Ghent University, Faculty of Veterinary Medicine, Department of Pathology, Bacteriology and Avian Diseases, Merelbeke, Belgium.
PLoS One. 2011;6(8):e24120. doi: 10.1371/journal.pone.0024120. Epub 2011 Aug 24.
Salmonellosis caused by Salmonella Typhimurium is one of the most important bacterial zoonotic diseases. The bacterium persists in pigs resulting in asymptomatic 'carrier pigs', generating a major source for Salmonella contamination of pork. Until now, very little is known concerning the mechanisms used by Salmonella Typhimurium during persistence in pigs. Using in vivo expression technology (IVET), a promoter-trap method based on ΔpurA attenuation of the parent strain, we identified 37 Salmonella Typhimurium genes that were expressed 3 weeks post oral inoculation in the tonsils, ileum and ileocaecal lymph nodes of pigs. Several genes were expressed in all three analyzed organs, while other genes were only expressed in one or two organs. Subsequently, the identified IVET transformants were pooled and reintroduced in pigs to detect tissue-specific gene expression patterns. We found that efp and rpoZ were specifically expressed in the ileocaecal lymph nodes during Salmonella peristence in pigs. Furthermore, we compared the persistence ability of substitution mutants for the IVET-identified genes sifB and STM4067 to that of the wild type in a mixed infection model. The ΔSTM4067::kanR was significantly attenuated in the ileum contents, caecum and caecum contents and faeces of pigs 3 weeks post inoculation, while deletion of the SPI-2 effector gene sifB did not affect Salmonella Typhimurium persistence. Although our list of identified genes is not exhaustive, we found that efp and rpoZ were specifically expressed in the ileocaecal lymph nodes of pigs and we identified STM4067 as a factor involved in Salmonella persistence in pigs. To our knowledge, our study is the first to identify Salmonella Typhimurium genes expressed during persistence in pigs.
鼠伤寒沙门氏菌引起的沙门氏菌病是最重要的细菌性人畜共患病之一。该细菌在猪体内持续存在,导致无症状的“带菌猪”,成为猪肉中沙门氏菌污染的主要来源。到目前为止,人们对鼠伤寒沙门氏菌在猪体内持续存在时所使用的机制知之甚少。本研究使用体内表达技术(IVET),一种基于亲本菌株ΔpurA 衰减的启动子陷阱方法,鉴定了 37 个在猪扁桃体、回肠和回盲淋巴结中经口服接种 3 周后表达的鼠伤寒沙门氏菌基因。一些基因在所有三个分析器官中都表达,而其他基因仅在一个或两个器官中表达。随后,将鉴定的 IVET 转化子汇集并重新引入猪体内,以检测组织特异性基因表达模式。结果发现,efp 和 rpoZ 在沙门氏菌在猪体内持续存在期间特异性表达于回盲淋巴结。此外,我们将 IVET 鉴定的基因 sifB 和 STM4067 的替代突变体与野生型在混合感染模型中的持久性能力进行了比较。与野生型相比,ΔSTM4067::kanR 在接种后 3 周的猪回肠内容物、盲肠和盲肠内容物以及粪便中的毒力显著减弱,而 SPI-2 效应基因 sifB 的缺失并不影响鼠伤寒沙门氏菌的持续存在。尽管我们鉴定的基因列表并不详尽,但我们发现 efp 和 rpoZ 特异性表达于猪的回盲淋巴结,并鉴定 STM4067 为参与鼠伤寒沙门氏菌在猪体内持续存在的因素。据我们所知,我们的研究首次鉴定了在猪体内持续存在时表达的鼠伤寒沙门氏菌基因。