Department of Molecular Biosciences, The University of Texas at Austin, Austin, Texas, USA.
mBio. 2022 Oct 26;13(5):e0236022. doi: 10.1128/mbio.02360-22. Epub 2022 Sep 14.
The role of the gut microbiota in the pathogenesis of Shigella flexneri remains largely unknown. To understand the impact of the gut microbiota on S. flexneri virulence, we examined the effect of interspecies interactions with Bacteroides thetaiotaomicron, a prominent member of the gut microbiota, on S. flexneri invasion. When grown in B. thetaiotaomicron-conditioned medium, S. flexneri showed reduced invasion of human epithelial cells. This decrease in invasiveness of S. flexneri resulted from a reduction in the level of the S. flexneri master virulence regulator VirF. Reduction of VirF corresponded with a decrease in expression of a secondary virulence regulator, , as well as expression of S. flexneri virulence genes required for invasion, intracellular motility, and spread. Repression of S. flexneri virulence factors by B. thetaiotaomicron-conditioned medium was not caused by either a secreted metabolite or secreted protein but rather was due to the presence of B. thetaiotaomicron outer membrane vesicles (OMVs) in the conditioned medium. The addition of purified B. thetaiotaomicron OMVs to S. flexneri growth medium recapitulated the inhibitory effects of B. thetaiotaomicron-conditioned medium on invasion, virulence gene expression, and virulence protein levels. Total lipids extracted from either B. thetaiotaomicron cells or B. thetaiotaomicron OMVs also recapitulated the effects of B. thetaiotaomicron-conditioned medium on expression of the S. flexneri virulence factor IpaC, indicating that B. thetaiotaomicron OMV lipids, rather than a cargo contained in the vesicles, are the active factor responsible for the inhibition of S. flexneri virulence. Shigella flexneri is the causative agent of bacillary dysentery in humans. spp. are one of the leading causes of diarrheal morbidity and mortality, especially among children in low- and middle-income countries. The rise of antimicrobial resistance combined with the lack of an effective vaccine for heightens the importance of studies aimed at better understanding previously uncharacterized aspects of pathogenesis. Here, we show that conditioned growth medium from the commensal bacterium Bacteroides thetaiotaomicron represses the invasion of S. flexneri. This repression is due to the presence of B. thetaiotaomicron outer membrane vesicles. These findings establish a role for interspecies interactions with a prominent member of the gut microbiota in modulating the virulence of S. flexneri and identify a novel function of outer membrane vesicles in interbacterial signaling between members of the gut microbiota and an enteric pathogen.
肠道微生物群在福氏志贺菌发病机制中的作用在很大程度上尚不清楚。为了了解肠道微生物群对福氏志贺菌毒力的影响,我们研究了与肠道微生物群中突出成员拟杆菌属(Bacteroides thetaiotaomicron)的种间相互作用对福氏志贺菌侵袭的影响。当在拟杆菌属条件培养基中生长时,福氏志贺菌对人上皮细胞的侵袭能力降低。福氏志贺菌侵袭力的这种降低是由于其主要毒力调节因子 VirF 的水平降低所致。VirF 的减少与次要毒力调节因子的表达减少以及侵袭、细胞内运动和扩散所需的福氏志贺菌毒力基因的表达减少有关。拟杆菌属条件培养基对福氏志贺菌毒力因子的抑制作用不是由分泌代谢物或分泌蛋白引起的,而是由于条件培养基中存在拟杆菌属外膜囊泡(OMVs)。将纯化的拟杆菌属 OMVs 添加到福氏志贺菌生长培养基中,可再现拟杆菌属条件培养基对侵袭、毒力基因表达和毒力蛋白水平的抑制作用。从拟杆菌属细胞或拟杆菌属 OMVs 中提取的总脂质也再现了拟杆菌属条件培养基对福氏志贺菌毒力因子 IpaC 表达的影响,表明拟杆菌属 OMV 脂质而不是囊泡中的货物,是负责抑制福氏志贺菌毒力的活性因子。福氏志贺菌是人类细菌性痢疾的病原体。 spp. 是导致腹泻发病率和死亡率的主要原因之一,尤其是在中低收入国家的儿童中。抗生素耐药性的出现加上缺乏针对的有效疫苗,增加了深入研究志贺菌发病机制中以前未被描述的方面的重要性。在这里,我们表明,共生细菌拟杆菌属(Bacteroides thetaiotaomicron)的条件生长培养基抑制了福氏志贺菌的侵袭。这种抑制作用是由于拟杆菌属外膜囊泡的存在。这些发现确立了与肠道微生物群中突出成员的种间相互作用在调节福氏志贺菌毒力方面的作用,并确定了外膜囊泡在肠道微生物群成员与肠道病原体之间的种间信号传递中的新功能。