Monecke Stefan, Müller Elke, Büchler Joseph, Stieber Bettina, Ehricht Ralf
Alere Technologies GmbH, Jena, Germany; Institute for Medical Microbiology and Hygiene, Technische Universität Dresden, Dresden, Germany.
Alere Technologies GmbH, Jena, Germany.
PLoS One. 2014 Jun 18;9(6):e100427. doi: 10.1371/journal.pone.0100427. eCollection 2014.
The alpha toxin of Staphylococcus aureus is a pore forming toxin that penetrates host cell membranes causing osmotic swelling, rupture, lysis and subsequently cell death. Haemolysin alpha is toxic to a wide range of different mammalian cells; i.e., neurotoxic, dermonecrotic, haemolytic, and it can cause lethality in a wide variety of animals. In this study, the in vitro alpha toxin production of 648 previously genotyped isolates of S. aureus was measured quantitatively using antibody microarrays. Isolates originated from medical and veterinary settings and were selected in order to represent diverse clonal complexes and defined clinical conditions. Generally, the production of alpha toxin in vitro is related to the clonal complex affiliation. For clonal complexes CC22, CC30, CC45, CC479, CC705 and others, invariably no alpha toxin production was noted under the given in vitro conditions, while others, such as CC1, CC5, CC8, CC15 or CC96 secreted variable or high levels of alpha toxin. There was no correlation between alpha toxin yield and clinical course of the disease, or between alpha toxin yield and host species.
金黄色葡萄球菌的α毒素是一种形成孔道的毒素,它能穿透宿主细胞膜,导致渗透性肿胀、破裂、溶解,随后细胞死亡。溶血素α对多种不同的哺乳动物细胞有毒性;即具有神经毒性、皮肤坏死性、溶血作用,并且能在多种动物中引起致死性。在本研究中,使用抗体微阵列对648株先前已进行基因分型的金黄色葡萄球菌分离株的体外α毒素产生情况进行了定量测定。分离株来源于医学和兽医领域,为了代表不同的克隆复合体和明确的临床情况而进行选择。一般来说,体外α毒素的产生与克隆复合体归属有关。对于克隆复合体CC22、CC30、CC45、CC479、CC705及其他复合体,在给定的体外条件下始终未检测到α毒素产生,而其他一些复合体,如CC1、CC5、CC8、CC15或CC96则分泌可变或高水平的α毒素。α毒素产量与疾病临床过程之间,或α毒素产量与宿主物种之间均无相关性。