Mastomys natalensis is a possible natural rodent reservoir for encephalomyocarditis virus
Encephalomyocarditis virus (EMCV) infects a wide range of hosts and can cause encephalitis, myocarditis, reproductive disorders and diabetes mellitus in selected mammalian species. As for humans, EMCV infection seems to occur by the contact with animals and can cause febrile illnesses in some infect...
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Published in | Journal of general virology Vol. 102; no. 3 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
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01.03.2021
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Abstract | Encephalomyocarditis virus (EMCV) infects a wide range of hosts and can cause encephalitis, myocarditis, reproductive disorders and diabetes mellitus in selected mammalian species. As for humans, EMCV infection seems to occur by the contact with animals and can cause febrile illnesses in some infected patients. Here we isolated EMCV strain ZM12/14 from a natal multimammate mouse (
Mastomys natalensis: M. natalensis
) in Zambia. Pairwise sequence similarity of the ZM12/14 P1 region consisting of antigenic capsid proteins showed the highest similarity of nucleotide (80.7 %) and amino acid (96.2%) sequence with EMCV serotype 1 (EMCV-1). Phylogenetic analysis revealed that ZM12/14 clustered into EMCV-1 at the P1 and P3 regions but segregated from known EMCV strains at the P2 region, suggesting a unique evolutionary history. Reverse transcription PCR (RT-PCR) screening and neutralizing antibody assays for EMCV were performed using collected tissues and serum from various rodents (
n
=179) captured in different areas in Zambia. We detected the EMCV genome in 19
M
.
natalensis
(19/179=10.6 %) and neutralizing antibody for EMCV in 33
M
.
natalensis
(33/179=18.4 %). However, we did not detect either the genome or neutralizing antibody in other rodent species. High neutralizing antibody litres (≧320) were observed in both RT-PCR-negative and -positive animals. Inoculation of ZM12/14 caused asymptomatic persistent infection in BALB/c mice with high antibody titres and high viral loads in some organs, consistent with the above epidemiological results. This study is the first report of the isolation of EMCV in Zambia, suggesting that
M. natalensis
may play a role as a natural reservoir of infection. |
---|---|
AbstractList | Encephalomyocarditis virus (EMCV) infects a wide range of hosts and can cause encephalitis, myocarditis, reproductive disorders and diabetes mellitus in selected mammalian species. As for humans, EMCV infection seems to occur by the contact with animals and can cause febrile illnesses in some infected patients. Here we isolated EMCV strain ZM12/14 from a natal multimammate mouse (
Mastomys natalensis: M. natalensis
) in Zambia. Pairwise sequence similarity of the ZM12/14 P1 region consisting of antigenic capsid proteins showed the highest similarity of nucleotide (80.7 %) and amino acid (96.2%) sequence with EMCV serotype 1 (EMCV-1). Phylogenetic analysis revealed that ZM12/14 clustered into EMCV-1 at the P1 and P3 regions but segregated from known EMCV strains at the P2 region, suggesting a unique evolutionary history. Reverse transcription PCR (RT-PCR) screening and neutralizing antibody assays for EMCV were performed using collected tissues and serum from various rodents (
n
=179) captured in different areas in Zambia. We detected the EMCV genome in 19
M
.
natalensis
(19/179=10.6 %) and neutralizing antibody for EMCV in 33
M
.
natalensis
(33/179=18.4 %). However, we did not detect either the genome or neutralizing antibody in other rodent species. High neutralizing antibody litres (≧320) were observed in both RT-PCR-negative and -positive animals. Inoculation of ZM12/14 caused asymptomatic persistent infection in BALB/c mice with high antibody titres and high viral loads in some organs, consistent with the above epidemiological results. This study is the first report of the isolation of EMCV in Zambia, suggesting that
M. natalensis
may play a role as a natural reservoir of infection. Encephalomyocarditis virus (EMCV) infects a wide range of hosts and can cause encephalitis, myocarditis, reproductive disorders and diabetes mellitus in selected mammalian species. As for humans, EMCV infection seems to occur by the contact with animals and can cause febrile illnesses in some infected patients. Here we isolated EMCV strain ZM12/14 from a natal multimammate mouse ( ) in Zambia. Pairwise sequence similarity of the ZM12/14 P1 region consisting of antigenic capsid proteins showed the highest similarity of nucleotide (80.7 %) and amino acid (96.2%) sequence with EMCV serotype 1 (EMCV-1). Phylogenetic analysis revealed that ZM12/14 clustered into EMCV-1 at the P1 and P3 regions but segregated from known EMCV strains at the P2 region, suggesting a unique evolutionary history. Reverse transcription PCR (RT-PCR) screening and neutralizing antibody assays for EMCV were performed using collected tissues and serum from various rodents ( =179) captured in different areas in Zambia. We detected the EMCV genome in 19 . (19/179=10.6 %) and neutralizing antibody for EMCV in 33 . (33/179=18.4 %). However, we did not detect either the genome or neutralizing antibody in other rodent species. High neutralizing antibody litres (≧320) were observed in both RT-PCR-negative and -positive animals. Inoculation of ZM12/14 caused asymptomatic persistent infection in BALB/c mice with high antibody titres and high viral loads in some organs, consistent with the above epidemiological results. This study is the first report of the isolation of EMCV in Zambia, suggesting that may play a role as a natural reservoir of infection. Encephalomyocarditis virus (EMCV) infects a wide range of hosts and can cause encephalitis, myocarditis, reproductive disorders and diabetes mellitus in selected mammalian species. As for humans, EMCV infection seems to occur by the contact with animals and can cause febrile illnesses in some infected patients. Here we isolated EMCV strain ZM12/14 from a natal multimammate mouse (Mastomys natalensis: M. natalensis) in Zambia. Pairwise sequence similarity of the ZM12/14 P1 region consisting of antigenic capsid proteins showed the highest similarity of nucleotide (80.7 %) and amino acid (96.2%) sequence with EMCV serotype 1 (EMCV-1). Phylogenetic analysis revealed that ZM12/14 clustered into EMCV-1 at the P1 and P3 regions but segregated from known EMCV strains at the P2 region, suggesting a unique evolutionary history. Reverse transcription PCR (RT-PCR) screening and neutralizing antibody assays for EMCV were performed using collected tissues and serum from various rodents (n=179) captured in different areas in Zambia. We detected the EMCV genome in 19 M. natalensis (19/179=10.6 %) and neutralizing antibody for EMCV in 33 M. natalensis (33/179=18.4 %). However, we did not detect either the genome or neutralizing antibody in other rodent species. High neutralizing antibody litres (≧320) were observed in both RT-PCR-negative and -positive animals. Inoculation of ZM12/14 caused asymptomatic persistent infection in BALB/c mice with high antibody titres and high viral loads in some organs, consistent with the above epidemiological results. This study is the first report of the isolation of EMCV in Zambia, suggesting that M. natalensis may play a role as a natural reservoir of infection.Encephalomyocarditis virus (EMCV) infects a wide range of hosts and can cause encephalitis, myocarditis, reproductive disorders and diabetes mellitus in selected mammalian species. As for humans, EMCV infection seems to occur by the contact with animals and can cause febrile illnesses in some infected patients. Here we isolated EMCV strain ZM12/14 from a natal multimammate mouse (Mastomys natalensis: M. natalensis) in Zambia. Pairwise sequence similarity of the ZM12/14 P1 region consisting of antigenic capsid proteins showed the highest similarity of nucleotide (80.7 %) and amino acid (96.2%) sequence with EMCV serotype 1 (EMCV-1). Phylogenetic analysis revealed that ZM12/14 clustered into EMCV-1 at the P1 and P3 regions but segregated from known EMCV strains at the P2 region, suggesting a unique evolutionary history. Reverse transcription PCR (RT-PCR) screening and neutralizing antibody assays for EMCV were performed using collected tissues and serum from various rodents (n=179) captured in different areas in Zambia. We detected the EMCV genome in 19 M. natalensis (19/179=10.6 %) and neutralizing antibody for EMCV in 33 M. natalensis (33/179=18.4 %). However, we did not detect either the genome or neutralizing antibody in other rodent species. High neutralizing antibody litres (≧320) were observed in both RT-PCR-negative and -positive animals. Inoculation of ZM12/14 caused asymptomatic persistent infection in BALB/c mice with high antibody titres and high viral loads in some organs, consistent with the above epidemiological results. This study is the first report of the isolation of EMCV in Zambia, suggesting that M. natalensis may play a role as a natural reservoir of infection. |
Author | Orba, Yasuko Sawa, Hirofumi Hang’ombe, Bernard M. Kishimoto, Mai Hall, William W. Sasaki, Michihito |
Author_xml | – sequence: 1 givenname: Mai surname: Kishimoto fullname: Kishimoto, Mai organization: Division of Molecular Pathobiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan – sequence: 2 givenname: Bernard M. surname: Hang’ombe fullname: Hang’ombe, Bernard M. organization: Africa Center of Excellence for Infectious Diseases of Humans and Animals, University of Zambia, Lusaka, Zambia, Department of Para-clinical Studies, School of Veterinary and Medicine, University of Zambia, Lusaka, Zambia – sequence: 3 givenname: William W. surname: Hall fullname: Hall, William W. organization: Centre for Research in Infectious Diseases, School of Medicine, University College Dublin, Dublin, Ireland, International Collaboration Unit, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan, National Virus Reference Laboratory, School of Medicine, University College Dublin, Dublin, Ireland, Global Virus Network, Baltimore, MD, USA – sequence: 4 givenname: Yasuko orcidid: 0000-0001-9910-3912 surname: Orba fullname: Orba, Yasuko organization: International Collaboration Unit, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan, Division of Molecular Pathobiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan – sequence: 5 givenname: Hirofumi orcidid: 0000-0003-2569-2755 surname: Sawa fullname: Sawa, Hirofumi organization: Global Virus Network, Baltimore, MD, USA, Division of Molecular Pathobiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan, International Collaboration Unit, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan – sequence: 6 givenname: Michihito orcidid: 0000-0003-1607-2175 surname: Sasaki fullname: Sasaki, Michihito organization: Division of Molecular Pathobiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan |
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SubjectTerms | Animals Antibodies, Neutralizing - blood Antibodies, Viral - blood Cardiovirus Infections - epidemiology Cardiovirus Infections - veterinary Cardiovirus Infections - virology Disease Reservoirs - virology Encephalomyocarditis virus - genetics Encephalomyocarditis virus - immunology Encephalomyocarditis virus - isolation & purification Encephalomyocarditis virus - pathogenicity Evolution, Molecular Genome, Viral Mice, Inbred BALB C Murinae - virology Phylogeny Prevalence Shrews - virology Zambia - epidemiology |
Title | Mastomys natalensis is a possible natural rodent reservoir for encephalomyocarditis virus |
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