Zoonotic potential of a novel bat morbillivirus

Ikegame, S.; Carmichael, J. C.; Wells, H.; Furler, R. L.; Acklin, J. A.; Chiu, H.-P.; Oguntuyo, K. Y.; Cox, R. M.; Patel, A. R.; Kowdle, S.; Stevens, C. S.; Eckley, M.; Zhan, S.; Lim, J. K.; Hashiguchi, T.; Durigon, E. L.; Schountz, T.; Epstein, J. E.; Plemper, R. K.; Daszak, P.; Anthony, S. J.; Lee, B.

doi:10.1101/2021.09.17.460143

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bioRxiv · 10.1101/2021.09.17.460143

Zoonotic potential of a novel bat morbillivirus

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Abstract

Morbilliviruses are amongst the most contagious viral pathogens that infect mammals. Metagenomic surveys have identified numerous morbillivirus sequences in bats, but no full-length authentic morbillivirus has been isolated or characterized from bats. Here we detail the discovery of full-length Myotis Bat Morbillivirus (MBaMV) from a bat surveillance program in Brazil. After determining that MBaMV utilizes bat CD150 but not human CD150 as an entry receptor, we generated an infectious clone of MBaMV using reverse genetics. MBaMV exhibited features consistent with other morbilliviruses, including pleomorphic virions, P-editing and the rule-of-six. MBaMV replicated well in human epithelial cell lines in a nectin-4 dependent manner. Surprisingly, MBaMV was able to infect human macrophages in a CD150-independent manner. However, MBaMV was restricted by cross-neutralizing human sera and did not evade the human innate immune system, indicating that while zoonotic spillover into humans may be possible, MBaMV replication in humans would likely be restricted.

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Ikegame, S., Carmichael, J. C., Wells, H., Furler, R. L., Acklin, J. A., Chiu, H.-P., Oguntuyo, K. Y., Cox, R. M., Patel, A. R., Kowdle, S., Stevens, C. S., Eckley, M., Zhan, S., Lim, J. K., Hashiguchi, T., Durigon, E. L., Schountz, T., Epstein, J. E., Plemper, R. K., Daszak, P., Anthony, S. J., Lee, B.. 2021-09-17. Zoonotic potential of a novel bat morbillivirus. https://doi.org/10.1101/2021.09.17.460143

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