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Mendenhall, I. H.

Publications and source records attributed to Mendenhall, I. H..

2 recordsLinked to original sources

Genetic introgression is a catalyst for diversification in an Old World fruit bat radiation

Genetic introgression, the exchange of genes between closely related species, was once thought to be rare and counterproductive to species differentiation until more recent evidence showed that introgression is pervasive in nature and may even facilitate the transfer of important functional traits among species. However, evidence for the role of introgression in facilitating speciation in natural systems is rare. In this study, we investigated the role of introgression in accelerating trait sharing and speciation in a poorly understood group of South and Southeast Asian fruit bats of the genus Cynopterus using genome-wide DNA from 93 individuals, including both fresh and historic museum specimens. We uncovered substantial new species level diversity within the genus and retrieved multiple strong signatures of complex genetic introgression, including two putative events of hybrid speciation within this radiation. In the genomic areas implicated in most of these introgression events, we identified a locus potentially linked to sperm integrity and fusion of egg and sperm. Further, we observed high between-species divergence in an area of the genome linked to skull development. The Cynopterus radiation augments a small but growing list of examples showing that genetic introgression - rather than forming an impediment against differentiation - is likely to boost and reinforce diversification processes, for example through the transfer of functional loci that may facilitate innovations. Our study also highlights the importance of museum collections in understanding cryptic diversity and speciation in complex biogeographic settings.

evolutionary biology↗

Spike independent replication of human coronavirus in bat cells

Bats are the reservoir for numerous human pathogens including coronaviruses. The factors leading to the emergence and sustained transmission of coronaviruses in humans are poorly understood. An outstanding question is how coronaviruses can accomplish a host switch with a likely mismatch between the surface protein spike of a bat virus and the human cellular receptor at the time of zoonotic virus transmission. To identify potential novel evolutionary pathways for zoonotic virus emergence, we serially passaged six human 229E isolates in a newly established Rhinolophus lepidus (horseshoe bat) kidney cells and analyzed viral genetic changes. Here we observed extensive deletions within the spike and ORF4 genes of five 229E viruses after passaging in bat cells. As a result, spike protein expression and infectivity of human cells was lost in 5 of 6 viruses but the capability to infect bat cells was maintained. Only viruses that expressed the spike protein could be neutralized by 229E spike-specific antibodies in human cells, whereas there was no neutralizing effect on viruses that do not express the spike protein inoculated on bat cells. However, one isolate acquired an early stop codon abrogating spike expression but maintaining infection in bat cells. Upon passaging this isolate in human cells, spike expression was restored due to acquisition of nucleotide insertions amongst virus subpopulations. Spike-independent infection of coronaviruses provides an alternative mechanism for viral maintenance in bats that does not rely on the compatibility of viral surface proteins and cellular entry receptors.

microbiology↗