmons, Heather A. Flores Insects.2020; 11(11): 735. CrossRef
The limited knowledge of placental damage due to neglected infections: ongoing problems in Latin America Isabela Moreti Ribeiro, Paula Cristina Souza Souto, Alexandre U. Borbely, Eloiza Lopes Lira Tanabe, Angela Cadavid, Angela M. Alvarez, Julio Bueno, Olga Agudelo, Reggie García Robles, Paola Ayala-Ramírez, Flavia Sacerdoti, Theodora Szasz, Alicia E. Damian Systems Biology in Reproductive Medicine.2020; 66(3): 151. CrossRef
The prevention of arboviral diseases using mobile devices: a preliminary study of the attitudes and behaviour change produced by educational interventions Francisco Fernandes Abel Mangueira, Roberta Smania‐Marques, Izabelly Dutra Fernandes, Victor Alves Albino, Ricardo Olinda, Tais Acácia Santos‐Silva, John Traxler, David Matheson, Silvana Santos Tropical Medicine & International Health.2019; 24(12): 1411. CrossRef
Influence of directional positive Darwinian selection-driven evolution on arboviruses Dengue and Zika virulence and pathogenesis Ricardo Durães-Carvalho, Louisa F. Ludwig-Begall, Marco Salemi, Roberto D. Lins, Ernesto T.A. Marques Molecular Phylogenetics and Evolution.2019; 140: 106607. CrossRef
Designing Paper-Based Immunoassays for Biomedical Applications Delyan R. Hristov, Cristina Rodriguez-Quijada, Jose Gomez-Marquez, Kimberly Hamad-Schifferli Sensors.2019; 19(3): 554. CrossRef
Concurrent Guillain-Barré syndrome, transverse myelitis and encephalitis post-Zika: A case report and review of the pathogenic role of multiple arboviral immunity Gustavo C. Román, Juan-Manuel Anaya, Óscar Mancera-Páez, Rodrigo Pardo-Turriago, Yohan Rodríguez Journal of the Neurological Sciences.2019; 396: 84. CrossRef
Multiplexed kit based on Luminex technology and achievements in synthetic biology discriminates Zika, chikungunya, and dengue viruses in mosquitoes Lyudmyla G. Glushakova, Barry W. Alto, Myong-Sang Kim, Daniel Hutter, Andrea Bradley, Kevin M. Bradley, Nathan D. Burkett-Cadena, Steven A. Benner BMC Infectious Diseases.2019;[Epub] CrossRef
Zika Virus Vaccines: Challenges and Perspectives Raquel Das Neves Almeida, Trina Racine, Kelly G. Magalhães, Gary P. Kobinger Vaccines.2018; 6(3): 62. CrossRef
Emerging sexually transmitted viral infections: 2. Review of Zika virus disease RJ Caswell, K Manavi International Journal of STD & AIDS.2018; 29(12): 1238. CrossRef
Identification of AaAtg8 as a marker of autophagy and a functional autophagy-related protein in Aedes albopictus Jialu Qiao, Dandan Zhang, Yu Wang, Xiaomei Li, Shengya Wang, Qingzhen Liu PeerJ.2018; 6: e5988. CrossRef
Vertical Transmission of the Zika Virus Causes Neurological Disorders in Mouse Offspring Yingchao Shi, Shihua Li, Qian Wu, Le Sun, Junjing Zhang, Na Pan, Qihui Wang, Yuhai Bi, Jing An, Xuancheng Lu, George Fu Gao, Xiaoqun Wang Scientific Reports.2018;[Epub] CrossRef
Diagnosis and outcomes of pregnant women with Zika virus infection in two municipalities of Risaralda, Colombia: Second report of the ZIKERNCOL study Alfonso J. Rodriguez-Morales, Jaime A. Cardona-Ospina, Valeria Ramirez-Jaramillo, Javier A. Gaviria, Gloria María González-Moreno, Juan D. Castrillón-Spitia, Alejandra López-Villegas, Estefania Morales-Jiménez, Valentina Ramírez-Zapata, German Eduardo Rue Travel Medicine and Infectious Disease.2018; 25: 20. CrossRef
A review of selected Arboviruses during pregnancy Penélope Saldanha Marinho, Antonio José Cunha, Joffre Amim Junior, Arnaldo Prata-Barbosa Maternal Health, Neonatology and Perinatology.2017;[Epub] CrossRef
In vitro study of Zika virus infection in boar semen Natthanej Luplertlop, San Suwanmanee, Sumate Ampawong, Sompong Vongpunsawad, Yong Poovorawan Archives of Virology.2017; 162(10): 3209. CrossRef
After the epidemic: Zika virus projections for Latin America and the Caribbean Felipe J. Colón-González, Carlos A. Peres, Christine Steiner São Bernardo, Paul R. Hunter, Iain R. Lake, Uwem Friday Ekpo PLOS Neglected Tropical Diseases.2017; 11(11): e0006007. CrossRef
Specific Biomarkers Associated With Neurological Complications and Congenital Central Nervous System Abnormalities From Zika Virus–Infected Patients in Brazil Yiu-Wing Kam, Juliana Almeida Leite, Fok-Moon Lum, Jeslin J L Tan, Bernett Lee, Carla C Judice, Daniel Augusto de Toledo Teixeira, Robert Andreata-Santos, Marco A Vinolo, Rodrigo Angerami, Mariangela Ribeiro Resende, Andre Ricardo Ribas Freitas, Eliana Am The Journal of Infectious Diseases.2017; 216(2): 172. CrossRef
An aerobic, Gram-negative bacterium, designated strain
SD70T, was isolated from sea cucumber aquaculture farm
sediment in Taean, Korea, and its taxonomic status was established
by undertaking a polyphasic study. Cells of strain
SD70T were non-motile, catalase-, and oxidase-positive, nonspore-
forming, and horseshoe-shaped. Optimal growth was
observed under 25–30°C, pH 7.0–8.0, and 3.0–5.0% (w/v)
NaCl conditions. Phylogenetic analyses based on 16S rRNA
gene sequences revealed that strain SD70T fell within an
evolutionary group comprising species of the genus Cyclobacterium.
Strain SD70T shared 92.1–98.5% 16S rRNA sequence
similarity values with the type strains of species of the
genus Cyclobacterium. Relatively low levels of DNA-DNA
relatedness were found between strain SD70T and C. marinum
DSM 745T (40.2%) and C. amurskyense KMM 6143T
(15.8%). The predominant cellular fatty acids were iso-C15:0
(32.1%), and anteiso-C15:0 (9.1%). Menaquinone MK-7 was
the only respiratory quinone. The G+C content of the genomic
DNA was 36 mol%. The polar lipids were phosphatidylcholine,
phosphatidylethanolamine, phosphatidylglycerol,
and seven unidentified lipids. On the basis of phenotypic and
genotypic data, strain SD70T represents a novel species of the
genus Cyclobacterium, for which the name Cyclobacterium
sediminis sp. nov. is proposed. An emended description of
the genus Cyclobacterium is also provided.
Citations
Citations to this article as recorded by
Taxogenomics of the Genus Cyclobacterium: Cyclobacterium xiamenense and Cyclobacterium halophilum as Synonyms and Description of Cyclobacterium plantarum sp. nov. Azadeh Shahinpei, Mohammad Ali Amoozegar, Leila Mirfeizi, Mahdi Moshtaghi Nikou, Antonio Ventosa, Cristina Sánchez-Porro Microorganisms.2020; 8(4): 610. CrossRef
Cyclobacterium salsum sp. nov. and Cyclobacterium roseum sp. nov., isolated from a saline lake Yong-Hong Liu, Yuan-Guo Xie, Li Li, Hong-Chen Jiang, Osama Abdalla Abdelshafy Mohamad, Wael Hozzein, Bao-Zhu Fang, Wen-Jun Li
International Journal of Systematic and Evolutionary Microbiology
.2020; 70(6): 3785. CrossRef
Glacial-interglacial transitions in microbiomes recorded in deep-sea sediments from the western equatorial Atlantic Lucas Freitas, Luciana Appolinario, Gabriela Calegario, Mariana Campeão, Diogo Tschoeke, Gizele Garcia, Igor Martins Venancio, Carlos A.N. Cosenza, Luciana Leomil, Marcelo Bernardes, Ana Luiza Albuquerque, Cristiane Thompson, Fabiano Thompson Science of The Total Environment.2020; 746: 140904. CrossRef
Analysis of 1,000 Type-Strain Genomes Improves Taxonomic Classification of Bacteroidetes Marina García-López, Jan P. Meier-Kolthoff, Brian J. Tindall, Sabine Gronow, Tanja Woyke, Nikos C. Kyrpides, Richard L. Hahnke, Markus Göker Frontiers in Microbiology.2019;[Epub] CrossRef
Notification of changes in taxonomic opinion previously published outside the IJSEM Aharon Oren, George M. Garrity
International Journal of Systematic and Evolutionary Microbiology
.2017; 67(7): 2081. CrossRef
To clarify the interactions between a common food spoilage
yeast and two pathogenic bacteria involved in outbreaks associated
with fruit juices, the present paper studies the effect
of the interplay of Candida krusei, collected from UF membranes,
with Escherichia coli O157:H7 and Salmonella enterica
in the overall process of adhesion and colonization of
abiotic surfaces. Two different cases were tested: a) co-adhesion
by pathogenic bacteria and yeasts, and b) incorporation
of bacteria to pre-adhered C. krusei cells. Cultures were made
on stainless steel at 25°C using apple juice as culture medium.
After 24 h of co-adhesion with C. krusei, both E. coli O157:H7
and S. enterica increased their counts 1.05 and 1.11 log CFU
cm2, respectively. Similar increases were obtained when incorporating
bacteria to pre-adhered cells of Candida. Nevertheless
C. krusei counts decreased in both experimental conditions,
in a) 0.40 log CFU cm2 and 0.55 log CFU cm2 when
exposed to E. coli O157:H7 and S. enterica and in b) 0.18 and
0.68 log CFU cm2, respectively. This suggests that C. krusei,
E. coli O157:H7, and S. enterica have a complex relationship
involving physical and chemical interactions on food contact
surfaces. This study supports the possibility that pathogen
interactions with members of spoilage microbiota, such
as C. krusei, might play an important role for the survival and
dissemination of E. coli O157:H7 and Salmonella enterica in
food-processing environments. Based on the data obtained
from the present study, much more attention should be given
to prevent the contamination of these pathogens in acidic
drinks.
Citations
Citations to this article as recorded by
Effectiveness of sodium hypochlorite and benzalkonium chloride in reducing spoilage yeast biofilms on food contact surfaces Manuel Alejandro Palencia Díaz, María Clara Tarifa, Patricia Liliana Marucci, Diego Bautista Genovese, Lorena Inés Brugnoni Biofouling.2024; 40(10): 964. CrossRef
Application of natamycin and farnesol as bioprotection agents to inhibit biofilm formation of yeasts and foodborne bacterial pathogens in apple juice processing lines María del Rosario Agustín, María Clara Tarifa, María Soledad Vela-Gurovic, Lorena Inés Brugnoni Food Microbiology.2023; 109: 104123. CrossRef
Candida krusei is the major contaminant of ultrafiltration and reverse osmosis membranes used for cranberry juice production Sherazade Fikri, Marie-Hélène Lessard, Véronique Perreault, Alain Doyen, Steve Labrie Food Microbiology.2023; 109: 104146. CrossRef
Application of Natamycin and Farnesol as Biocontrol Agents of Multi-Species Biofilms on Industrial Surfaces in Apple Juice María del Rosario Agustín, Maria Clara Tarifa, Maria Soledad Vela-Gurovic, Lorena Ines Brugnoni SSRN Electronic Journal .2022;[Epub] CrossRef
Enhanced microbial inactivation by carbon dioxide through mechanical effects Ratka Hoferick, Angelos Ntovas, Qasim Alhusaini, Mareike Müller, Stéphan Barbe, Holger Schönherr The Journal of Supercritical Fluids.2021; 175: 105273. CrossRef
Yeast biofilm in food realms: occurrence and control Giacomo Zara, Marilena Budroni, Ilaria Mannazzu, Francesco Fancello, Severino Zara World Journal of Microbiology and Biotechnology.2020;[Epub] CrossRef
Disinfection efficacy over yeast biofilms of juice processing industries María C. Tarifa, Jorge E. Lozano, Lorena I. Brugnoni Food Research International.2018; 105: 473. CrossRef
Identification des espèces de levures isolées de l’attiéké commercialisé sur les marchés à Abidjan (Côte d’Ivoire) : étude préliminaire C.G. Kouadio-Yapo, G.S.P. Dou, N.A.D. Aka, K.D. Zika, K.D. Adoubryn, M. Dosso Journal de Mycologie Médicale.2018; 28(2): 305. CrossRef
Multispecies biofilms between Listeria monocytogenes and Listeria innocua with resident microbiota isolated from apple juice processing equipment María del Rosario Agustín, Lorena Brugnoni Journal of Food Safety.2018;[Epub] CrossRef
Efficiency of Enterobacter cloacae KU923381 isolated from
petroleum hydrocarbon contaminated soil was evaluated in
batch culture and bioreactor mode. The isolate were screened
for biofilm formation using qualitative and quantitative assays.
Response surface methodology (RSM) was used to study the
effect of pH, temperature, glucose concentration, and sodium
chloride on diesel degradation. The predicted values for
diesel oil degradation efficiency by the statistical designs are
in a close agreement with experimental data (R2 = 99.66%).
Degradation efficiency is increased by 36.78% at pH = 7,
temperature = 35°C, glucose = 5%, and sodium chloride concentration
= 5%. Under the optimized conditions, the experiments
were performed for diesel oil degradation by gas chromatographic
mass spectrometric analysis (GC-MS). GC-MS
analysis confirmed that E. cloacae had highly degrade hexadecane,
heptadecane, tridecane, and docosane by 99.71%,
99.23%, 99.66%, and 98.34% respectively. This study shows
that rapid bioremoval of hydrocarbons in diesel oil is acheived
by E. cloacae with abet of biofilm formation. The potential
use of the biofilms for preparing trickling filters (gravel particles)
for the degradation of hydrocarbons from petroleum
wastes before their disposal in the open environment is highly
suggested. This is the first successful attempt for artificially
establishing petroleum hydrocarbon degrading bacterial biofilm
on solid substrates in bioreactor.
Citations
Citations to this article as recorded by
Biodegradation of crude oil using bacterial strains isolated from the oil contaminated soil of Shakar Dara oil fields of Pakistan Shahrukh Bahar, Abdul Rehman, Muhammad Saqib Malik, Iffat Naz, Muhammad Jamil, Muhammad Anees Bioremediation Journal.2024; : 1. CrossRef
Oilfield Carbonated Produced Water Recycling Coupled to Exopolysaccharide Transformation by Lelliottia amnigena Igor Carvalho Fontes Sampaio, Joalene de Azevedo Santos Ferreira, Pedro Jorge Louro Crugeira, Ian Mascena da Silva Oliveira, Jacson Nunes dos Santos, Josilene Borges Torres Lima Matos, Antonio Luiz Barbosa Pinheiro, Paulo Fernando de Almeida Waste and Biomass Valorization.2024; 15(3): 1309. CrossRef
Increasing in situ bioremediation effectiveness through field-scale application of molecular biological tools Andrew S. Madison, Skyler J. Sorsby, Yingnan Wang, Trent A. Key Frontiers in Microbiology.2023;[Epub] CrossRef
Genomic and biotechnological potential of a novel oil-degrading strain Enterobacter kobei DH7 isolated from petroleum-contaminated soil Muhammad Zohaib Nawaz, Chunyan Xu, Majjid A. Qaria, Syed Zeeshan Haider, Hafiz Rameez Khalid, Huda Ahmed Alghamdi, Iqrar Ahmad Khan, Daochen Zhu Chemosphere.2023; 340: 139815. CrossRef
Bioremediation of diesel oil: potential use of bacteria consortium Lactobacillus fermentum and Clostridium beijerinckii in degrading Total Petroleum Hydrocarbon (TPH) Naomi Oshin Laurensa Sipahutar, Lutfia Rahmiyati, Astri Rinanti, Melati Ferianita Fachrul, Astari Minarti IOP Conference Series: Earth and Environmental Science.2023; 1239(1): 012037. CrossRef
Coupled reduction of structural Fe(III) in nontronite and oxidation of petroleum hydrocarbons Yuan Liu, Shengbao Shi, Qiang Zeng, Yang Li, Yu Chen, Dongyi Guo, Dafu Hu, Hailiang Dong Geochimica et Cosmochimica Acta.2023; 344: 103. CrossRef
Advanced bioremediation by an amalgamation of nanotechnology and modern artificial intelligence for efficient restoration of crude petroleum oil-contaminated sites: a prospective study Rupshikha Patowary, Arundhuti Devi, Ashis K. Mukherjee Environmental Science and Pollution Research.2023; 30(30): 74459. CrossRef
Enhanced petroleum removal with a novel biosurfactant producer consortium isolated from drilling cuttings of offshore Akçakoca-5 in the Black Sea Sezen Bilen Ozyurek Geoenergy Science and Engineering.2023; 231: 212348. CrossRef
Mycoremediation as a Potentially Promising Technology: Current Status and Prospects—A Review Stephen Okiemute Akpasi, Ifeanyi Michael Smarte Anekwe, Emmanuel Kweinor Tetteh, Ubani Oluwaseun Amune, Hassan Oriyomi Shoyiga, Thembisile Patience Mahlangu, Sammy Lewis Kiambi Applied Sciences.2023; 13(8): 4978. CrossRef
Potential Egyptian bacterial consortium for oil spill treatment: A laboratory simulation Aya Elkemary, Samia S. Abouelkheir, Mostafa AbdelHakim, Soraya A. Sabry, Hanan A. Ghozlan Case Studies in Chemical and Environmental Engineering.2023; 7: 100278. CrossRef
Use of Taguchi design for optimization of diesel-oil biodegradation using consortium of Pseudomonas stutzeri, Cellulosimicrobium cellulans, Acinetobacter baumannii and Pseudomonas balearica isolated from tarball in Terengganu Beach, Malaysia Bruno Martins Nkem, Normala Halimoon, Fatimah Md Yusoff, Wan Lutfi Wan Johari Journal of Environmental Health Science and Engineering.2022; 20(2): 729. CrossRef
Optimization of the Biodegradation of Aliphatic, Aromatic, and UCM Hydrocarbons from Light Crude Oil in Marine Sediment Using Response Surface Methodology (RSM) Itzá García-Bautista, Ulises García-Cruz, Neith Pacheco, José Q. García-Maldonado, M. Leopoldina Aguirre-Macedo Bulletin of Environmental Contamination and Toxicology.2022; 108(1): 107. CrossRef
ACTIVIDAD ANTIFÚNGICA Y CARACTERÍSTICAS DE PROMOCIÓN DE CRECIMIENTO VEGETAL DE Pseudomonas aeruginosa y Enterobacter sp. DEGRADADORAS DE HIDROCARBUROS AISLADAS DE SUELO CONTAMINADO Luis Enrique Flores Pantoja, Everardo Briseño Silva, Pedro Damián Loeza Lara, Rafael Jiménez Mejía Acta Biológica Colombiana.2022;[Epub] CrossRef
Rhodococcus: A promising genus of actinomycetes for the bioremediation of organic and inorganic contaminants Mateus Torres Nazari, Viviane Simon, Bruna Strieder Machado, Larissa Crestani, Giovana Marchezi, Gustavo Concolato, Valdecir Ferrari, Luciane Maria Colla, Jeferson Steffanello Piccin Journal of Environmental Management.2022; 323: 116220. CrossRef
Diesel degradation efficiency of Enterobacter sp., Acinetobacter sp., and Cedecea sp. isolated from petroleum waste dumping site: a bioremediation view point Israt Jerin, Md. Sifat Rahi, Tanjia Sultan, Md. Shihabul Islam, Salek Ahmed Sajib, Kazi Md. Faisal Hoque, Md Abu Reza Archives of Microbiology.2021; 203(8): 5075. CrossRef
Bacteria, Fungi and Microalgae for the Bioremediation of Marine Sediments Contaminated by Petroleum Hydrocarbons in the Omics Era Filippo Dell’ Anno, Eugenio Rastelli, Clementina Sansone, Christophe Brunet, Adrianna Ianora, Antonio Dell’ Anno Microorganisms.2021; 9(8): 1695. CrossRef
Isolation and Characterization of Oil-Degrading Enterobacter sp. from Naturally Hydrocarbon-Contaminated Soils and Their Potential Use against the Bioremediation of Crude Oil Mukkaram Ejaz, Baowei Zhao, Xiukang Wang, Safdar Bashir, Fasih Ullah Haider, Zubair Aslam, Muhammad Imran Khan, Muhammad Shabaan, Muhammad Naveed, Adnan Mustafa Applied Sciences.2021; 11(8): 3504. CrossRef
Biodegradation of n-alkanes in crude oil by three identified bacterial strains Yuan Liu, Yun Yang Wan, Chunjiang Wang, Zheyu Ma, Xiaoli Liu, Shengjin Li Fuel.2020; 275: 117897. CrossRef
Bioremoval of Acephate by biofilm-forming Enterobacter cloacae – VITDAJ8 in a vertical packed bed biofilm bioreactor Dipti Mayee Dash, Ankita Itusha, Jabez W Osborne Asia Pacific Journal of Molecular Biology and Biotechnology.2020; : 68. CrossRef
Rapid biodegradation and biofilm-mediated bioremoval of organophosphorus pesticides using an indigenous Kosakonia oryzae strain -VITPSCQ3 in a Vertical-flow Packed Bed Biofilm Bioreactor Dipti Mayee Dash, W. Jabez Osborne Ecotoxicology and Environmental Safety.2020; 192: 110290. CrossRef
Optimization of carbofuran insecticide degradation by Enterobacter sp. using response surface methodology (RSM) Mohammed Umar Mustapha, Normala Halimoon, Wan Lutfi Wan Johari, Mohd Yunus abd shokur Journal of King Saud University - Science.2020; 32(3): 2254. CrossRef
Hexadecane biodegradation of high efficiency by bacterial isolates from Santos Basin sediments Vitor B. Ferrari, Augusto Cesar, Rodrigo Cayô, Rodrigo B. Choueri, Débora N. Okamoto, Juliana G. Freitas, Mariana Favero, Ana C. Gales, Cristina V. Niero, Flavia T. Saia, Suzan P. de Vasconcellos Marine Pollution Bulletin.2019; 142: 309. CrossRef
Analysis of petroleum biodegradation by a bacterial consortium isolated from worms of the polychaeta class (Annelida): Implications for NPK fertilizer supplementation Carla Jaqueline Silva Sampaio, José Roberto Bispo de Souza, Gilson Correia de Carvalho, Cristina Maria Quintella, Milton Ricardo de Abreu Roque Journal of Environmental Management.2019; 246: 617. CrossRef
Potential of bacteria isolated from diesel-contaminated seawater in diesel biodegradation Muhammad Fauzul Imron, Setyo Budi Kurniawan, Harmin Sulistiyaning Titah Environmental Technology & Innovation.2019; 14: 100368. CrossRef
Isolation, identification, and characterization of diesel‐oil‐degrading bacterial strains indigenous to Changqing oil field, China Wuyang Sun, Imran Ali, Jiwei Liu, Min Dai, Wenrui Cao, Mingyu Jiang, Gaowa Saren, Xinke Yu, Changsheng Peng, Iffat Naz Journal of Basic Microbiology.2019; 59(7): 723. CrossRef
The coordinated action of RNase III and RNase G controls enolase expression in response to oxygen availability in Escherichia coli Minho Lee, Minju Joo, Minji Sim, Se-Hoon Sim, Hyun-Lee Kim, Jaejin Lee, Minkyung Ryu, Ji-Hyun Yeom, Yoonsoo Hahn, Nam-Chul Ha, Jang-Cheon Cho, Kangseok Lee Scientific Reports.2019;[Epub] CrossRef
RNase G controls tpiA mRNA abundance in response to oxygen availability in Escherichia coli Jaejin Lee, Dong-Ho Lee, Che Ok Jeon, Kangseok Lee Journal of Microbiology.2019; 57(10): 910. CrossRef
Construction of potential bacterial consortia for efficient hydrocarbon degradation Kasturi Poddar, Debapriya Sarkar, Angana Sarkar International Biodeterioration & Biodegradation.2019; 144: 104770. CrossRef
Optimization of diesel biodegradation by Vibrio alginolyticus using Box-Behnken design Muhammad Fauzul Imron, Harmin Sulistiyaning Titah Environmental Engineering Research.2018; 23(4): 374. CrossRef
Process optimization of butachlor bioremediation by Enterobacter cloacae using Plackett Burman design and response surface methodology Satya Sundar Mohanty, Hara Mohan Jena Process Safety and Environmental Protection.2018; 119: 198. CrossRef
Optimization of biodegradation of polycyclic aromatic sulfur heterocycles in soil using response surface methodology Shuiquan Chen, Shuo Sun, Chaocheng Zhao, Meng Zang, Qian Wang, Qiyou Liu, Lin Li Petroleum Science and Technology.2018; 36(22): 1883. CrossRef
Fast Biodegradation of Diesel Hydrocarbons at High Concentration by the Sophorolipid-Producing Yeast Candida catenulata KP324968 Faezeh Babaei, Alireza Habibi Microbial Physiology.2018; 28(5): 240. CrossRef
Coliform Bacteria for Bioremediation of Waste Hydrocarbons Majida Khanafer, Husain Al-Awadhi, Samir Radwan BioMed Research International.2017; 2017: 1. CrossRef
Degradation of diesel-oil by a newly isolated Kocuria sediminis DDK6 Y. Z. Khalifa Ashraf African Journal of Microbiology Research.2017; 11(10): 400. CrossRef
Lipid droplets consist of a core of neutral lipids surrounded
by a phospholipid monolayer with bound proteins. Much of
the information on lipid droplet function comes from proteomic
and lipodomic studies that identify the components
of droplets isolated from organisms throughout the phylogenetic
tree. Here, we add to that important inventory by reporting
lipid droplet factors from the fission yeast, Schizosaccharomyces
pombe. Unique to this study was the fact that cells were
cultured in three different environments: 1) late log growth
phase in glucose-based media, 2) stationary phase in glucosebased
media, and 3) late log growth phase in media containing
oleic acid. We confirmed colocalization of major factors
with lipid droplets using live-cell fluorescent microscopy. We
also analyzed droplets from each of the three conditions for
sterol ester (SE) and triacylglycerol (TAG) content, along
with their respective fatty acid compositions. We identified
a previously undiscovered lipid droplet protein, Vip1p, which
affects droplet size distribution. The results provide further
insight into the workings of these ubiquitous organelles.
Citations
Citations to this article as recorded by
Cbf11 and Mga2 function together to activate transcription of lipid metabolism genes and promote mitotic fidelity in fission yeast Anna Marešová, Michaela Grulyová, Miluše Hradilová, Viacheslav Zemlianski, Jarmila Princová, Martin Převorovský, Cathy Savage-Dunn PLOS Genetics.2024; 20(12): e1011509. CrossRef
Mild Heat Stress Alters the Physical State and Structure of Membranes in Triacylglycerol-Deficient Fission Yeast, Schizosaccharomyces pombe Péter Gudmann, Imre Gombos, Mária Péter, Gábor Balogh, Zsolt Török, László Vígh, Attila Glatz Cells.2024; 13(18): 1543. CrossRef
Lipid droplets: a cellular organelle vital in cancer cells Yi Jin, Yanjie Tan, Jian Wu, Zhuqing Ren Cell Death Discovery.2023;[Epub] CrossRef
Oleaginous yeasts: Time to rethink the definition? José Manuel Salvador López, Meriam Vandeputte, Inge N. A. Van Bogaert Yeast.2022; 39(11-12): 553. CrossRef
Proteomic and lipidomic analyses of lipid droplets in Aurantiochytrium limacinum ATCC MYA-1381 Kohei Yoneda, Yohei Ishibashi, Masaki Yoshida, Makoto M. Watanabe, Makoto Ito, Iwane Suzuki Algal Research.2022; 67: 102844. CrossRef
ER-localized phosphatidylethanolamine synthase plays a conserved role in lipid droplet formation Mehmet Oguz Gok, Natalie Ortiz Speer, W. Mike Henne, Jonathan R. Friedman, James Olzmann Molecular Biology of the Cell.2022;[Epub] CrossRef
Lipid Droplet Nucleation Abdou Rachid Thiam, Elina Ikonen Trends in Cell Biology.2021; 31(2): 108. CrossRef
Metabolism of Storage Lipids and the Role of Lipid Droplets in the Yeast Schizosaccharomyces pombe Ivan Hapala, Peter Griac, Roman Holic Lipids.2020; 55(5): 513. CrossRef
Lipid Droplets in Neurodegenerative Disorders Brandon C. Farmer, Adeline E. Walsh, Jude C. Kluemper, Lance A. Johnson Frontiers in Neuroscience.2020;[Epub] CrossRef
Harnessing the Power of Mutagenesis and Adaptive Laboratory Evolution for High Lipid Production by Oleaginous Microalgae and Yeasts Neha Arora, Hong-Wei Yen, George P. Philippidis Sustainability.2020; 12(12): 5125. CrossRef
Mechanisms of protein targeting to lipid droplets: A unified cell biological and biophysical perspective Ravi Dhiman, Stefanie Caesar, Abdou Rachid Thiam, Bianca Schrul Seminars in Cell & Developmental Biology.2020; 108: 4. CrossRef
The New Face of the Lipid Droplet: Lipid Droplet Proteins Congyan Zhang, Pingsheng Liu PROTEOMICS.2019;[Epub] CrossRef
Effect of Selenium on Lipid and Amino Acid Metabolism in Yeast Cells Marek Kieliszek, Stanisław Błażejak, Anna Bzducha-Wróbel, Anna M. Kot Biological Trace Element Research.2019; 187(1): 316. CrossRef
The Peroxygenase Activity of the Aspergillus flavus Caleosin, AfPXG, Modulates the Biosynthesis of Aflatoxins and Their Trafficking and Extracellular Secretion via Lipid Droplets Abdulsamie Hanano, Mari Alkara, Ibrahem Almousally, Mouhnad Shaban, Farzana Rahman, Mehedi Hassan, Denis J. Murphy Frontiers in Microbiology.2018;[Epub] CrossRef
Mitotic defects in fission yeast lipid metabolism ‘cut’ mutants are suppressed by ammonium chloride Róbert Zach, Jarmila Tvarůžková, Martin Schätz, Ondřej Ťupa, Beáta Grallert, Martin Převorovský FEMS Yeast Research.2018;[Epub] CrossRef
Lipid Droplets: Formation to Breakdown Alex Meyers, Taylor M. Weiskittel, Paul Dalhaimer Lipids.2017; 52(6): 465. CrossRef
Silent information regulator 2 (Sir2), which is the founding
member of the sirtuin family of proteins, is a pro-longevity
factor for replicative lifespan (RLS) in Saccharomyces cerevisiae.
Sir2 is required for transcriptional silencing at mating
type loci, telomeres, and rDNA loci. Sir2 also represses transcription
of highly expressed growth-related genes, such as
PMA1 and some ribosomal protein genes. Although the Sir2
paralogues Hst1, Hst2, Hst3, and Hst4 occur in S. cerevisiae,
none of them could replace the transcriptional regulation of
PMA1 by Sir2 in the wild type. In this study, we demonstrate
that Hst1, the closest Sir2 paralogue, deacetylates the acetylated
lysine 16 of histone H4 (H4K16Ac) and represses PMA1
transcription in the sir2Δ pde2Δ mutant. We further show
that Hst1 plays a role in extending the RLS of the sir2Δ pde2Δ
mutant. Collectively, our results suggest that Hst1 can substitute
for Sir2 by deacetylating H4K16Ac only in the sir2Δ
pde2Δ.
Citations
Citations to this article as recorded by
Selective production, relationship and controversy between Monascus pigments and citrinin Xueling Qin, Bin Xie, Xuanli Zong, Xiang Yu, Yanli Feng Food Bioscience.2023; 56: 103233. CrossRef
Gene repression in S. cerevisiae—looking beyond Sir-dependent gene silencing Safia Mahabub Sauty, Kholoud Shaban, Krassimir Yankulov Current Genetics.2021; 67(1): 3. CrossRef
Characterization of Resveratrol, Oxyresveratrol, Piceatannol and Roflumilast as Modulators of Phosphodiesterase Activity. Study of Yeast Lifespan Adrián Matencio, Francisco García-Carmona, José Manuel López-Nicolás Pharmaceuticals.2020; 13(9): 225. CrossRef
NAD+-dependent HDAC inhibitor stimulates Monascus pigment production but inhibit citrinin Yan Hu, Youxiang Zhou, Zejing Mao, Huihui Li, Fusheng Chen, Yanchun Shao AMB Express.2017;[Epub] CrossRef
Efflux pumps play an important role in antimicrobial resistance
for Acinetobacter baumannii. However, the function of
the Emr pump system and the relationship between Emr and
drug resistance has not been characterized in A. baumannii.
In this study, four possible groups of emr-like genes were
found by searching a genome database. Among them, A1S_
1772 (emrB) and A1S_1773 (emrA) were demonstrated to be
co-transcribed as a single operon. Moreover, during osmotic
stress, A1S_1772 showed the largest change in gene expression
compared to the other emrB-like genes, and deletion of
A1S_1772 (AB ΔemrB) significantly slowed cell growth in
20% sucrose. Using a phenotypic microarray analysis, the AB
ΔemrB mutant was more susceptible to colistin and nafcillin,
paromomycin, spiramycin, and D,L-serine hydroxmate than
the wild type. The spot assay, time kill assay and minimal
inhibition concentration determination also indicated that
the wild type could tolerate colistin better than the AB ΔemrB
mutant. Finally, the increased expression levels of all emrBlike
genes, including A1S_0775, A1S_0909, A1S_1772, and
A1S_1799, in colistin resistance-induced A. baumannii further
supported the possible involvement of the emrB genes
in A. baumannii colistin resistance. Together, the Emr pump
systems in A. baumannii contribute to adaptation to osmotic
stress and resistance to colistin.
Citations
Citations to this article as recorded by
Prevalence of antibiotic-resistant Acinetobacter spp. on soil and crops collected from agricultural fields in South Korea Su Min Son, Eunbyeol Ahn, Sojin Ahn, Seoae Cho, Sangryeol Ryu Food Science and Biotechnology.2024; 33(8): 1931. CrossRef
Fitness trade-offs of multidrug efflux pumps in
Escherichia coli
K-12 in acid or base, and with aromatic phytochemicals
Yangyang Liu, Andrew M. Van Horn, Minh T. N. Pham, Bao Ngoc N. Dinh, Rachel Chen, Slaybrina D. R. Raphael, Alejandro Paulino, Kavya Thaker, Aaryan Somadder, Dominick J. Frost, Chelsea C. Menke, Zachary C. Slimak, Joan L. Slonczewski, Ning-Yi Zhou Applied and Environmental Microbiology.2024;[Epub] CrossRef
Alteration in the Morphological and Transcriptomic Profiles of Acinetobacter baumannii after Exposure to Colistin Eun-Jeong Yoon, Jun Won Mo, Jee-woong Kim, Min Chul Jeong, Jung Sik Yoo Microorganisms.2024; 12(8): 1644. CrossRef
Diclofenac sensitizes multi-drug resistant Acinetobacter baumannii to colistin Fabiana Bisaro, Clay D. Jackson-Litteken, Jenna C. McGuffey, Anna J. Hooppaw, Sophie Bodrog, Leila Jebeli, Manon Janet-Maitre, Juan C. Ortiz-Marquez, Tim van Opijnen, Nichollas E. Scott, Gisela Di Venanzio, Mario F. Feldman, Daria Van Tyne PLOS Pathogens.2024; 20(11): e1012705. CrossRef
Deciphering the inhibitory mechanism of antimicrobial peptide pexiganan conjugated with sodium-alginate chitosan-cholesterol nanoparticle against the opportunistic pathogen Acinetobacter baumannii Sujata Saha, Rishav Kar, Kunal Sikder, Dipak Manna, Ritesh Ranjan Pal, Soumyananda Chakraborti, Ali Hossain Khan, Sourav Barman, Amit Ranjan Maity, Arnab Basu Journal of Drug Delivery Science and Technology.2024; 101: 106305. CrossRef
Efflux pumps as potential targets for biofilm inhibition Jingyi Ren, Meijuan Wang, Wenjuan Zhou, Zhonghao Liu Frontiers in Microbiology.2024;[Epub] CrossRef
Pan-Genome Plasticity and Virulence Factors: A Natural Treasure Trove for Acinetobacter baumannii Theodoros Karampatakis, Katerina Tsergouli, Payam Behzadi Antibiotics.2024; 13(3): 257. CrossRef
Colistin: Lights and Shadows of an Older Antibiotic Erica Diani, Gabriele Bianco, Milo Gatti, Davide Gibellini, Paolo Gaibani Molecules.2024; 29(13): 2969. CrossRef
Multidrug‐resistant Stenotrophomonas maltophilia in residential aged care facilities: An emerging threat Sylvia A. Sapula, Bradley J. Hart, Naomi L. Siderius, Anteneh Amsalu, Jack M. Blaikie, Henrietta Venter MicrobiologyOpen.2024;[Epub] CrossRef
Types and Mechanisms of Efflux Pump Systems and the Potential of Efflux Pump Inhibitors in the Restoration of Antimicrobial Susceptibility, with a Special Reference to Acinetobacter baumannii Kira M. Zack, Trent Sorenson, Suresh G. Joshi Pathogens.2024; 13(3): 197. CrossRef
Acinetobacter baumannii: an evolving and cunning opponent Jingchao Shi, Jianghao Cheng, Shourong Liu, Yufeng Zhu, Mingli Zhu Frontiers in Microbiology.2024;[Epub] CrossRef
Colistin Resistance Mechanism and Management Strategies of Colistin-Resistant Acinetobacter baumannii Infections Md Minarul Islam, Da Eun Jung, Woo Shik Shin, Man Hwan Oh Pathogens.2024; 13(12): 1049. CrossRef
Response of Paenibacillus polymyxa SC2 to the stress of polymyxin B and a key ABC transporter YwjA involved Hui Li, Wenhui E, Dongying Zhao, Haiyang Liu, Jian Pei, Binghai Du, Kai Liu, Xueming Zhu, Chengqiang Wang Applied Microbiology and Biotechnology.2024;[Epub] CrossRef
A molecular overview of the polymyxin-LPS interaction in the context of its mode of action and resistance development Indira Padhy, Sambit K. Dwibedy, Saswat S. Mohapatra Microbiological Research.2024; 283: 127679. CrossRef
Colistin Resistance in Acinetobacter baumannii: Molecular Mechanisms and Epidemiology Katarina Novović, Branko Jovčić Antibiotics.2023; 12(3): 516. CrossRef
Comparative genomics and molecular epidemiology of colistin-resistant Acinetobacter baumannii Jovana Kabic, Katarina Novovic, Dusan Kekic, Anika Trudic, Natasa Opavski, Ivica Dimkic, Branko Jovcic, Ina Gajic Computational and Structural Biotechnology Journal.2023; 21: 574. CrossRef
Novel approaches to overcome Colistin resistance in Acinetobacter baumannii: Exploring quorum quenching as a potential solution Reza Khoshbakht, Susan Panahi, Alireza Neshani, Mahdis Ghavidel, Kiarash Ghazvini Microbial Pathogenesis.2023; 182: 106264. CrossRef
Carbonyl Cyanide 3-Chloro Phenyl Hydrazone (CCCP) Restores the Colistin Sensitivity in Brucella intermedia Malak Zoaiter, Zaher Zeaiter, Oleg Mediannikov, Cheikh Sokhna, Pierre-Edouard Fournier International Journal of Molecular Sciences.2023; 24(3): 2106. CrossRef
Role of efflux pumps, their inhibitors, and regulators in colistin resistance Yinhuan Ding, Jingchen Hao, Weijia Xiao, Caihong Ye, Xue Xiao, Chunxia Jian, Min Tang, Guangrong Li, Jinbo Liu, Zhangrui Zeng Frontiers in Microbiology.2023;[Epub] CrossRef
Acinetobacter baumannii Survival under Infection-Associated Stresses Depends on the Expression of Resistance–Nodulation–Division and Major Facilitator Superfamily Efflux Pumps Inga V. Leus, Marcela Olvera, Justyna W. Adamiak, Lauren L. Nguyen, Helen I. Zgurskaya Antibiotics.2023; 13(1): 7. CrossRef
Comparative genotypic characterization related to antibiotic resistance phenotypes of clinical carbapenem-resistant Acinetobacter baumannii MTC1106 (ST2) and MTC0619 (ST25) Made Rai Dwitya Wiradiputra, Krit Thirapanmethee, Piyatip Khuntayaporn, Pagakrong Wanapaisan, Mullika Traidej Chomnawang BMC Genomics.2023;[Epub] CrossRef
Efflux-mediated tolerance to cationic biocides, a cause for concern?
Matthew E. Wand, J. Mark Sutton
Microbiology
.2022;[Epub] CrossRef
Acetylome and Succinylome Profiling of Edwardsiella tarda Reveals Key Roles of Both Lysine Acylations in Bacterial Antibiotic Resistance Yuying Fu, Lishan Zhang, Huanhuan Song, Junyan Liao, Li Lin, Wenjia Jiang, Xiaoyun Wu, Guibin Wang Antibiotics.2022; 11(7): 841. CrossRef
The role of bacterial transport systems in the removal of host antimicrobial peptides in Gram-negative bacteria Jessica M A Blair, Kornelius Zeth, Vassiliy N Bavro, Enea Sancho-Vaello FEMS Microbiology Reviews.2022;[Epub] CrossRef
Overcoming addition of phosphoethanolamine to lipid A mediated colistin resistance in Acinetobacter baumannii clinical isolates with colistin–sulbactam combination therapy Sukrit Srisakul, Dhammika Leshan Wannigama, Paul G. Higgins, Cameron Hurst, Shuichi Abe, Parichart Hongsing, Thammakorn Saethang, Sirirat Luk-in, Tingting Liao, Naris Kueakulpattana, Aye Mya Sithu Shein, Lin Gan, Rosalyn Kupwiwat, Chanikan Tanasatitchai, Scientific Reports.2022;[Epub] CrossRef
Acinetobacter baumannii complex, national laboratory-based surveillance in South Africa, 2017 to 2019 Olga Perovic, Adrian Duse, Vindana Chibabhai, Marianne Black, Mohamed Said, Elizabeth Prentice, Jeannette Wadula, Yesholata Mahabeer, K. Swe Swe Han, Ruth Mogokotleng, Wilhelmina Strasheim, Michelle Lowe, Sabelle Jallow, Husna Ismail, Daniel M. Czyz PLOS ONE.2022; 17(8): e0271355. CrossRef
Formic acid, an organic acid food preservative, induces viable-but-non-culturable state, and triggers new Antimicrobial Resistance traits in Acinetobacter baumannii and Klebsiella pneumoniae Manisha Yadav, Samridhi Dhyani, Pooja Joshi, Sakshi Awasthi, Subhash Tanwar, Vishal Gupta, Deepak K. Rathore, Susmita Chaudhuri Frontiers in Microbiology.2022;[Epub] CrossRef
MacAB-TolC Contributes to the Development of Acinetobacter baumannii Biofilm at the Solid–Liquid Interface Brandon Robin, Marion Nicol, Hung Le, Ali Tahrioui, Annick Schaumann, Jean-Baptiste Vuillemenot, Delphine Vergoz, Olivier Lesouhaitier, Thierry Jouenne, Julie Hardouin, Anaïs Potron, Valérie Perrot, Emmanuelle Dé Frontiers in Microbiology.2022;[Epub] CrossRef
Whole-genome sequencing for the characterization of resistance mechanisms and epidemiology of colistin-resistant Acinetobacter baumannii Chorong Hahm, Hae-Sun Chung, Miae Lee, Iddya Karunasagar PLOS ONE.2022; 17(3): e0264335. CrossRef
Rescuing humanity by antimicrobial peptides against colistin-resistant bacteria Majid Taati Moghadam, Ali Mojtahedi, Mehrdad Moosazadeh Moghaddam, Mahdi Fasihi-Ramandi, Reza Mirnejad Applied Microbiology and Biotechnology.2022; 106(11): 3879. CrossRef
Colistin Resistance and Management of Drug Resistant Infections Juhi Sharma, Divakar Sharma, Amit Singh, Kumari Sunita, Matthew Gavino Donadu Canadian Journal of Infectious Diseases and Medical Microbiology.2022; 2022: 1. CrossRef
Immunoinformatics-guided designing of epitope-based subunit vaccine from Pilus assembly protein of Acinetobacter baumannii bacteria Soumya Ranjan Mahapatra, Jyotirmayee Dey, Aryan Jaiswal, Riya Roy, Namrata Misra, Mrutyunjay Suar Journal of Immunological Methods.2022; 508: 113325. CrossRef
The ABC-Type Efflux Pump MacAB Is Involved in Protection of Serratia marcescens against Aminoglycoside Antibiotics, Polymyxins, and Oxidative Stress Tatiana V. Shirshikova, Cecilia G. Sierra-Bakhshi, Leisan K. Kamaletdinova, Lilia E. Matrosova, Nailya N. Khabipova, Vladimir G. Evtugyn, Irina V. Khilyas, Iuliia V. Danilova, Ayslu M. Mardanova, Margarita R. Sharipova, Lydia M. Bogomolnaya, Ana Cristina mSphere.2021;[Epub] CrossRef
Bacteriophage as a Novel Therapeutic Weapon for Killing Colistin-Resistant Multi-Drug-Resistant and Extensively Drug-Resistant Gram-Negative Bacteria Seyed Mohammad Mousavi, Sajad Babakhani, Leila Moradi, Saina Karami, Mahsa Shahbandeh, Maryam Mirshekar, Samane Mohebi, Majid Taati Moghadam Current Microbiology.2021; 78(12): 4023. CrossRef
Colistin and Carbapenem-Resistant Acinetobacter baumannii Aci46 in Thailand: Genome Analysis and Antibiotic Resistance Profiling Nalumon Thadtapong, Soraya Chaturongakul, Sunhapas Soodvilai, Padungsri Dubbs Antibiotics.2021; 10(9): 1054. CrossRef
Antimicrobial Resistance Mechanisms and Virulence of Colistin- and Carbapenem-Resistant Acinetobacter baumannii Isolated from a Teaching Hospital in Taiwan Noor Andryan Ilsan, Yuarn-Jang Lee, Shu-Chen Kuo, I-Hui Lee, Tzu-Wen Huang Microorganisms.2021; 9(6): 1295. CrossRef
The Challenge of Global Emergence of Novel Colistin-Resistant Escherichia coli ST131 Majid Taati Moghadam, Mehrnaz Mirzaei, Mozhdeh Fazel Tehrani Moghaddam, Sajad Babakhani, Omid Yeganeh, Sajad Asgharzadeh, Hamed Eraghiye Farahani, Shahla Shahbazi Microbial Drug Resistance.2021; 27(11): 1513. CrossRef
Acinetobacter baumannii: An Ancient Commensal with Weapons of a Pathogen Meysam Sarshar, Payam Behzadi, Daniela Scribano, Anna Teresa Palamara, Cecilia Ambrosi Pathogens.2021; 10(4): 387. CrossRef
Current Update on Intrinsic and Acquired Colistin Resistance Mechanisms in Bacteria Firdoos Ahmad Gogry, Mohammad Tahir Siddiqui, Insha Sultan, Qazi Mohd. Rizwanul Haq Frontiers in Medicine.2021;[Epub] CrossRef
Oxacillinase Gene Distribution, Antibiotic Resistance, and Their Correlation with Biofilm Formation in Acinetobacter baumannii Bloodstream Isolates Ceren Özkul, Gülşen Hazırolan Microbial Drug Resistance.2021; 27(5): 637. CrossRef
MALDI-TOF Mass Spectrometry Technology as a Tool for the Rapid Diagnosis of Antimicrobial Resistance in Bacteria Eun-Jeong Yoon, Seok Hoon Jeong Antibiotics.2021; 10(8): 982. CrossRef
Effects of colistin and tigecycline on multidrug-resistant Acinetobacter baumannii biofilms: advantages and disadvantages of their combination Yoshinori Sato, Tsuneyuki Ubagai, Shigeru Tansho-Nagakawa, Yusuke Yoshino, Yasuo Ono Scientific Reports.2021;[Epub] CrossRef
Genomic Insights into Drug Resistance Determinants in Cedecea neteri, A Rare Opportunistic Pathogen Dorothea K. Thompson, Stephen M. Sharkady Microorganisms.2021; 9(8): 1741. CrossRef
Overexpression of Efflux Pumps Mediate Pan Resistance of Klebsiella pneumoniae Sequence Type 11 Fei Lv, Jingjing Cai, Qixia He, WeiQi Wang, Yi Luo, Xin Wang, Na Mi, Zuguo Zhao, Guoming Li, Wenying Luo Microbial Drug Resistance.2021; 27(10): 1405. CrossRef
Colistin resistance in Gram-negative bacteria analysed by five phenotypic assays and inference of the underlying genomic mechanisms Diana Albertos Torres, Helena M. B. Seth-Smith, Nicole Joosse, Claudia Lang, Olivier Dubuis, Magdalena Nüesch-Inderbinen, Vladimira Hinic, Adrian Egli BMC Microbiology.2021;[Epub] CrossRef
Detection of mobile colistin-resistance gene variants (mcr-1andmcr-2) in urinary tract pathogens in Bangladesh: the last resort of infectious disease management colistin efficacy is under threat Bayasrin Ara, Umme Laila Urmi, Tanjum Ara Haque, Shamsun Nahar, Adity Rumnaz, Tamanna Ali, Mohammed Shah Alam, Abu Syed Md. Mosaddek, nor Azlina a Rahman, Mainul Haque, Salequl Islam Expert Review of Clinical Pharmacology.2021; 14(4): 513. CrossRef
In vitro and in vivo efficacy of combinations of colistin and different endolysins against clinical strains of multi-drug resistant pathogens Lucia Blasco, Anton Ambroa, Rocio Trastoy, Ines Bleriot, Miriam Moscoso, Laura Fernández-Garcia, Elena Perez-Nadales, Felipe Fernández-Cuenca, Julian Torre-Cisneros, Jesus Oteo-Iglesias, Antonio Oliver, Rafael Canton, Tim Kidd, Ferran Navarro, Elisenda Mi Scientific Reports.2020;[Epub] CrossRef
Characterization of biofilm production in different strains of Acinetobacter baumannii and the effects of chemical compounds on biofilm formation Ming-Feng Lin, Yun-You Lin, Chung-Yu Lan PeerJ.2020; 8: e9020. CrossRef
Identification of novel in vitro antibacterial action of cloprostenol and evaluation of other non-antibiotics against multi-drug resistant A. baumannii Shakeel Shahzad, Mark Willcox, Aqeel Shahzad The Journal of Antibiotics.2020; 73(1): 72. CrossRef
Molecular characterization of lpxACD and pmrA/B two-component regulatory system in the colistin resistance Acinetobacter baumannii clinical isolates Mohammad Reza Kandehkar Ghahraman, Hossein Hosseini-Nave, Omid Azizi, Mohammad Reza Shakibaie, Hamid Reza Mollaie, Samane Shakibaie Gene Reports.2020; 21: 100952. CrossRef
The clue is in the lipid A: Rapid detection of colistin resistance R. Christopher D. Furniss, Markus Kostrzewa, Despoina A. I. Mavridou, Gerald Larrouy-Maumus, John M. Leong PLOS Pathogens.2020; 16(4): e1008331. CrossRef
Diversity of amino acid substitutions in PmrCAB associated with colistin resistance in clinical isolates of Acinetobacter baumannii Stefanie Gerson, Kai Lucaßen, Julia Wille, Carolina S. Nodari, Danuta Stefanik, Jennifer Nowak, Thorsten Wille, Jonathan W. Betts, Ignasi Roca, Jordi Vila, Jose M. Cisneros, Harald Seifert, Paul G. Higgins International Journal of Antimicrobial Agents.2020; 55(3): 105862. CrossRef
Colistin and its role in the Era of antibiotic resistance: an extended review (2000–2019) Mohamed Abd El-Gawad El-Sayed Ahmed, Lan-Lan Zhong, Cong Shen, Yongqiang Yang, Yohei Doi, Guo-Bao Tian Emerging Microbes & Infections.2020; 9(1): 868. CrossRef
First report on the characterization of pathogenic Rahnella aquatilis KCL‐5 from crucian carp: Revealed by genomic and proteomic analyses Jing Liang, Xiucai Hu, Aijun Lü, Jingfeng Sun Journal of Fish Diseases.2020; 43(8): 889. CrossRef
Colistin Induced Assortment of Antimicrobial Resistance in a Clinical Isolate of Acinetobacter baumannii SD01 Debarati Paul, Swarupa Mallick, Swati Das, Suman Saha, Ananta K. Ghosh, Santi M. Mandal Infectious Disorders - Drug Targets.2020; 20(4): 501. CrossRef
Emergence of mcr- and fosA3-mediated colistin and fosfomycin resistance among carbapenem-resistant Acinetobacter baumannii in Iraq Sawsan Mohammed Kareem Meta Gene.2020; 25: 100708. CrossRef
PmrB mutations including a novel 10-amino acid repeat sequence insertion associated with low-level colistin resistance in carbapenem-resistant Acinetobacter baumannii Kamonwan Lunha, Khin Thet Thet, Arisa Ngudsuntia, Nicha Charoensri, Aroonlug Lulitanond, Ratree Tavichakorntrakool, Lumyai Wonglakorn, Kiatichai Faksri, Aroonwadee Chanawong Infection, Genetics and Evolution.2020; 85: 104577. CrossRef
Clinical and laboratory-induced colistin-resistance mechanisms in Acinetobacter baumannii
Christine J. Boinett, Amy K. Cain, Jane Hawkey, Nhu Tran Do Hoang, Nhu Nguyen Thi Khanh, Duy Pham Thanh, Janina Dordel, James I. Campbell, Nguyen Phu Huong Lan, Matthew Mayho, Gemma C. Langridge, James Hadfield, Nguyen Van Vinh Chau, Guy E. Thwaites, Juli
Microbial Genomics
.2019;[Epub] CrossRef
Can Nebulised Colistin Therapy Improve Outcomes in Critically Ill Children with Multi-Drug Resistant Gram-Negative Bacterial Pneumonia? Fatih Aygun, Fatma Deniz Aygun, Fatih Varol, Cansu Durak, Haluk Cokugraş, Yildiz Camcioglu, Halit Cam Antibiotics.2019; 8(2): 40. CrossRef
Coping with low water activities and osmotic stress in Acinetobacter baumannii: significance, current status and perspectives Sabine Zeidler, Volker Müller Environmental Microbiology.2019; 21(7): 2212. CrossRef
Molecular mechanisms of antimicrobial resistance in Acinetobacter baumannii, with a special focus on its epidemiology in Lebanon Sabah Jamal, Ahmad Al Atrouni, Rayane Rafei, Fouad Dabboussi, Monzer Hamze, Marwan Osman Journal of Global Antimicrobial Resistance.2018; 15: 154. CrossRef
Chromosomally encoded and plasmid-mediated polymyxins resistance in Acinetobacter baumannii: a huge public health threat William Gustavo Lima, Mara Cristina Alves, Waleska Stephanie Cruz, Magna Cristina Paiva European Journal of Clinical Microbiology & Infectious Diseases.2018; 37(6): 1009. CrossRef
Contribution of efflux to colistin heteroresistance in a multidrug resistant Acinetobacter baumannii clinical isolate Diana Machado, Jéssica Antunes, Ana Simões, João Perdigão, Isabel Couto, Matthew McCusker, Marta Martins, Isabel Portugal, Teresa Pacheco, Judite Batista, Cristina Toscano, Miguel Viveiros
Journal of Medical Microbiology
.2018; 67(6): 740. CrossRef
Curcumin alleviates persistence of Acinetobacter baumannii against colistin Amanjot Kaur, Prince Sharma, Neena Capalash Scientific Reports.2018;[Epub] CrossRef
Functional Characterization of AbaQ, a Novel Efflux Pump Mediating Quinolone Resistance in Acinetobacter baumannii María Pérez-Varela, Jordi Corral, Jesús Aranda, Jordi Barbé Antimicrobial Agents and Chemotherapy.2018;[Epub] CrossRef
Antibiotic resistance of pathogenic Acinetobacter species and emerging combination therapy Bora Shin, Woojun Park Journal of Microbiology.2017; 55(11): 837. CrossRef
Differences in Gene Expression Profiles between Early and Late Isolates in Monospecies Achromobacter Biofilm Signe Nielsen, Rikke Meyer, Niels Nørskov-Lauritsen Pathogens.2017; 6(2): 20. CrossRef
Molecular Characterization of Reduced Susceptibility to Biocides in Clinical Isolates of Acinetobacter baumannii Fei Lin, Ying Xu, Yaowen Chang, Chao Liu, Xu Jia, Baodong Ling Frontiers in Microbiology.2017;[Epub] CrossRef
A cystine-dependent anti-oxidative stress response is characterized
in Deinococcus geothermalis for the first time. Nevertheless,
the same transcriptional directed Δdgeo_1985F mutant
strain was revealed to have an identical phenotype to the
wild-type strain, while the reverse transcriptional directed
Δdgeo_1985R mutant strain was more resistant to oxidative
stress at a certain concentration of H2O2 than the wild-type
strain. The wild-type and mutant strains expressed equal levels
of superoxide dismutase and catalase under H2O2-induced
stress. Although the expression levels of the general DNAdamage
response-related genes recA, pprA, ddrA, and ddrB
were up-regulated by more than five-fold in the wild-type
strain relative to the Δdgeo_1985R mutant strain, the mutant
strain had a higher survival rate than the wild-type under
H2O2 stress. The Δdgeo_1985R mutant strain highly expressed
a cystine-transporter gene (dgeo_1986), at levels 150-fold
higher than the wild-type strain, leading to the conclusion
that this cystine transporter might be involved in the defensive
response to H2O2 stress. In this study, the cystine transporter
was identified and characterized through membrane
protein expression analysis, a cystine-binding assay, and assays
of intracellular H2O2, cysteine, and thiol levels. The genedisrupted
mutant strain of the cystine importer revealed high
sensitivity to H2O2 and less absorbed cystine, resulting in low
concentrations of total thiol. Thus, the absorbed cystine via
this cystine-specific importer may be converted into cysteine,
which acts as a primitive defense substrate that non-enzymatically
scavenges oxidative stress agents in D. geothermalis.
Citations
Citations to this article as recorded by
The Mechanism of Zinc Oxide in Alleviating Diarrhea in Piglets after Weaning: A Review from the Perspective of Intestinal Barrier Function Xiaopeng Tang, Kangning Xiong, Yan Zeng, Rejun Fang International Journal of Molecular Sciences.2024; 25(18): 10040. CrossRef
The Transposition of Insertion Sequences in Sigma-Factor- and LysR-Deficient Mutants of Deinococcus geothermalis Ji Hyun Park, Sohee Lee, Eunjung Shin, Sama Abdi Nansa, Sung-Jae Lee Microorganisms.2024; 12(2): 328. CrossRef
Transposition of insertion sequences by dielectric barrier discharge plasma and gamma irradiation in the radiation-resistant bacterium Deinococcus geothermalis Qianying Ye, Eunjung Shin, Chanjae Lee, Nakjun Choi, Yeonho Kim, Ki Sun Yoon, Sung-Jae Lee Journal of Microbiological Methods.2022; 196: 106473. CrossRef
Proteomic profiling of Deinococcus radiodurans with response to thioredoxin reductase inhibitor and ionizing radiation treatment Sudharsan M, Rajendra Prasad N, Anindita Chakraborty, Saravanan Rajendrasozhan Journal of Proteomics.2022; 267: 104697. CrossRef
Influence of Redox Imbalances on the Transposition of Insertion Sequences in Deinococcus geothermalis Qianying Ye, Chanjae Lee, Eunjung Shin, Sung-Jae Lee Antioxidants.2021; 10(10): 1623. CrossRef
Active Transposition of Insertion Sequences by Oxidative Stress in Deinococcus geothermalis Chanjae Lee, Kyungsil Choo, Sung-Jae Lee Frontiers in Microbiology.2020;[Epub] CrossRef
Oxidative stress-mediated genotoxic effect of zinc oxide nanoparticles on Deinococcus radiodurans Ragini Singh, Shuang Cheng, Sanjay Singh 3 Biotech.2020;[Epub] CrossRef
Redox potential change by the cystine importer affected on enzymatic antioxidant protection in Deinococcus geothermalis Kyungsil Choo, Minwook Kim, Sama Abdi Nansa, Min K. Bae, Chanjae Lee, Sung-Jae Lee Antonie van Leeuwenhoek.2020; 113(6): 779. CrossRef
Transposition of Insertion Sequences was Triggered by Oxidative Stress in Radiation-Resistant Bacterium Deinococcus geothermalis Chanjae Lee, Nakjun Choi, Min K. Bae, Kyungsil Choo, Sung-Jae Lee Microorganisms.2019; 7(10): 446. CrossRef
Conservation and diversity of radiation and oxidative stress resistance mechanisms inDeinococcusspecies Sangyong Lim, Jong-Hyun Jung, Laurence Blanchard, Arjan de Groot FEMS Microbiology Reviews.2019; 43(1): 19. CrossRef
Metabolic Alternations of Amino Acids, γ-Aminobutyric Acid, and Salicylic Acid in Solanum lycopersicum (L.) Following Preplanting Seedling Spray with Salicylic Acid Hari C. Meher, Ghanendra Singh, Gautam Chawla Journal of Agricultural and Food Chemistry.2018; 66(46): 12236. CrossRef
γ-Glutamyltranspeptidase (GGT) catalyzes the cleavage of γ-
glutamyl compounds and the transfer of γ-glutamyl moiety
to water or to amino acid/peptide acceptors. GGT can be utilized
for the generation of γ-glutamyl peptides or glutamic
acid, which are used as food taste enhancers. In the present
study, Bacillus amyloliquefaciens SMB469 with high GGT activity
was isolated from Doenjang, a traditional fermented soy
food of Korea. The gene encoding GGT from B. amyloliquefaciens
SMB469 (BaGGT469) was cloned from the isolate, and
heterologously expressed in E. coli and B. subtilis. For comparison,
three additional GGT genes were cloned from B.
subtilis 168, B. licheniformis DSM 13, and B. amyloliquefaciens
FZB42. The BaGGT469 protein was composed of 591
amino acids. The final protein comprises two separate polypeptide
chains of 45.7 and 19.7 kDa, generated via autocatalytic
cleavage. The specific activity of BaGGT469 was determined
to be 17.8 U/mg with γ-L-glutamyl-p-nitroanilide
as the substrate and diglycine as the acceptor. GGTs from B.
amyloliquefaciens showed 1.4- and 1.7-fold higher transpeptidase
activities than those from B. subtilis and B. licheniformis,
respectively. Especially, recombinant B. subtilis expressing
BaGGT469 demonstrated 11- and 23-fold higher GGT
activity than recombinant E. coli and the native B. amyloliquefaciens,
respectively, did. These results suggest that BaGGT469
can be utilized for the enzymatic production of various γ-
glutamyl compounds.
Citations
Citations to this article as recorded by
Exploring the capacity of Bacillus species for production of kokumi γ-glutamyl peptides: A comparative study Qian Li, Longteng Zhang, Dennis Sandris Nielsen, Lene Jespersen, René Lametsch LWT.2024; 206: 116542. CrossRef
Functional connexion of bacterioferritin in antibiotic production and morphological differentiation in Streptomyces coelicolor Javier García-Martín, Laura García-Abad, Ramón I. Santamaría, Margarita Díaz Microbial Cell Factories.2024;[Epub] CrossRef
Efficient expression of γ-glutamyl transpeptidase in Bacillus subtilis via CRISPR/Cas9n and its immobilization Qianlin Chen, Bin Wang, Li Pan Applied Microbiology and Biotechnology.2024;[Epub] CrossRef
Biochemical Characterization of γ-Glutamyl Transpeptidase from Bacillus altitudinis IHB B1644 and Its Application in the Synthesis of l-Theanine Eshita Sharma, Milan Kumar Lal, Arvind Gulati, Ashu Gulati Journal of Agricultural and Food Chemistry.2023; 71(14): 5592. CrossRef
Characterization of alkaline Bacillus amyloliquefaciens γ-glutamyltranspeptidase expressed in Bacillus subtilis and its application in enzymatic synthesis of L‑Theanine Ran Zhang, Luhua Zheng, Licheng Zhou, Longbei Xiang, Bo Jiang, Tao Zhang, Jingjing Chen Process Biochemistry.2023; 131: 125. CrossRef
Heterologous expression, on-column refolding and characterization of gamma-glutamyl transpeptidase gene from Bacillus altitudinis IHB B1644: A microbial bioresource from Western Himalayas Eshita Sharma, Milan Kumar Lal, Arvind Gulati, Ashu Gulati Process Biochemistry.2022; 116: 126. CrossRef
Expression of Bacillus amyloliquefaciens γ-Glutamyltransferase in Lactococcus lactis and Immobilization on Magnetic Nanoparticles Tiange Ma, Xingjiang Li, Xuefeng Wu, Suwei Jiang, Zhi Zheng, Dongdong Mu ACS Food Science & Technology.2021; 1(5): 778. CrossRef
Bacterial Gamma-Glutamyl Transpeptidase, an Emerging Biocatalyst: Insights Into Structure–Function Relationship and Its Biotechnological Applications Meenu Saini, Amuliya Kashyap, Shruti Bindal, Kuldeep Saini, Rani Gupta Frontiers in Microbiology.2021;[Epub] CrossRef
A chemical screening method for menaquinone-producing strains based on HPLC-UV technology Sheng Cao, Xia Du, Pingyi Li, Ganjun Yuan, Shanjun Chen, Weiping Chen, Xiaoyuan Song, Bingdi Kuang Journal of Microbiological Methods.2020; 172: 105907. CrossRef
γ-Glutamyltranspeptidase from Bacillus amyloliquefaciens: transpeptidation activity enhancement and L-theanine production Zelong Li, Runtao Zhu, Yongqi Liu, Jiaqi Li, Haofeng Gao, Nan Hu Enzyme and Microbial Technology.2020; 140: 109644. CrossRef
Secretion of Bacillus amyloliquefaciens γ-Glutamyltranspeptidase from Bacillus subtilis and Its Application in Enzymatic Synthesis of l-Theanine Dongdong Mu, Haowen Li, Qi Chen, Jing Zhu, Xuefeng Wu, Shuizhong Luo, Yanyan Zhao, Lei Wang, Shaotong Jiang, Xingjiang Li, Zhi Zheng Journal of Agricultural and Food Chemistry.2019; 67(51): 14129. CrossRef
High level extracellular production of recombinant γ-glutamyl transpeptidase from Bacillus licheniformis in Escherichia coli fed-batch culture Shruti Bindal, Vikas Kumar Dagar, Meenu Saini, Yogender Pal Khasa, Rani Gupta Enzyme and Microbial Technology.2018; 116: 23. CrossRef
γ-Glutamyl Cysteine Ligase of Lactobacillus reuteri Synthesizes γ-Glutamyl Dipeptides in Sourdough Bowen Yan, Yuan Yao Chen, Weilan Wang, Jianxin Zhao, Wei Chen, Michael Gänzle Journal of Agricultural and Food Chemistry.2018; 66(46): 12368. CrossRef
Inference of sigma factor controlled networks by using numerical modeling applied to microarray time series data of the germinating prokaryote E. Strakova, A. Zikova, J. Vohradsky Nucleic Acids Research.2014; 42(2): 748. CrossRef
The effectiveness of novel bacteriocin derived from Escherichia coli colonized in the fermented pineapple Ananas comosus (L.) Merr. against pathogenic bacteria isolated from aquaculture sites S. W. Lee, W. Wendy, L. Montira, A. U. Siti Hazirah Veterinary World.2014; 7(11): 1014. CrossRef
Daptomycin (DAP) has potent activity in vitro and in vivo
against both methicillin-susceptible Staphylococcus aureus
(MSSA) and methicillin-resistant S. aureus (MRSA) strains.
DAP-resistance (DAP-R) in S. aureus has been mainly observed
in MRSA strains, and has been linked to single nucleotide
polymorphisms (SNPs) within the mprF gene leading
to altered cell membrane (CM) phospholipid (PL) profiles,
enhanced positive surface charge, and changes in CM
fluidity. The current study was designed to delineate whether
these same genotypic and phenotypic perturbations are demonstrated
in clinically-derived DAP-R MSSA strains. We
used three isogenic DAP-susceptible (DAP-S)/DAP-R strainpairs
and compared: (i) presence of mprF SNPs, (ii) temporal
expression profiles of the two key determinants (mprF and
dltABCD) of net positive surface charge, (iii) increased production
of mprF-dependent lysinylated-phosphatidylglycerol
(L-PG), (iv) positive surface charge assays, and (v) susceptibility
to cationic host defense peptides (HDPs) of neutrophil
and platelet origins. Similar to prior data in MRSA, DAP-R
(vs DAP-S) MSSA strains exhibited hallmark hot-spot SNPs
in mprF, enhanced and dysregulated expression of both mprF
and dltA, L-PG overproduction, HDP resistance and enhanced
positive surface charge profiles. However, in contrast to most
DAP-R MRSA strains, there were no changes in CM fluidity
seen. Thus, charge repulsion via mprF- and dlt-mediated enhancement
of positive surface charge may be the main mechanism
to explain DAP-R in MSSA strains.
Citations
Citations to this article as recorded by
The Effect of Shock Gentamicin Concentrations on the Formation of Resistance and Small Colony Variants in Staphylococcus aureus V. V. Gostev, O. S. Kalinogorskaya, O. S. Sulian, P. S. Chulkova, J. V. Sopova, M. E. Velizhanina, V. Yu. Pleshkov, V. A. Ageevets, S. V. Sidorenko Antibiotics and Chemotherapy.2024; 68(9-10): 25. CrossRef
Investigating a possible link between antiseptic treatment and the increased occurrence of daptomycin-resistant Staphylococcus aureus Andreas F. Wendel, Robin Otchwemah, Franziska Layer-Nicolaou, Frauke Mattner, Carlos J. Tellez-Castillo, Robert Skov, Henrik Oberländer, Guido Werner, Birgit Strommenger Clinical Microbiology and Infection.2023; 29(10): 1334.e1. CrossRef
Acquisition of Daptomycin Resistance by Enterococcus faecium Confers Collateral Sensitivity to Glycopeptides Weiliang Zeng, Luozhu Feng, Changrui Qian, Tao Chen, Sipei Wang, Ying Zhang, Xiangkuo Zheng, Lingbo Wang, Shixing Liu, Tieli Zhou, Yao Sun Frontiers in Microbiology.2022;[Epub] CrossRef
A Decade of Research on Daptomycin Scott D. Taylor Synlett.2022; 33(17): 1695. CrossRef
Establishing the Structure–Activity Relationship between Phosphatidylglycerol and Daptomycin Ryan Moreira, Scott D. Taylor ACS Infectious Diseases.2022; 8(8): 1674. CrossRef
Polymyxin and lipopeptide antibiotics: membrane-targeting drugs of last resort
Elizabeth V. K. Ledger, Akshay Sabnis, Andrew M. Edwards
Microbiology
.2022;[Epub] CrossRef
Evaluating the Rapid Emergence of Daptomycin Resistance in
Corynebacterium
: a Multicenter Study
Kaitlin F. Mitchell, Erin McElvania, Meghan A. Wallace, Lauren E. Droske, Amy E. Robertson, Lars F. Westblade, Carey-Ann D. Burnham, Patricia J. Simner Journal of Clinical Microbiology.2021;[Epub] CrossRef
Novel Daptomycin Tolerance and Resistance Mutations in Methicillin-Resistant Staphylococcus aureus from Adaptive Laboratory Evolution Jordy Evan Sulaiman, Henry Lam, Patricia A. Bradford mSphere.2021;[Epub] CrossRef
A narrative review of single-nucleotide polymorphism detection methods and their application in studies of
Staphylococcus aureus
Ying Jian, Min Li Journal of Bio-X Research.2021; 04(01): 1. CrossRef
Prolonged Exposure to β-Lactam Antibiotics Reestablishes Susceptibility of Daptomycin-Nonsusceptible Staphylococcus aureus to Daptomycin Rachel E. Jenson, Sarah L. Baines, Benjamin P. Howden, Nagendra N. Mishra, Sabrina Farah, Cassandra Lew, Andrew D. Berti, Sanjay K. Shukla, Arnold S. Bayer, Warren E. Rose Antimicrobial Agents and Chemotherapy.2020;[Epub] CrossRef
Selection of Resistance to Daptomycin in Methicillin-Resistant Staphylococcus aureus: Role of Homo- and Hetero-Mutations V. V. Gostev, Yu. V. Sopova, O. S. Kalinogorskaya, I. A. Tsvetkova, S. V. Sidorenko Russian Journal of Genetics.2020; 56(3): 289. CrossRef
Association of mprF mutations with cross-resistance to daptomycin and vancomycin in methicillin-resistant Staphylococcus aureus (MRSA) Kanate Thitiananpakorn, Yoshifumi Aiba, Xin-Ee Tan, Shinya Watanabe, Kotaro Kiga, Yusuke Sato’o, Tanit Boonsiri, Feng-Yu Li, Teppei Sasahara, Yusuke Taki, Aa Haeruman Azam, Yuancheng Zhang, Longzhu Cui Scientific Reports.2020;[Epub] CrossRef
Multidrug-Resistant Bacteria and Alternative Methods to Control Them: An Overview Roberto Vivas, Ana Andréa Teixeira Barbosa, Silvio Santana Dolabela, Sona Jain Microbial Drug Resistance.2019; 25(6): 890. CrossRef
Insights Into the Evolution of Staphylococcus aureus Daptomycin Resistance From an in vitro Bioreactor Model Erica Lasek-Nesselquist, Jackson Lu, Ryan Schneider, Zhuo Ma, Vincenzo Russo, Smruti Mishra, Manjunath P. Pai, Janice D. Pata, Kathleen A. McDonough, Meenakshi Malik Frontiers in Microbiology.2019;[Epub] CrossRef
Antibiotic Resistance and the MRSA Problem Martin Vestergaard, Dorte Frees, Hanne Ingmer, Vincent A. Fischetti, Richard P. Novick, Joseph J. Ferretti, Daniel A. Portnoy, Miriam Braunstein, Julian I. Rood Microbiology Spectrum.2019;[Epub] CrossRef
An entirely fmoc solid phase approach to the synthesis of daptomycin analogs Ghufran Barnawi, Michael Noden, Robert Taylor, Chuda Lohani, David Beriashvili, Michael Palmer, Scott D. Taylor Peptide Science.2019;[Epub] CrossRef
One Drug Multiple Targets: An Approach To Predict Drug Efficacies on Bacterial Strains Differing in Membrane Composition Ayan Majumder, Malay Ranjan Biswal, Meher K. Prakash ACS Omega.2019; 4(3): 4977. CrossRef
Daptomycin resistance in methicillin-resistant Staphylococcus aureus is conferred by IS256 insertion in the promoter of mprF along with mutations in mprF and walK Yuyao Yin, Hongbin Chen, Shuguang Li, Hua Gao, Shijun Sun, Henan Li, Ruobing Wang, Longyang Jin, Yudong Liu, Hui Wang International Journal of Antimicrobial Agents.2019; 54(6): 673. CrossRef
IS256-Mediated Overexpression of the WalKR Two-Component System Regulon Contributes to Reduced Vancomycin Susceptibility in a Staphylococcus aureus Clinical Isolate Makoto Kuroda, Tsuyoshi Sekizuka, Hidehito Matsui, Jun Ohsuga, Toshio Ohshima, Hideaki Hanaki Frontiers in Microbiology.2019;[Epub] CrossRef
A partial reconstitution implicates DltD in catalyzing lipoteichoic acid d-alanylation B. McKay Wood, John P. Santa Maria, Leigh M. Matano, Christopher R. Vickery, Suzanne Walker Journal of Biological Chemistry.2018; 293(46): 17985. CrossRef
Daptomycin Resistant Staphylococcus aureus Clinical Strain With Novel Non-synonymous Mutations in the mprF and vraS Genes: A New Insight Into Daptomycin Resistance Artur J. Sabat, Marco Tinelli, Hajo Grundmann, Viktoria Akkerboom, Monica Monaco, Maria Del Grosso, Giulia Errico, Annalisa Pantosti, Alexander W. Friedrich Frontiers in Microbiology.2018;[Epub] CrossRef
Daptomycin: New Insights into an Antibiotic of Last Resort Vera Pader, Andrew M Edwards Future Microbiology.2017; 12(6): 461. CrossRef
Md Bashir Uddin , Byeong-Hoon Lee , Chamilani Nikapitiya , Jae-Hoon Kim , Tae-Hwan Kim , Hyun-Cheol Lee , Choul Goo Kim , Jong-Soo Lee , Chul-Joong Kim
In the article by Uddin et al. published in Journal of Microbiology 2016; 54, 853–866, the Protocol number on page 856 and 865 should be corrected as below.