Watson P R, Galyov E E, Paulin S M, Jones P W, Wallis T S
Institute for Animal Health, Newbury, Berkshire, United Kingdom.
Infect Immun. 1998 Apr;66(4):1432-8. doi: 10.1128/IAI.66.4.1432-1438.1998.
The induction of secretory and inflammatory responses in calves by Salmonella typhimurium and Salmonella dublin strains was compared, and the effects of mutations in the invH and stn genes were assessed. S. typhimurium induced greater secretory and inflammatory responses than S. dublin in bovine ileal loops, despite the fact that these serotypes were recovered from bovine ileal mucosa in comparable numbers (P. R. Watson, S. M. Paulin, A. P. Bland, P. W. Jones, and T. S. Wallis, Infect. Immun. 63:2743-2754, 1995). These results implicate serotype-specific factors other than, or in addition to, intestinal invasion in the induction of enteritis. The secretory and inflammatory responses induced by S. typhimurium and S. dublin in bovine ligated ileal loops were not significantly altered by mutation of stn, which suggests that stn does not have a major role in Salmonella-induced enteritis. The invH mutation significantly reduced the secretory and inflammatory responses induced in bovine ileal loops, and this correlated with a reduction in the severity of enteritis following oral inoculation of calves. The attenuation associated with the invH mutation did not appear to be due to an increased susceptibility to the innate host defense mechanisms, because the resistance of S. typhimurium to the bactericidal action of either bovine polymorphonuclear leukocytes or bovine serum was not significantly altered. However, lysis of macrophages following infection with S. typhimurium was significantly reduced by the invH mutation. The invH mutation prevented the normal secretion of several proteins, including SipC, by S. typhimurium, indicating that the function of the inv-spa-encoded type III protein secretion system was disrupted. Taken together, these observations implicate inv-spa-dependent effectors in mediation of Salmonella-induced enteritis in cattle. Clearly, however, other undefined serotype-specific virulence factors are also involved in Salmonella-induced enteritis.
比较了鼠伤寒沙门氏菌和都柏林沙门氏菌菌株对犊牛分泌和炎症反应的诱导作用,并评估了invH和stn基因突变的影响。尽管从牛回肠黏膜中回收的这些血清型数量相当,但在牛回肠肠袢中,鼠伤寒沙门氏菌诱导的分泌和炎症反应比都柏林沙门氏菌更强(P. R. 沃森、S. M. 保林、A. P. 布兰德、P. W. 琼斯和T. S. 沃利斯,《感染与免疫》63:2743 - 2754,1995)。这些结果表明,除了肠道侵袭之外,或者除肠道侵袭之外还存在血清型特异性因素参与肠炎的诱导。stn基因突变并未显著改变鼠伤寒沙门氏菌和都柏林沙门氏菌在牛结扎回肠肠袢中诱导的分泌和炎症反应,这表明stn在沙门氏菌诱导的肠炎中不发挥主要作用。invH基因突变显著降低了在牛回肠肠袢中诱导的分泌和炎症反应,这与犊牛口服接种后肠炎严重程度的降低相关。与invH基因突变相关的减毒似乎并非由于对宿主固有防御机制的易感性增加,因为鼠伤寒沙门氏菌对牛多形核白细胞或牛血清杀菌作用的抗性并未显著改变。然而,invH基因突变显著降低了感染鼠伤寒沙门氏菌后巨噬细胞的裂解。invH基因突变阻止了鼠伤寒沙门氏菌正常分泌包括SipC在内的几种蛋白质,表明inv - spa编码的III型蛋白分泌系统的功能被破坏。综上所述,这些观察结果表明inv - spa依赖性效应子参与介导牛的沙门氏菌诱导的肠炎。然而,显然其他未明确的血清型特异性毒力因子也参与沙门氏菌诱导的肠炎。