共 50 条
Emergence of a mupirocin-resistant, methicillin-susceptible Staphylococcus aureus clone associated with skin and soft tissue infections in Greece
被引:2
|作者:
Giormezis, Nikolaos
[1
,2
]
Doudoulakakis, Anastassios
[3
]
Tsilipounidaki, Katerina
[4
]
Militsopoulou, Maria
[5
]
Kalogeras, George
[3
]
Stamouli, Vasiliki
[5
]
Kolonitsiou, Fevronia
[1
]
Petinaki, Efthimia
[4
]
Lebessi, Evangelia
[3
]
Spiliopoulou, Iris
[1
,2
]
机构:
[1] Univ Patras, Sch Med, Dept Microbiol, Patras 26504, Greece
[2] Univ Patras, Natl Reference Lab Staphylococci, Patras, Greece
[3] Kyriakou Childrens Hosp, Dept Microbiol P&A, Athens, Greece
[4] Univ Thessaly, Sch Med, Dept Microbiol, Larisa, Greece
[5] Univ Gen Hosp Patras, Dept Microbiol, Patras, Greece
关键词:
MSSA;
SSTIs;
Mupirocin-resistant;
ST121;
Exfoliative toxins;
Greece;
VIRULENCE FACTORS;
GENES;
D O I:
10.1186/s12866-021-02272-5
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Background Staphylococcus aureus causes various infections, including skin and soft tissue infections (SSTIs). In this study, methicillin-susceptible S. aureus (MSSA) from SSTIs among patients in three tertiary-care hospitals in Greece were studied in terms of antimicrobial resistance, clonal distribution, toxin and adhesin genes carriage. Results During a five-year period (2014-2018), 6145 S. aureus were recovered from 13,244 patients with SSTIs and tested for antimicrobial susceptibility. MSSA were 4806 (78.21 %) including 1484 isolates with mupirocin minimum inhibitory concentration (MIC) > 64 mg/L (30.88 %). Two hundred and sixty representative mupirocin-resistant MSSA were analyzed for genes encoding Panton-Valentine leukocidin (PVL, lukS/lukF-PV), exfoliative toxins (eta, etb), adhesin FnbA (fnbA) and resistance genes mupA (high-level resistance to mupirocin), fusB (fusidic acid), aminoglycosides' modifying enzymes, ermA, ermC and msrA (macrolides/lincosamides) by PCRs. Strains were classified into clones by PFGE and MLST. All mupirocin-resistant MSSA were penicillin-resistant; 92.7 % expressed resistance to fusidic acid and 88.9 % to tobramycin. All 260 molecularly analyzed isolates were mupA-positive; all fusidic acid-resistant (241/260) carried fusB whereas, the tobramycin-resistant ones (230), ant(4 ')-Ia. The majority carried eta (93.85 %), etb (98.08 %) and fnbA (88.85 %). PFGE typing revealed a mostly unvarying population; 260 MSSA were grouped into three types. One major eta/etb-positive clone comprising of 258/260 strains (99.2 %), PFGE type 1, was classified as ST121, including nine strains co-carrying PVL. Another PVL-positive strain was identified as ST1, and one toxins-negative as ST21. Conclusions A mupirocin-resistant MSSA clone, ST121, carrying resistance, exfoliative toxins and adhesin genes, was spread and predominated in SSTIs from patients in Greece during the five-year studied period.
引用
收藏
页数:10
相关论文