Thornbrough Joshua M, Gopinath Adarsh, Hundley Tom, Worley Micah J
Department of Biology, University of Louisville, Louisville, KY, 40292, United States of America.
Department of Microbiology and Immunology, University of Louisville, Louisville, KY, 40202, United States of America.
PLoS One. 2016 Nov 23;11(11):e0166916. doi: 10.1371/journal.pone.0166916. eCollection 2016.
Salmonella enterica can actively invade the gastro-intestinal epithelium. This frequently leads to diarrheal disease, and also gives the pathogen access to phagocytes that can serve as vehicles for dissemination into deeper tissue. The ability to invade host cells is also important in maintaining the carrier state. While much is known about the bacterial factors that promote invasion, relatively little is known about the host factors involved. To gain insight into how Salmonella enterica serovar Typhimurium is able to invade normally non-phagocytic cells, we undertook a global RNAi screen with S. Typhimurium-infected human epithelial cells. In all, we identified 633 genes as contributing to bacterial internalization. These genes fall into a diverse group of functional categories revealing that cytoskeletal regulators are not the only factors that modulate invasion. In fact, potassium ion transport was the most enriched molecular function category in our screen, reinforcing a link between potassium and internalization. In addition to providing new insights into the molecular mechanisms underlying the ability of pathogens to invade host cells, all 633 host factors identified are candidates for new anti-microbial targets for treating Salmonella infections, and may be useful in curtailing infections with other pathogens as well.
肠炎沙门氏菌能够主动侵入胃肠道上皮。这常常导致腹泻疾病,并且还使该病原体能够接触吞噬细胞,而吞噬细胞可作为传播至更深层组织的载体。侵入宿主细胞的能力在维持携带状态方面也很重要。虽然人们对促进侵入的细菌因素了解很多,但对其中涉及的宿主因素却知之甚少。为了深入了解鼠伤寒沙门氏菌如何能够侵入正常的非吞噬细胞,我们对感染了鼠伤寒沙门氏菌的人类上皮细胞进行了全基因组RNA干扰筛选。我们总共鉴定出633个有助于细菌内化的基因。这些基因分属于不同的功能类别,这表明细胞骨架调节因子并非调节侵入的唯一因素。事实上,钾离子转运是我们筛选中富集程度最高的分子功能类别,这强化了钾与内化之间的联系。除了为病原体侵入宿主细胞能力背后的分子机制提供新见解外,所鉴定出的所有633个宿主因子都是治疗沙门氏菌感染新抗菌靶点的候选者,并且可能也有助于减少其他病原体的感染。