Ponnusamy Duraisamy, Clinkenbeard Kenneth D
Department of Veterinary Pathobiology, Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, OK 74078, United States of America.
PLoS One. 2015 Nov 4;10(11):e0141984. doi: 10.1371/journal.pone.0141984. eCollection 2015.
Yersinia pestis initiates infection by parasitism of host macrophages. In response to macrophage infections, intracellular Y. pestis can assume a filamentous cellular morphology which may mediate resistance to host cell innate immune responses. We previously observed the expression of Y. pestis tellurite resistance proteins TerD and TerE from the terZABCDE operon during macrophage infections. Others have observed a filamentous response associated with expression of tellurite resistance operon in Escherichia coli exposed to tellurite. Therefore, in this study we examine the potential role of Y. pestis tellurite resistance operon in filamentous cellular morphology during macrophage infections.
In vitro treatment of Y. pestis culture with sodium tellurite (Na2TeO3) caused the bacterial cells to assume a filamentous phenotype similar to the filamentous phenotype observed during macrophage infections. A deletion mutant for genes terZAB abolished the filamentous morphologic response to tellurite exposure or intracellular parasitism, but without affecting tellurite resistance. However, a terZABCDE deletion mutant abolished both filamentous morphologic response and tellurite resistance. Complementation of the terZABCDE deletion mutant with terCDE, but not terZAB, partially restored tellurite resistance. When the terZABCDE deletion mutant was complemented with terZAB or terCDE, Y. pestis exhibited filamentous morphology during macrophage infections as well as while these complemented genes were being expressed under an in vitro condition. Further in E. coli, expression of Y. pestis terZAB, but not terCDE, conferred a filamentous phenotype.
These findings support the role of Y. pestis terZAB mediation of the filamentous response phenotype; whereas, terCDE confers tellurite resistance. Although the beneficial role of filamentous morphological responses by Y. pestis during macrophage infections is yet to be fully defined, it may be a bacterial adaptive strategy to macrophage associated stresses.
鼠疫耶尔森菌通过寄生于宿主巨噬细胞引发感染。作为对巨噬细胞感染的反应,胞内鼠疫耶尔森菌可呈现丝状细胞形态,这可能介导对宿主细胞固有免疫反应的抗性。我们之前观察到在巨噬细胞感染期间,鼠疫耶尔森菌来自terZABCDE操纵子的亚碲酸盐抗性蛋白TerD和TerE的表达。其他人观察到在暴露于亚碲酸盐的大肠杆菌中,与亚碲酸盐抗性操纵子表达相关的丝状反应。因此,在本研究中,我们研究了鼠疫耶尔森菌亚碲酸盐抗性操纵子在巨噬细胞感染期间丝状细胞形态中的潜在作用。
用亚碲酸钠(Na2TeO3)对鼠疫耶尔森菌培养物进行体外处理,导致细菌细胞呈现与巨噬细胞感染期间观察到的丝状表型相似的丝状表型。terZAB基因的缺失突变体消除了对亚碲酸盐暴露或胞内寄生的丝状形态反应,但不影响亚碲酸盐抗性。然而,terZABCDE缺失突变体消除了丝状形态反应和亚碲酸盐抗性。用terCDE而不是terZAB对terZABCDE缺失突变体进行互补,部分恢复了亚碲酸盐抗性。当用terZAB或terCDE对terZABCDE缺失突变体进行互补时,鼠疫耶尔森菌在巨噬细胞感染期间以及这些互补基因在体外条件下表达时均呈现丝状形态。此外,在大肠杆菌中,鼠疫耶尔森菌terZAB而非terCDE的表达赋予了丝状表型。
这些发现支持鼠疫耶尔森菌terZAB介导丝状反应表型的作用;而terCDE赋予亚碲酸盐抗性。尽管鼠疫耶尔森菌在巨噬细胞感染期间丝状形态反应的有益作用尚未完全明确,但它可能是细菌对巨噬细胞相关应激的一种适应性策略。