Department of Microbiology and Immunology, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.
Faculty of Pharmacy, King Salman International University, South Sinai, Ras-Sudr, Egypt.
Ann Clin Microbiol Antimicrob. 2023 Apr 3;22(1):23. doi: 10.1186/s12941-023-00574-2.
Methicillin-Resistant Staphylococcus aureus (MRSA) causes life-threatening infections, with narrow therapeutic options including: vancomycin and linezolid. Accordingly, this study aimed to characterize phenotypically and genotypically, the most relevant means of linezolid resistance among some MRSA clinical isolates.
A total of 159 methicillin-resistant clinical isolates were collected, of which 146 were indentified microscopically and biochemically as MRSA. Both biofilm formation and efflux pump activity were assessed for linezolid-resistant MRSA (LR-MRSA) using the microtiter plate and carbonyl cyanide 3-chlorophenylhydrazone (CCCP) methods, respectively. Linezolid resistance was further characterized by polymerase chain reaction (PCR) amplification and sequencing of domain V of 23 S rRNA; rplC; rplD;and rplV genes. Meanwhile, some resistance genes were investigated: cfr; cfr(B); optrA; msrA;mecA; and vanA genes. To combat LR-MRSA, the effect of combining linezolid with each of 6 different antimicrobials was investigated using the checkerboard assay.
Out of the collected MRSA isolates (n = 146), 5.48% (n = 8) were LR-MRSA and 18.49% (n = 27) were vancomycin-resistant (VRSA). It is worth noting that all LR-MRSA isolates were also vancomycin-resistant. All LR-MRSA isolates were biofilm producers (r = 0.915, p = 0.001), while efflux pumps upregulation showed no significant contribution to development of resistance (t = 1.374, p = 0.212). Both mecA and vanA genes were detected in 92.45% (n = 147) and 6.92% (n = 11) of methicillin-resistant isolates, respectively. In LR-MRSA isolates, some 23 S rRNA domain V mutations were observed: A2338T and C2610G (in 5 isolates); T2504C and G2528C (in 2 isolates); and G2576T (in 1 isolate). Amino acids substitutions were detected: in L3 protein (rplC gene) of (3 isolates) and in L4 protein (rplD gene) of (4 isolates). In addition, cfr(B) gene was detected (in 3 isolates). In 5 isolates, synergism was recorded when linezolid was combined with chloramphenicol, erythromycin, or ciprofloxacin. Reversal of linezolid resistance was observed in some LR-MRSA isolates when linezolid was combined with gentamicin or vancomycin.
LR-MRSA biofilm producers' phenotypes evolved in the clinical settings in Egypt. Various antibiotic combinations with linezolid were evaluated in vitro and showed synergistic effects.
耐甲氧西林金黄色葡萄球菌(MRSA)可引起危及生命的感染,其治疗方法有限,包括:万古霉素和利奈唑胺。因此,本研究旨在对一些 MRSA 临床分离株中与利奈唑胺耐药相关的最主要表型和基因型进行特征描述。
共收集了 159 株耐甲氧西林的临床分离株,其中 146 株经显微镜和生化鉴定为 MRSA。分别使用微孔板和碳酰氰基-3-氯苯腙(CCCP)方法评估利奈唑胺耐药 MRSA(LR-MRSA)的生物膜形成和外排泵活性。通过聚合酶链反应(PCR)扩增和 23S rRNA 结构域 V、rplC、rplD 和 rplV 基因的测序进一步表征利奈唑胺耐药性。同时,还研究了一些耐药基因:cfr;cfr(B);optrA;msrA;mecA 和 vanA 基因。为了对抗 LR-MRSA,使用棋盘微量稀释法评估了利奈唑胺与 6 种不同抗菌药物联合使用的效果。
在所收集的 MRSA 分离株(n=146)中,有 5.48%(n=8)为 LR-MRSA,18.49%(n=27)为万古霉素耐药(VRSA)。值得注意的是,所有 LR-MRSA 分离株均对万古霉素耐药。所有 LR-MRSA 分离株均为生物膜产生菌(r=0.915,p=0.001),而外排泵上调对耐药性的发展没有显著贡献(t=1.374,p=0.212)。在 147 株耐甲氧西林分离株中分别检测到 mecA 和 vanA 基因的存在,其阳性率分别为 92.45%(n=147)和 6.92%(n=11)。在 LR-MRSA 分离株中观察到 23S rRNA 结构域 V 的一些突变:A2338T 和 C2610G(5 株);T2504C 和 G2528C(2 株);和 G2576T(1 株)。检测到 L3 蛋白(rplC 基因)和 L4 蛋白(rplD 基因)中的氨基酸取代(3 株和 4 株)。此外,还检测到 cfr(B)基因(3 株)。在 5 株分离株中,当利奈唑胺与氯霉素、红霉素或环丙沙星联合使用时,记录到协同作用。当利奈唑胺与庆大霉素或万古霉素联合使用时,一些 LR-MRSA 分离株的利奈唑胺耐药性被逆转。
LR-MRSA 生物膜产生菌在埃及临床环境中发生了进化。对利奈唑胺与不同抗生素的联合使用进行了体外评估,显示出协同作用。