Journal Article
- Phenotypic and genotypic correlates of daptomycin-resistant methicillin-susceptible Staphylococcus aureus clinical isolates
-
Kyoung-Mi Kang , Nagendra N. Mishra , Kun Taek Park , Gi-Yong Lee , Yong Ho Park , Arnold S. Bayer , Soo-Jin Yang
-
J. Microbiol. 2017;55(2):153-159. Published online January 26, 2017
-
DOI: https://doi.org/10.1007/s12275-017-6509-1
-
-
46
View
-
0
Download
-
22
Crossref
-
Abstract
-
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
Research Support, Non-U.S. Gov'ts
- NOTE] Next-Generation Sequencing-Based Genome-Wide Mutation Analysis of L-Lysine-Producing Corynebacterium glutamicum ATCC 21300 Strain
-
Chang-Soo Lee , Jae-Young Nam , Eun-Suk Son , O-chul Kwon , Woorijarang Han , Jae-Yong Cho , Young-Jin Park
-
J. Microbiol. 2012;50(5):860-863. Published online November 4, 2012
-
DOI: https://doi.org/10.1007/s12275-012-2109-2
-
-
30
View
-
0
Download
-
13
Scopus
-
Abstract
-
In order to identify single nucleotide polymorphism and insertion/deletion mutations, we performed whole-genome re-sequencing of the enhanced L-lysine-producing Corynebacterium glutamicum ATCC 21300 strain. In total, 142 single nucleotide polymorphisms and 477 insertion/deletion mutations were identified in the ATCC 21300 strain when compared to 3,434 predicted genes of the wild-type C. glutamicum ATCC 13032 strain. Among them, 110 transitions and 29 transversions of single nucleotide polymorphisms were found from genes of the ATCC 21300 strain. In addition, 11 genes, involved in the L-lysine biosynthetic pathway and central carbohydrate metabolism, contained mutations including single nucleotide polymorphisms and insertions/deletions. Interestingly, RT-PCR analysis of these 11 genes indicated that they were normally expressed in the ATCC 21300 strain. This information of genome-wide gene-associated variations will be useful for genome breeding of C. glutamicum in order to develop an industrial amino acidproducing strain with minimal mutation.
- Characterization of a Baculovirus Newly Isolated from the Tea Slug Moth, Iragoidae fasciata
-
Li-Rong Yang , Xiao Qiang , Bao-Qin Zhang , Mei-Jun Tang , Chuan-Xi Zhang
-
J. Microbiol. 2009;47(2):208-213. Published online May 2, 2009
-
DOI: https://doi.org/10.1007/s12275-008-0253-5
-
-
36
View
-
0
Download
-
4
Crossref
-
Abstract
-
The tea slug moth Iragoidae fasciata (Lepidoptera, Eucleidae) is one of the main insect pests that attack tea bushes. A new nucleopolyhedrovirus (NPV) called Iragoidae fasciata NPV (IrfaNPV) was recently isolated from diseased larvae. An 11,626 bp fragment of the viral genomic DNA containing the polyhedrin gene and other 12 genes was cloned and sequenced. Gene comparison and phylogenetic analysis showed that IrfaNPV is a member of the Group I NPVs. However, the genomic organization of IrfaNPV is highly distinct. In addition, electron microscopy analysis showed that IrfaNPV is a single nucleocapsid NPV (SNPV). An inoculation assay showed that IrfaNPV is semi-permissive in the Trichoplusia ni cell line Tn-5B1-4. Bioassays on lethal concentration (LC50) and lethal time (LT50) were conducted to test the susceptibility of I. fasciata larvae to the virus.
-
Citations
Citations to this article as recorded by

- Granulovirus GP37 Facilitated ODVs Cross Insect Peritrophic Membranes and Fuse with Epithelia
Xiangyang Liu, Wei Fang, Rui Fan, Linna Zhang, Chengfeng Lei, Jingjing Zhang, Wenkai Nian, Tao Dou, Shiheng An, Lin Zhou, Xiulian Sun
Toxins.2019; 11(3): 145. CrossRef - Microbial management of arthropod pests of tea: current state and prospects
Somnath Roy, Narayanannair Muraleedharan
Applied Microbiology and Biotechnology.2014; 98(12): 5375. CrossRef - Molecular Characterization of a Nucleopolyhedrovirus Newly Isolated from Ophiusa disjungens in China
Tong Lin, Li Liu, Runlei Chang, Guojun Lang, Wen Xu
Indian Journal of Virology.2012; 23(3): 379. CrossRef - Synergistic effects of Cydia pomonella granulovirus GP37 on the infectivity of nucleopolyhedroviruses and the lethality of Bacillus thuringiensis
Xiangyang Liu, Xiaohe Ma, Chengfeng Lei, Yuzhou Xiao, Zhongxin Zhang, Xiulian Sun
Archives of Virology.2011; 156(10): 1707. CrossRef