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Distribution of genes encoding resistance to aminoglycoside modifying enzymes in methicillin-resistant Staphylococcus aureus (MRSA) strains

机译:耐甲氧西林的金黄色葡萄球菌(MRSA)菌株对氨基糖苷修饰酶的抗性编码基因的分布

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Today Methicillin-Resistant Staphylococcus aureus (MRSA) have acquired multiple resistance to a wide range of antibiotics including aminoglycosides. So, this study was aimed to investigate the rate of aminoglycoside resistance and the frequency of aminoglycoside resistance mediated genes of aac(Ia)-2 , aph(3)-IIIa and ant(4′)-Ia among MRSA strains. A total of 467 staphylococci isolates were collected from various clinical samples. S. aureus strains were identified by standard culture and identification criteria and investigating of presence of 16S rRNA and nuc genes. Cefoxitin disk diffusion, and oxacillin-salt agar screening methods were used to detect the MRSA strains with subsequent molecular identification for the presence of mecA gene. Antibiotic susceptibility of MRSA strains against aminoglycoside antibiotics was evaluated by using agar disk diffusion method. Multiplex PCR for the presence of aac(Ia)-2 , aph(3)-IIIa and ant(4′)-Ia encoding genes for aminoglycosides were performed for MRSA strains. From total staphylococci tested isolates, 262 (56.1%) were identified as S. aureus , of which 161 (61.45%) were detected as MRSA and all comprised mecA gene. The resistance pattern of MRSA strains to aminoglycoside antibiotics were: gentamicin 136 (84.5%); amikacin 125 (77.6%); kanamycin 139 (86.3%); tobramycin 132 (82%); and neomycin 155 (96.3%). The frequency of aac(Ia)-2 , aph(3)-IIIa , and ant(4′)-Ia genes among MRSA strains, were 64%, 42% and 11.8% respectively. In conclusion, as MRSA strains are of great concern in human infections, the results of present study could provide a useful resource for health sectors for choosing appropriate antibiotics for the effective treatment of infections due to MRSA strains.
机译:如今,耐甲氧西林金黄色葡萄球菌(MRSA)已对包括氨基糖苷在内的多种抗生素产生了多重耐药性。因此,本研究旨在探讨MRSA菌株中aac(Ia)-2,aph(3)-IIIa和ant(4')-Ia的氨基糖苷抗性介导的频率和频率。从各种临床样品中总共收集了467株葡萄球菌分离株。通过标准的培养和鉴定标准以及研究16S rRNA和nuc基因的存在来鉴定金黄色葡萄球菌菌株。头孢西丁圆盘扩散法和奥沙西林盐琼脂筛选方法用于检测MRSA菌株,随后通过分子鉴定是否存在mecA基因。采用琼脂圆盘扩散法评价了MRSA菌株对氨基糖苷类抗生素的敏感性。对MRSA菌株进行了存在aac(Ia)-2,aph(3)-IIIa和ant(4')-Ia编码氨基糖苷酸基因的多重PCR。从总的葡萄球菌分离株中,有262个(56.1%)被鉴定为金黄色葡萄球菌,其中有161个(61.45%)被检测为MRSA,均包含mecA基因。 MRSA菌株对氨基糖苷类抗生素的耐药模式为:庆大霉素136(84.5%);阿米卡星125(77.6%);卡那霉素139(86.3%);妥布霉素132(82%);新霉素155(96.3%)。 MRSA菌株中aac(Ia)-2,aph(3)-IIIa和ant(4')-Ia基因的频率分别为64%,42%和11.8%。总之,由于MRSA菌株在人类感染中引起极大关注,因此本研究结果可为卫生部门提供有用的资源,以选择合适的抗生素来有效治疗MRSA菌株引起的感染。

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