AI Article Synopsis

  • Bats are considered the primary hosts for many coronaviruses, particularly Betacoronaviruses, which can cause severe respiratory diseases in humans.
  • Research showed that Egyptian fruit bats were more susceptible to respiratory infections (like SARS-CoV-2) compared to oral infections, with significant differences in virus shedding and immune response.
  • The study suggests that SARS-CoV-2 is likely inactivated in the bats' stomachs, making oral infections less effective, highlighting the unique pathology of coronavirus infections in bats.

Article 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 (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 TCID 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 TCID, 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 , 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11598992PMC
http://dx.doi.org/10.3390/v16111717DOI Listing

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