Increased Susceptibility of Rousettus aegyptiacus Bats to Respiratory SARS-CoV-2 Challenge Despite Its Distinct Tropism for Gut Epithelia in Bats

Increasing evidence suggests bats are the ancestral hosts of the majority of coronaviruses. In general, coronaviruses primarily target the gastrointestinal system, while some strains, especially Betacoronaviruses with the most relevant representatives SARS-CoV, MERS-CoV, and SARS-CoV-2, also cause severe respiratory disease in humans and other mammals. We previously reported the susceptibility of <i>Rousettus aegyptiacus</i> (Egyptian fruit bats) to intranasal SARS-CoV-2 infection. Here, we compared their permissiveness to an oral infection versus respiratory challenge (intranasal or orotracheal) by assessing virus shedding, host immune responses, tissue-specific pathology, and physiological parameters. While respiratory challenge with a moderate infection dose of 1 × 10<sup>4</sup> TCID<sub>50</sub> caused a systemic infection with oral and nasal shedding of replication-competent virus, the oral challenge only induced nasal shedding of low levels of viral RNA. Even after a challenge with a higher infection dose of 1 × 10<sup>6</sup> TCID<sub>50</sub>, no replication-competent virus was detectable in any of the samples of the orally challenged bats. We postulate that SARS-CoV-2 is inactivated by HCl and digested by pepsin in the stomach of <i>R. aegyptiacus</i>, thereby decreasing the efficiency of an oral infection. Therefore, fecal shedding of RNA seems to depend on systemic dissemination upon respiratory infection. These findings may influence our general understanding of the pathophysiology of coronavirus infections in bats.

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Journal
Viruses
Published
2024-10-31
DOI
https://doi.org/10.3390/v16111717
Citations
3
Primary Topic
Bat Biology and Ecology Studies
Type
article
Field-Weighted Citation Impact
3.09
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article

Increased Susceptibility of Rousettus aegyptiacus Bats to Respiratory SARS-CoV-2 Challenge Despite Its Distinct Tropism for Gut Epithelia in Bats

Marcel Bokelmann, Alexander Riek, Gang Pei, Angele Breithaupt et al.
3 citations
Viruses
Bat Biology and Ecology Studies
3.09
article

Increased Susceptibility of Rousettus aegyptiacus Bats to Respiratory SARS-CoV-2 Challenge Despite Its Distinct Tropism for Gut Epithelia in Bats

Marcel Bokelmann, Alexander Riek, Gang Pei, Angele Breithaupt, Anca Dorhoi, Anne Balkema‐Buschmann, Balal Sadeghi, John R. Speakman, Claudia Blaurock, Catherine Hambly, Björn-Patrick Mohl
article en
3 citations

Abstract

Increasing evidence suggests bats are the ancestral hosts of the majority of coronaviruses. In general, coronaviruses primarily target the gastrointestinal system, while some strains, especially Betacoronaviruses with the most relevant representatives SARS-CoV, MERS-CoV, and SARS-CoV-2, also cause severe respiratory disease in humans and other mammals. We previously reported the susceptibility of <i>Rousettus aegyptiacus</i> (Egyptian fruit bats) to intranasal SARS-CoV-2 infection. Here, we compared their permissiveness to an oral infection versus respiratory challenge (intranasal or orotracheal) by assessing virus shedding, host immune responses, tissue-specific pathology, and physiological parameters. While respiratory challenge with a moderate infection dose of 1 × 10<sup>4</sup> TCID<sub>50</sub> caused a systemic infection with oral and nasal shedding of replication-competent virus, the oral challenge only induced nasal shedding of low levels of viral RNA. Even after a challenge with a higher infection dose of 1 × 10<sup>6</sup> TCID<sub>50</sub>, no replication-competent virus was detectable in any of the samples of the orally challenged bats. We postulate that SARS-CoV-2 is inactivated by HCl and digested by pepsin in the stomach of <i>R. aegyptiacus</i>, thereby decreasing the efficiency of an oral infection. Therefore, fecal shedding of RNA seems to depend on systemic dissemination upon respiratory infection. These findings may influence our general understanding of the pathophysiology of coronavirus infections in bats.

VirusesVol. 16(11)
Friedrich-Loeffler-Institut (DE), University of Aberdeen (GB), Robert Koch Institute (DE)
Good health and well-being
Openalex Percentile: Top 8%
Bat Biology and Ecology Studies
3.09
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