Pumirat Pornpan, Broek Charles Vander, Juntawieng Niramol, Muangsombut Veerachat, Kiratisin Pattarachai, Pattanapanyasat Kovit, Stevens Joanne M, Stevens Mark P, Korbsrisate Sunee
Department of Microbiology and Immunology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand; Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, United Kingdom.
PLoS One. 2014 May 8;9(5):e96298. doi: 10.1371/journal.pone.0096298. eCollection 2014.
Enteropathogenic and enterohaemorrhagic Escherichia coli express a cell cycle-inhibiting factor (Cif), that is injected into host cells via a Type III secretion system (T3SS) leading to arrest of cell division, delayed apoptosis and cytoskeletal rearrangements. A homologue of Cif has been identified in Burkholderia pseudomallei (CHBP; Cif homologue in B. pseudomallei; BPSS1385), which shares catalytic activity, but its prevalence, secretion and function are ill-defined. Among 43 available B. pseudomallei genome sequences, 33 genomes (76.7%) harbor the gene encoding CHBP. Western blot analysis using antiserum raised to a synthetic CHBP peptide detected CHBP in 46.6% (7/15) of clinical B. pseudomallei isolates from the endemic area. Secretion of CHBP into bacterial culture supernatant could not be detected under conditions where a known effector (BopE) was secreted in a manner dependent on the Bsa T3SS. In contrast, CHBP could be detected in U937 cells infected with B. pseudomallei by immunofluorescence microscopy and Western blotting in a manner dependent on bsaQ. Unlike E. coli Cif, CHBP was localized within the cytoplasm of B. pseudomallei-infected cells. A B. pseudomallei chbP insertion mutant showed a significant reduction in cytotoxicity and plaque formation compared to the wild-type strain that could be restored by plasmid-mediated trans-complementation. However, there was no defect in actin-based motility or multinucleated giant cell formation by the chbP mutant. The data suggest that the level or timing of CHBP secretion differs from a known Bsa-secreted effector and that CHBP is required for selected virulence-associated phenotypes in vitro.
肠道致病性大肠杆菌和肠出血性大肠杆菌表达一种细胞周期抑制因子(Cif),该因子通过III型分泌系统(T3SS)注入宿主细胞,导致细胞分裂停滞、凋亡延迟和细胞骨架重排。在类鼻疽伯克霍尔德菌中已鉴定出Cif的同源物(CHBP;类鼻疽伯克霍尔德菌中的Cif同源物;BPSS1385),其具有催化活性,但其流行情况、分泌和功能尚不明确。在43个可用的类鼻疽伯克霍尔德菌基因组序列中,33个基因组(76.7%)含有编码CHBP的基因。使用针对合成CHBP肽产生的抗血清进行的蛋白质印迹分析在来自流行地区的46.6%(7/15)的临床类鼻疽伯克霍尔德菌分离株中检测到了CHBP。在已知效应蛋白(BopE)以依赖于Bsa T3SS的方式分泌的条件下,未检测到CHBP分泌到细菌培养上清液中。相比之下,通过免疫荧光显微镜和蛋白质印迹法,在感染类鼻疽伯克霍尔德菌的U937细胞中可以检测到CHBP,其方式依赖于bsaQ。与大肠杆菌Cif不同,CHBP定位于感染类鼻疽伯克霍尔德菌的细胞的细胞质内。与野生型菌株相比,类鼻疽伯克霍尔德菌chbP插入突变体的细胞毒性和噬菌斑形成显著降低,质粒介导的反式互补可恢复这种降低。然而,chbP突变体在基于肌动蛋白的运动性或多核巨细胞形成方面没有缺陷。数据表明,CHBP分泌的水平或时间与已知的Bsa分泌效应蛋白不同,并且CHBP是体外选定的毒力相关表型所必需的。