Phenotypic and genotypic determinants of mupirocin resistance among Staphylococcus aureus isolates recovered from clinical samples of children: an Iranian hospital-based study

被引:10
作者
Mahmoudi, Shima [1 ]
Mamishi, Setareh [1 ,2 ]
Mohammadi, Mohsen [2 ]
Banar, Maryam [1 ]
Ashtiani, Mohammad Taghi Haghi [3 ]
Mahzari, Masoumeh [2 ]
Bahador, Abbas [4 ]
Pourakbari, Babak [1 ]
机构
[1] Univ Tehran Med Sci, Pediat Infect Dis Res Ctr, Tehran, Iran
[2] Univ Tehran Med Sci, Sch Med, Dept Infect Dis, Tehran, Iran
[3] Univ Tehran Med Sci, Sch Med, Dept Pathol, Tehran, Iran
[4] Univ Tehran Med Sci, Sch Med, Dept Microbiol, Tehran, Iran
来源
INFECTION AND DRUG RESISTANCE | 2019年 / 12卷
关键词
methicillin-resistant Staphylococcus aureus; mupirocin; PCR; children; HIGH PREVALENCE; ANTIMICROBIAL RESISTANCE; SKIN; SUSCEPTIBILITY; INFECTIONS; EMERGENCE; STRAINS; CHLORHEXIDINE; CLINDAMYCIN; GENES;
D O I
10.2147/IDR.S185610
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Backgrounds: The aim of this study was to evaluate both phenotypic and genotypic determinants of mupirocin resistance among methicillin-resistant Staphylococcus aureus (MRSA) and methicillin susceptible S. aureus (MSSA) strains recovered from different clinical samples of children who were admitted to the Children's Medical Center (CMC) Hospital, Tehran, Iran. Materials and methods: A total of 120 clinical isolates of S. aureus were collected from the microbiology laboratory of CMC Hospital. Antimicrobial susceptibility of the isolates to different antimicrobial agents was determined by disk diffusion method. The methicillin resistance phenotype (MRSA) was identified using a 30 mu g cefoxitin disk. The minimum inhibitory concentration (MIC) of mupirocin was determined by broth microdilution method. Strains with mupirocin MIC between 8 and 256 mu g/mL were considered as low-level mupirocin resistant (LLMR), and strains with an MIC >= 512 mu g/mL were considered as high-level mupirocin resistant (HLMR). The presence of genes encoding HLMR (ie, mupA and mupB genes) was evaluated by PCR method. Results: Four out of 120 isolates (3%) had mupirocin MIC >= 512 mu g/mL and were HLMR; however, no LLMR isolate was detected. Fifty-two isolates (43%) were MRSA, and there were no differences in the distribution of mupirocin resistance among MRSA and MSSA isolates (P>0.05). The PCR method identified mupA gene in two out of four HLMR isolates, and mupB gene was not detected in any HLMR isolates. Conclusion: Because of discrepancies between the phenotypic and genotypic patterns of mupirocin resistance and due to the avoidance of false-negative results, it is better to determine the mupirocin resistance by both antibiotic susceptibility tests and PCR method. Considering the increasing need of mupirocin for the control of S. aureus infections, continuous checking of its susceptibility status is necessary.
引用
收藏
页码:137 / 143
页数:7
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