Bacteriological Study of Carbapenem and Aminoglycoside Resistance in Staphylococcus Aureus Recovered from Patient in Baghdad Province

H. Anwar, Maliha Masaoud, A. Salim
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Abstract

Background: In population- and hospital-acquired infections, Staphylococcus aureus is one of the most powerful causative agents. Aminoglycosides are active bactericidal drugs and are frequently used to treat staphylococcal infections in conjunction with beta-lactams or glycopeptides. Staphylococcus aureus is immune to carbapenems and other beta-lactams A different mechanism that can lead to carbapenem resistance is the active expulsion of carbapenems from the periplasmic space after their entry, due to the high distribution of these bacteria that are now immune to other antibiotics, it has become more difficult to treat these drug-resistant strains. Materials and Methods: A total of 130 staph.aureus isolates were isolated from different clinical samples in some public & private hospitals in Baghdad city during the period from November to December 2019. Bacterial identification was done using conventional cultural & chemical methods & and VITEk 2 cards for identification (GP), while the minimum inhibitory concentration (MIC) testing was performed using disk diffusion & (AST-GP30) cards in VITEK 2 automated system. Results: By using disk duffusion test out of 130 of Staph.aureus isolate, 76(58.4%) were resistant to aminoglycosids antibiotics (gentamicin) while 29(22.3%) were resistant to carbapenem antibiotics (imipenem) The MIC of different antibiotics was performed on 26 isolates using (VITEK2AST-GP30) showed that 18(69.2%) were resistant to aminoglycosids antibiotics (gentamicin) while 26(100%) were resistant to carbapenem antibiotics (imipenem). Conclusion: The MIC of different antibiotics By using disk duffusion the Staph.aureus isolate resistant to gentamicin 76(58.4%) and 29(22.3%) were resistant to imipenem, while, by VITEK2AST-GP30 showed 18(69.2%) were resistant to gentamicin , while 26(100% were resistant to imipenem.
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巴格达省金黄色葡萄球菌对碳青霉烯类和氨基糖苷类耐药的细菌学研究
背景:在人群和医院获得性感染中,金黄色葡萄球菌是最强大的病原体之一。氨基糖苷是有效的杀菌药物,常与β -内酰胺或糖肽联合用于治疗葡萄球菌感染。金黄色葡萄球菌对碳青霉烯类和其他β -内酰胺类免疫,另一种导致碳青霉烯类耐药的机制是碳青霉烯类在进入质周间隙后被主动排出,由于这些细菌的高度分布现在对其他抗生素免疫,因此治疗这些耐药菌株变得更加困难。材料与方法:共130株葡萄球菌。2019年11 - 12月在巴格达市部分公立和私立医院的不同临床样本中分离到金黄色葡萄球菌。细菌鉴定采用传统的培养和化学方法和VITEk 2卡进行鉴定(GP),最低抑制浓度(MIC)测试采用VITEk 2自动化系统中的磁盘扩散和(AST-GP30)卡进行。结果:对130株葡萄球菌进行了磁盘扩散试验。对氨基糖苷类抗生素(庆大霉素)耐药76株(58.4%),对碳青霉烯类抗生素(亚胺培南)耐药29株(22.3%)。采用VITEK2AST-GP30对26株不同抗生素进行MIC检测,结果显示,对氨基糖苷类抗生素(庆大霉素)耐药18株(69.2%),对碳青霉烯类抗生素(亚胺培南)耐药26株(100%)。结论:不同抗生素的MIC采用圆盘扩散法对葡萄球菌进行扩散。对庆大霉素耐药的金黄色葡萄球菌有76株(58.4%)和29株(22.3%),对亚胺培南耐药的金黄色葡萄球菌有18株(69.2%),对亚胺培南耐药的金黄色葡萄球菌有26株(100%)。
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