Department of Veterinary Pathobiology, Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, Oklahoma, United States of America.
PLoS One. 2012;7(7):e42211. doi: 10.1371/journal.pone.0042211. Epub 2012 Jul 27.
Yersinia pestis causes severe disease in natural rodent hosts, but mild to inapparent disease in certain rodent predators such as dogs. Y. pestis initiates infection in susceptible hosts by parasitizing and multiplying intracellularly in local macrophages prior to systemic dissemination. Thus, we hypothesize that Y. pestis disease severity may depend on the degree to which intracellular Y. pestis overcomes the initial host macrophage imposed stress.
METHODOLOGY/PRINCIPAL FINDINGS: To test this hypothesis, the progression of in vitro infection by Y. pestis KIM62053.1+ of mouse splenic and RAW264.7 tissue culture macrophages and dog peripheral blood-derived and DH82 tissue culture macrophages was studied using microscopy and various parameters of infection. The study showed that during the early stage of infection, intracellular Y. pestis assumed filamentous cellular morphology with multiple copies of the genome per bacterium in both mouse and dog macrophages. Later, in mouse macrophages, the infection elicited spacious vacuolar extension of Yersinia containing vacuoles (YCV), and the filamentous Y. pestis reverted to coccobacillary morphology with genomic equivalents approximately equaling colony forming units. In contrast, Y. pestis infected dog macrophages did not show noticeable extension of YCV, and intracellular Y. pestis retained the filamentous cellular morphology for the entire experiment in DH82 cells or were killed by blood-derived macrophages. In addition, during the later stage of infection, Y. pestis infected mouse macrophages exhibited cell lysis whereas dog macrophages did not.
CONCLUSION/SIGNIFICANCE: Overall, these results support our hypothesis that Y. pestis in mouse macrophages can overcome the initial intracellular stress necessary for subsequent systemic infection. However, in dogs, failure of Y. pestis to overcome macrophage imposed stress may result in mild or in apparent disease in dogs.
鼠疫耶尔森菌在天然啮齿动物宿主中引起严重疾病,但在某些啮齿动物捕食者(如狗)中则引起轻度至无明显症状的疾病。鼠疫耶尔森菌通过在局部巨噬细胞中寄生和增殖,在系统性传播之前引起易感宿主的感染。因此,我们假设鼠疫耶尔森菌疾病的严重程度可能取决于细胞内鼠疫耶尔森菌克服宿主巨噬细胞最初施加的应激的程度。
方法/主要发现:为了验证这一假设,研究了 Y. pestis KIM62053.1+在体外感染小鼠脾脏和 RAW264.7 组织培养巨噬细胞以及狗外周血衍生和 DH82 组织培养巨噬细胞的过程,使用显微镜和感染的各种参数进行了研究。研究表明,在感染的早期阶段,细胞内鼠疫耶尔森菌在鼠和犬巨噬细胞中都呈现出丝状细胞形态,每个细菌的基因组有多个拷贝。后来,在鼠巨噬细胞中,感染引起了 Yersinia 包含空泡(YCV)的广泛空泡扩张,而丝状鼠疫耶尔森菌恢复为短杆状形态,基因组当量约等于菌落形成单位。相比之下,感染犬巨噬细胞的鼠疫耶尔森菌没有明显的 YCV 扩张,并且在 DH82 细胞中或被血液衍生的巨噬细胞杀死的整个实验过程中,细胞内鼠疫耶尔森菌保持丝状细胞形态。此外,在感染的后期阶段,感染鼠疫耶尔森菌的鼠巨噬细胞发生细胞溶解,而犬巨噬细胞则没有。
结论/意义:总体而言,这些结果支持我们的假设,即鼠巨噬细胞中的鼠疫耶尔森菌可以克服随后系统性感染所需的初始细胞内应激。然而,在狗中,鼠疫耶尔森菌未能克服巨噬细胞施加的应激可能导致狗的轻度或无明显疾病。