Sydney School of Veterinary Science, University of Sydney, NSW, Australia.
Department of Microbiology and Immunology, The University of Melbourne at the Peter Doherty Institute for Infection and Immunity, VIC, Australia.
mSphere. 2018 Nov 7;3(6):e00491-18. doi: 10.1128/mSphere.00491-18.
We examined the oxacillin resistance phenotype and genomic structure of staphylococcal cassette chromosome (SCC) elements from 77 veterinary methicillin-resistant (MRSP) isolates. Isolates were characterized by oxacillin broth microdilution, whole-genome sequencing, and bioformatics analysis. Five previously described SCC elements, and a sixth novel element, were identified: SCC III (also known as II-III), ΨSCC, and SCC (a SCC VII variant), all previously described in MRSP, and SCC IVg and SCC V, previously described in both methicillin-resistant (MRSA) and MRSP. The sixth element was novel and found among nine geographically clustered isolates. This novel pseudostaphylococcal cassette chromosome (ΨSCC) contained a class A gene complex but lacked genes. It also harbored heavy metal (cadmium) resistance determinants. The median oxacillin MIC values among ΨSCC, SCC III, and SCC V isolates were significantly higher than those determined for the SCC VII variant isolates and ΨSCC and SCC IVg isolates. ΨSCC was found exclusively in sequence type 497 (ST497), an MRSP clone that is locally successful in Victoria, Australia. Future studies are necessary to determine if this clone has disseminated further afield and if ΨSCC has moved into other MRSP lineages or staphylococcal species. is a significant veterinary pathogen and occasional cause of infections in humans. β-Lactams are an important group of antimicrobials used to treat staphylococcal infections in humans and animals. However, when staphylococci become methicillin resistant via the acquisition of a mobile genetic element called staphylococcal cassette chromosome (SCC), they become resistant to all β-lactams. This study detected a novel SCC element among a cluster of methicillin-resistant isolates from animals in Australia. It also detected SCC elements in that had high similarity to those identified in methicillin-resistant , demonstrating how human and animal pathogens can share the same resistance determinants.
我们研究了 77 株兽医耐甲氧西林金黄色葡萄球菌(MRSP)分离株的苯唑西林耐药表型和葡萄球菌盒染色体(SCC)元件的基因组结构。通过苯唑西林肉汤微量稀释法、全基因组测序和生物信息学分析对分离株进行了特征描述。确定了五个先前描述的 SCC 元件和第六个新元件:SCC III(也称为 II-III)、ΨSCC 和 SCC(SCC VII 变体),这些都曾在 MRSP 中描述过,还有 SCC IVg 和 SCC V,这些都曾在耐甲氧西林金黄色葡萄球菌(MRSA)和 MRSP 中描述过。第六个元件是新发现的,存在于 9 个地理聚类的分离株中。这个新的伪葡萄球菌盒染色体(ΨSCC)含有一个 A 类基因复合物,但缺乏 基因。它还携带重金属(镉)耐药决定因素。ΨSCC、SCC III 和 SCC V 分离株的苯唑西林 MIC 值中位数明显高于 SCC VII 变体分离株、ΨSCC 和 SCC IVg 分离株的 MIC 值中位数。ΨSCC 仅在序列型 497(ST497)中发现,ST497 是一种在澳大利亚维多利亚州成功的 MRSP 克隆。未来的研究有必要确定该克隆是否已进一步传播,以及 ΨSCC 是否已转移到其他 MRSP 谱系或葡萄球菌物种中。是一种重要的兽医病原体,偶尔也是人类感染的原因。β-内酰胺类抗生素是一类重要的抗生素,用于治疗人类和动物的葡萄球菌感染。然而,当葡萄球菌通过获得一种称为葡萄球菌盒染色体(SCC)的移动遗传元件而对甲氧西林产生耐药性时,它们对所有β-内酰胺类抗生素都产生耐药性。本研究在来自澳大利亚动物的一组耐甲氧西林分离株中检测到一种新型 SCC 元件。它还在与耐甲氧西林 具有高度相似性的分离株中检测到 SCC 元件,表明人类和动物病原体如何共享相同的耐药决定因素。