Center for Infectious and Inflammatory Diseases, Institute of Biosciences and Technology, Texas A&M University Health Science Center, Houston, Texas, USA.
Department of Infectious Diseases, Division of Internal Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
mBio. 2020 Feb 18;11(1):e02911-19. doi: 10.1128/mBio.02911-19.
is a leading cause of nosocomial infections in patients with a compromised immune system and/or an implanted medical device. Seventy to 90% of clinical isolates are methicillin resistant and carry the gene, present in a mobile genetic element (MGE) called the staphylococcal cassette chromosome (SCC) element. Along with the presence of antibiotic and heavy metal resistance genes, MGEs can also contain genes encoding secreted or cell wall-anchored virulence factors. In our earlier studies of clinical isolates, we discovered surface protein J (SesJ), a prototype of a recently discovered subfamily of the microbial surface component recognizing adhesive matrix molecule (MSCRAMM) group. MSCRAMMs are major virulence factors of pathogenic Gram-positive bacteria. Here, we report that the gene is always accompanied by two glycosyltransferase genes, and , and is present in two MGEs, called the arginine catabolic mobile element (ACME) and the staphylococcal cassette chromosome (SCC) element. The presence of the gene was associated with the left-hand direct repeat DR_B or DR_E. When inserted via DR_E, the gene was encoded in the SCC element. When inserted via DR_B, the gene was accompanied by the genes for the type 1 restriction modification system and was encoded in the ACME. Additionally, the SCC element and ACME carry different isoforms of the SesJ protein. To date, the genes encoding MSCRAMMs have been seen to be located in the bacterial core genome. Here, we report the presence of an MSCRAMM in an MGE in clinical isolates. is an opportunistic bacterium that has established itself as a successful nosocomial pathogen. The modern era of novel therapeutics and medical devices has extended the longevity of human life, but at the same time, we also witness the evolution of pathogens to adapt to newly available niches in the host. Increasing antibiotic resistance among pathogens provides an example of such pathogen adaptation. With limited opportunities to modify the core genome, most of the adaptation occurs by acquiring new genes, such as virulence factors and antibiotic resistance determinants present in MGEs. In this study, we describe that the gene, encoding a recently discovered cell wall-anchored protein in , is present in both ACME and the SCC element. The presence of virulence factors in MGEs can influence the virulence potential of a specific strain. Therefore, it is critical to study the virulence factors found in MGEs in emerging pathogenic bacteria or strains to understand the mechanisms used by these bacteria to cause infections.
是一种导致免疫系统受损和/或植入医疗设备的患者发生医院获得性感染的主要病原体。70%至 90%的临床分离株对甲氧西林耐药,且携带 基因,该基因存在于一种称为葡萄球菌盒染色体 (SCC)元件的移动遗传元件 (MGE)中。除了携带抗生素和重金属耐药基因外,MGE 还可能包含编码分泌或细胞壁锚定毒力因子的基因。在我们之前对临床分离株的研究中,我们发现了表面蛋白 J(SesJ),它是最近发现的微生物表面成分识别黏附基质分子 (MSCRAMM)亚家族的原型。MSCRAMM 是致病性革兰氏阳性菌的主要毒力因子。在这里,我们报告 基因总是伴随着两个糖基转移酶基因 和 ,并且存在于两个 MGE 中,称为精氨酸分解代谢移动元件 (ACME)和葡萄球菌盒染色体 (SCC)元件。 基因的存在与左手重复 DR_B 或 DR_E 有关。当通过 DR_E 插入时, 基因编码在 SCC 元件中。当通过 DR_B 插入时, 基因伴随着 I 型限制修饰系统的基因,并编码在 ACME 中。此外,SCC 元件和 ACME 携带不同的 SesJ 蛋白同工型。迄今为止,编码 MSCRAMM 的基因已被视为位于细菌核心基因组中。在这里,我们报告了在 临床分离株中存在一种位于 MGE 中的 MSCRAMM。是一种机会性病原体,已成为成功的医院获得性病原体。新型治疗方法和医疗设备的现代时代延长了人类的寿命,但与此同时,我们也见证了病原体为适应宿主中可用的新小生境而进化。病原体对抗生素的耐药性增加就是这种病原体适应的一个例子。由于对核心基因组进行修改的机会有限,大多数适应是通过获得新基因来实现的,例如 MGE 中存在的毒力因子和抗生素耐药决定因子。在这项研究中,我们描述了 基因,该基因编码 中的一种新发现的细胞壁锚定蛋白,存在于 ACME 和 SCC 元件中。MGE 中存在毒力因子会影响特定菌株的毒力潜力。因此,研究新兴致病菌或菌株中发现的 MGE 中的毒力因子对于了解这些细菌引起感染的机制至关重要。