Genotypic and phenotypic changes of Staphylococcus epidermidis during relapse episodes in prosthetic joint infections

被引:6
作者
Ortega-Pena, Silvestre [1 ,2 ]
Franco-Cendejas, Rafael [1 ]
Aquino-Andrade, Alejandra [3 ]
Betanzos-Cabrera, Gabriel [4 ,5 ]
Sharma, Ashutosh [4 ]
Rodriguez-Martinez, Sandra [2 ]
Cancino-Diaz, Mario E. [2 ]
Carlos Cancino-Diaz, Juan [2 ]
机构
[1] Inst Nacl Rehabil Luis Guillermo Ibarra Ibarra, Lab Infectol, Mexico City 11340, DF, Mexico
[2] Inst Politecn Nacl, Microbiol & Immunol Dept, Escuela Nacl Ciencias Biol, Carpio & Plan Ayala S-N, Mexico City, DF, Mexico
[3] Inst Nacl Pediat, Lab Mol Microbiol, Mexico City, DF, Mexico
[4] Tecnol Monterrey, Sch Engn & Sci, Campus Queretaro, Queretaro, Mexico
[5] Univ Autonoma Estado Hidalgo, Inst Ciencias Salud, Rea Acad Nutr & Toxicol Clin, Pachuca, Hidalgo, Mexico
关键词
Staphylococcus epidermidis; Prosthetic joint infection; Relapse; Biofilm; Clone; Subclone; SMALL-COLONY VARIANTS; MOLECULAR-BASIS; AUREUS; RESISTANCE; ADHERENCE; PATTERNS; ADHESION; GENES;
D O I
10.1007/s42770-019-00190-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Staphylococcus epidermidis is a coagulase-negative bacterium capable of causing recurrent relapses in prosthetic joint infection (PJI). The aim of this study was to determine if Staphylococcus epidermidis isolates from patients with recurrent relapses of prosthetic joint infection (PJI) changed genotypically (pulsed-field gel electrophoresis (PFGE) pattern analysis and genes involved in biofilm formation) and phenotypically (antimicrobial resistance, biofilm formation) during the different episodes. Four patients with PJI recurrent relapses were evaluated clinically and microbiologically. Genotypic and phenotypic characteristics of 31 S. epidermidis isolates were determined. In all cases, PJI was treated with antimicrobial therapy and resection of the prosthesis without reimplantation. Months later, all patients had a relapse episode and treated with rifampin plus vancomycin and surgical debridement. Changes in the antibiotics resistance profile in isolates from patients 1 and 2 were observed in the two episodes. Patient 1 had four clones A, B, C, and D that were distributed differentially in the two episodes. Similarly, patients 2 and 3 had two clones and subclones (E-E1 and F-F1, respectively), and patient 4 had only the clone G in both episodes. The clone F formed small-colony variants (SCVs). High level of biofilm formation was found in all clones, except for clones D and G. Clones/subclones showed a genotypic variation in icaA, sdrF, bap, sesI, and embp genes. The principal coordinate analysis showed that all clones/subclones were different. These results showed that the initial infective clone of S. epidermidis from PJI, changed genotypically and phenotypically after a second relapse as a response to the treatment.
引用
收藏
页码:601 / 612
页数:12
相关论文
共 41 条
[1]   Prosthetic Joint Infections: an Update [J].
Abad, C. L. ;
Haleem, A. .
CURRENT INFECTIOUS DISEASE REPORTS, 2018, 20 (07)
[2]  
[Anonymous], 2017, M100S22 CLSI
[3]   Coagulase-Negative Staphylococci Pathogenomics [J].
Argemi, Xavier ;
Hansmann, Yves ;
Prola, Kevin ;
Prevost, Gilles .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (05)
[4]   An invasive marker Staphylococcus epidermidis surface protein I (SesI) harboured by a ST239 methicillin-resistant Staphylococcus aureus [J].
Bakthavatchalam, Yamuna Devi ;
Arumugam, Amala ;
Veeraraghavan, Balaji .
JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE, 2019, 18 :122-125
[5]   Characterization of Staphylococcus epidermidis and Staphyloccocus warneri small-colony variants associated with prosthetic-joint infections [J].
Bogut, Agnieszka ;
Niedzwiadek, Justyna ;
Koziol-Montewka, Maria ;
Strzelec-Nowak, Dagmara ;
Blacha, Jan ;
Mazurkiewicz, Tomasz ;
Marczynski, Wojciech ;
Plewik, Dorota .
JOURNAL OF MEDICAL MICROBIOLOGY, 2014, 63 :176-185
[6]   Pathogenic Mechanisms and Host Interactions in Staphylococcus epidermidis Device-Related Infection [J].
Bresco, Marina Sabate ;
Harris, Llinos G. ;
Thompson, Keith ;
Stanic, Barbara ;
Morgenstern, Mario ;
O'Mahony, Liam ;
Richards, R. Geoff ;
Moriarty, T. Fintan .
FRONTIERS IN MICROBIOLOGY, 2017, 8
[7]   ADHERENCE OF COAGULASE-NEGATIVE STAPHYLOCOCCI TO PLASTIC TISSUE-CULTURE PLATES - A QUANTITATIVE MODEL FOR THE ADHERENCE OF STAPHYLOCOCCI TO MEDICAL DEVICES [J].
CHRISTENSEN, GD ;
SIMPSON, WA ;
YOUNGER, JJ ;
BADDOUR, LM ;
BARRETT, FF ;
MELTON, DM ;
BEACHEY, EH .
JOURNAL OF CLINICAL MICROBIOLOGY, 1985, 22 (06) :996-1006
[8]   The giant extracellular matrix-binding protein of Staphylococcus epidermidis mediates biofilm accumulation and attachment to fibronectin [J].
Christner, Martin ;
Franke, Gefion C. ;
Schommer, Nina N. ;
Wendt, Ulrike ;
Wegert, Kim ;
Pehle, Philip ;
Kroll, Gesche ;
Schulze, Christian ;
Buck, Friedrich ;
Mack, Dietrich ;
Aepfelbacher, Martin ;
Rohde, Holger .
MOLECULAR MICROBIOLOGY, 2010, 75 (01) :187-207
[9]   Clonal dissemination of epidemic methicillin-resistant Staphylococcus aureus in Belgium and neighboring countries [J].
Deplano, A ;
Witte, W ;
Van Leeuwen, WJ ;
Brun, Y ;
Struelens, MJ .
CLINICAL MICROBIOLOGY AND INFECTION, 2000, 6 (05) :239-245
[10]   Biofilm formation by ica-positive and ica-negative strains of Staphylococcus epidermidis in vitro [J].
Dice, Bethany ;
Stoodley, P. ;
Buchinsky, Farrel ;
Metha, Nalini ;
Ehrlich, Garth D. ;
Hu, Fen Z. .
BIOFOULING, 2009, 25 (04) :367-375