TY - JOUR
T1 - Genomic epidemiology and evolutionary analysis of Lassa virus from small mammals suggest bidirectional viral movement across humans and animals
AU - Happi, Anise N.
AU - Ogunsanya, Olusola A.
AU - Sijuwola, Ayotunde E.
AU - Saibu, Femi M.
AU - Akano, Kazeem
AU - Ayinla, Akeemat O.
AU - Daodu, Richard O.
AU - Page, Brady
AU - Olumade, Testimony J.
AU - Oguzie, Judith U.
AU - Oluniyi, Paul E.
AU - Adedokun, Oluwatobi A.
AU - Fadele, John
AU - Nwofoke, Cecilia
AU - Elias, Obineche T.
AU - Ogundana, Kehinde E.
AU - Lawal, Omolola Z.
AU - Nosamiefan, Iguosadolo
AU - Okolie, Johnson
AU - Adelabu, Ademola
AU - Lombardi, Kara
AU - Eller, Leigh A.
AU - Broach, Erica
AU - Prins, Petra A.
AU - Heeney, Jonathan L.
AU - Modjarrad, Kayvon
AU - Njatou, Thierry L.F.A.
AU - Parker, Zahra F.
AU - McCauley, Melanie
AU - Vasan, Sandhya
AU - Parker, Edyth
AU - Collins, Natalie D.
AU - Michael, Nelson L.
AU - Happi, Christian T.
N1 - Publisher Copyright:
© The Author(s) 2026. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact [email protected] for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact [email protected].
PY - 2026
Y1 - 2026
N2 - Lassa fever is a viral haemorrhagic fever that poses a persistent public health threat in several West African countries, particularly Nigeria. The scarcity of Lassa virus (LASV) sequences isolated from small mammal reservoirs limits our knowledge and understanding of LASV genomic diversity and transmission dynamics. To address this knowledge gap, we sampled 1189 small mammals, including mice, rats, and shrews, from two LASV-endemic states in southern Nigeria (Ondo and Ebonyi States) and tested them for the presence of LASV RNA using reverse transcription-quantitative polymerase chain reaction. Selected quantitative polymerase chain reaction-positive samples were subjected to whole genome sequencing and small mammal speciation through next-generation sequencing outputs. We recorded an overall polymerase chain reaction positivity rate of 61.6%, with rat species demonstrating the highest LASV prevalence. We also conducted a serosurvey of 269 small rodents using indirect Enzyme-Linked Immunosorbent Assay (ELISA) and obtained an overall anti-LASV seroprevalence of 45%. Using the Nextera XT metagenomic sequencing protocol, we produced 55 LASV partial (n = 28) and full-length genomes (n = 27) from small mammals sampled, all of which clustered within sublineage 2g. LASV sequences generated from this study suggest that LASV variation is mostly driven by location, as isolates from this study tend to cluster more closely with other isolates collected from within the same region, rather than by collection date or host. However, samples collected from Ebonyi State were more closely related to isolates collected in Ondo State than to isolates from Edo, despite a larger physical distance. Overall, the data from this study suggest free movement of the virus across states in Nigeria, among humans and various non-human taxa. The finding of LASV in additional small mammal hosts suggests that the virus reservoir is vast and may include many small mammals not well-characterized.
AB - Lassa fever is a viral haemorrhagic fever that poses a persistent public health threat in several West African countries, particularly Nigeria. The scarcity of Lassa virus (LASV) sequences isolated from small mammal reservoirs limits our knowledge and understanding of LASV genomic diversity and transmission dynamics. To address this knowledge gap, we sampled 1189 small mammals, including mice, rats, and shrews, from two LASV-endemic states in southern Nigeria (Ondo and Ebonyi States) and tested them for the presence of LASV RNA using reverse transcription-quantitative polymerase chain reaction. Selected quantitative polymerase chain reaction-positive samples were subjected to whole genome sequencing and small mammal speciation through next-generation sequencing outputs. We recorded an overall polymerase chain reaction positivity rate of 61.6%, with rat species demonstrating the highest LASV prevalence. We also conducted a serosurvey of 269 small rodents using indirect Enzyme-Linked Immunosorbent Assay (ELISA) and obtained an overall anti-LASV seroprevalence of 45%. Using the Nextera XT metagenomic sequencing protocol, we produced 55 LASV partial (n = 28) and full-length genomes (n = 27) from small mammals sampled, all of which clustered within sublineage 2g. LASV sequences generated from this study suggest that LASV variation is mostly driven by location, as isolates from this study tend to cluster more closely with other isolates collected from within the same region, rather than by collection date or host. However, samples collected from Ebonyi State were more closely related to isolates collected in Ondo State than to isolates from Edo, despite a larger physical distance. Overall, the data from this study suggest free movement of the virus across states in Nigeria, among humans and various non-human taxa. The finding of LASV in additional small mammal hosts suggests that the virus reservoir is vast and may include many small mammals not well-characterized.
KW - Lassa virus genomes
KW - LASV genomic diversity
KW - LASV IgM and IgG
KW - Nigeria
KW - small mammals
UR - https://www.scopus.com/pages/publications/105042475083
U2 - 10.1093/ve/veag032
DO - 10.1093/ve/veag032
M3 - Article
AN - SCOPUS:105042475083
SN - 2057-1577
VL - 12
JO - Virus Evolution
JF - Virus Evolution
IS - 1
M1 - veag032
ER -