Laboratory of Veterinary Public Health, Department of Veterinary Medicine, Faculty of Agriculture, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065, Japan.
Vet Microbiol. 2010 Sep 28;145(1-2):76-83. doi: 10.1016/j.vetmic.2010.02.035. Epub 2010 Mar 3.
During 2005-2008, a longitudinal study was conducted in southern Japan to detect and characterize multidrug-resistant Salmonella enterica serovars recovered from cattle diagnostic specimens. Determination of antimicrobial resistance phenotypes and genotypes, identification of Salmonella genomic island 1 (SGI1), detection of virulence genes, plasmid analysis, conjugal transfer experiments, and sequencing of class 1 integrons were conducted. Multidrug-resistant Salmonella detected were serovars Stanley, Typhimurium, and O4:d. Salmonella Stanley isolates exhibited resistance to ampicillin, chloramphenicol, streptomycin, sulfamethoxazole, oxytetracycline, trimethoprim, and kanamycin (ACSSuT+) encoded by bla(TEM), catA, aadA2, tetA, sul1, dfrA12, and aphA1 genes, respectively. Sequencing analysis revealed that aadA2 and dfrA12 were integrated as gene cassettes within the class 1 integrons of 1.5kb size. Importantly, the isolates harboured easily transferable plasmids of ca. 210kb with the potential of transmitting resistance phenotype and genotype detected in the donor isolates. Moreover, Salmonella Typhimurium DT104 isolates with typical SGI1 were detected and presented ACSSuT+ resistance phenotype encoded by bla(PSE-1) and bla(TEM); floR; aadA1; sul1; and tetA and tetG, respectively. Salmonella Typhimurium isolates carried plasmids of variable sizes ranging from 3.5 to 100 kb with DT104 isolates harbouring plasmids of ca. 90 kb. Salmonella serovar O4:d had ACSSuT+ resistance phenotype mediated by bla(TEM), catA, aadA1, sul1, tetA, and aphA1 genes. A virulence gene invA was found in all multidrug-resistant Salmonella Typhimurium, Stanley and O4:d clinical isolates. In conclusion, this is the first report describing the occurrence of multidrug-resistant Salmonella Stanley from bovine species. The emergence of Salmonella Stanley isolates exhibiting plasmid-encoded high-level multidrug resistance is an important health concern because this new pathogenecity was associated with mortality in cattle.
2005-2008 年,在日本南部进行了一项纵向研究,以检测和鉴定从牛诊断标本中分离出的多重耐药沙门氏菌血清型。进行了抗生素耐药表型和基因型的测定、沙门氏菌基因组岛 1(SGI1)的鉴定、毒力基因的检测、质粒分析、接合转移实验以及 class 1 整合子的测序。检测到的多重耐药沙门氏菌血清型为 Stanley、Typhimurium 和 O4:d。Stanley 分离株对氨苄西林、氯霉素、链霉素、磺胺甲恶唑、土霉素、甲氧苄啶和卡那霉素(ACSSuT+)表现出耐药性,分别由 bla(TEM)、catA、aadA2、tetA、sul1、dfrA12 和 aphA1 基因编码。测序分析显示,aadA2 和 dfrA12 作为基因盒整合到大小为 1.5kb 的 class 1 整合子中。重要的是,这些分离株携带约 210kb 的可转移质粒,具有在供体分离株中检测到的耐药表型和基因型的潜在转移能力。此外,还检测到携带典型 SGI1 的 Salmonella Typhimurium DT104 分离株,并呈现由 bla(PSE-1)和 bla(TEM)、floR、aadA1、sul1 和 tetA 和 tetG 编码的 ACSSuT+耐药表型。携带的质粒大小从 3.5 到 100kb 不等,DT104 分离株携带约 90kb 的质粒。O4:d 血清型沙门氏菌具有由 bla(TEM)、catA、aadA1、sul1、tetA 和 aphA1 基因介导的 ACSSuT+耐药表型。所有多重耐药 Salmonella Typhimurium、Stanley 和 O4:d 临床分离株均发现了毒力基因 invA。总之,这是首次报道从牛种中分离出多重耐药 Salmonella Stanley。Stanley 分离株表现出质粒编码的高水平多重耐药性,这是一个重要的健康关注点,因为这种新的病原体与牛的死亡率有关。