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YspM,一种新鉴定出的小肠结肠炎耶尔森菌的YsaⅢ型分泌蛋白。

YspM, a newly identified Ysa type III secreted protein of Yersinia enterocolitica.

作者信息

Witowski Sarah E, Walker Kimberly A, Miller Virginia L

机构信息

Department of Microbiology and Immunology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Bacteriol. 2008 Nov;190(22):7315-25. doi: 10.1128/JB.00861-08. Epub 2008 Sep 19.

Abstract

Yersinia enterocolitica has three type three secretion systems, the flagellar, the plasmid Ysc type III secretion system (T3SS), and the chromosomal Ysa T3SS. The Ysc T3SS, through the proteins it secretes (Yops), prevents phagocytosis of Y. enterocolitica and is required for disease processes in the mouse host. Recent data demonstrate a role for the Ysa T3SS during initial colonization of the mouse via secretion of Ysps (Yersinia secreted proteins). This work characterizes the discovery of a newly identified Ysa type III secreted protein, YspM. Expression of yspM is regulated by temperature, NaCl concentration, and other known regulators of the ysa system. In addition, YspM is translocated into host cells via the Ysa T3SS. YspM is homologous to proteins classified as GDSL bacterial lipases, which possess a catalytic triad of amino acids (Ser, Asp, and His) located in three of five blocks of amino acid identity. Sequence analysis of the JB580v strain of Y. enterocolitica shows that, due to a premature stop codon, it no longer encodes the fifth block of amino acid identity containing the predicted catalytic histidine. However, seven other biotype 1B strains sequenced did possess the domain. A functional difference between the forms was revealed when YspM was expressed in Saccharomyces cerevisiae. Yeast growth was uninhibited when YspM from JB580v was expressed but greatly inhibited when YspM from Y295 (YspM(Y295)) was expressed. Site-directed mutagenesis of the histidine of YspM(Y295) ablated the toxic effects. These results indicate that YspM is secreted by the Ysa T3SS and that, possibly due to lipase activity, it targets eukaryotic cellular component(s).

摘要

小肠结肠炎耶尔森菌有三种三型分泌系统,即鞭毛三型分泌系统、质粒Ysc三型分泌系统(T3SS)和染色体Ysa T3SS。Ysc T3SS通过其分泌的蛋白质(Yops)来防止小肠结肠炎耶尔森菌被吞噬,并且是小鼠宿主疾病进程所必需的。最近的数据表明,Ysa T3SS通过分泌Ysps(耶尔森菌分泌蛋白)在小鼠的初始定植过程中发挥作用。这项工作描述了一种新鉴定的Ysa三型分泌蛋白YspM的发现。yspM的表达受温度、NaCl浓度以及ysa系统其他已知调节因子的调控。此外,YspM通过Ysa T3SS转运到宿主细胞中。YspM与归类为GDSL细菌脂肪酶的蛋白质同源,这些蛋白质在五个氨基酸一致性区域中的三个区域具有催化三联体氨基酸(丝氨酸、天冬氨酸和组氨酸)。小肠结肠炎耶尔森菌JB580v菌株的序列分析表明,由于一个提前的终止密码子,它不再编码包含预测催化组氨酸的第五个氨基酸一致性区域。然而,测序的其他7个生物型1B菌株确实具有该结构域。当YspM在酿酒酵母中表达时,揭示了这两种形式之间的功能差异。当表达来自JB580v的YspM时,酵母生长不受抑制,但当表达来自Y295的YspM(YspM(Y295))时,酵母生长受到极大抑制。对YspM(Y295)的组氨酸进行定点诱变消除了毒性作用。这些结果表明,YspM由Ysa T3SS分泌,并且可能由于脂肪酶活性,它靶向真核细胞成分。

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