Genome-Wide Analysis of Staphylococcus aureus Sequence Type 72 Isolates Provides Insights Into Resistance Against Antimicrobial Agents and Virulence Potential

被引:13
作者
Batool, Nayab [1 ]
Shamim, Amen [1 ]
Chaurasia, Akhilesh Kumar [1 ,2 ]
Kim, Kyeong Kyu [1 ,2 ,3 ]
机构
[1] Sungkyunkwan Univ, Dept Precis Med, Sch Med, Suwon, South Korea
[2] Sungkyunkwan Univ SKKU, Inst Antimicrobial Resistance & Therapeut IAMRT, Suwon, South Korea
[3] Sungkyunkwan Univ, Samsung Adv Inst Hlth Sci & Technol SAIHST, Samsung Med Ctr SMC, Sch Med, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Staphylococcus aureus; sequence type 72; antibiotics resistance; virulence factors; subtractive genomics; CATABOLIC MOBILE ELEMENT; REGULATED VIRULENCE; GALLERIA-MELLONELLA; COMMUNITY; GENES; CLONE; MECHANISMS; EXPRESSION; MACROLIDE; USA300;
D O I
10.3389/fmicb.2020.613800
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus aureus sequence type 72 (ST72) is a major community-associated (CA) methicillin-resistant Staphylococcus aureus (MRSA) that has rapidly entered the hospital setting in Korea, causing mild superficial skin wounds to severe bloodstream infections. In this study, we sequenced and analyzed the genomes of one methicillin-resistant human isolate and one methicillin-sensitive human isolate of ST72 from Korea, K07-204 and K07-561, respectively. We used a subtractive genomics approach to compare these two isolates to other 27 ST72 isolates to investigate antimicrobial resistance (AMR) and virulence potential. Furthermore, we validated genotypic differences by phenotypic characteristics analysis. Comparative and subtractive genomics analysis revealed that K07-204 contains methicillin (mecA), ampicillin (blaZ), erythromycin (ermC), aminoglycoside (aadD), and tetracycline (tet38, tetracycline efflux pump) resistance genes while K07-561 has ampicillin (blaZ) and tetracycline (tet38) resistance genes. In addition to antibiotics, K07-204 was reported to show resistance to lysostaphin treatment. K07-204 also has additional virulence genes (adsA, aur, hysA, icaABCDR, lip, lukD, sdrC, and sdrE) compared to K07-561, which may explain the differential virulence potential of these human isolates of ST72. Unexpectedly, the virulence potential of K07-561 was higher in an in vivo wax-worm infection model than that of K07-204, putatively due to the presence of a 20-fold higher staphyloxanthin concentration than K07-204. Comprehensive genomic analysis of these two human isolates, with 27 ST72 isolates, and S. aureus USA300 (ST8) suggested that acquisition of both virulence and antibiotics resistance genes by ST72 isolates might have facilitated their adaptation from a community to a hospital setting where the selective pressure imposed by antibiotics selects for more resistant and virulent isolates. Taken together, the results of the current study provide insight into the genotypic and phenotypic features of various ST72 clones across the globe, delivering more options for developing therapeutics and rapid molecular diagnostic tools to detect resistant bacteria.
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页数:12
相关论文
共 68 条
[1]   Glyceryl trinitrate blocks staphyloxanthin and biofilm formation in Staphylococcus aureus [J].
Abbas, Hisham A. ;
Elsherbini, Ahmed M. ;
Shaldam, Moutaz A. .
AFRICAN HEALTH SCIENCES, 2019, 19 (01) :1376-1384
[2]   Genotypes, Exotoxin Gene Content, and Antimicrobial Resistance of Staphylococcus aureus Strains Recovered from Foods and Food Handlers [J].
Argudin, M. A. ;
Mendoza, M. C. ;
Gonzalez-Hevia, M. A. ;
Bances, M. ;
Guerra, B. ;
Rodicio, M. R. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2012, 78 (08) :2930-2935
[3]   Draft Genome Sequences of Lysostaphin-Resistant (K07-204) and Lysostaphin-Susceptible (K07-561) Staphylococcus aureus Sequence Type 72 Strains Isolated from Patients in South Korea [J].
Batool, Nayab ;
Ko, Kwan Soo ;
Chaurasia, Akhilesh Kumar ;
Kim, Kyeong Kyu .
MICROBIOLOGY RESOURCE ANNOUNCEMENTS, 2020, 9 (49)
[4]   Functional Identification of Serine Hydroxymethyltransferase as a Key Gene Involved in Lysostaphin Resistance and Virulence Potential of Staphylococcus aureus Strains [J].
Batool, Nayab ;
Ko, Kwan Soo ;
Chaurasia, Akhilesh Kumar ;
Kim, Kyeong Kyu .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (23) :1-20
[5]   Molecular mechanisms of antibiotic resistance [J].
Blair, Jessica M. A. ;
Webber, Mark A. ;
Baylay, Alison J. ;
Ogbolu, David O. ;
Piddock, Laura J. V. .
NATURE REVIEWS MICROBIOLOGY, 2015, 13 (01) :42-51
[6]   Absence of Protein A Expression Is Associated With Higher Capsule Production in Staphylococcal Isolates [J].
Brignoli, Tarcisio ;
Manetti, Andrea G. O. ;
Rosini, Roberto ;
Haag, Andreas F. ;
Scarlato, Vincenzo ;
Bagnoli, Fabio ;
Delany, Isabel .
FRONTIERS IN MICROBIOLOGY, 2019, 10
[7]   LYSOSTAPHIN - ENZYMATIC MODE OF ACTION [J].
BROWDER, HP ;
ZYGMUNT, WA ;
YOUNG, JR ;
TAVORMIN.PA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1965, 19 (03) :383-&
[8]   4',4'' ADENYLTRANSFERASE ACTIVITY ON CONJUGATIVE PLASMIDS ISOLATED FROM STAPHYLOCOCCUS-AUREUS IS ENCODED ON AN INTEGRATED COPY OF PUB110 [J].
BYRNE, ME ;
GILLESPIE, MT ;
SKURRAY, RA .
PLASMID, 1991, 25 (01) :70-75
[9]   Phylogenomic Classification and the Evolution of Clonal Complex 5 Methicillin-Resistant Staphylococcus aureus in the Western Hemisphere [J].
Challagundla, Lavanya ;
Reyes, Jinnethe ;
Rafiqullah, Iftekhar ;
Sordelli, Daniel O. ;
Echaniz-Aviles, Gabriela ;
Velazquez-Meza, Maria E. ;
Castillo-Ramirez, Santiago ;
Fittipaldi, Nahuel ;
Feldgarden, Michael ;
Chapman, Sinead B. ;
Calderwood, Michael S. ;
Carvajal, Lina P. ;
Rincon, Sandra ;
Hanson, Blake ;
Planet, Paul J. ;
Arias, Cesar A. ;
Diaz, Lorena ;
Robinson, D. Ashley .
FRONTIERS IN MICROBIOLOGY, 2018, 9
[10]  
Chen FF, 2016, NAT CHEM BIOL, V12, P174, DOI [10.1038/NCHEMBIO.2003, 10.1038/nchembio.2003]