Review
	
	
				- Structural Insights into the Lipopolysaccharide Transport (Lpt) System as a Novel Antibiotic Target
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		Yurim Yoon, Saemee Song		
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			J. Microbiol. 2024;62(4):261-275.   Published online May 31, 2024		
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							DOI: https://doi.org/10.1007/s12275-024-00137-w
					
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						 Abstract Abstract PDF PDF
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		Lipopolysaccharide (LPS) is a critical component of the extracellular leaflet within the bacterial outer membrane, forming an effective physical barrier against environmental threats in Gram-negative bacteria. After LPS is synthesized and matured in the bacterial cytoplasm and the inner membrane (IM), LPS is inserted into the outer membrane (OM) through the ATP-driven LPS transport (Lpt) pathway, which is an energy-intensive process. A trans-envelope complex that contains seven Lpt proteins (LptA-LptG) is crucial for extracting LPS from the IM and transporting it across the periplasm to the OM. The last step in LPS transport involves the mediation of the LptDE complex, facilitating the insertion of LPS into the outer leaflet of the OM. As the Lpt system plays an essential role in maintaining the impermeability of the OM via LPS decoration, the interactions between these interconnected subunits, which are meticulously regulated, may be potential targets for the development of new antibiotics to combat multidrug-resistant Gram-negative bacteria. In this review, we aimed to provide an overview of current research concerning the structural interactions within the Lpt system and their implications to clarify the function and regulation of LPS transport in the overall process of OM biogenesis.
Additionally, we explored studies on the development of therapeutic inhibitors of LPS transport, the factors that limit success, and future prospects.	
		
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			Citations Citations to this article as recorded by    
- Boosting the Antimicrobial Activity of Quaternary Ammonium Photosensitizers by Janus‐Type AIE Luminogens
 Dongyang Fan, Meng Li, Zipeng Shen, Ying Li, Jingjing Guo, Dong Wang, Ting Han, Ben Zhong Tang
 Aggregate.2025;[Epub]     CrossRef
- Functional Versatility of Vibrio cholerae Outer Membrane Proteins
 Annabelle Mathieu-Denoncourt, Marylise Duperthuy
 Applied Microbiology.2025; 5(3): 64.     CrossRef
- Integrated Omics-Based Discovery of Bioactive Halogenated Metabolites from the Deep-Sea Streptomyces sp. B188M101
 Emmanuel Tope Oluwabusola, Stephen A. Jackson, Cristina Brunati, Stefanie Gackstatter, Hannah Vedder, Marianna Iorio, Gargee Chawande, Lekha Menon Margassery, Giang-Son Nguyen, David J. Clarke, Rainer Ebel, Marcel Jaspars, Alan D. W. Dobson
 Marine Drugs.2025; 23(9): 362.     CrossRef
 
 Journal Articles
	
	
				- [Protocol] Use of Cas9 Targeting and Red Recombination for Designer Phage Engineering
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		Shin-Yae Choi , Danitza Xiomara Romero-Calle , Han-Gyu Cho , Hee-Won Bae , You-Hee Cho 		
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			J. Microbiol. 2024;62(1):1-10.   Published online February 1, 2024		
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							DOI: https://doi.org/10.1007/s12275-024-00107-2
					
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						 Abstract Abstract PDF PDF
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		Bacteriophages (phages) are natural antibiotics and biological nanoparticles, whose application is significantly boosted by
recent advances of synthetic biology tools. Designer phages are synthetic phages created by genome engineering in a way
to increase the benefits or decrease the drawbacks of natural phages. Here we report the development of a straightforward
genome engineering method to efficiently obtain engineered phages in a model bacterial pathogen, Pseudomonas aeruginosa.
This was achieved by eliminating the wild type phages based on the Streptococcus pyogenes Cas9 (SpCas9) and facilitating
the recombinant generation based on the Red recombination system of the coliphage λ (λRed). The producer (PD) cells of
P. aeruginosa strain PAO1 was created by miniTn7-based chromosomal integration of the genes for SpCas9 and λRed under
an inducible promoter. To validate the efficiency of the recombinant generation, we created the fluorescent phages from a
temperate phage MP29. A plasmid bearing the single guide RNA (sgRNA) gene for selectively targeting the wild type gp35
gene and the editing template for tagging the Gp35 with superfolder green fluorescent protein (sfGFP) was introduced into
the PD cells by electroporation. We found that the targeting efficiency was affected by the position and number of sgRNA.
The fluorescent phage particles were efficiently recovered from the culture of the PD cells expressing dual sgRNA molecules.
This protocol can be used to create designer phages in P. aeruginosa for both application and research purposes.	
		
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			Citations Citations to this article as recorded by    
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            Pilin regions that select for the small RNA phages in
            Pseudomonas aeruginosa
            type IV pilus
          
 Hee-Won Bae, Hyeong-Jun Ki, Shin-Yae Choi, You-Hee Cho, Kristin N. Parent
 Journal of Virology.2025;[Epub]     CrossRef
- Synthetic and Functional Engineering of Bacteriophages: Approaches for Tailored Bactericidal, Diagnostic, and Delivery Platforms
 Ola Alessa, Yoshifumi Aiba, Mahmoud Arbaah, Yuya Hidaka, Shinya Watanabe, Kazuhiko Miyanaga, Dhammika Leshan Wannigama, Longzhu Cui
 Molecules.2025; 30(15): 3132.     CrossRef
- Characteristics of bioaerosols under high-ozone periods, haze episodes, dust storms, and normal days in Xi’an, China
 Yiming Yang, Liu Yang, Xiaoyan Hu, Zhenxing Shen
 Particuology.2024; 90: 140.     CrossRef
- Airborne desert dust and aeromicrobiology over the Turkish Mediterranean coastline
 Dale W. Griffin, Nilgün Kubilay, Mustafa Koçak, Mike A. Gray, Timothy C. Borden, Eugene A. Shinn
 Atmospheric Environment.2007; 41(19): 4050.     CrossRef
 
 
	
	
				- Alpha‑Hemolysin from Staphylococcus aureus Obstructs Yeast‑Hyphae Switching and Diminishes Pathogenicity in Candida albicans
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		Xiaoyu Yu , Yinhe Mao , Guangbo Li , Xianwei Wu , Qiankun Xuan , Simin Yang , Xiaoqing Chen , Qi Cao , Jian Guo , Jinhu Guo , Wenjuan Wu 		
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			J. Microbiol. 2023;61(2):233-243.   Published online February 9, 2023		
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							DOI: https://doi.org/10.1007/s12275-022-00006-4
					
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						 Abstract Abstract PDF PDF
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		The use of antibiotics can disrupt the body’s natural balance and increase the susteptibility of patients towards fungal infections.
Candida albicans is a dimorphic opportunistic fungal pathogen with niches similar to those of bacteria. Our aim was
to study the interaction between this pathogen and bacteria to facilitate the control of C. albicans infection. Alpha-hemolysin
(Hla), a protein secreted from Staphylococcus aureus, causes cell wall damage and impedes the yeast–hyphae transition in
C. albicans. Mechanistically, Hla stimulation triggered the formation of reactive oxygen species that damaged the cell wall
and mitochondria of C. albicans. The cell cycle was arrested in the G0/G1 phase, CDC42 was downregulated, and Ywp1
was upregulated, disrupting yeast hyphae switching. Subsequently, hyphae development was inhibited. In mouse models,
C. albicans pretreated with Hla reduced the C. albicans burden in skin and vaginal mucosal infections, suggesting that S.
aureus Hla can inhibit hyphal development and reduce the pathogenicity of candidiasis in vivo.	
		
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			Citations Citations to this article as recorded by    
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            Candida albicans
            and
            Candida glabrata
            : global priority pathogens
          
 Myrto Katsipoulaki, Mark H. T. Stappers, Dhara Malavia-Jones, Sascha Brunke, Bernhard Hube, Neil A. R. Gow, Joseph Heitman
 Microbiology and Molecular Biology Reviews.2024;[Epub]     CrossRef
 
 
	
	
				- PROTOCOL] Applications of different solvents and conditions for differential extraction of lipopolysaccharide in Gram-negative bacteria
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		Mai Phuong Nguyen , Le Viet Ha Tran , Hyun Namgoong , Yong-Hak Kim 		
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			J. Microbiol. 2019;57(8):644-654.   Published online May 23, 2019		
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							DOI: https://doi.org/10.1007/s12275-019-9116-5
					
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						 Abstract Abstract PDF PDF
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		Lipopolysaccharide (LPS) is one of the major components in
the outer membrane of Gram-negative bacteria. However,
its heterogeneity and variability in different bacteria and differentiation
conditions make it difficult to extract all of the
structural variants. We designed a solution to improve quality
and biological activity of LPS extracted from various bacteria
with different types of LPS, as compared to conventional
 methods
 . We introduced a quality index as a simple measure
of LPS purity in terms of a degree of polysaccharide content
detected by absorbance at 204 nm. Further experiments using
gel electrophoresis, endotoxin test, and macrophage activation
test were performed to evaluate the performance and reliability
of a proposed ‘T-sol’ method and the biological effectiveness
and character of the LPS products. We presented
that the T-sol method had differential effects on extraction of
a RAW 264.7 cell-activating LPS, which was effective in the
macrophage activation with similar effects in stimulating
the production of TNF-alpha. In conclusion, the T-sol method
provides a simple way to improve quality and biological activity
of LPS with high yield.
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			Citations Citations to this article as recorded by    
- Effective Modalities of Periodontitis Induction in Rat Model
 Fazle Khuda, Badiah Baharin, Nur Najmi Mohamad Anuar, Bellen Sharon Fred Satimin, Nurrul Shaqinah Nasruddin
 Journal of Veterinary Dentistry.2024; 41(1): 49.     CrossRef
- LPS-Induced Mortality in Zebrafish: Preliminary Characterisation of Common Fish Pathogens
 Rafaela A. Santos, Cláudia Cardoso, Neide Pedrosa, Gabriela Gonçalves, Jorge Matinha-Cardoso, Filipe Coutinho, António P. Carvalho, Paula Tamagnini, Aires Oliva-Teles, Paulo Oliveira, Cláudia R. Serra
 Microorganisms.2023; 11(9): 2205.     CrossRef
- Heterogeneity of Lipopolysaccharide as Source of Variability in Bioassays and LPS-Binding Proteins as Remedy
 Alexandra C. Fux, Cristiane Casonato Melo, Sara Michelini, Benjamin J. Swartzwelter, Andreas Neusch, Paola Italiani, Martin Himly
 International Journal of Molecular Sciences.2023; 24(9): 8395.     CrossRef
- Identification workflow of endotoxins by pyrolysis–gas chromatography–mass spectrometry based on a database and chemometrics
 Jackie Jackie, Chun Kiang Chua, Norrapat Shih, Sam Fong Yau Li
 Journal of Analytical and Applied Pyrolysis.2022; 165: 105547.     CrossRef
- Exploring the Lipidome: Current Lipid Extraction Techniques for Mass Spectrometry Analysis
 Julian Aldana, Adriana Romero-Otero, Mónica P. Cala
 Metabolites.2020; 10(6): 231.     CrossRef
- The outer membrane glycolipids of bacteria from cold environments: isolation, characterization, and biological activity
 Angela Casillo, Ermenegilda Parrilli, Maria Luisa Tutino, Maria Michela Corsaro
 FEMS Microbiology Ecology.2019;[Epub]     CrossRef
 
 
	
	
				- Antagonistic effect of peptidoglycan of Streptococcus sanguinis on lipopolysaccharide of major periodontal pathogens
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		Sung-Hoon Lee 		
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			J. Microbiol. 2015;53(8):553-560.   Published online July 31, 2015		
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							DOI: https://doi.org/10.1007/s12275-015-5319-6
					
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						 Abstract Abstract
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		Streptococcus sanguinis is often found in subgingival biofilm
including periodontopathogens, and is correlated with
a delay in colonization by periodontopathogens. However,
the effect of S. sanguinis on inflammation induced by periodontopathogens
is poorly understood. Thus, this study investigated
the effect of S. sanguinis peptidoglycan (PGN) on
induction of TNF-α, IL-6, and IL-8 expression by lipopolysaccharide
(LPS) of periodontal pathogens. LPS was extracted
from Aggregatibacter actinomycetemcomitans, Porphyromonas
gingivalis, and Tannerella forsythia, and PGN was isolated
from S. sanguinis. THP-1 cells, a monocytic cell-line, were cotreated
with LPS of the periodontal pathogens and S. sanguinis
PGN, and then the expression of inflammatory cytokines
was analyzed by real-time RT-PCR. To analyze the underlying
mechanism, the binding assay of the LPS to CD14
or LPS-binding protein (LBP) was performed in the presence
or absence of the PGN after coating recombinant human
CD14 and LBP on EIA plate. The PGN inhibited the binding
of LPS to CD14 and LBP in a dose-dependent manner.
Also, THP-1 cells were co-treated with the LPS in the presence
of N-acetylmuramic acid and N-acetylglucosamine,
as components of PGN, and the competition binding assay
to CD14 and LBP was performed. N-acetylmuramic acid inhibited
the induction of inflammatory cytokine expression
by LPS and the binding of LPS to CD14 or LBP whereas Nacetylglucosamine
did not show such effect. Collectively, the
 results
 suggest that S. sanguinis PGN inhibited the cytokine
expression induced by the LPS of periodontopathogens due
to the inhibition of LPS binding to LBP and CD14. N-acetylmuramic
acid of PGN may play a role in inhibition of
the LPS binding of periodontopathogens to CD14 and LBP.
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			Citations Citations to this article as recorded by    
- Inflammasome regulation by the cell surface ecto-5′-nucleotidase of the oral commensal, Streptococcus oralis
 Natsuno Nakamura, Hirobumi Morisaki, Momoe Itsumi, Nobuo Okahashi, Haruka Fukamachi, Ayako Sato, Miki Kadena, Mariko Kikuchi, Shohei Matsui, Takahiro Funatsu, Hirotaka Kuwata
 Biochemical and Biophysical Research Communications.2025; 744: 151206.     CrossRef
- New putative periodontopathogens and periodontal health‐associated species: A systematic review and meta‐analysis
 Angéline Antezack, Damien Etchecopar‐Etchart, Bernard La Scola, Virginie Monnet‐Corti
 Journal of Periodontal Research.2023; 58(5): 893.     CrossRef
- Correlation and mechanism between cardiac magnetic resonance imaging and oral streptococcus count in patients with primary microvascular angina pectoris
 Qi Huang, Shi Sheng Wang, Rong Hua Luo
 Medicine.2022; 101(12): e29060.     CrossRef
- Oral ecological environment modifications by hard-cheese: from pH to microbiome: a prospective cohort study based on 16S rRNA metabarcoding approach
 Erna Cecilia Lorenzini, Barbara Lazzari, Gianluca Martino Tartaglia, Giampietro Farronato, Valentina Lanteri, Sara Botti, Filippo Biscarini, Paolo Cozzi, Alessandra Stella
 Journal of Translational Medicine.2022;[Epub]     CrossRef
- Biofilm growth and IL-8 & TNF-α-inducing properties of Candida albicans in the presence of oral gram-positive and gram-negative bacteria
 Radhika G. Bhardwaj, Arjuna Ellepolla, Hana Drobiova, Maribasappa Karched
 BMC Microbiology.2020;[Epub]     CrossRef
- Genetics ofsanguinis-Group Streptococci in Health and Disease
 Angela Nobbs, Jens Kreth, Vincent A. Fischetti, Richard P. Novick, Joseph J. Ferretti, Daniel A. Portnoy, Miriam Braunstein, Julian I. Rood
 Microbiology Spectrum.2019;[Epub]     CrossRef
- Influence of a light‐activated glaze on the adhesion of Streptococcus sanguinis to the surface of polymers used in fabrication of interim prostheses
 Daniela Micheline dos Santos, Betina Chiarelo Commar, Emily Vivianne Freitas da Silva, Valentim Adelino Ricardo Barão, Adaias Oliveira Matos, Marcelo Coelho Goiato
 Journal of Investigative and Clinical Dentistry.2019;[Epub]     CrossRef
- Novel nanotechnology and near-infrared photodynamic therapy to kill periodontitis-related biofilm pathogens and protect the periodontium
 Manlin Qi, Xue Li, Xiaolin Sun, Chunyan Li, Franklin R. Tay, Michael D. Weir, Biao Dong, Yanmin Zhou, Lin Wang, Hockin H.K. Xu
 Dental Materials.2019; 35(11): 1665.     CrossRef
- A wear-resistant TiO2 nanoceramic coating on titanium implants for visible-light photocatalytic removal of organic residues
 Hao Wu, Li Xie, Min He, Ruitao Zhang, Yuan Tian, Suru Liu, Tao Gong, Fangjun Huo, Ting Yang, Qingyuan Zhang, Shujuan Guo, Weidong Tian
 Acta Biomaterialia.2019; 97: 597.     CrossRef
- Activity of the Chimeric Lysin ClyR against Common Gram-Positive Oral Microbes and Its Anticaries Efficacy in Rat Models
 Jingjing Xu, Hang Yang, Yongli Bi, Wuyou Li, Hongping Wei, Yuhong Li
 Viruses.2018; 10(7): 380.     CrossRef
- Bacterial Adhesion on Lithium Disilicate Ceramic Surface Exposed to Different Hydrofluoric Solutions
 Daniela Micheline dos Santos, Emily Vivianne Freitas da Silva, Adaias Oliveira Matos, Beatriz Cristiane Zuin Monteiro, Rodrigo Antonio de Medeiros, Sandro Basso Bitencourt, Valentim Adelino Ricardo Barão, Elidiane Cipriano Rangel, Marcelo Coelho Goiato
 Ceramics.2018; 1(1): 145.     CrossRef
- Inhibitory effect of Lactococcus lactis on the bioactivity of periodontopathogens
 Hyun-Seung Shin, Dong-Heon Baek, Sung-Hoon Lee
 The Journal of General and Applied Microbiology.2018; 64(2): 55.     CrossRef
- The road less traveled – defining molecular commensalism with Streptococcus sanguinis
 J. Kreth, R.A. Giacaman, R. Raghavan, J. Merritt
 Molecular Oral Microbiology.2017; 32(3): 181.     CrossRef
- Buckyballs conjugated with nucleic acid sequences identifies microorganisms in live cell assays
 Qingsu Cheng, Bahram Parvin
 Journal of Nanobiotechnology.2017;[Epub]     CrossRef
- Antimicrobial activity and regulation of CXCL9 and CXCL10 in oral keratinocytes
 Alison Marshall, Antonio Celentano, Nicola Cirillo, Michele D. Mignogna, Michael McCullough, Stephen Porter
 European Journal of Oral Sciences.2016; 124(5): 433.     CrossRef
 
 
	
	
				- Reducing the Bioactivity of Tannerella forsythia Lipopolysaccharide by Porphyromonas gingivalis
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		Young-Jae Kim , Sung-Hoon Lee 		
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			J. Microbiol. 2014;52(8):702-708.   Published online August 1, 2014		
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							DOI: https://doi.org/10.1007/s12275-014-4324-5
					
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						 Abstract Abstract PDF PDF
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		Tannerella forsythia is considered a pathogen of periodontitis and forms a biofilm with multi-species bacteria in oral cavity. Lipopolysaccharide is a powerful immunostimulator and induces inflammation and shock. The purpose of this study was to investigate the characteristics of T. forsythia LPS in its co-cultivation with Fusobacterium nucleatum or Porphyromonas gingivalis. T. forsythia was co-cultured in the presence and absence of F. nucleatum and P. gingivalis and then T. forsythia LPS was extracted. The extracts were analyzed by SDS-PAGE and NF-κB reporter CHO cell lines. THP-1 cells were treated with the LPS and evaluated induction
of cytokine expression by real-time RT-PCR and ELISA. For analysis of the bioactivity of T. forsythia LPS, the binding assay on LPS-binding protein (LBP) and CD14 was processed. The extracts did not contaminate other molecules except LPS and showed TLR4 agonists. Co-cultured T. forsythia LPS with P. gingivalis exhibited a lower level of induction of TNF-α, IL-1β, and IL-6 expression than singleor co-cultured T. forsythia LPS with F. nucleatum in the conditions of human serum. However, the three T. forsythia LPS did not show difference of cytokine induction in the serum free conditions. Co-cultured T. forsythia LPS with
P. gingivalis exhibited a lower affinity to LBP and CD14 as binding site of O-antigen and attached at a lower level to THP-1 cells compared to single- or co-cultured T. forsythia LPS with F. nucleatum. The virulence of T. forsythia LPS was decreased by co-culturing with P. gingivalis and their affinity to LBP and CD14 was reduced, which may due to modification of O-antigen chain by P. gingivalis.	
		
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			Citations Citations to this article as recorded by    
- Anti-Inflammatory Efficacy of Human-Derived Streptococcus salivarius on Periodontopathogen-Induced Inflammation
 Dong-Heon Baek, Sung-Hoon Lee
 Journal of Microbiology and Biotechnology.2023; 33(8): 998.     CrossRef
- Virulence of Filifactor alocis lipoteichoic acid on human gingival fibroblast
 Hyun-Jun Yoo, Sung-Hoon Lee
 Archives of Oral Biology.2022; 135: 105370.     CrossRef
- Effects of Shiitake mushroom extract on antimicrobial activity against periodontopathogens and inflammatory condition of human gingival fibroblast
 Yeol-Mae Jeon
 Journal of Dental Rehabilitation and Applied Science.2022; 38(2): 90.     CrossRef
- Characteristics of Treponema denticola lipooligosaccharide in presence of hemin and quorum-sensing molecule
 Dong-Heon Baek, Sung-Hoon Lee
 Archives of Oral Biology.2021; 124: 105062.     CrossRef
- The Associations of Periodontopathic Bacteria and Oral Candida with Periodontal Inflamed Surface Area in Older Adults Receiving Supportive Periodontal Therapy
 Hideo Shigeishi, Mariko Nakamura, Iori Oka, Cheng-Yih Su, Kanako Yano, Momoko Ishikawa, Yoshino Kaneyasu, Masaru Sugiyama, Kouji Ohta
 Diagnostics.2021; 11(8): 1397.     CrossRef
- Efficacy of β-caryophyllene for periodontal disease related factors
 Hyun-Jun Yoo, Su-Kyung Jwa
 Archives of Oral Biology.2019; 100: 113.     CrossRef
- Inhibitory effect of Lactococcus lactis on the bioactivity of periodontopathogens
 Hyun-Seung Shin, Dong-Heon Baek, Sung-Hoon Lee
 The Journal of General and Applied Microbiology.2018; 64(2): 55.     CrossRef
- Consistent and reproducible long-term in vitro growth of health and disease-associated oral subgingival biofilms
 Irina M. Velsko, Luciana M. Shaddox
 BMC Microbiology.2018;[Epub]     CrossRef
- Quantification by qPCR of Pathobionts in Chronic Periodontitis: Development of Predictive Models of Disease Severity at Site-Specific Level
 Inmaculada Tomás, Alba Regueira-Iglesias, Maria López, Nora Arias-Bujanda, Lourdes Novoa, Carlos Balsa-Castro, Maria Tomás
 Frontiers in Microbiology.2017;[Epub]     CrossRef
- Gingipain‐dependent augmentation by Porphyromonas gingivalis of phagocytosis of Tannerella forsythia
 Y.‐J. Jung, H.‐K. Jun, B.‐K. Choi
 Molecular Oral Microbiology.2016; 31(6): 457.     CrossRef
- Development of Filifactor alocis media for single- and co-cultivation with periodontopathogens
 조인우,  이성훈
 Oral Biology Research.2016; 40(4): 193.     CrossRef
- Antagonistic effect of peptidoglycan of Streptococcus sanguinis on lipopolysaccharide of major periodontal pathogens
 Sung-Hoon Lee
 Journal of Microbiology.2015; 53(8): 553.     CrossRef
- Polymicrobial Oral Infection with Four Periodontal Bacteria Orchestrates a Distinct Inflammatory Response and Atherosclerosis in ApoEnull Mice
 Sasanka S. Chukkapalli, Irina M. Velsko, Mercedes F. Rivera-Kweh, Donghang Zheng, Alexandra R. Lucas, Lakshmyya Kesavalu, Salomon Amar
 PLOS ONE.2015; 10(11): e0143291.     CrossRef
 
 
	
	
				- Porphyromonas gingivalis-Derived Lipopolysaccharide-Mediated Activation of MAPK Signaling Regulates Inflammatory Response and Differentiation in Human Periodontal Ligament Fibroblasts
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		Taegun Seo , Seho Cha , Tae-Il Kim , Hee-Jung Park , Jeong-Soon Lee , Kyung Mi Woo 		
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			J. Microbiol. 2012;50(2):311-319.   Published online April 27, 2012		
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							DOI: https://doi.org/10.1007/s12275-012-2146-x
					
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						 Abstract Abstract PDF PDF
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		Porphyromonas gingivalis (P.g.), which is a potential pathogen
for periodontal diseases, contains lipopolysaccharide
(LPS), and this endotoxin stimulates a variety of cellular
responses. At present, P.g.-derived LPS-induced cellular responses
in human periodontal ligament fibroblasts (PDLFs)
are not well characterized. Here, we demonstrate that P.gderived
LPS regulates inflammatory responses, apoptosis
and differentiation in PDLFs. Interleukin-6 (IL-6) and -8
(IL-8) were effectively upregulated by treatment of P.g.-derived
LPS, and we confirmed apoptosis markers including
elevated cytochrome c levels, active caspase-3 and morphological
change in the presence of P.g.-derived LPS. Moreover,
when PDLFs were cultured with differentiation media, P.g.-
derived LPS reduced the expression of differentiation marker
genes, as well as reducing alkaline phosphatase (ALP) activity
and mineralization. P.g.-derived LPS-mediated these
cellular responses were effectively abolished by treatment
of mitogen-activated protein kinase (MAPK) inhibitors.
Taken together, our results suggest that P.g.-derived LPS
regulates several cellular responses via activation of MAPK
signaling pathways in PDLFs.	
		
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			Citations Citations to this article as recorded by    
- Biofilms and oral health: nanotechnology for biofilm control
 Deenadayalan Karaiyagowder Govindarajan, Maline Mohanarangam, Lohita Kadirvelu, Sowmiya Sri Sivaramalingam, Deepsikha Jothivel, Anand Ravichandran, Saravanan Periasamy, Kumaravel Kandaswamy
 Discover Nano.2025;[Epub]     CrossRef
- Evaluation of the role of mitofusin‐1 and mitofusin‐2 in periodontal disease
 Ömer Alperen Kırmızıgül, Arife Sabanci, Faruk Dişli, Sedat Yıldız, Michael R. Milward, Kübra Aral
 Journal of Periodontology.2024; 95(1): 64.     CrossRef
- Programmed cell death of periodontal ligament cells
 Wei He, Yu Fu, Song Yao, Lan Huang
 Journal of Cellular Physiology.2023; 238(8): 1768.     CrossRef
- Porphyromonas gingivalis lipopolysaccharide promotes T-hel per17 cell differentiation by upregulating Delta-like ligand 4 expression on CD14+ monocytes
 Chi Zhang, Chenrong Xu, Li Gao, Xiting Li, Chuanjiang Zhao
 PeerJ.2021; 9: e11094.     CrossRef
- Gene expression profiles of mitochondria-endoplasmic reticulum tethering in human gingival fibroblasts in response to periodontal pathogens
 Kübra Aral, Michael R. Milward, Paul R. Cooper
 Archives of Oral Biology.2021; 128: 105173.     CrossRef
- Ginsenoside Rb3 Inhibits Pro-Inflammatory Cytokines via MAPK/AKT/NF-κB Pathways and Attenuates Rat Alveolar Bone Resorption in Response to Porphyromonas gingivalis LPS
 Minmin Sun, Yaoting Ji, Zhen Li, Rourong Chen, Shuhui Zhou, Chang Liu, Minquan Du
 Molecules.2020; 25(20): 4815.     CrossRef
- Low-intensity pulsed ultrasound upregulates osteogenesis under inflammatory conditions in periodontal ligament stem cells through unfolded protein response
 Han Li, Yuejia Deng, Minmin Tan, Ge Feng, Yunchun Kuang, Jie Li, Jinlin Song
 Stem Cell Research & Therapy.2020;[Epub]     CrossRef
- Effect of ScLL and 15d-PGJ2 on viability and cytokine release in LPS-stimulated fibroblasts: an in vitro study
 Manuella Verdinelli de Paula REIS, Gabriela Leite de SOUZA, Priscilla Barbosa Ferreira SOARES, Maria Aparecida de SOUZA, Carlos José SOARES, Camilla Christian Gomes MOURA
 Brazilian Oral Research.2020;[Epub]     CrossRef
- TLR activation inhibits the osteogenic potential of human periodontal ligament stem cells through Akt signaling in a Myd88‐ or TRIF‐dependent manner
 Yunyan Zhu, Qian Li, Yanheng Zhou, Weiran Li
 Journal of Periodontology.2019; 90(4): 400.     CrossRef
- Low‐intensity pulsed ultrasound promotes bone morphogenic protein 9‐induced osteogenesis and suppresses inhibitory effects of inflammatory cytokines on cellular responses via Rho‐associated kinase 1 in human periodontal ligament fibroblasts
 Joji Kusuyama, Toshiaki Nakamura, Tomokazu Ohnishi, Brent G. Albertson, Yukari Ebe, Nahoko Eiraku, Kazuyuki Noguchi, Tetsuya Matsuguchi
 Journal of Cellular Biochemistry.2019; 120(9): 14657.     CrossRef
- Periodontal bacterial supernatants modify differentiation, migration and inflammatory cytokine expression in human periodontal ligament stem cells
 Liza L. Ramenzoni, Giancarlo Russo, Maria D. Moccia, Thomas Attin, Patrick R. Schmidlin, Alain Haziot
 PLOS ONE.2019; 14(7): e0219181.     CrossRef
- Necrostatin-1 promotes ectopic periodontal tissue like structure regeneration in LPS-treated PDLSCs
 Bingbing Yan, Hongmei Zhang, Taiqiang Dai, Yongchun Gu, Xinyu Qiu, Cheng Hu, Yan Liu, Kewen Wei, Dehua Li, Motohiro Komaki
 PLOS ONE.2018; 13(11): e0207760.     CrossRef
- TGF-β2 downregulates osteogenesis under inflammatory conditions in dental follicle stem cells
 Soyoun Um, Joo-Hee Lee, Byoung-Moo Seo
 International Journal of Oral Science.2018;[Epub]     CrossRef
- Periostin promotes migration and osteogenic differentiation of human periodontal ligament mesenchymal stem cells via the Jun amino‐terminal kinases (JNK) pathway under inflammatory conditions
 Yi Tang, Lin Liu, Pei Wang, Donglei Chen, Ziqiang Wu, Chunbo Tang
 Cell Proliferation.2017;[Epub]     CrossRef
- Osteogenic potential of periodontal ligament stem cells are unaffected after exposure to lipopolysaccharides
 Mayra Laino ALBIERO, Bruna Rabelo AMORIM, Márcio Zaffalon CASATI, Enilson Antonio SALLUM, Francisco Humberto NOCITI JUNIOR, Karina Gonzales SILVÉRIO
 Brazilian Oral Research.2017;[Epub]     CrossRef
- Periodontal-Derived Mesenchymal Cell Sheets Promote Periodontal Regeneration in Inflammatory Microenvironment
 Shujuan Guo, Jian Kang, Baohui Ji, Weihua Guo, Yi Ding, Yafei Wu, Weidong Tian
 Tissue Engineering Part A.2017; 23(13-14): 585.     CrossRef
- Hypoxia enhances the effect of lipopolysaccharide-stimulated IL-1β expression in human periodontal ligament cells
 Jittima Pumklin, Kanokporn Bhalang, Prasit Pavasant
 Odontology.2016; 104(3): 338.     CrossRef
- Effect of lectin (ScLL) on fibroblasts stimulated with LPS - an in vitro study
 Manuella Verdinelli de Paula REIS, Camilla Christian Gomes MOURA, Marcus Vinicius da SILVA, Maria Aparecida de SOUZA, Priscilla Barbosa Ferreira SOARES, Carlos José SOARES
 Brazilian Oral Research.2016;[Epub]     CrossRef
- Leukocyte Inclusion within a Platelet Rich Plasma-Derived Fibrin Scaffold Stimulates a More Pro-Inflammatory Environment and Alters Fibrin Properties
 Eduardo Anitua, Mar Zalduendo, María Troya, Sabino Padilla, Gorka Orive, Paula A. da Costa Martins
 PLOS ONE.2015; 10(3): e0121713.     CrossRef
- The negative feedback regulation of microRNA-146a in human periodontal ligament cells after Porphyromonas gingivalis lipopolysaccharide stimulation
 Shao-Yun Jiang, Dong Xue, Yu-Feng Xie, Dong-Wang Zhu, Yun-Yun Dong, Cong-Cong Wei, Jia-Yin Deng
 Inflammation Research.2015; 64(6): 441.     CrossRef
- IL-1R/TLR2 through MyD88 Divergently Modulates Osteoclastogenesis through Regulation of Nuclear Factor of Activated T Cells c1 (NFATc1) and B Lymphocyte-induced Maturation Protein-1 (Blimp1)
 Zhihong Chen, Lingkai Su, Qingan Xu, Jenny Katz, Suzanne M. Michalek, Mingwen Fan, Xu Feng, Ping Zhang
 Journal of Biological Chemistry.2015; 290(50): 30163.     CrossRef
- Effects of Streptococcus thermophilus on volatile sulfur compounds produced by Porphyromonas gingivalis
 Sung-Hoon Lee, Dong-Heon Baek
 Archives of Oral Biology.2014; 59(11): 1205.     CrossRef
- Porphyromonas gingivalis LPS inhibits osteoblastic differentiation and promotes pro-inflammatory cytokine production in human periodontal ligament stem cells
 Hirohito Kato, Yoichiro Taguchi, Kazuya Tominaga, Makoto Umeda, Akio Tanaka
 Archives of Oral Biology.2014; 59(2): 167.     CrossRef
- Effect of epithelial rests of Malassez’ cells on RANKL mRNA expression and ALP activity by periodontal ligament fibroblasts stimulated with sonicated Porphyromonas gingivalis in vitro
 Kenichi Matsuzaka, Eitoyo Kokubu, Takashi Inoue
 Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology.2014; 26(4): 554.     CrossRef
- Effects of Enterococcus faecalis lipoteichoic acid on receptor activator of nuclear factor‐κB ligand and osteoprotegerin expression in periodontal ligament fibroblasts
 L. Zhao, J. Chen, L. Cheng, X. Wang, J. Du, F. Wang, Z. Peng
 International Endodontic Journal.2014; 47(2): 163.     CrossRef
- Apoptosis: an underlying factor for accelerated periodontal disease associated with diabetes in rats
 Mustafa Tunalı, Tamer Ataoğlu, Ilhami Çelik
 Clinical Oral Investigations.2014; 18(7): 1825.     CrossRef
- Reducing the bioactivity of Tannerella forsythia lipopolysaccharide by Porphyromonas gingivalis
 Young-Jae Kim, Sung-Hoon Lee
 Journal of Microbiology.2014; 52(8): 702.     CrossRef
- Bambusae Caulis in Taeniam modulates neuroprotective and anti-neuroinflammatory effects in hippocampal and microglial cells via HO-1- and Nrf-2-mediated pathways
 HYE WON EOM, SUN YOUNG PARK, YOUNG HUN KIM, SU JIN SEONG, MEI LING JIN, EUN YEON RYU, MIN JU KIM, SANG JOON LEE
 International Journal of Molecular Medicine.2012; 30(6): 1512.     CrossRef
- Baicalin Downregulates Porphyromonas gingivalis Lipopolysaccharide-Upregulated IL-6 and IL-8 Expression in Human Oral Keratinocytes by Negative Regulation of TLR Signaling
 Wei Luo, Cun-Yu Wang, Lijian Jin, Anne Wertheimer
 PLoS ONE.2012; 7(12): e51008.     CrossRef
 
 Research Support, Non-U.S. Gov't
	
	
				- Acinetobacter baumannii Outer Membrane Protein A Modulates the Biogenesis of Outer Membrane Vesicles
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		Dong Chan Moon , Chul Hee Choi , Jung Hwa Lee , Chi-Won Choi , Hye-Yeon Kim , Jeong Soon Park , Seung Il Kim , Je Chul Lee 		
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			J. Microbiol. 2012;50(1):155-160.   Published online February 27, 2012		
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							DOI: https://doi.org/10.1007/s12275-012-1589-4
					
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						 Abstract Abstract PDF PDF
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		Acinetobacter baumannii secretes outer membrane vesicles
(OMVs) during both in vitro and in vivo growth, but the
biogenesis mechanism by which A. baumannii produces
OMVs remains undefined. Outer membrane protein A of
A. baumannii (AbOmpA) is a major protein in the outer
membrane and the C-terminus of AbOmpA interacts with
diaminopimelate of peptidoglycan. This study investigated
the role of AbOmpA in the biogenesis of A. baumannii
OMVs. Quantitative and qualitative approaches were used
to analyze OMV biogenesis in A. baumannii ATCC 19606T
and an isogenic ΔAbOmpA mutant. OMV production was
significantly increased in the ΔAbOmpA mutant compared
to wild-type bacteria as demonstrated by quantitation of
proteins and lipopolysaccharides (LPS) packaged in OMVs.
LPS profiles prepared from OMVs from wild-type bacteria
and the ΔAbOmpA mutant had identical patterns, but
proteomic analysis showed different protein constituents in
OMVs from wild-type bacteria compared to the ΔAbOmpA
mutant. In conclusion, AbOmpA influences OMV biogenesis
by controlling OMV production and protein composition.	
		
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			Citations Citations to this article as recorded by    
- Brucella suis ΔmapB outer membrane vesicles as an acellular vaccine against systemic and mucosal B. suis infection
 Florencia Muñoz González, Magali G. Bialer, Maria L. Cerutti, Silvia M. Estein, Lila Y. Ramis, Pablo C. Baldi, Ángeles Zorreguieta, Mariana C. Ferrero
 Frontiers in Immunology.2025;[Epub]     CrossRef
- Exploring the Multifaceted Genus Acinetobacter: the Facts, the Concerns and the Oppoptunities the Dualistic Geuns Acinetobacter
 Tsvetana Muleshkova, Inga Bazukyan, Konstantinos Papadimitriou, Velitchka Gotcheva, Angel Angelov, Svetoslav G. Dimov
 Journal of Microbiology and Biotechnology.2025;[Epub]     CrossRef
- Engineering bacterial membrane vesicles: A new paradigm in biomedical innovation
 Xiao Xu, Limei Xu, Caining Wen, Yuanmin Zhang, Jiang Xia, Yujie Liang
 Coordination Chemistry Reviews.2025; 543: 216895.     CrossRef
- AbOmpA in Acinetobacter baumannii: exploring virulence mechanisms of outer membrane-integrated and outer membrane vesicle-associated AbOmpA and developing anti-infective agents targeting AbOmpA
 Man Hwan Oh, Md Minarul Islam, Nayeong Kim, Chul Hee Choi, Minsang Shin, Woo Shik Shin, Je Chul Lee
 Journal of Biomedical Science.2025;[Epub]     CrossRef
- Engineered bacterial extracellular vesicles for gastrointestinal diseases
 Xinke Nie, Qiqiong Li, Ying He, Yushan Xu, Shanfeng Qiao, Xingdong Wang, Fan Meng, Junhua Xie, Shaoping Nie
 Journal of Controlled Release.2025; 385: 113972.     CrossRef
- Cas3 of type I-Fa CRISPR-Cas system upregulates bacterial biofilm formation and virulence in Acinetobacter baumannii
 Tingting Guo, Jie Yang, Na Zhou, Xiaoli Sun, Changchao Huan, Tao Lin, Guangyu Bao, Jian Hu, Guocai Li
 Communications Biology.2025;[Epub]     CrossRef
- Signaling in Acinetobacter baumannii: Quorum sensing and nucleotide second messengers
 Binbin Cui, Ganjin Peng, Liu-En Wang, Yinyue Deng
 Computational and Structural Biotechnology Journal.2025; 27: 2168.     CrossRef
- Engineered Membrane Vesicle Production via oprF or oprI Deletion Has Distinct Phenotypic Effects in Pseudomonas putida
 Rebecca A. Wilkes, Tarryn E. Miller, Jacob Waldbauer, Nanqing Zhou, Lichun Zhang, Beth N. DiBiase, Neha P. Kamat, Ludmilla Aristilde, Gregg T. Beckham, Allison Z. Werner
 ACS Synthetic Biology.2025; 14(7): 2739.     CrossRef
- Engineered Bacterial Extracellular Besicles: Developments, Challenges, and Opportunities
 Qiqiong Li, Xinyang Chen, Junhua Xie, Shaoping Nie
 Engineering.2025;[Epub]     CrossRef
- The aryl hydrocarbon receptor and FOS mediate cytotoxicity induced by Acinetobacter baumannii
 Chun Kew, Cristian Prieto-Garcia, Anshu Bhattacharya, Manuela Tietgen, Craig R. MacNair, Lindsey A. Carfrae, João Mello-Vieira, Stephan Klatt, Yi-Lin Cheng, Rajeshwari Rathore, Elise Gradhand, Ingrid Fleming, Man-Wah Tan, Stephan Göttig, Volkhard A. J. Ke
 Nature Communications.2024;[Epub]     CrossRef
- 
            Pathogenicity and virulence of
            Acinetobacter baumannii
            : Factors contributing to the fitness in healthcare settings and the infected host
          
 Massimiliano Lucidi, Daniela Visaggio, Antonella Migliaccio, Giulia Capecchi, Paolo Visca, Francesco Imperi, Raffaele Zarrilli
 Virulence.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
- Characterization and immunological effect of outer membrane vesicles from Pasteurella multocida on macrophages
 Jiaying Sun, Yee Huang, Xuefeng Li, Xiangfei Xu, Xuemei Cui, Fangjiao Hao, Quanan Ji, Chun Chen, Guolian Bao, Yan Liu
 Applied Microbiology and Biotechnology.2024;[Epub]     CrossRef
- An in-depth exploration of the multifaceted roles of EVs in the context of pathogenic single-cell microorganisms
 Anna Sophia Feix, Emily Z. Tabaie, Aarshi N. Singh, Nathan J. Wittenberg, Emma H. Wilson, Anja Joachim, Melissa Bruckner Lodoen
 Microbiology and Molecular Biology Reviews.2024;[Epub]     CrossRef
- Antimicrobial Resistance in Acinetobacter baumannii: A Challenge to Clinical Settings
 Shilpa Sharma, Amandeep Kaur, Renuka Bajaj, Kanwardeep Singh, Sarika Sharma, Sandeep Sharma
 Molecular Genetics, Microbiology and Virology.2024; 39(3): 219.     CrossRef
- 
            Outer membrane vesicles from genetically engineered
            Salmonella enterica
            serovar Typhimurium presenting
            Helicobacter pylori
            antigens UreB and CagA induce protection against
            Helicobact
 Qiong Liu, Yinpan Shang, Lu Shen, Xiaomin Yu, Yanli Cao, Lingbing Zeng, Hanchi Zhang, Zirong Rao, Yi Li, Ziwei Tao, Zhili Liu, Xiaotian Huang
 Virulence.2024;[Epub]     CrossRef
- The role of extracellular vesicles in pyroptosis-mediated infectious and non-infectious diseases
 Cai-Hua Zhang, Ding-Ci Lu, Ying Liu, Lingzhi Wang, Gautam Sethi, Zhaowu Ma
 International Immunopharmacology.2024; 138: 112633.     CrossRef
- Loss of Lipooligosaccharide Synthesis in Acinetobacter baumannii Produces Changes in Outer Membrane Vesicle Protein Content
 Beatriz Cano-Castaño, Andrés Corral-Lugo, Eva Gato, María C. Terrón, Antonio J. Martín-Galiano, Javier Sotillo, Astrid Pérez, Michael J. McConnell
 International Journal of Molecular Sciences.2024; 25(17): 9272.     CrossRef
- The Role of Bacterial Extracellular Vesicles in the Immune Response to Pathogens, and Therapeutic Opportunities
 Eliud S. Peregrino, Jessica Castañeda-Casimiro, Luis Vázquez-Flores, Sergio Estrada-Parra, Carlos Wong-Baeza, Jeanet Serafín-López, Isabel Wong-Baeza
 International Journal of Molecular Sciences.2024; 25(11): 6210.     CrossRef
- A genetic engineering strategy to enhance outer membrane vesicle-mediated extracellular electron transfer of Geobacter sulfurreducens
 Yanlun Fang, Guiqin Yang, Xian Wu, Canfen Lin, Baoli Qin, Li Zhuang
 Biosensors and Bioelectronics.2024; 250: 116068.     CrossRef
- Bacterial extracellular vesicles: Emerging nanoplatforms for biomedical applications
 Sangiliyandi Gurunathan, Jin-Hoi Kim
 Microbial Pathogenesis.2023; 183: 106308.     CrossRef
- Outer Membrane Vesicles from Acinetobacter baumannii: Biogenesis, Functions, and Vaccine Application
 Zheqi Weng, Ning Yang, Shujun Shi, Zining Xu, Zixu Chen, Chen Liang, Xiuwei Zhang, Xingran Du
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- Non-typeable Haemophilus influenzae major outer membrane protein P5 contributes to bacterial membrane stability, and affects the membrane protein composition crucial for interactions with the human host
 Yu-Ching Su, Mahendar Kadari, Megan L. Straw, Martina Janoušková, Sandra Jonsson, Oskar Thofte, Farshid Jalalvand, Erika Matuschek, Linda Sandblad, Ákos Végvári, Roman A. Zubarev, Kristian Riesbeck
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- Acinetobacter baumannii in the critically ill: complex infections get complicated
 Ilaria Cavallo, Alessandra Oliva, Rebecca Pages, Francesca Sivori, Mauro Truglio, Giorgia Fabrizio, Martina Pasqua, Fulvia Pimpinelli, Enea Gino Di Domenico
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- Outer Membrane Porins Contribute to Antimicrobial Resistance in Gram-Negative Bacteria
 Gang Zhou, Qian Wang, Yingsi Wang, Xia Wen, Hong Peng, Ruqun Peng, Qingshan Shi, Xiaobao Xie, Liangqiu Li
 Microorganisms.2023; 11(7): 1690.     CrossRef
- Deciphering the virulence factors, regulation, and immune response to Acinetobacter baumannii infection
 Afreen Shadan, Avik Pathak, Ying Ma, Ranjana Pathania, Rajnish Prakash Singh
 Frontiers in Cellular and Infection Microbiology.2023;[Epub]     CrossRef
- 
            Bacterial outer membrane vesicles provide an alternative pathway for trafficking of
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 Natalie Sirisaengtaksin, Eloise J. O'Donoghue, Sara Jabbari, Andrew J. Roe, Anne Marie Krachler, Craig D. Ellermeier
 mSphere.2023;[Epub]     CrossRef
- Microbiota and plant-derived vesicles that serve as therapeutic agents and delivery carriers to regulate metabolic syndrome
 Guanting Niu, Tunyu Jian, Yanan Gai, Jian Chen
 Advanced Drug Delivery Reviews.2023; 196: 114774.     CrossRef
- Bacterial extracellular vesicles and their interplay with the immune system
 Etienne Doré, Eric Boilard
 Pharmacology & Therapeutics.2023; 247: 108443.     CrossRef
- An Explorative Review on Advanced Approaches to Overcome Bacterial Resistance by Curbing Bacterial Biofilm Formation
 F Mohamad, Raghad R Alzahrani, Ahlam Alsaadi, Bahauddeen M Alrfaei, Alaa Eldeen B Yassin, Manal M Alkhulaifi, Majed Halwani
 Infection and Drug Resistance.2023; Volume 16: 19.     CrossRef
- The Two Faces of Bacterial Membrane Vesicles: Pathophysiological Roles and Therapeutic Opportunities
 Himadri B. Thapa, Stephan P. Ebenberger, Stefan Schild
 Antibiotics.2023; 12(6): 1045.     CrossRef
- Bacterial outer membrane vesicles in cancer: Biogenesis, pathogenesis, and clinical application
 Deming Li, Lisi Zhu, Yuxiao Wang, Xiangyu Zhou, Yan Li
 Biomedicine & Pharmacotherapy.2023; 165: 115120.     CrossRef
- Bacterial Outer Membrane Vesicles Promote Lung Inflammatory Responses and Macrophage Activation via Multi-Signaling Pathways
 Sunhyo Ryu, Kareemah Ni, Chenghao Wang, Ayyanar Sivanantham, Jonathan M. Carnino, Hong-Long Ji, Yang Jin
 Biomedicines.2023; 11(2): 568.     CrossRef
- Vaccine development to control the rising scourge of antibiotic-resistant Acinetobacter baumannii: a systematic review
 Ravinder Singh, Neena Capalash, Prince Sharma
 3 Biotech.2022;[Epub]     CrossRef
- Advances of bacteria-based delivery systems for modulating tumor microenvironment
 Shuping Li, Hua Yue, Shuang Wang, Xin Li, Xiaojun Wang, Peilin Guo, Guanghui Ma, Wei Wei
 Advanced Drug Delivery Reviews.2022; 188: 114444.     CrossRef
- Engineered bacterial membrane vesicles are promising carriers for vaccine design and tumor immunotherapy
 Qiong Long, Peng Zheng, Xiao Zheng, Weiran Li, Liangqun Hua, Zhongqian Yang, Weiwei Huang, Yanbing Ma
 Advanced Drug Delivery Reviews.2022; 186: 114321.     CrossRef
- 
            Outer Membrane Vesicles of
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 Ganeshwari Dhurve, Ashok Kumar Madikonda, Medicharla Venkata Jagannadham, Dayananda Siddavattam, Ayush Kumar
 Microbiology Spectrum.2022;[Epub]     CrossRef
- Peptidoglycan Recycling Promotes Outer Membrane Integrity and Carbapenem Tolerance in Acinetobacter baumannii
 Nowrosh Islam, Misha I. Kazi, Katie N. Kang, Jacob Biboy, Joe Gray, Feroz Ahmed, Richard D. Schargel, Cara C. Boutte, Tobias Dörr, Waldemar Vollmer, Joseph M. Boll, Vanessa Sperandio
 mBio.2022;[Epub]     CrossRef
- Outer Membrane Vesicles: Biogenesis, Functions, and Issues
 Rokas Juodeikis, Simon R. Carding
 Microbiology and Molecular Biology Reviews.2022;[Epub]     CrossRef
- Thioredoxin-mediated alteration of protein content and cytotoxicity of Acinetobacter baumannii outer membrane vesicles
 Swathi Shrihari, Holly C May, Jieh-Juen Yu, Sara B Papp, James P Chambers, M Neal Guentzel, Bernard P Arulanandam
 Experimental Biology and Medicine.2022; 247(3): 282.     CrossRef
- Raman Microspectroscopy Imaging Analysis of Extracellular Vesicles Biogenesis by Filamentous Fungus Penicilium chrysogenum
 Ashok Zachariah Samuel, Shumpei Horii, Takuji Nakashima, Naoko Shibata, Masahiro Ando, Haruko Takeyama
 Advanced Biology.2022;[Epub]     CrossRef
- The Discovery of the Role of Outer Membrane Vesicles against Bacteria
 Sofia Combo, Sérgio Mendes, Kaare Magne Nielsen, Gabriela Jorge da Silva, Sara Domingues
 Biomedicines.2022; 10(10): 2399.     CrossRef
- Enhancement of Acinetobacter baumannii biofilm growth by cephem antibiotics via enrichment of protein and extracellular DNA in the biofilm matrices
 Kaoru Yamabe, Yukio Arakawa, Masaki Shoji, Katsushiro Miyamoto, Takahiro Tsuchiya, Katsuhiko Minoura, Yukihiro Akeda, Kazunori Tomono, Mitsuko Onda
 Journal of Applied Microbiology.2022; 133(3): 2002.     CrossRef
- The role of Zur-regulated lipoprotein A in bacterial morphology, antimicrobial susceptibility, and production of outer membrane vesicles in Acinetobacter baumannii
 Nayeong Kim, Hyo Jeong Kim, Man Hwan Oh, Se Yeon Kim, Mi Hyun Kim, Joo Hee Son, Seung Il Kim, Minsang Shin, Yoo Chul Lee, Je Chul Lee
 BMC Microbiology.2021;[Epub]     CrossRef
- Host immunity and cellular responses to bacterial outer membrane vesicles
 Varnesh Tiku, Man-Wah Tan
 Trends in Immunology.2021; 42(11): 1024.     CrossRef
- Outer membrane vesicles mediated horizontal transfer of an aerobic denitrification gene between Escherichia coli
 Weichuan Qiao, Lianjie Wang, Yang Luo, Jiahui Miao
 Biodegradation.2021; 32(4): 435.     CrossRef
- Comparative Analysis of Outer Membrane Vesicle Isolation Methods With an Escherichia coli tolA Mutant Reveals a Hypervesiculating Phenotype With Outer-Inner Membrane Vesicle Content
 Shelby L. Reimer, Daniel R. Beniac, Shannon L. Hiebert, Timothy F. Booth, Patrick M. Chong, Garrett R. Westmacott, George G. Zhanel, Denice C. Bay
 Frontiers in Microbiology.2021;[Epub]     CrossRef
- Engineered Remolding and Application of Bacterial Membrane Vesicles
 Li Qiao, Yifan Rao, Keting Zhu, Xiancai Rao, Renjie Zhou
 Frontiers in Microbiology.2021;[Epub]     CrossRef
- Inhibition of Virulence Factors and Biofilm Formation ofAcinetobacter Baumanniiby Naturally-derived and Synthetic Drugs
 Nilushi Indika Bamunuarachchi, Fazlurrahman Khan, Young-Mog Kim
 Current Drug Targets.2021; 22(7): 734.     CrossRef
- Gut Microbiota Extracellular Vesicles as Signaling Molecules Mediating Host-Microbiota Communications
 Salma Sultan, Walid Mottawea, JuDong Yeo, Riadh Hammami
 International Journal of Molecular Sciences.2021; 22(23): 13166.     CrossRef
- Mycobacterium tuberculosis extracellular vesicles: exploitation for vaccine technology and diagnostic methods
 Roghayeh Mohammadzadeh, Kiarash Ghazvini, Hadi Farsiani, Saman Soleimanpour
 Critical Reviews in Microbiology.2021; 47(1): 13.     CrossRef
- Methoxy‐Substituted Hydroxychalcone Reduces Biofilm Production, Adhesion and Surface Motility of Acinetobacter baumannii by Inhibiting ompA Gene Expression
 Dušan Ušjak, Miroslav Dinić, Katarina Novović, Branka Ivković, Nenad Filipović, Magdalena Stevanović, Marina T. Milenković
 Chemistry & Biodiversity.2021;[Epub]     CrossRef
- 
            New Provisional Function of OmpA from
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 Shahab Shahryari, Mahbubeh Talaee, Kamahldin Haghbeen, Lorenz Adrian, Hojatollah Vali, Hossein Shahbani Zahiri, Kambiz Akbari Noghabi, Jack A. Gilbert
 mSystems.2021;[Epub]     CrossRef
- The extracellular vesicle generation paradox: a bacterial point of view
 Hannah M McMillan, Meta J Kuehn
 The EMBO Journal.2021;[Epub]     CrossRef
- Bacteria- and host-derived extracellular vesicles – two sides of the same coin?
 Jeffrey S. Schorey, Yong Cheng, William R. McManus
 Journal of Cell Science.2021;[Epub]     CrossRef
- INSIGHTS INTO THE VIRULENCE FACTORS OF ACINETOBACTER BAUMANNII AND THEIR ROLES IN PERSISTENCE AND INFECTIOUS PROCESS
 Al Shaikhli Nawfal Haitham, Irina Gheorghe, Andreea Gheorghe
 Romanian Archives of Microbiology and Immunology.2021; 80(2): 141.     CrossRef
- Screening of small molecules attenuating biofilm formation of Acinetobacter baumannii by inhibition of ompA promoter activity
 Seok Hyeon Na, Hyejin Jeon, Man Hwan Oh, Yoo Jeong Kim, Je Chul Lee
 Journal of Microbiology.2021; 59(9): 871.     CrossRef
- Membrane Vesicle Production as a Bacterial Defense Against Stress
 Negar Mozaheb, Marie-Paule Mingeot-Leclercq
 Frontiers in Microbiology.2020;[Epub]     CrossRef
- Extracellular Vesicles: An Overlooked Secretion System in Cyanobacteria
 Steeve Lima, Jorge Matinha-Cardoso, Paula Tamagnini, Paulo Oliveira
 Life.2020; 10(8): 129.     CrossRef
- The Outer Membrane Proteins OmpA, CarO, and OprD of Acinetobacter baumannii Confer a Two-Pronged Defense in Facilitating Its Success as a Potent Human Pathogen
 Siva R. Uppalapati, Abhiroop Sett, Ranjana Pathania
 Frontiers in Microbiology.2020;[Epub]     CrossRef
- Microevolution in the major outer membrane protein OmpA of Acinetobacter baumannii
         
 Alejandro M. Viale, Benjamin A. Evans
 Microbial Genomics
.2020;[Epub]     CrossRef
- Small RNAs in Outer Membrane Vesicles and Their Function in Host-Microbe Interactions
 Sara Ahmadi Badi, Stefania Paola Bruno, Arfa Moshiri, Samira Tarashi, Seyed Davar Siadat, Andrea Masotti
 Frontiers in Microbiology.2020;[Epub]     CrossRef
- Engineered Bacterial Outer Membrane Vesicles as Multifunctional Delivery Platforms
 Ruizhen Li, Qiong Liu
 Frontiers in Materials.2020;[Epub]     CrossRef
- Outer Membrane Lipid Secretion and the Innate Immune Response to Gram-Negative Bacteria
 Nicole P. Giordano, Melina B. Cian, Zachary D. Dalebroux, Anthony R. Richardson
 Infection and Immunity.2020;[Epub]     CrossRef
- The Role of Bacterial Membrane Vesicles in the Dissemination of Antibiotic Resistance and as Promising Carriers for Therapeutic Agent Delivery
 Md Jalal Uddin, Jirapat Dawan, Gibeom Jeon, Tao Yu, Xinlong He, Juhee Ahn
 Microorganisms.2020; 8(5): 670.     CrossRef
- The Mutation of Conservative Asp268 Residue in the Peptidoglycan-Associated Domain of the OmpA Protein Affects Multiple Acinetobacter baumannii Virulence Characteristics
 Jūratė Skerniškytė, Emilija Karazijaitė, Julien Deschamps, Renatas Krasauskas, Romain Briandet, Edita Sužiedėlienė
 Molecules.2019; 24(10): 1972.     CrossRef
- Role of OmpA1 and OmpA2 in Aggregatibacter actinomycetemcomitans and Aggregatibacter aphrophilus serum resistance
 Mark Lindholm, Kyaw Min Aung, Sun Nyunt Wai, Jan Oscarsson
 Journal of Oral Microbiology.2019; 11(1): 1536192.     CrossRef
- Studies on the mechanism of multidrug resistance of Acinetobacter baumannii by proteomic analysis of the outer membrane vesicles of the bacterium
 Bina Agarwal, Raman Karthikeyan, P. Gayathri, B. RameshBabu, G. Ahmed, M. V. Jagannadham
 Journal of Proteins and Proteomics.2019; 10(1): 1.     CrossRef
- Toll-Like Receptors 2 and 4 Modulate Pulmonary Inflammation and Host Factors Mediated by Outer Membrane Vesicles Derived from Acinetobacter baumannii
 Chad R. Marion, Jaewook Lee, Lokesh Sharma, Kyong-Su Park, Changjin Lee, Wei Liu, Pei Liu, Jingjing Feng, Yong Song Gho, Charles S. Dela Cruz, Vincent B. Young
 Infection and Immunity.2019;[Epub]     CrossRef
- The sensor kinase BfmS controls production of outer membrane vesicles in Acinetobacter baumannii
 Se Yeon Kim, Mi Hyun Kim, Seung Il Kim, Joo Hee Son, Shukho Kim, Yoo Chul Lee, Minsang Shin, Man Hwan Oh, Je Chul Lee
 BMC Microbiology.2019;[Epub]     CrossRef
- The Mechanisms of Disease Caused by Acinetobacter baumannii
 Faye C. Morris, Carina Dexter, Xenia Kostoulias, Muhammad Ikhtear Uddin, Anton Y. Peleg
 Frontiers in Microbiology.2019;[Epub]     CrossRef
- Human pleural fluid triggers global changes in the transcriptional landscape of Acinetobacter baumannii as an adaptive response to stress
 Jasmine Martinez, Jennifer S. Fernandez, Christine Liu, Amparo Hoard, Anthony Mendoza, Jun Nakanouchi, Nyah Rodman, Robert Courville, Marisel R. Tuttobene, Carolina Lopez, Lisandro J. Gonzalez, Parvin Shahrestani, Krisztina M. Papp-Wallace, Alejandro J. V
 Scientific Reports.2019;[Epub]     CrossRef
- Synergistic activity of an OmpA inhibitor and colistin against colistin-resistant Acinetobacter baumannii: mechanistic analysis and in vivo efficacy
 Raquel Parra-Millán, Xavier Vila-Farrés, Rafael Ayerbe-Algaba, Monica Varese, Viviana Sánchez-Encinales, Nuría Bayó, María Eugenia Pachón-Ibáñez, Meritxell Teixidó, Jordi Vila, Jerónimo Pachón, Ernest Giralt, Younes Smani
 Journal of Antimicrobial Chemotherapy.2018;[Epub]     CrossRef
- 
            Acinetobacter
            : an emerging pathogen with a versatile secretome
          
 Noha M. Elhosseiny, Ahmed S. Attia
 Emerging Microbes & Infections.2018; 7(1): 1.     CrossRef
- Gram-negative bacterial membrane vesicle release in response to the host-environment: different threats, same trick?
 Charlotte Volgers, Paul H. M. Savelkoul, Frank R. M. Stassen
 Critical Reviews in Microbiology.2018; 44(3): 258.     CrossRef
- Versatile effects of bacterium-released membrane vesicles on mammalian cells and infectious/inflammatory diseases
 You-jiang Yu, Xiao-hong Wang, Guo-Chang Fan
 Acta Pharmacologica Sinica.2018; 39(4): 514.     CrossRef
- Tug of war betweenAcinetobacter baumanniiand host immune responses
 Fei-Ju Li, Lora Starrs, Gaetan Burgio
 Pathogens and Disease.2018;[Epub]     CrossRef
- Outer Membrane Vesicles (OMVs) of Gram-negative Bacteria: A Perspective Update
 Arif Tasleem Jan
 Frontiers in Microbiology.2017;[Epub]     CrossRef
- The Secrets of Acinetobacter Secretion
 Brent S. Weber, Rachel L. Kinsella, Christian M. Harding, Mario F. Feldman
 Trends in Microbiology.2017; 25(7): 532.     CrossRef
- Biology of Acinetobacter baumannii: Pathogenesis, Antibiotic Resistance Mechanisms, and Prospective Treatment Options
 Chang-Ro Lee, Jung Hun Lee, Moonhee Park, Kwang Seung Park, Il Kwon Bae, Young Bae Kim, Chang-Jun Cha, Byeong Chul Jeong, Sang Hee Lee
 Frontiers in Cellular and Infection Microbiology.2017;[Epub]     CrossRef
- 
            LPS Remodeling Triggers Formation of Outer Membrane Vesicles in
            Salmonella
          
 Wael Elhenawy, Michael Bording-Jorgensen, Ezequiel Valguarnera, M. Florencia Haurat, Eytan Wine, Mario F. Feldman, John J. Mekalanos
 mBio.2016;[Epub]     CrossRef
- Pangenome and immuno-proteomics analysis of Acinetobacter baumannii strains revealed the core peptide vaccine targets
 Afreenish Hassan, Anam Naz, Ayesha Obaid, Rehan Zafar Paracha, Kanwal Naz, Faryal Mehwish Awan, Syed Aun Muhmmad, Hussnain Ahmed Janjua, Jamil Ahmad, Amjad Ali
 BMC Genomics.2016;[Epub]     CrossRef
- Proteomic profiling of Gram‐negative bacterial outer membrane vesicles: Current perspectives
 Jaewook Lee, Oh Youn Kim, Yong Song Gho
 PROTEOMICS – Clinical Applications.2016; 10(9-10): 897.     CrossRef
- Outer membrane Protein A plays a role in pathogenesis ofAcinetobacter nosocomialis
 Sang Woo Kim, Man Hwan Oh, So Hyun Jun, Hyejin Jeon, Seung Il Kim, Kwangho Kim, Yoo Chul Lee, Je Chul Lee
 Virulence.2016; 7(4): 413.     CrossRef
- Bacterial membrane vesicles: Biogenesis, immune regulation and pathogenesis
 Rishi D. Pathirana, Maria Kaparakis-Liaskos
 Cellular Microbiology.2016; 18(11): 1518.     CrossRef
- Membrane Vesicles Released by a hypervesiculating Escherichia coli Nissle 1917 tolR Mutant Are Highly Heterogeneous and Show Reduced Capacity for Epithelial Cell Interaction and Entry
 Carla Pérez-Cruz, María-Alexandra Cañas, Rosa Giménez, Josefa Badia, Elena Mercade, Laura Baldomà, Laura Aguilera, Maria Kaparakis-Liaskos
 PLOS ONE.2016; 11(12): e0169186.     CrossRef
- Outer membrane vesicles of Lysobacter sp. XL1: biogenesis, functions, and applied prospects
 Irina V. Kudryakova, Nina A. Shishkova, Natalia V. Vasilyeva
 Applied Microbiology and Biotechnology.2016; 100(11): 4791.     CrossRef
- Immunization with a 22-kDa outer membrane protein elicits protective immunity to multidrug-resistant Acinetobacter baumannii
 Weiwei Huang, Yufeng Yao, Shijie Wang, Ye Xia, Xu Yang, Qiong Long, Wenjia Sun, Cunbao Liu, Yang Li, Xiaojie Chu, Hongmei Bai, Yueting Yao, Yanbing Ma
 Scientific Reports.2016;[Epub]     CrossRef
- Bacterial outer membrane vesicles: New insights and applications
 Deepak Anand, Arunima Chaudhuri
 Molecular Membrane Biology.2016; 33(6-8): 125.     CrossRef
- Pathogenic Acinetobacter: from the Cell Surface to Infinity and Beyond
 Brent S. Weber, Christian M. Harding, Mario F. Feldman, W. Margolin
 Journal of Bacteriology.2016; 198(6): 880.     CrossRef
- Biogenesis ofLysobactersp. XL1 vesicles
 Irina V. Kudryakova, Natalia E. Suzina, Natalia V. Vasilyeva, Klaus Hantke
 FEMS Microbiology Letters.2015; 362(18): fnv137.     CrossRef
- Roles of bacterial membrane vesicles
 Eric Daniel Avila-Calderón, Minerva Georgina Araiza-Villanueva, Juan Carlos Cancino-Diaz, Edgar Oliver López-Villegas, Nammalwar Sriranganathan, Stephen M. Boyle, Araceli Contreras-Rodríguez
 Archives of Microbiology.2015; 197(1): 1.     CrossRef
- Outer-membrane vesicles from Gram-negative bacteria: biogenesis and functions
 Carmen Schwechheimer, Meta J. Kuehn
 Nature Reviews Microbiology.2015; 13(10): 605.     CrossRef
- OmpA Binding Mediates the Effect of Antimicrobial Peptide LL-37 on Acinetobacter baumannii
 Ming-Feng Lin, Pei-Wen Tsai, Jeng-Yi Chen, Yun-You Lin, Chung-Yu Lan, Surajit Bhattacharjya
 PLOS ONE.2015; 10(10): e0141107.     CrossRef
- Bacterial outer membrane nanovesicles: Structure, biogenesis, functions, and application in biotechnology and medicine (Review)
 K. A. Lusta
 Applied Biochemistry and Microbiology.2015; 51(5): 485.     CrossRef
- Outer membrane vesicles as platform vaccine technology
 Leo van der Pol, Michiel Stork, Peter van der Ley
 Biotechnology Journal.2015; 10(11): 1689.     CrossRef
- Modulation of bacterial outer membrane vesicle production by envelope structure and content
 Carmen Schwechheimer, Adam Kulp, Meta J Kuehn
 BMC Microbiology.2014;[Epub]     CrossRef
- Gene Transfer Potential of Outer Membrane Vesicles of Acinetobacter baylyi and Effects of Stress on Vesiculation
 Shweta Fulsundar, Klaus Harms, Gøril E. Flaten, Pål J. Johnsen, Balu Ananda Chopade, Kaare M. Nielsen, M. Kivisaar
 Applied and Environmental Microbiology.2014; 80(11): 3469.     CrossRef
- Acinetobacter baumannii Outer Membrane Vesicles Elicit a Potent Innate Immune Response via Membrane Proteins
 So Hyun Jun, Jung Hwa Lee, Bo Ra Kim, Seung Il Kim, Tae In Park, Je Chul Lee, Yoo Chul Lee, Özlem Yilmaz
 PLoS ONE.2013; 8(8): e71751.     CrossRef
- Molecular paleontology and complexity in the last eukaryotic common ancestor
 V. Lila Koumandou, Bill Wickstead, Michael L. Ginger, Mark van der Giezen, Joel B. Dacks, Mark C. Field
 Critical Reviews in Biochemistry and Molecular Biology.2013; 48(4): 373.     CrossRef
- Host-microbe interactions that shape the pathogenesis ofAcinetobacter baumanniiinfection
 Brittany L. Mortensen, Eric P. Skaar
 Cellular Microbiology.2012; 14(9): 1336.     CrossRef