Detection of rat hepatitis E virus, but not human pathogenic hepatitis E virus genotype 1–4 infections in wild rats from Lithuania

•Rat HEV infects Black (Rattus rattus) and Norway (R. norvegicus) rats from Lithuania.•Partial ORF1-derived sequences of rat HEV show geographically-related clustering.•Prevalence of anti-rat HEV antibodies indicates a high-rate of virus circulation in rats.•The low level of parallel rat HEV RNA and...

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Veröffentlicht in:Veterinary microbiology 2018-07, Vol.221, p.129-133
Hauptverfasser: Simanavicius, Martynas, Juskaite, Karolina, Verbickaite, Arune, Jasiulionis, Marius, Tamosiunas, Paulius Lukas, Petraityte-Burneikiene, Rasa, Zvirbliene, Aurelija, Ulrich, Rainer G., Kucinskaite-Kodze, Indre
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container_start_page 129
container_title Veterinary microbiology
container_volume 221
creator Simanavicius, Martynas
Juskaite, Karolina
Verbickaite, Arune
Jasiulionis, Marius
Tamosiunas, Paulius Lukas
Petraityte-Burneikiene, Rasa
Zvirbliene, Aurelija
Ulrich, Rainer G.
Kucinskaite-Kodze, Indre
description •Rat HEV infects Black (Rattus rattus) and Norway (R. norvegicus) rats from Lithuania.•Partial ORF1-derived sequences of rat HEV show geographically-related clustering.•Prevalence of anti-rat HEV antibodies indicates a high-rate of virus circulation in rats.•The low level of parallel rat HEV RNA and anti-rat HEV antibody detection suggest a non-persistent infection. Rat hepatitis E virus (HEV) is an orthohepevirus which is related to other HEV found in humans and other mammals. It was first identified in Norway rats (Rattus norvegicus) from Germany in 2010, and later it has been detected in Black rats (Rattus rattus) and Norway rats from USA, China, Indonesia, Vietnam and many European countries. In this study, we describe molecular and serological investigations of Black and Norway rats trapped in Lithuania, Eastern Europe, for infections with rat HEV and human HEV genotypes 1–4. Rat HEV-specific real-time reverse transcription-PCR (RT-qPCR) analysis of rat liver samples revealed the presence of rat HEV in 9 of 109 (8.3%) samples. In contrast, a RT-qPCR specific for HEV genotypes 1–4 did not reveal any positive samples. A nested broad spectrum RT-PCR was used for a confirmation of rat HEV infection with a subsequent sequencing of the amplified rat HEV genome fragment. Phylogenetic analysis revealed a clustering of all newly identified rat HEV sequences with Norway rat-derived rat HEV sequences from Germany within the species Orthohepevirus C. An indirect ELISA using a yeast-expressed truncated rat HEV capsid protein variant revealed 31.2% seropositive samples indicating a high rate of rat HEV circulation in the rat population examined. In conclusion, the current investigation confirms rat HEV infections in Norway and Black rats in Lithuania, Eastern Europe, and the non-persistent nature of HEV infection.
doi_str_mv 10.1016/j.vetmic.2018.06.014
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Rat hepatitis E virus (HEV) is an orthohepevirus which is related to other HEV found in humans and other mammals. It was first identified in Norway rats (Rattus norvegicus) from Germany in 2010, and later it has been detected in Black rats (Rattus rattus) and Norway rats from USA, China, Indonesia, Vietnam and many European countries. In this study, we describe molecular and serological investigations of Black and Norway rats trapped in Lithuania, Eastern Europe, for infections with rat HEV and human HEV genotypes 1–4. Rat HEV-specific real-time reverse transcription-PCR (RT-qPCR) analysis of rat liver samples revealed the presence of rat HEV in 9 of 109 (8.3%) samples. In contrast, a RT-qPCR specific for HEV genotypes 1–4 did not reveal any positive samples. A nested broad spectrum RT-PCR was used for a confirmation of rat HEV infection with a subsequent sequencing of the amplified rat HEV genome fragment. Phylogenetic analysis revealed a clustering of all newly identified rat HEV sequences with Norway rat-derived rat HEV sequences from Germany within the species Orthohepevirus C. An indirect ELISA using a yeast-expressed truncated rat HEV capsid protein variant revealed 31.2% seropositive samples indicating a high rate of rat HEV circulation in the rat population examined. 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Rat hepatitis E virus (HEV) is an orthohepevirus which is related to other HEV found in humans and other mammals. It was first identified in Norway rats (Rattus norvegicus) from Germany in 2010, and later it has been detected in Black rats (Rattus rattus) and Norway rats from USA, China, Indonesia, Vietnam and many European countries. In this study, we describe molecular and serological investigations of Black and Norway rats trapped in Lithuania, Eastern Europe, for infections with rat HEV and human HEV genotypes 1–4. Rat HEV-specific real-time reverse transcription-PCR (RT-qPCR) analysis of rat liver samples revealed the presence of rat HEV in 9 of 109 (8.3%) samples. In contrast, a RT-qPCR specific for HEV genotypes 1–4 did not reveal any positive samples. A nested broad spectrum RT-PCR was used for a confirmation of rat HEV infection with a subsequent sequencing of the amplified rat HEV genome fragment. Phylogenetic analysis revealed a clustering of all newly identified rat HEV sequences with Norway rat-derived rat HEV sequences from Germany within the species Orthohepevirus C. An indirect ELISA using a yeast-expressed truncated rat HEV capsid protein variant revealed 31.2% seropositive samples indicating a high rate of rat HEV circulation in the rat population examined. 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Rat hepatitis E virus (HEV) is an orthohepevirus which is related to other HEV found in humans and other mammals. It was first identified in Norway rats (Rattus norvegicus) from Germany in 2010, and later it has been detected in Black rats (Rattus rattus) and Norway rats from USA, China, Indonesia, Vietnam and many European countries. In this study, we describe molecular and serological investigations of Black and Norway rats trapped in Lithuania, Eastern Europe, for infections with rat HEV and human HEV genotypes 1–4. Rat HEV-specific real-time reverse transcription-PCR (RT-qPCR) analysis of rat liver samples revealed the presence of rat HEV in 9 of 109 (8.3%) samples. In contrast, a RT-qPCR specific for HEV genotypes 1–4 did not reveal any positive samples. A nested broad spectrum RT-PCR was used for a confirmation of rat HEV infection with a subsequent sequencing of the amplified rat HEV genome fragment. Phylogenetic analysis revealed a clustering of all newly identified rat HEV sequences with Norway rat-derived rat HEV sequences from Germany within the species Orthohepevirus C. An indirect ELISA using a yeast-expressed truncated rat HEV capsid protein variant revealed 31.2% seropositive samples indicating a high rate of rat HEV circulation in the rat population examined. In conclusion, the current investigation confirms rat HEV infections in Norway and Black rats in Lithuania, Eastern Europe, and the non-persistent nature of HEV infection.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29981698</pmid><doi>10.1016/j.vetmic.2018.06.014</doi><tpages>5</tpages></addata></record>
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identifier ISSN: 0378-1135
ispartof Veterinary microbiology, 2018-07, Vol.221, p.129-133
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language eng
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Animals, Wild - virology
Capsid protein
Enzyme-linked immunosorbent assay
Genomes
Genotype
Genotype C1
Genotypes
Hepatitis
Hepatitis Antibodies
Hepatitis E - epidemiology
Hepatitis E - veterinary
Hepatitis E - virology
Hepatitis E virus (HEV)
Hepatitis E virus - classification
Infections
Lithuania - epidemiology
Liver
Mammals
Phylogeny
Polymerase chain reaction
Rat HEV
Rats
Rattus norvegicus
Reverse Transcriptase Polymerase Chain Reaction
Reverse transcription
Rodent Diseases - epidemiology
Rodent Diseases - virology
Rodents
Viruses
title Detection of rat hepatitis E virus, but not human pathogenic hepatitis E virus genotype 1–4 infections in wild rats from Lithuania
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