4.6 Article

Ectopic expression of murine CD163 enables cell-culture isolation of lactate dehydrogenase-elevating virus 63 years after its discovery

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JOURNAL OF VIROLOGY
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AMER SOC MICROBIOLOGY
DOI: 10.1128/jvi.00930-23

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lactate dehydrogenase-elevating virus; arterivirus; CD163; porcine reproductive and respiratory syndrome virus; simian hemorrhagic fever virus; PRRSV; SHFV

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Arteriviruses, including lactate dehydrogenase-elevating virus (LDV), have been identified as RNA viruses related to coronaviruses. LDV is a valuable model for studying immune failure and viral persistence in immunocompetent mice. This study demonstrates that the macrophage marker CD163 is essential for LDV infection and the establishment of an immortalized cell-culture system. Additionally, LDV infection can be completely resisted in knockout mice lacking the expression of mCD163. The findings contribute to the understanding of arterivirus infection and highlight the significance of CD163 utilization in this virus family.
Arteriviruses are RNA viruses related to coronaviruses but have not yet been associated with human infection. A murine arterivirus, lactate dehydrogenase-elevating virus (LDV), was first described in 1960 and quickly became a promising model for understanding immune failure due to its unique ability to persist in immunocompetent adult mice. However, the inability to culture LDV in vitro ultimately limited this system. Here, we demonstrate that the macrophage marker CD163 is essential for LDV infection. Expression of the murine homolog (mCD163) in otherwise mCD163-negative cell lines from mice and nonhuman primates enables productive LDV infection, creating the first immortalized cell-culture system. We also show that mCD163-knockout mice are completely resistant to LDV infection. These findings advance LDV as a model of arterivirus infection and viral persistence while adding to a growing body of literature suggesting that CD163 utilization is a broad feature of arteriviruses.

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