Cargando…
A Novel Marsupial Hepatitis A Virus Corroborates Complex Evolutionary Patterns Shaping the Genus Hepatovirus
The discovery of highly diverse nonprimate hepatoviruses illuminated the evolutionary origins of hepatitis A virus (HAV) ancestors in mammals other than primates. Marsupials are ancient mammals that diverged from other Eutheria during the Jurassic. Viruses from marsupials may thus provide important...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002732/ https://www.ncbi.nlm.nih.gov/pubmed/29695421 http://dx.doi.org/10.1128/JVI.00082-18 |
_version_ | 1783332262668926976 |
---|---|
author | de Oliveira Carneiro, Ianei Sander, Anna-Lena Silva, Namá Moreira-Soto, Andres Normann, Andrea Flehmig, Bertram Lukashev, Alexander N. Dotzauer, Andreas Wieseke, Nicolas Franke, Carlos Roberto Drexler, Jan Felix |
author_facet | de Oliveira Carneiro, Ianei Sander, Anna-Lena Silva, Namá Moreira-Soto, Andres Normann, Andrea Flehmig, Bertram Lukashev, Alexander N. Dotzauer, Andreas Wieseke, Nicolas Franke, Carlos Roberto Drexler, Jan Felix |
author_sort | de Oliveira Carneiro, Ianei |
collection | PubMed |
description | The discovery of highly diverse nonprimate hepatoviruses illuminated the evolutionary origins of hepatitis A virus (HAV) ancestors in mammals other than primates. Marsupials are ancient mammals that diverged from other Eutheria during the Jurassic. Viruses from marsupials may thus provide important insight into virus evolution. To investigate Hepatovirus macroevolutionary patterns, we sampled 112 opossums in northeastern Brazil. A novel marsupial HAV (MHAV) in the Brazilian common opossum (Didelphis aurita) was detected by nested reverse transcription-PCR (RT-PCR). MHAV concentration in the liver was high, at 2.5 × 10(9) RNA copies/g, and at least 300-fold higher than those in other solid organs, suggesting hepatotropism. Hepatovirus seroprevalence in D. aurita was 26.6% as determined using an enzyme-linked immunosorbent assay (ELISA). Endpoint titers in confirmatory immunofluorescence assays were high, and marsupial antibodies colocalized with anti-HAV control sera, suggesting specificity of serological detection and considerable antigenic relatedness between HAV and MHAV. MHAV showed all genomic hallmarks defining hepatoviruses, including late-domain motifs likely involved in quasi-envelope acquisition, a predicted C-terminal pX extension of VP1, strong avoidance of CpG dinucleotides, and a type 3 internal ribosomal entry site. Translated polyprotein gene sequence distances of at least 23.7% from other hepatoviruses suggested that MHAV represents a novel Hepatovirus species. Conserved predicted cleavage sites suggested similarities in polyprotein processing between HAV and MHAV. MHAV was nested within rodent hepatoviruses in phylogenetic reconstructions, suggesting an ancestral hepatovirus host switch from rodents into marsupials. Cophylogenetic reconciliations of host and hepatovirus phylogenies confirmed that host-independent macroevolutionary patterns shaped the phylogenetic relationships of extant hepatoviruses. Although marsupials are synanthropic and consumed as wild game in Brazil, HAV community protective immunity may limit the zoonotic potential of MHAV. IMPORTANCE Hepatitis A virus (HAV) is a ubiquitous cause of acute hepatitis in humans. Recent findings revealed the evolutionary origins of HAV and the genus Hepatovirus defined by HAV in mammals other than primates in general and in small mammals in particular. The factors shaping the genealogy of extant hepatoviruses are unclear. We sampled marsupials, one of the most ancient mammalian lineages, and identified a novel marsupial HAV (MHAV). The novel MHAV shared specific features with HAV, including hepatotropism, antigenicity, genome structure, and a common ancestor in phylogenetic reconstructions. Coevolutionary analyses revealed that host-independent evolutionary patterns contributed most to the current phylogeny of hepatoviruses and that MHAV was the most drastic example of a cross-order host switch of any hepatovirus observed so far. The divergence of marsupials from other mammals offers unique opportunities to investigate HAV species barriers and whether mechanisms of HAV immune control are evolutionarily conserved. |
format | Online Article Text |
id | pubmed-6002732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-60027322018-06-27 A Novel Marsupial Hepatitis A Virus Corroborates Complex Evolutionary Patterns Shaping the Genus Hepatovirus de Oliveira Carneiro, Ianei Sander, Anna-Lena Silva, Namá Moreira-Soto, Andres Normann, Andrea Flehmig, Bertram Lukashev, Alexander N. Dotzauer, Andreas Wieseke, Nicolas Franke, Carlos Roberto Drexler, Jan Felix J Virol Genetic Diversity and Evolution The discovery of highly diverse nonprimate hepatoviruses illuminated the evolutionary origins of hepatitis A virus (HAV) ancestors in mammals other than primates. Marsupials are ancient mammals that diverged from other Eutheria during the Jurassic. Viruses from marsupials may thus provide important insight into virus evolution. To investigate Hepatovirus macroevolutionary patterns, we sampled 112 opossums in northeastern Brazil. A novel marsupial HAV (MHAV) in the Brazilian common opossum (Didelphis aurita) was detected by nested reverse transcription-PCR (RT-PCR). MHAV concentration in the liver was high, at 2.5 × 10(9) RNA copies/g, and at least 300-fold higher than those in other solid organs, suggesting hepatotropism. Hepatovirus seroprevalence in D. aurita was 26.6% as determined using an enzyme-linked immunosorbent assay (ELISA). Endpoint titers in confirmatory immunofluorescence assays were high, and marsupial antibodies colocalized with anti-HAV control sera, suggesting specificity of serological detection and considerable antigenic relatedness between HAV and MHAV. MHAV showed all genomic hallmarks defining hepatoviruses, including late-domain motifs likely involved in quasi-envelope acquisition, a predicted C-terminal pX extension of VP1, strong avoidance of CpG dinucleotides, and a type 3 internal ribosomal entry site. Translated polyprotein gene sequence distances of at least 23.7% from other hepatoviruses suggested that MHAV represents a novel Hepatovirus species. Conserved predicted cleavage sites suggested similarities in polyprotein processing between HAV and MHAV. MHAV was nested within rodent hepatoviruses in phylogenetic reconstructions, suggesting an ancestral hepatovirus host switch from rodents into marsupials. Cophylogenetic reconciliations of host and hepatovirus phylogenies confirmed that host-independent macroevolutionary patterns shaped the phylogenetic relationships of extant hepatoviruses. Although marsupials are synanthropic and consumed as wild game in Brazil, HAV community protective immunity may limit the zoonotic potential of MHAV. IMPORTANCE Hepatitis A virus (HAV) is a ubiquitous cause of acute hepatitis in humans. Recent findings revealed the evolutionary origins of HAV and the genus Hepatovirus defined by HAV in mammals other than primates in general and in small mammals in particular. The factors shaping the genealogy of extant hepatoviruses are unclear. We sampled marsupials, one of the most ancient mammalian lineages, and identified a novel marsupial HAV (MHAV). The novel MHAV shared specific features with HAV, including hepatotropism, antigenicity, genome structure, and a common ancestor in phylogenetic reconstructions. Coevolutionary analyses revealed that host-independent evolutionary patterns contributed most to the current phylogeny of hepatoviruses and that MHAV was the most drastic example of a cross-order host switch of any hepatovirus observed so far. The divergence of marsupials from other mammals offers unique opportunities to investigate HAV species barriers and whether mechanisms of HAV immune control are evolutionarily conserved. American Society for Microbiology 2018-06-13 /pmc/articles/PMC6002732/ /pubmed/29695421 http://dx.doi.org/10.1128/JVI.00082-18 Text en Copyright © 2018 de Oliveira Carneiro et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Genetic Diversity and Evolution de Oliveira Carneiro, Ianei Sander, Anna-Lena Silva, Namá Moreira-Soto, Andres Normann, Andrea Flehmig, Bertram Lukashev, Alexander N. Dotzauer, Andreas Wieseke, Nicolas Franke, Carlos Roberto Drexler, Jan Felix A Novel Marsupial Hepatitis A Virus Corroborates Complex Evolutionary Patterns Shaping the Genus Hepatovirus |
title | A Novel Marsupial Hepatitis A Virus Corroborates Complex Evolutionary Patterns Shaping the Genus Hepatovirus |
title_full | A Novel Marsupial Hepatitis A Virus Corroborates Complex Evolutionary Patterns Shaping the Genus Hepatovirus |
title_fullStr | A Novel Marsupial Hepatitis A Virus Corroborates Complex Evolutionary Patterns Shaping the Genus Hepatovirus |
title_full_unstemmed | A Novel Marsupial Hepatitis A Virus Corroborates Complex Evolutionary Patterns Shaping the Genus Hepatovirus |
title_short | A Novel Marsupial Hepatitis A Virus Corroborates Complex Evolutionary Patterns Shaping the Genus Hepatovirus |
title_sort | novel marsupial hepatitis a virus corroborates complex evolutionary patterns shaping the genus hepatovirus |
topic | Genetic Diversity and Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6002732/ https://www.ncbi.nlm.nih.gov/pubmed/29695421 http://dx.doi.org/10.1128/JVI.00082-18 |
work_keys_str_mv | AT deoliveiracarneiroianei anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT sanderannalena anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT silvanama anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT moreirasotoandres anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT normannandrea anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT flehmigbertram anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT lukashevalexandern anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT dotzauerandreas anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT wiesekenicolas anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT frankecarlosroberto anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT drexlerjanfelix anovelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT deoliveiracarneiroianei novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT sanderannalena novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT silvanama novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT moreirasotoandres novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT normannandrea novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT flehmigbertram novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT lukashevalexandern novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT dotzauerandreas novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT wiesekenicolas novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT frankecarlosroberto novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus AT drexlerjanfelix novelmarsupialhepatitisaviruscorroboratescomplexevolutionarypatternsshapingthegenushepatovirus |