Area of Biochemistry and Molecular Biology, OneHealth-UR Research Group, University of La Rioja, 26006, Logroño, Spain.
Department of Medical Laboratory Science, Faculty of Allied Health Sciences, College of Medical Sciences, Ahmadu Bello University, PMB 05 , Zaria, Nigeria.
Curr Microbiol. 2024 Jun 14;81(8):225. doi: 10.1007/s00284-024-03737-2.
Linezolid resistance in Enterococcus spp. is increasingly considered critically important and a public health threat which mandates the need to understand their genomic contents and dissemination patterns. Here, we used whole-genome sequencing to characterize the resistome, virulome and mobile genetic elements of nine linezolid-resistant (LZD) enterococci (seven optrA-E. faecalis, one poxtA-E. faecium and one optrA-E. casseliflavus) previously obtained from the nares of healthy dogs, pigs, pig farmers and tracheal samples of nestling storks in Spain. Also, the relatedness of the isolates with publicly available genomes was accessed by core-genome single nucleotide polymorphism (SNP) analysis. The optrA gene of the E. faecalis and E. casseliflavus isolates was located downstream of the fexA gene. The optrA gene in the E. casseliflavus isolate was carried in a plasmid (pURX4962), while those in the seven E. faecalis isolates were chromosomally located. The OptrA proteins were mostly variants of wild type (DP-2: Y176D/T481P; RDK: I104R/Y176D/E256K; DD-3: Y176D/G393D; and EDD: K3E/Y176D/G393D), except two that were wild type (one E. faecalis and one E. casseliflavus). The poxtA gene in the E. faecium isolate was found alone within its contig. The cfrD was upstream of ermB gene in the E. casseliflavus isolate and flanked by ISNCY and IS1216. All the LZD enterococci carried plasmid rep genes (2-3) containing tetracycline, chloramphenicol and aminoglycoside resistance genes. All isolates except E. casseliflavus carried at least one intact prophage, of which E. faecalis-ST330 (X4957) from a pig carried the highest (n = 5). Tn6260 was associated with lnuG in E. faecalis-ST330 while Tn554 was with fexA in E. feaecalis-ST59 isolates. All except E. casseliflavus (n = 0) carried at least two metal resistance genes (MRGs), of which poxtA-carrying E. faecium-ST1739 isolate contained the most (arsA, copA, fief, ziaA, znuA, zosA, zupT, and zur). SNP-based analyses identified closely related optrA-E. faecalis isolates from a pig and a pig farmer on the same farm (SNP = 4). Moreover, optrA- carrying E. faecalis-ST32, -ST59, and -ST474 isolates from pigs were related to those previously described from humans (sick and healthy) and cattle in Spain, Belgium, and Switzerland (SNP range 43-86). These findings strongly suggest the transmission of LZD-E. faecalis between a pig and a pig farmer and potential inter-country dissemination. These highlight the need to strengthen molecular surveillance of LZD enterococci in all ecological niches and body parts to direct appropriate control strategies.
屎肠球菌属中的利奈唑胺耐药性日益被认为至关重要,是一种公共卫生威胁,这就要求我们必须了解其基因组内容和传播模式。在这里,我们使用全基因组测序技术来描述 9 株耐利奈唑胺(LZD)肠球菌(7 株 optrA-粪肠球菌、1 株 poxtA-屎肠球菌和 1 株 optrA-解没食子酸链球菌)的耐药组、毒力组和移动遗传元件,这些菌株先前从西班牙健康狗、猪、猪农的鼻腔和鹳雏鸟的气管样本中获得。此外,通过核心基因组单核苷酸多态性(SNP)分析,还评估了这些分离株与公开可用基因组的相关性。E. faecalis 和 E. casseliflavus 分离株的 optrA 基因位于 fexA 基因下游。E. casseliflavus 分离株的 optrA 基因位于质粒(pURX4962)上,而 7 株 E. faecalis 分离株的 optrA 基因位于染色体上。OptrA 蛋白大多是野生型的变异体(DP-2:Y176D/T481P;RDK:I104R/Y176D/E256K;DD-3:Y176D/G393D;和 EDD:K3E/Y176D/G393D),只有两种是野生型(一种 E. faecalis 和一种 E. casseliflavus)。E. faecium 分离株的 poxtA 基因单独位于其基因序列内。E. casseliflavus 分离株的 cfrD 基因位于 ermB 基因上游,由 ISNCY 和 IS1216 侧翼。所有 LZD 肠球菌均携带含有四环素、氯霉素和氨基糖苷类耐药基因的质粒 rep 基因(2-3)。除 E. casseliflavus 外,所有分离株都至少携带一个完整的噬菌体,其中来自猪的 E. faecalis-ST330(X4957)携带的最多(n=5)。Tn6260 与 E. faecalis-ST330 中的 lnuG 相关,而 Tn554 与 E. feaecalis-ST59 分离株中的 fexA 相关。除 E. casseliflavus(n=0)外,所有分离株都至少携带两个金属耐药基因(MRGs),其中携带 poxtA 的 E. faecium-ST1739 分离株含有最多的(arsA、copA、fief、ziaA、znuA、zosA、zupT 和 zur)。基于 SNP 的分析鉴定了来自同一农场的猪和猪农的密切相关的 optrA-粪肠球菌分离株(SNP=4)。此外,来自猪的携带 optrA 的 E. faecalis-ST32、-ST59 和 -ST474 分离株与之前在西班牙、比利时和瑞士从人和牛描述的分离株有关(SNP 范围 43-86)。这些发现强烈表明 LZD-粪肠球菌在猪和猪农之间传播,以及潜在的国家间传播。这些发现突出了需要加强对所有生态位和身体部位的 LZD 肠球菌的分子监测,以指导采取适当的控制策略。