Equine pegiviruses cause persistent infection of bone marrow and are not associated with hepatitis
Pegiviruses frequently cause persistent infection (as defined by >6 months), but unlike most other Flaviviridae members, no apparent clinical disease. Human pegivirus (HPgV, previously GBV-C) is detectable in 1-4% of healthy individuals and another 5-13% are seropositive. Some evidence for infect...
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creator | Tomlinson, Joy E. Wolfisberg, Raphael Fahnoe, Ulrik Sharma, Himanshu Renshaw, Randall W. Nielsen, Louise Nishiuchi, Eiko Holm, Christina Dubovi, Edward Rosenberg, Brad R. Tennant, Bud C. Bukh, Jens Kapoor, Amit Divers, Thomas J. Rice, Charles M. Van de Walle, Gerlinde R. Scheel, Troels K. H. |
description | Pegiviruses frequently cause persistent infection (as defined by >6 months), but unlike most other Flaviviridae members, no apparent clinical disease. Human pegivirus (HPgV, previously GBV-C) is detectable in 1-4% of healthy individuals and another 5-13% are seropositive. Some evidence for infection of bone marrow and spleen exists. Equine pegivirus 1 (EPgV-1) is not linked to disease, whereas another pegivirus, Theiler's disease-associated virus (TDAV), was identified in an outbreak of acute serum hepatitis (Theiler's disease) in horses. Although no subsequent reports link TDAV to disease, any association with hepatitis has not been formally examined. Here, we characterized EPgV-1 and TDAV tropism, sequence diversity, persistence and association with liver disease in horses. Among more than 20 tissue types, we consistently detected high viral loads only in serum, bone marrow and spleen, and viral RNA replication was consistently identified in bone marrow. PBMCs and lymph nodes, but not liver, were sporadically positive. To exclude potential effects of co-infecting agents in experimental infections, we constructed full-length consensus cDNA clones; this was enabled by determination of the complete viral genomes, including a novel TDAV 3' terminus. Clone derived RNA transcripts were used for direct intrasplenic inoculation of healthy horses. This led to productive infection detectable from week 2-3 and persisting beyond the 28 weeks of study. We did not observe any clinical signs of illness or elevation of circulating liver enzymes. The polyprotein consensus sequences did not change, suggesting that both clones were fully functional. To our knowledge, this is the first successful extrahepatic viral RNA launch and the first robust reverse genetics system for a pegivirus. In conclusion, equine pegiviruses are bone marrow tropic, cause persistent infection in horses, and are not associated with hepatitis. Based on these findings, it may be appropriate to rename the group of TDAV and related viruses as EPgV-2.
Author summary Transmissible hepatitis in horses (Theiler's disease) has been known for 100 years without knowledge of causative infectious agents. Recently, two novel equine pegiviruses (EPgV) were discovered. Whereas EPgV-1 was not associated to disease, the other was identified in an outbreak of acute serum hepatitis and therefore named Theiler's disease-associated virus (TDAV). This finding was surprising since human and monkey pegiviruses typically c |
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Author summary Transmissible hepatitis in horses (Theiler's disease) has been known for 100 years without knowledge of causative infectious agents. Recently, two novel equine pegiviruses (EPgV) were discovered. Whereas EPgV-1 was not associated to disease, the other was identified in an outbreak of acute serum hepatitis and therefore named Theiler's disease-associated virus (TDAV). This finding was surprising since human and monkey pegiviruses typically cause long-term infection without associated clinical disease. Whereas no subsequent reports link TDAV to disease, the original association to hepatitis has not been formally examined. Here, we studied EPgV-1 and TDAV and found that their natural history of infection in horses were remarkably similar. Examination of various tissues identified the bone marrow as the primary site of replication for both viruses with no evidence of replication in the liver. To exclude potential effects of other infectious agents, we developed molecular full-length clones for EPgV-1 and TDAV and were able to initiate infection in horses using derived synthetic viral genetic material. This demonstrated long-term infection, but no association with hepatitis. These findings call into question the connection between TDAV, liver infection, and hepatitis in horses.</description><identifier>ISSN: 1553-7366</identifier><identifier>ISSN: 1553-7374</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1008677</identifier><identifier>PMID: 32649726</identifier><language>eng</language><publisher>SAN FRANCISCO: Public Library Science</publisher><subject>Animals ; Biology and Life Sciences ; Bone marrow ; Bone Marrow - virology ; Care and treatment ; Development and progression ; Flaviviridae ; Flavivirus infections ; Flavivirus Infections - veterinary ; Flavivirus Infections - virology ; Funding ; Genetics ; Genomes ; Hepatitis ; Hepatitis C ; Hepatitis, Viral, Animal - virology ; HIV ; Horse Diseases - virology ; Horses ; Hospitals ; Human immunodeficiency virus ; Immunology ; Infections ; Infectious diseases ; Inoculation ; Laboratories ; Life Sciences & Biomedicine ; Liver ; Liver diseases ; Lymph nodes ; Medicine and Health Sciences ; Microbiology ; Observations ; Parasitology ; Persistent infection ; Physiological aspects ; Research and analysis methods ; Ribonucleic acid ; RNA ; Science & Technology ; Spleen ; Supervision ; Tropism ; Vaccines ; Veterinary colleges ; Veterinary medicine ; Viral hepatitis ; Virology ; Viruses</subject><ispartof>PLoS pathogens, 2020-07, Vol.16 (7), p.e1008677-e1008677, Article 1008677</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><rights>2020 Tomlinson et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 Tomlinson et al 2020 Tomlinson et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>16</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000552678800001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c661t-d60629131cd671e60944be658e4b855f357ecb28351293eccb7f7c96fff45653</citedby><cites>FETCH-LOGICAL-c661t-d60629131cd671e60944be658e4b855f357ecb28351293eccb7f7c96fff45653</cites><orcidid>0000-0003-1545-4067 ; 0000-0002-2527-5751 ; 0000-0001-7365-3967 ; 0000-0002-5885-1276 ; 0000-0002-6191-2084 ; 0000-0002-7815-4806 ; 0000-0002-8117-7347 ; 0000-0003-3087-8079 ; 0000-0002-2064-8029 ; 0000-0003-1679-1591 ; 0000-0002-2444-1383</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375656/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375656/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2106,2118,2932,23875,27933,27934,28257,53800,53802</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32649726$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>O'Connor, David H.</contributor><creatorcontrib>Tomlinson, Joy E.</creatorcontrib><creatorcontrib>Wolfisberg, Raphael</creatorcontrib><creatorcontrib>Fahnoe, Ulrik</creatorcontrib><creatorcontrib>Sharma, Himanshu</creatorcontrib><creatorcontrib>Renshaw, Randall W.</creatorcontrib><creatorcontrib>Nielsen, Louise</creatorcontrib><creatorcontrib>Nishiuchi, Eiko</creatorcontrib><creatorcontrib>Holm, Christina</creatorcontrib><creatorcontrib>Dubovi, Edward</creatorcontrib><creatorcontrib>Rosenberg, Brad R.</creatorcontrib><creatorcontrib>Tennant, Bud C.</creatorcontrib><creatorcontrib>Bukh, Jens</creatorcontrib><creatorcontrib>Kapoor, Amit</creatorcontrib><creatorcontrib>Divers, Thomas J.</creatorcontrib><creatorcontrib>Rice, Charles M.</creatorcontrib><creatorcontrib>Van de Walle, Gerlinde R.</creatorcontrib><creatorcontrib>Scheel, Troels K. H.</creatorcontrib><title>Equine pegiviruses cause persistent infection of bone marrow and are not associated with hepatitis</title><title>PLoS pathogens</title><addtitle>PLOS PATHOG</addtitle><addtitle>PLoS Pathog</addtitle><description>Pegiviruses frequently cause persistent infection (as defined by >6 months), but unlike most other Flaviviridae members, no apparent clinical disease. Human pegivirus (HPgV, previously GBV-C) is detectable in 1-4% of healthy individuals and another 5-13% are seropositive. Some evidence for infection of bone marrow and spleen exists. Equine pegivirus 1 (EPgV-1) is not linked to disease, whereas another pegivirus, Theiler's disease-associated virus (TDAV), was identified in an outbreak of acute serum hepatitis (Theiler's disease) in horses. Although no subsequent reports link TDAV to disease, any association with hepatitis has not been formally examined. Here, we characterized EPgV-1 and TDAV tropism, sequence diversity, persistence and association with liver disease in horses. Among more than 20 tissue types, we consistently detected high viral loads only in serum, bone marrow and spleen, and viral RNA replication was consistently identified in bone marrow. PBMCs and lymph nodes, but not liver, were sporadically positive. To exclude potential effects of co-infecting agents in experimental infections, we constructed full-length consensus cDNA clones; this was enabled by determination of the complete viral genomes, including a novel TDAV 3' terminus. Clone derived RNA transcripts were used for direct intrasplenic inoculation of healthy horses. This led to productive infection detectable from week 2-3 and persisting beyond the 28 weeks of study. We did not observe any clinical signs of illness or elevation of circulating liver enzymes. The polyprotein consensus sequences did not change, suggesting that both clones were fully functional. To our knowledge, this is the first successful extrahepatic viral RNA launch and the first robust reverse genetics system for a pegivirus. In conclusion, equine pegiviruses are bone marrow tropic, cause persistent infection in horses, and are not associated with hepatitis. Based on these findings, it may be appropriate to rename the group of TDAV and related viruses as EPgV-2.
Author summary Transmissible hepatitis in horses (Theiler's disease) has been known for 100 years without knowledge of causative infectious agents. Recently, two novel equine pegiviruses (EPgV) were discovered. Whereas EPgV-1 was not associated to disease, the other was identified in an outbreak of acute serum hepatitis and therefore named Theiler's disease-associated virus (TDAV). This finding was surprising since human and monkey pegiviruses typically cause long-term infection without associated clinical disease. Whereas no subsequent reports link TDAV to disease, the original association to hepatitis has not been formally examined. Here, we studied EPgV-1 and TDAV and found that their natural history of infection in horses were remarkably similar. Examination of various tissues identified the bone marrow as the primary site of replication for both viruses with no evidence of replication in the liver. To exclude potential effects of other infectious agents, we developed molecular full-length clones for EPgV-1 and TDAV and were able to initiate infection in horses using derived synthetic viral genetic material. This demonstrated long-term infection, but no association with hepatitis. These findings call into question the connection between TDAV, liver infection, and hepatitis in horses.</description><subject>Animals</subject><subject>Biology and Life Sciences</subject><subject>Bone marrow</subject><subject>Bone Marrow - virology</subject><subject>Care and treatment</subject><subject>Development and progression</subject><subject>Flaviviridae</subject><subject>Flavivirus infections</subject><subject>Flavivirus Infections - veterinary</subject><subject>Flavivirus Infections - virology</subject><subject>Funding</subject><subject>Genetics</subject><subject>Genomes</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Hepatitis, Viral, Animal - virology</subject><subject>HIV</subject><subject>Horse Diseases - virology</subject><subject>Horses</subject><subject>Hospitals</subject><subject>Human immunodeficiency virus</subject><subject>Immunology</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Inoculation</subject><subject>Laboratories</subject><subject>Life Sciences & Biomedicine</subject><subject>Liver</subject><subject>Liver diseases</subject><subject>Lymph nodes</subject><subject>Medicine and Health Sciences</subject><subject>Microbiology</subject><subject>Observations</subject><subject>Parasitology</subject><subject>Persistent infection</subject><subject>Physiological aspects</subject><subject>Research and analysis methods</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>Science & Technology</subject><subject>Spleen</subject><subject>Supervision</subject><subject>Tropism</subject><subject>Vaccines</subject><subject>Veterinary colleges</subject><subject>Veterinary medicine</subject><subject>Viral hepatitis</subject><subject>Virology</subject><subject>Viruses</subject><issn>1553-7366</issn><issn>1553-7374</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqVk11v0zAUhiMEYmPwDxBE4gaEWvzt5GbSVA2oNIEEu7cc57j1lMad7azw73FoVlG0C5AvbB0_5_X5clG8xGiOqcQfbvwQet3Nt1ud5hihSkj5qDjFnNOZpJI9PpyFOCmexXiDEMMUi6fFCSWC1ZKI06K5vB1cD-UWVu7OhSFCLI3OW7aE6GKCPpWut2CS833pbdn4jG90CH5X6r4tdYCy96nUMXrjdIK23Lm0LteQA3PJxefFE6u7CC-m_ay4_nh5vfg8u_r6abm4uJoZIXCatQIJUucATSskBoFqxhoQvALWVJxbyiWYhlSUY1JTMKaRVppaWGsZF5yeFa_3stvORzVVJyrCKBtzZSITyz3Ren2jtsHlLH4qr536bfBhpXRIznSgKtEISVthWq4Zt6RG2gitEZUUA5Eka51Prw3NBlqTyxR0dyR6fNO7tVr5O5Vbk6Mdg3k7CQR_O0BMauOiga7TPfhhjJtQJDjCdUbf_IU-nN1ErXROILfM53fNKKouBMWE1jUZqzR_gMqrhY0zubXWZfuRw7sjh8wk-JFWeUaiWn7_9h_sl2OW7VkTfIwB7KF2GKlxwO-TVOOAq2nAs9urP-t-cLqf6Ay83wM7aLyNxkFv4IAhhDgnQlZVPiGc6erf6YVLevwFCz_0if4CoTgXeQ</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Tomlinson, Joy E.</creator><creator>Wolfisberg, Raphael</creator><creator>Fahnoe, Ulrik</creator><creator>Sharma, Himanshu</creator><creator>Renshaw, Randall W.</creator><creator>Nielsen, Louise</creator><creator>Nishiuchi, Eiko</creator><creator>Holm, Christina</creator><creator>Dubovi, Edward</creator><creator>Rosenberg, Brad R.</creator><creator>Tennant, Bud C.</creator><creator>Bukh, Jens</creator><creator>Kapoor, Amit</creator><creator>Divers, Thomas J.</creator><creator>Rice, Charles M.</creator><creator>Van de Walle, Gerlinde R.</creator><creator>Scheel, Troels K. H.</creator><general>Public Library Science</general><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1545-4067</orcidid><orcidid>https://orcid.org/0000-0002-2527-5751</orcidid><orcidid>https://orcid.org/0000-0001-7365-3967</orcidid><orcidid>https://orcid.org/0000-0002-5885-1276</orcidid><orcidid>https://orcid.org/0000-0002-6191-2084</orcidid><orcidid>https://orcid.org/0000-0002-7815-4806</orcidid><orcidid>https://orcid.org/0000-0002-8117-7347</orcidid><orcidid>https://orcid.org/0000-0003-3087-8079</orcidid><orcidid>https://orcid.org/0000-0002-2064-8029</orcidid><orcidid>https://orcid.org/0000-0003-1679-1591</orcidid><orcidid>https://orcid.org/0000-0002-2444-1383</orcidid></search><sort><creationdate>20200701</creationdate><title>Equine pegiviruses cause persistent infection of bone marrow and are not associated with hepatitis</title><author>Tomlinson, Joy E. ; Wolfisberg, Raphael ; Fahnoe, Ulrik ; Sharma, Himanshu ; Renshaw, Randall W. ; Nielsen, Louise ; Nishiuchi, Eiko ; Holm, Christina ; Dubovi, Edward ; Rosenberg, Brad R. ; Tennant, Bud C. ; Bukh, Jens ; Kapoor, Amit ; Divers, Thomas J. ; Rice, Charles M. ; Van de Walle, Gerlinde R. ; Scheel, Troels K. H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c661t-d60629131cd671e60944be658e4b855f357ecb28351293eccb7f7c96fff45653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Biology and Life Sciences</topic><topic>Bone marrow</topic><topic>Bone Marrow - virology</topic><topic>Care and treatment</topic><topic>Development and progression</topic><topic>Flaviviridae</topic><topic>Flavivirus infections</topic><topic>Flavivirus Infections - veterinary</topic><topic>Flavivirus Infections - virology</topic><topic>Funding</topic><topic>Genetics</topic><topic>Genomes</topic><topic>Hepatitis</topic><topic>Hepatitis C</topic><topic>Hepatitis, Viral, Animal - virology</topic><topic>HIV</topic><topic>Horse Diseases - virology</topic><topic>Horses</topic><topic>Hospitals</topic><topic>Human immunodeficiency virus</topic><topic>Immunology</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Inoculation</topic><topic>Laboratories</topic><topic>Life Sciences & Biomedicine</topic><topic>Liver</topic><topic>Liver diseases</topic><topic>Lymph nodes</topic><topic>Medicine and Health Sciences</topic><topic>Microbiology</topic><topic>Observations</topic><topic>Parasitology</topic><topic>Persistent infection</topic><topic>Physiological aspects</topic><topic>Research and analysis methods</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>Science & Technology</topic><topic>Spleen</topic><topic>Supervision</topic><topic>Tropism</topic><topic>Vaccines</topic><topic>Veterinary colleges</topic><topic>Veterinary medicine</topic><topic>Viral hepatitis</topic><topic>Virology</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tomlinson, Joy E.</creatorcontrib><creatorcontrib>Wolfisberg, Raphael</creatorcontrib><creatorcontrib>Fahnoe, Ulrik</creatorcontrib><creatorcontrib>Sharma, Himanshu</creatorcontrib><creatorcontrib>Renshaw, Randall W.</creatorcontrib><creatorcontrib>Nielsen, Louise</creatorcontrib><creatorcontrib>Nishiuchi, Eiko</creatorcontrib><creatorcontrib>Holm, Christina</creatorcontrib><creatorcontrib>Dubovi, Edward</creatorcontrib><creatorcontrib>Rosenberg, Brad R.</creatorcontrib><creatorcontrib>Tennant, Bud C.</creatorcontrib><creatorcontrib>Bukh, Jens</creatorcontrib><creatorcontrib>Kapoor, Amit</creatorcontrib><creatorcontrib>Divers, Thomas J.</creatorcontrib><creatorcontrib>Rice, Charles M.</creatorcontrib><creatorcontrib>Van de Walle, Gerlinde R.</creatorcontrib><creatorcontrib>Scheel, Troels K. H.</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tomlinson, Joy E.</au><au>Wolfisberg, Raphael</au><au>Fahnoe, Ulrik</au><au>Sharma, Himanshu</au><au>Renshaw, Randall W.</au><au>Nielsen, Louise</au><au>Nishiuchi, Eiko</au><au>Holm, Christina</au><au>Dubovi, Edward</au><au>Rosenberg, Brad R.</au><au>Tennant, Bud C.</au><au>Bukh, Jens</au><au>Kapoor, Amit</au><au>Divers, Thomas J.</au><au>Rice, Charles M.</au><au>Van de Walle, Gerlinde R.</au><au>Scheel, Troels K. H.</au><au>O'Connor, David H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Equine pegiviruses cause persistent infection of bone marrow and are not associated with hepatitis</atitle><jtitle>PLoS pathogens</jtitle><stitle>PLOS PATHOG</stitle><addtitle>PLoS Pathog</addtitle><date>2020-07-01</date><risdate>2020</risdate><volume>16</volume><issue>7</issue><spage>e1008677</spage><epage>e1008677</epage><pages>e1008677-e1008677</pages><artnum>1008677</artnum><issn>1553-7366</issn><issn>1553-7374</issn><eissn>1553-7374</eissn><abstract>Pegiviruses frequently cause persistent infection (as defined by >6 months), but unlike most other Flaviviridae members, no apparent clinical disease. Human pegivirus (HPgV, previously GBV-C) is detectable in 1-4% of healthy individuals and another 5-13% are seropositive. Some evidence for infection of bone marrow and spleen exists. Equine pegivirus 1 (EPgV-1) is not linked to disease, whereas another pegivirus, Theiler's disease-associated virus (TDAV), was identified in an outbreak of acute serum hepatitis (Theiler's disease) in horses. Although no subsequent reports link TDAV to disease, any association with hepatitis has not been formally examined. Here, we characterized EPgV-1 and TDAV tropism, sequence diversity, persistence and association with liver disease in horses. Among more than 20 tissue types, we consistently detected high viral loads only in serum, bone marrow and spleen, and viral RNA replication was consistently identified in bone marrow. PBMCs and lymph nodes, but not liver, were sporadically positive. To exclude potential effects of co-infecting agents in experimental infections, we constructed full-length consensus cDNA clones; this was enabled by determination of the complete viral genomes, including a novel TDAV 3' terminus. Clone derived RNA transcripts were used for direct intrasplenic inoculation of healthy horses. This led to productive infection detectable from week 2-3 and persisting beyond the 28 weeks of study. We did not observe any clinical signs of illness or elevation of circulating liver enzymes. The polyprotein consensus sequences did not change, suggesting that both clones were fully functional. To our knowledge, this is the first successful extrahepatic viral RNA launch and the first robust reverse genetics system for a pegivirus. In conclusion, equine pegiviruses are bone marrow tropic, cause persistent infection in horses, and are not associated with hepatitis. Based on these findings, it may be appropriate to rename the group of TDAV and related viruses as EPgV-2.
Author summary Transmissible hepatitis in horses (Theiler's disease) has been known for 100 years without knowledge of causative infectious agents. Recently, two novel equine pegiviruses (EPgV) were discovered. Whereas EPgV-1 was not associated to disease, the other was identified in an outbreak of acute serum hepatitis and therefore named Theiler's disease-associated virus (TDAV). This finding was surprising since human and monkey pegiviruses typically cause long-term infection without associated clinical disease. Whereas no subsequent reports link TDAV to disease, the original association to hepatitis has not been formally examined. Here, we studied EPgV-1 and TDAV and found that their natural history of infection in horses were remarkably similar. Examination of various tissues identified the bone marrow as the primary site of replication for both viruses with no evidence of replication in the liver. To exclude potential effects of other infectious agents, we developed molecular full-length clones for EPgV-1 and TDAV and were able to initiate infection in horses using derived synthetic viral genetic material. This demonstrated long-term infection, but no association with hepatitis. These findings call into question the connection between TDAV, liver infection, and hepatitis in horses.</abstract><cop>SAN FRANCISCO</cop><pub>Public Library Science</pub><pmid>32649726</pmid><doi>10.1371/journal.ppat.1008677</doi><tpages>23</tpages><orcidid>https://orcid.org/0000-0003-1545-4067</orcidid><orcidid>https://orcid.org/0000-0002-2527-5751</orcidid><orcidid>https://orcid.org/0000-0001-7365-3967</orcidid><orcidid>https://orcid.org/0000-0002-5885-1276</orcidid><orcidid>https://orcid.org/0000-0002-6191-2084</orcidid><orcidid>https://orcid.org/0000-0002-7815-4806</orcidid><orcidid>https://orcid.org/0000-0002-8117-7347</orcidid><orcidid>https://orcid.org/0000-0003-3087-8079</orcidid><orcidid>https://orcid.org/0000-0002-2064-8029</orcidid><orcidid>https://orcid.org/0000-0003-1679-1591</orcidid><orcidid>https://orcid.org/0000-0002-2444-1383</orcidid><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 1553-7366 |
ispartof | PLoS pathogens, 2020-07, Vol.16 (7), p.e1008677-e1008677, Article 1008677 |
issn | 1553-7366 1553-7374 1553-7374 |
language | eng |
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source | Public Library of Science (PLoS) Journals Open Access; MEDLINE; DOAJ Directory of Open Access Journals; Web of Science - Science Citation Index Expanded - 2020<img src="https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg" />; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access |
subjects | Animals Biology and Life Sciences Bone marrow Bone Marrow - virology Care and treatment Development and progression Flaviviridae Flavivirus infections Flavivirus Infections - veterinary Flavivirus Infections - virology Funding Genetics Genomes Hepatitis Hepatitis C Hepatitis, Viral, Animal - virology HIV Horse Diseases - virology Horses Hospitals Human immunodeficiency virus Immunology Infections Infectious diseases Inoculation Laboratories Life Sciences & Biomedicine Liver Liver diseases Lymph nodes Medicine and Health Sciences Microbiology Observations Parasitology Persistent infection Physiological aspects Research and analysis methods Ribonucleic acid RNA Science & Technology Spleen Supervision Tropism Vaccines Veterinary colleges Veterinary medicine Viral hepatitis Virology Viruses |
title | Equine pegiviruses cause persistent infection of bone marrow and are not associated with hepatitis |
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