TY - JOUR
T1 - Isolation and genome sequencing of cytomegaloviruses from Natal multimammate mice (Mastomys natalensis)
AU - Hansen, Frederick
AU - Vučak, Matej
AU - Nichols, Jenna
AU - Hughes, Joseph
AU - Bane, Sidy
AU - Camiolo, Salvatore
AU - da Silva Filipe, Ana
AU - Ostermann, Eleonore
AU - Staliunaite, Laura
AU - Chan, Baca
AU - Mauch, Thekla
AU - Sogoba, Nafomon
AU - Streblow, Daniel N.
AU - Voigt, Sebastian
AU - Oestereich, Lisa
AU - Ehlers, Bernhard
AU - Redwood, Alec J.
AU - Feldmann, Heinz
AU - Brune, Wolfram
AU - Rosenke, Kyle
AU - Jarvis, Michael A.
AU - Davison, Andrew J.
PY - 2023/8/29
Y1 - 2023/8/29
N2 - Distinct cytomegaloviruses (CMVs) are widely distributed across their mammalian hosts in a highly host species-restricted pattern. To date, evidence demonstrating this has been limited largely to PCR-based approaches targeting small, conserved genomic regions, and only a few complete genomes of isolated viruses representing distinct CMV species have been sequenced. We have now combined direct isolation of infectious viruses from tissues with complete genome sequencing to provide a view of CMV diversity in a wild animal population. We targeted Natal multimammate mice (Mastomys natalensis), which are common in sub-Saharan Africa, are known to carry a variety of zoonotic pathogens, and are regarded as the primary source of Lassa virus (LASV) spillover into humans. Using transformed epithelial cells prepared from M. natalensis kidneys, we isolated CMVs from the salivary gland tissue of 14 of 37 (36 %) animals from a field study site in Mali. Genome sequencing showed that these primary isolates represent three different M. natalensis CMVs (MnatCMVs: MnatCMV1, MnatCMV2 and MnatCMV3), with some animals carrying multiple MnatCMVs or multiple strains of a single MnatCMV presumably as a result of coinfection or superinfection. Including primary isolates and plaque-purified isolates, we sequenced and annotated the genomes of two MnatCMV1 strains (derived from sequencing 14 viruses), six MnatCMV2 strains (25 viruses) and ten MnatCMV3 strains (21 viruses), totalling 18 MnatCMV strains isolated as 60 infectious viruses. Phylogenetic analysis showed that these MnatCMVs group with other murid viruses in the genus Muromegalovirus (subfamily Betaherpesvirinae, family Orthoherpesviridae), and that MnatCMV1 and MnatCMV2 are more closely related to each other than to MnatCMV3. The availability of MnatCMV isolates and the characterization of their genomes will serve as the prelude to the generation of a MnatCMV-based vaccine to target LASV in the M. natalensis reservoir.
AB - Distinct cytomegaloviruses (CMVs) are widely distributed across their mammalian hosts in a highly host species-restricted pattern. To date, evidence demonstrating this has been limited largely to PCR-based approaches targeting small, conserved genomic regions, and only a few complete genomes of isolated viruses representing distinct CMV species have been sequenced. We have now combined direct isolation of infectious viruses from tissues with complete genome sequencing to provide a view of CMV diversity in a wild animal population. We targeted Natal multimammate mice (Mastomys natalensis), which are common in sub-Saharan Africa, are known to carry a variety of zoonotic pathogens, and are regarded as the primary source of Lassa virus (LASV) spillover into humans. Using transformed epithelial cells prepared from M. natalensis kidneys, we isolated CMVs from the salivary gland tissue of 14 of 37 (36 %) animals from a field study site in Mali. Genome sequencing showed that these primary isolates represent three different M. natalensis CMVs (MnatCMVs: MnatCMV1, MnatCMV2 and MnatCMV3), with some animals carrying multiple MnatCMVs or multiple strains of a single MnatCMV presumably as a result of coinfection or superinfection. Including primary isolates and plaque-purified isolates, we sequenced and annotated the genomes of two MnatCMV1 strains (derived from sequencing 14 viruses), six MnatCMV2 strains (25 viruses) and ten MnatCMV3 strains (21 viruses), totalling 18 MnatCMV strains isolated as 60 infectious viruses. Phylogenetic analysis showed that these MnatCMVs group with other murid viruses in the genus Muromegalovirus (subfamily Betaherpesvirinae, family Orthoherpesviridae), and that MnatCMV1 and MnatCMV2 are more closely related to each other than to MnatCMV3. The availability of MnatCMV isolates and the characterization of their genomes will serve as the prelude to the generation of a MnatCMV-based vaccine to target LASV in the M. natalensis reservoir.
KW - cytomegalovirus
KW - genome sequence
KW - herpesvirus
KW - Mastomys natalensis
KW - Mastomys natalensis cytomegalovirus
KW - muromegalovirus
UR - http://www.scopus.com/inward/record.url?scp=85168980860&partnerID=8YFLogxK
U2 - 10.1099/jgv.0.001873
DO - 10.1099/jgv.0.001873
M3 - Article
C2 - 37643006
AN - SCOPUS:85168980860
SN - 0022-1317
VL - 104
JO - The Journal of general virology
JF - The Journal of general virology
IS - 8
M1 - 001873
ER -