Peripheral immune responses to filoviruses in a reservoir versus spillover hosts reveal transcriptional correlates of disease

Several filoviruses, including Marburg virus (MARV), cause severe disease in humans and nonhuman primates (NHPs). However, the Egyptian rousette bat (ERB, ), the only known MARV reservoir, shows no overt illness upon natural or experimental infection, which, like other bat hosts of zoonoses, is due...

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Veröffentlicht in:Frontiers in immunology 2024-01, Vol.14, p.1306501
Hauptverfasser: Guito, Jonathan C, Arnold, Catherine E, Schuh, Amy J, Amman, Brian R, Sealy, Tara K, Spengler, Jessica R, Harmon, Jessica R, Coleman-McCray, Joann D, Sanchez-Lockhart, Mariano, Palacios, Gustavo F, Towner, Jonathan S, Prescott, Joseph B
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Sprache:eng
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Zusammenfassung:Several filoviruses, including Marburg virus (MARV), cause severe disease in humans and nonhuman primates (NHPs). However, the Egyptian rousette bat (ERB, ), the only known MARV reservoir, shows no overt illness upon natural or experimental infection, which, like other bat hosts of zoonoses, is due to well-adapted, likely species-specific immune features. Despite advances in understanding reservoir immune responses to filoviruses, ERB peripheral blood responses to MARV and how they compare to those of diseased filovirus-infected spillover hosts remain ill-defined. We thus conducted a longitudinal analysis of ERB blood gene responses during acute MARV infection. These data were then contrasted with a compilation of published primate blood response studies to elucidate gene correlates of filovirus protection versus disease. Our work expands on previous findings in MARV-infected ERBs by supporting both host resistance and disease tolerance mechanisms, offers insight into the peripheral immunocellular repertoire during infection, and provides the most direct known cross-examination between reservoir and spillover hosts of the most prevalently-regulated response genes, pathways and activities associated with differences in filovirus pathogenesis and pathogenicity.
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2023.1306501