A full genomic characterization of the development of a stable Small Colony Variant cell-type by a clinical Staphylococcus aureus strain

被引:30
作者
Bui, Long M. G. [1 ]
Kidd, Stephen P. [1 ]
机构
[1] Univ Adelaide, Dept Mol & Cellular Biol, Res Ctr Infect Dis, Adelaide, SA 5005, Australia
关键词
Staphylococcus aureus; Small Colony Variants; Whole genome sequencing; Methylome; Persister cells; MOBILE GENETIC ELEMENTS; SIGMA-FACTOR SIGMA(B); BIOFILM FORMATION; SUBSYSTEMS TECHNOLOGY; RECURRENT INFECTIONS; GLOBAL REGULATOR; BACTERIAL-GROWTH; VIRULENCE GENES; FUNCTIONAL RSBU; HEMB MUTANTS;
D O I
10.1016/j.meegid.2015.10.011
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A key to persistent and recurrent Staphylococcus aureus infections is its ability to adapt to diverse and toxic conditions. This ability includes a switch into a biofilm or to the quasi-dormant Small Colony Variant (SCV). The development and molecular attributes of SCVs have been difficult to study due to their rapid reversion to their parental cell-type. We recently described the unique induction of a matrix-embedded and stable SCV cell-type in a clinical S. aureus strain (WCH-SK2) by growing the cells with limiting conditions for a prolonged timeframe. Here we further study their characteristics. They possessed an increased viability in the presence of antibiotics compared to their non-SCV form. Their stability implied that there had been genetic changes; we therefore determined both the genome sequence of WCH-SK2 and its stable SCV format a single base resolution, employing Single Molecular Real-Time (SMRT) sequencing that enabled the methylome to also be determined. The genetic features of WCH-SK2 have been identified; the SCCmec type, the pathogenicity and genetic islands and virulence factors. The genetic changes that had occurred in the stable SCV form were identified; most notably being in MgrA, a global regulator, and RsbU, a phosphoserine phosphatase within the regulatory pathway of the sigma factor SigB. There was a shift in the methylomes of the non-SCV and stable SCV forms. We have also shown a similar induction of this cell-type in other S. aureus strains and performed a genetic comparison to these and other S. aureus genomes. We additionally map RNAseq data to the WCH-SK2 genome in a transcriptomic analysis of the parental, SCV and stable SCV cells. The results from this study represent the unique identification of a suite of epigenetic, genetic and transcriptional factors that are implicated in the switch in S. aureus to its persistent SCV form. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:345 / 355
页数:11
相关论文
共 90 条
[1]   Augmented expression of polysaccharide intercellular adhesin in a defined Staphylococcus epidermidis mutant with the small-colony-variant phenotype [J].
Al Laham, Nahed ;
Rohde, Holger ;
Sander, Gunnar ;
Fischer, Andreas ;
Hussain, Muzaffar ;
Heilmann, Christine ;
Mack, Dietrich ;
Proctor, Richard ;
Peters, Georg ;
Becker, Karsten ;
von Eiff, Christof .
JOURNAL OF BACTERIOLOGY, 2007, 189 (12) :4494-4501
[2]   Mutational analysis of MarR, the negative regulator of marRAB expression in Escherichia coli, suggests the presence of two regions required for DNA binding [J].
Alekshun, MN ;
Kim, YS ;
Levy, SB .
MOLECULAR MICROBIOLOGY, 2000, 35 (06) :1394-1404
[3]   Staphylococcus aureus mobile genetic elements [J].
Alibayov, Babek ;
Baba-Moussa, Lamine ;
Sina, Haziz ;
Zdenkova, Kamila ;
Demnerova, Katerina .
MOLECULAR BIOLOGY REPORTS, 2014, 41 (08) :5005-5018
[4]   BLAST Ring Image Generator (BRIG): simple prokaryote genome comparisons [J].
Alikhan, Nabil-Fareed ;
Petty, Nicola K. ;
Ben Zakour, Nouri L. ;
Beatson, Scott A. .
BMC GENOMICS, 2011, 12
[5]  
Atalla Heba, 2011, Animal Health Research Reviews, V12, P33, DOI 10.1017/S1466252311000065
[6]   The RAST server: Rapid annotations using subsystems technology [J].
Aziz, Ramy K. ;
Bartels, Daniela ;
Best, Aaron A. ;
DeJongh, Matthew ;
Disz, Terrence ;
Edwards, Robert A. ;
Formsma, Kevin ;
Gerdes, Svetlana ;
Glass, Elizabeth M. ;
Kubal, Michael ;
Meyer, Folker ;
Olsen, Gary J. ;
Olson, Robert ;
Osterman, Andrei L. ;
Overbeek, Ross A. ;
McNeil, Leslie K. ;
Paarmann, Daniel ;
Paczian, Tobias ;
Parrello, Bruce ;
Pusch, Gordon D. ;
Reich, Claudia ;
Stevens, Rick ;
Vassieva, Olga ;
Vonstein, Veronika ;
Wilke, Andreas ;
Zagnitko, Olga .
BMC GENOMICS, 2008, 9 (1)
[7]   SdrC induces staphylococcal biofilm formation through a homophilic interaction [J].
Barbu, E. Magda ;
Mackenzie, Chris ;
Foster, Timothy J. ;
HoeoeK, Magnus .
MOLECULAR MICROBIOLOGY, 2014, 94 (01) :172-185
[8]   Comparative Genome Sequencing of an Isogenic Pair of USA800 Clinical Methicillin-Resistant Staphylococcus aureus Isolates Obtained before and after Daptomycin Treatment Failure [J].
Boyle-Vavra, Susan ;
Jones, Marcus ;
Gourley, Brett L. ;
Holmes, Michael ;
Ruf, Rebecca ;
Balsam, Ashley R. ;
Boulware, David R. ;
Kline, Susan ;
Jawahir, Selina ;
DeVries, Aaron ;
Peterson, Scott N. ;
Daum, Robert S. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (05) :2018-2025
[9]   Contribution of glutathione peroxidase to the virulence of Streptococcus pyogenes [J].
Brenot, A ;
King, KY ;
Janowiak, B ;
Griffith, O ;
Caparon, MG .
INFECTION AND IMMUNITY, 2004, 72 (01) :408-413
[10]   The induction of Staphylococcus aureus biofilm formation or Small Colony Variants is a strain-specific response to host-generated chemical stresses [J].
Bui, Long M. G. ;
Turnidge, John D. ;
Kidd, Stephen P. .
MICROBES AND INFECTION, 2015, 17 (01) :77-82