Food Safety and Enteric Pathogens Research Unit, National Animal Disease Center, Agricultural Research Service , U.S. Department of Agriculture, Ames, IA 50010, USA.
Foodborne Pathog Dis. 2012 Apr;9(4):346-51. doi: 10.1089/fpd.2011.1021. Epub 2012 Mar 8.
The aims of this study were to determine whether Shigella species, which are human gastrointestinal pathogens, can adhere to cattle recto-anal junction squamous epithelial (RSE) cells using a recently standardized in vitro adherence assay, and to compare their adherence patterns with that of Escherichia coli O157. Shigella dysenteriae (serogroup A), S. flexneri (serogroup B), S. boydii (serogroup C), and S. sonnei (serogroup D) were tested in adherence assays using both RSE and HEp-2 cells, in the presence or absence of D+mannose. Escherichia coli O157, which adheres to RSE cells in a Type I fimbriae-independent manner, was used as a positive control. Shigella serogroups A, B, D, but not C adhered to RSE cells with distinct adherence patterns in the presence of D+mannose. No such distinction could be made between the four Shigella serogroups based on the HEp-2 cell adherence patterns. Thus, this study provides evidence that certain Shigella serogroups adhere to RSE cells in a manner that is similar to the adherence pattern of E. coli O157. These unexpected observations of in vitro binding of these foodborne human pathogens to cells of the bovine gastrointestinal tract warrant evaluation of Shigella carriage by cattle using both experimental and observational studies, especially for serogroups B and D. Such studies are currently underway.
本研究的目的是确定志贺氏菌(Shigella species),即人类胃肠道病原体,是否可以使用最近标准化的体外黏附试验黏附于牛直肠-肛门交界处的鳞状上皮(RSE)细胞,并比较其黏附模式与大肠杆菌 O157 的黏附模式。使用 RSE 和 HEp-2 细胞,在存在或不存在 D+甘露糖的情况下,对志贺氏菌血清型 A、B、C 和 D 进行黏附试验。大肠杆菌 O157 以非 I 型菌毛依赖的方式黏附于 RSE 细胞,作为阳性对照。在存在 D+甘露糖的情况下,志贺氏菌血清型 A、B 和 D 但不是 C 以独特的黏附模式黏附于 RSE 细胞。根据 HEp-2 细胞的黏附模式,无法在这四种志贺氏菌血清型之间做出区分。因此,本研究提供了证据表明,某些志贺氏菌血清型以类似于大肠杆菌 O157 黏附模式的方式黏附于 RSE 细胞。这些食源性人类病原体在体外与牛胃肠道细胞结合的意外观察结果表明,需要使用实验和观察研究来评估牛的志贺氏菌携带情况,尤其是血清型 B 和 D。此类研究正在进行中。