Department of Microbiology and Immunology, University of Louisville Health Sciences Center, 505 South Hancock Street Rm 622, Louisville, KY 40202, USA.
Center for Predictive Medicine for Biodefense and Emerging Infectious Diseases, Louisville, KY 40202, USA.
Viruses. 2018 Feb 10;10(2):75. doi: 10.3390/v10020075.
Mammarenavirusesare single-stranded RNA viruses with a bisegmented ambisense genome. Ingestion has been shown as a natural route of transmission for both Lassa virus (LASV) and Lymphocytic choriomeningitis virus (LCMV). Due to the mechanism of transmission, epithelial tissues are among the first host cells to come in contact with the viruses, and as such they potentially play a role in spread of virus to naïve hosts. The role of the intestinal epithelia during arenavirus infection remains to be uncharacterized. We have utilized a well-established cell culture model, Caco-2, to investigate the role of intestinal epithelia during intragastric infection. We found that LCMV-Armstrong, LCMV-WE, and Mopeia (MOPV) release infectious progeny via similar patterns. However, the reassortant virus, ML-29, containing the L segment of MOPV and S segment of LASV, exhibits a unique pattern of viral release relative to LCMV and MOPV. Furthermore, we have determined attachment efficacy to Caco-2 cells is potentially responsible for observed replication kinetics of these viruses in a polarized Caco-2 cell model. Collectively, our data shows that viral dissemination and interaction with intestinal epithelia may be host, tissue, and viral specific.
沙粒病毒是具有双节段反义基因组的单链 RNA 病毒。已证实摄入是拉沙病毒 (LASV) 和淋巴细胞性脉络丛脑膜炎病毒 (LCMV) 的两种自然传播途径。由于传播机制,上皮组织是首先与病毒接触的宿主细胞之一,因此它们可能在病毒向未感染的宿主传播中发挥作用。在沙粒病毒感染期间,肠道上皮的作用仍未被描述。我们利用成熟的细胞培养模型 Caco-2 来研究在胃内感染期间肠道上皮的作用。我们发现 LCMV-Armstrong、LCMV-WE 和 Mopeia(MOPV)通过相似的模式释放感染性后代。然而,包含 MOPV 的 L 节段和 LASV 的 S 节段的重组病毒 ML-29 相对于 LCMV 和 MOPV 表现出独特的病毒释放模式。此外,我们已经确定与 Caco-2 细胞的附着效力可能是导致这些病毒在极化的 Caco-2 细胞模型中观察到的复制动力学的原因。总之,我们的数据表明病毒传播和与肠道上皮的相互作用可能具有宿主、组织和病毒特异性。