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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Veröffentlicht in:PLoS pathogens 2020-07, Vol.16 (7), p.e1008677-e1008677, Article 1008677
Hauptverfasser: 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.
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container_issue 7
container_start_page e1008677
container_title PLoS pathogens
container_volume 16
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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H.</creator><contributor>O'Connor, David H.</contributor><creatorcontrib>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. ; O'Connor, David H.</creatorcontrib><description>Pegiviruses frequently cause persistent infection (as defined by &gt;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><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 &amp; 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 &amp; 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 &gt;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 &amp; 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 &amp; 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 &amp; 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 &amp; 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. 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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 &gt;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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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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