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Molecular characterization of carbapenemases of clinical Acinetobacter baumannii-calcoaceticus complex isolates from a University Hospital in Tunisia
被引:15
|作者:
Ben Cheikh, Hadhemi
[1
,2
,3
]
Domingues, Sara
[1
,4
]
Silveira, Eduarda
[1
]
Kadri, Yosr
[3
,5
]
Rosario, Natasha
[1
]
Mastouri, Maha
[3
,5
]
Da Silva, Gabriela Jorge
[1
,4
]
机构:
[1] Univ Coimbra, Fac Pharm, Coimbra, Portugal
[2] Bizerta Carthage Univ, Fac Sci, Bizerte, Tunisia
[3] Monastirs Pharm Fac, Lab Contagious Dis & Biol Act Subst LR99 ES27, Monastir, Tunisia
[4] Univ Coimbra, Fac Pharm, Ctr Neurosci & Cell Biol CNC, Lab Microbiol, Hlth Sci Campus, P-3000548 Coimbra, Portugal
[5] Fattouma Bourguiba Univ Hosp, Lab Microbiol, Monastir, Tunisia
来源:
关键词:
Acinetobacter;
Tn125;
Epidemiology;
Carbapenemases;
Natural transformation;
Antimicrobial resistance;
BETA-LACTAMASE;
MULTIPLEX PCR;
RESISTANT;
IDENTIFICATION;
GENE;
BLA(OXA-51-LIKE);
DISSEMINATION;
BLA(NDM-1);
EMERGENCE;
IMIPENEM;
D O I:
10.1007/s13205-018-1310-3
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The aim of this study was to identify the carbapenemases from clinical carbapenem-resistant Acinetobacter baumannii-calcoaceticus complex (CRABC) isolates and to assess their potential dissemination by conjugation and natural transformation. CRABC (n=101) were collected consecutively from inpatients of the University Hospital of Monastir, Tunisia, from 2013 to 2016. Antimicrobial susceptibility was determined by the disk diffusion method and E-test. Carbapenemase-encoding genes were screened by PCR. Genotyping was performed by Pasteur MLST scheme. Isolates were resistant to all beta-lactams, fluoroquinolones and aminoglycosides while 80 and 90% were susceptible to tigecycline and colistin, respectively. Resistance and intermediate resistance to imipenem were 87 and 13%, respectively. The genes bla(OXA-24)-like, bla(OXA-58)-like, blaca(OXA143)-like, bla(OXA-48)-like, bla(VIM), bla(IMP), and bla(KPC) were not found. The bla(OXA_51)-like and bla(OXA-23)-like genes were present in 100 and 82.17% isolates, respectively. One isolate (< 1%) carried bla(NDM_1) and bla(OXA-51)-like and belonged to Sequence Type 85 (ST85). Absence of transconjugants suggests a chromosomal location of NDM-1 determinant. The bla(NDM-1) gene was inserted in a truncated form of Tn125, which may explain the absence of bla(NDM_1) carrier-transformants. To our knowledge, this is the first report of the finding of NDM-positive A. baumannii in Tunisian territory. The study shows that despite the low prevalence and potential spread of NDM-1 enzyme among CRABC, continuous regional antimicrobial resistance surveillance and improved infection control measures are required in Tunisia to prevent further dissemination.
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