We describe the first known relatives of rubella virus ( Matonaviridae : Rubivirus ) 1 in Africa and Europe. Ruhugu virus, the closest relative of rubella virus, was found in apparently healthy cyclops leaf-nosed bats ( Hipposideros cyclops ) in Uganda. Rustrela virus, outgroup to the rubella/ruhugu clade of viruses, was found in acutely encephalitic placental and marsupial animals at a zoo in Germany and in wild yellow-necked field mice ( Apodemus flavicollis ) at and near the zoo. Ruhugu and rustrela viruses share an identical genomic architecture with rubella virus 2 , 3 . Amino acid sequences of rubella, ruhugu, and rustrela viruses are moderately to highly conserved within 4 putative B-cell epitopes in the fusion (EI) protein and, in the case of rubella and ruhugu viruses, within two putative T-cell epitopes in the capsid protein 4 – 6 . Modeling of E1 homotrimers in the post-fusion state predicts similar host-cell membrane fusion capacity for ruhugu and rubella viruses 5 . Together, these findings suggest show that some members of the Matonaviridae can cross wide host species barriers and that rubella virus likely had a zoonotic origin. Our findings raise concerns about future zoonotic transmission of rubella-like viruses but open doors for heretofore impossible comparative studies and novel animal models of rubella and congenital rubella syndrome.
Obligate hematophagous ectoparasitic flies of the superfamily Hippoboscoidea are distributed worldwide, but their role as vectors and reservoirs of viruses remains understudied. We examined hippoboscoid bat flies (family Nycteribiidae) parasitizing Angolan soft-furred fruit bats (Lissonycteris angolensis ruwenzorii) from Bundibugyo District, Uganda. Using metagenomic methods, we detected 21 variants of the rhabdovirid genus Ledantevirus, which contains medically important “bat-associated” viruses. These 21 viruses, representing at least two divergent viral lineages, infected 26 bat flies from 8 bats in a single roost. Cophylogenetic analyses of viruses and bat flies resulted in strong evidence of virus-host codivergence, indicating vertical transmission of bat fly ledanteviruses. Examination of oral swabs from bats revealed ledantevirus RNA in the saliva of 1 out of 11 bats, with no evidence of insect genetic material in the mouth of this bat. These data demonstrate that bat flies can harbor diverse ledanteviruses even in a single roost and that the predominant mode of transmission is likely vertical (among bat flies), but that bats can become infected and shed viruses orally. In conclusion, bat flies may serve as ectoparasitic reservoirs of “bat-associated” viruses that only transiently or sporadically infect bats.
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