Deletion of E184L, a Putative DIVA Target from the Pandemic Strain of African Swine Fever Virus, Produces a Reduction in Virulence and Protection against Virulent Challenge

African swine fever (ASF) is currently causing a major pandemic affecting the swine industry and protein availability from Central Europe to East and South Asia. No commercial vaccines are available, making disease control dependent on the elimination of affected animals. Here, we show that the dele...

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Veröffentlicht in:Journal of virology 2022-01, Vol.96 (1), p.e0141921-e0141921
Hauptverfasser: Ramirez-Medina, Elizabeth, Vuono, Elizabeth, Rai, Ayushi, Pruitt, Sarah, Espinoza, Nallely, Velazquez-Salinas, Lauro, Pina-Pedrero, Sonia, Zhu, James, Rodriguez, Fernando, Borca, Manuel V, Gladue, Douglas P
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container_issue 1
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container_title Journal of virology
container_volume 96
creator Ramirez-Medina, Elizabeth
Vuono, Elizabeth
Rai, Ayushi
Pruitt, Sarah
Espinoza, Nallely
Velazquez-Salinas, Lauro
Pina-Pedrero, Sonia
Zhu, James
Rodriguez, Fernando
Borca, Manuel V
Gladue, Douglas P
description African swine fever (ASF) is currently causing a major pandemic affecting the swine industry and protein availability from Central Europe to East and South Asia. No commercial vaccines are available, making disease control dependent on the elimination of affected animals. Here, we show that the deletion of the African swine fever virus (ASFV) E184L gene from the highly virulent ASFV Georgia 2010 (ASFV-G) isolate produces a reduction in virus virulence during the infection in swine. Of domestic pigs intramuscularly inoculated with a recombinant virus lacking the E184L gene (ASFV-G-ΔE184L), 40% experienced a significantly (5 days) delayed presentation of clinical disease and, overall, had a 60% rate of survival compared to animals inoculated with the virulent parental ASFV-G. Importantly, all animals surviving ASFV-G-ΔE184L infection developed a strong antibody response and were protected when challenged with ASFV-G. As expected, a pool of sera from ASFV-G-ΔE184L-inoculated animals lacked any detectable antibody response to peptides partially representing the E184L protein, while sera from animals inoculated with an efficacious vaccine candidate, ASFV-G-ΔMGF, strongly recognize the same set of peptides. These results support the potential use of the E184L deletion for the development of vaccines able to differentiate infected from vaccinated animals (DIVA). Therefore, it is shown here that the E184L gene is a novel ASFV determinant of virulence that can potentially be used to increase safety in preexisting vaccine candidates, as well as to provide them with DIVA capabilities. To our knowledge, E184L is the first ASFV gene product experimentally shown to be a functional DIVA antigenic marker. No commercial vaccines are available to prevent African swine fever (ASF). The ASF pandemic caused by the ASF virus Georgia 2010 (ASFV-G) strain is seriously affecting pork production in a contiguous geographical area from Central Europe to East Asia. The only effective experimental vaccines are viruses attenuated by deleting ASFV genes associated with virus virulence. Therefore, identification of such genes is of critical importance for vaccine development. Here, we report the discovery of a novel determinant of ASFV virulence, the E184L gene. Deletion of the E184L gene from the ASFV-G genome (ASFV-G-ΔE184L) produced a reduction in virus virulence, and importantly, animals surviving infection with ASFV-G-ΔE184L were protected from developing ASF after challenge with the
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No commercial vaccines are available, making disease control dependent on the elimination of affected animals. Here, we show that the deletion of the African swine fever virus (ASFV) E184L gene from the highly virulent ASFV Georgia 2010 (ASFV-G) isolate produces a reduction in virus virulence during the infection in swine. Of domestic pigs intramuscularly inoculated with a recombinant virus lacking the E184L gene (ASFV-G-ΔE184L), 40% experienced a significantly (5 days) delayed presentation of clinical disease and, overall, had a 60% rate of survival compared to animals inoculated with the virulent parental ASFV-G. Importantly, all animals surviving ASFV-G-ΔE184L infection developed a strong antibody response and were protected when challenged with ASFV-G. As expected, a pool of sera from ASFV-G-ΔE184L-inoculated animals lacked any detectable antibody response to peptides partially representing the E184L protein, while sera from animals inoculated with an efficacious vaccine candidate, ASFV-G-ΔMGF, strongly recognize the same set of peptides. These results support the potential use of the E184L deletion for the development of vaccines able to differentiate infected from vaccinated animals (DIVA). Therefore, it is shown here that the E184L gene is a novel ASFV determinant of virulence that can potentially be used to increase safety in preexisting vaccine candidates, as well as to provide them with DIVA capabilities. To our knowledge, E184L is the first ASFV gene product experimentally shown to be a functional DIVA antigenic marker. No commercial vaccines are available to prevent African swine fever (ASF). The ASF pandemic caused by the ASF virus Georgia 2010 (ASFV-G) strain is seriously affecting pork production in a contiguous geographical area from Central Europe to East Asia. The only effective experimental vaccines are viruses attenuated by deleting ASFV genes associated with virus virulence. Therefore, identification of such genes is of critical importance for vaccine development. Here, we report the discovery of a novel determinant of ASFV virulence, the E184L gene. Deletion of the E184L gene from the ASFV-G genome (ASFV-G-ΔE184L) produced a reduction in virus virulence, and importantly, animals surviving infection with ASFV-G-ΔE184L were protected from developing ASF after challenge with the virulent parental virus ASFV-G. Importantly, the virus protein encoded by E184L is highly immunogenic, making a virus lacking this gene a vaccine candidate that allows the differentiation of infected from vaccinated animals (DIVA). Here, we show that unlike what is observed in animals inoculated with the vaccine candidate ASFV-G-ΔMGF, ASFV-G-ΔE184L-inoculated animals do not mount a E184L-specific antibody response, indicating the feasibility of using the E184L deletion as the antigenic marker for the development of a DIVA vaccine in ASFV.</description><identifier>ISSN: 0022-538X</identifier><identifier>EISSN: 1098-5514</identifier><identifier>DOI: 10.1128/JVI.01419-21</identifier><identifier>PMID: 34668772</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>African swine fever ; African Swine Fever - diagnosis ; African Swine Fever - virology ; African Swine Fever Virus - classification ; African Swine Fever Virus - genetics ; Amino Acid Sequence ; Animals ; ASF ; ASFV ; BASIC BIOLOGICAL SCIENCES ; Body Temperature ; Conserved Sequence ; DIVA ; E184L ; Gene Expression Regulation, Viral ; Host-Pathogen Interactions ; Macrophages - immunology ; Macrophages - metabolism ; Macrophages - virology ; Pathogenesis and Immunity ; Phylogeny ; Sequence Deletion ; Swine ; Viral Proteins - chemistry ; Viral Proteins - genetics ; Viral Proteins - metabolism ; Viremia ; Virology ; Virulence ; Virulence Factors - chemistry ; Virulence Factors - genetics ; Virulence Factors - metabolism ; Virus Replication</subject><ispartof>Journal of virology, 2022-01, Vol.96 (1), p.e0141921-e0141921</ispartof><rights>Copyright © 2022 American Society for Microbiology.</rights><rights>Copyright © 2022 American Society for Microbiology. 2022 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a445t-5914c7a09bb43131acae092baad0241e31d269af5c500a519a4c7d72e1b2b9713</citedby><cites>FETCH-LOGICAL-a445t-5914c7a09bb43131acae092baad0241e31d269af5c500a519a4c7d72e1b2b9713</cites><orcidid>0000-0002-7894-0233 ; 0000000278940233</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/PMC8754217/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754217/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34668772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/servlets/purl/1983351$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><contributor>Heise, Mark T</contributor><contributor>Heise, Mark T.</contributor><creatorcontrib>Ramirez-Medina, Elizabeth</creatorcontrib><creatorcontrib>Vuono, Elizabeth</creatorcontrib><creatorcontrib>Rai, Ayushi</creatorcontrib><creatorcontrib>Pruitt, Sarah</creatorcontrib><creatorcontrib>Espinoza, Nallely</creatorcontrib><creatorcontrib>Velazquez-Salinas, Lauro</creatorcontrib><creatorcontrib>Pina-Pedrero, Sonia</creatorcontrib><creatorcontrib>Zhu, James</creatorcontrib><creatorcontrib>Rodriguez, Fernando</creatorcontrib><creatorcontrib>Borca, Manuel V</creatorcontrib><creatorcontrib>Gladue, Douglas P</creatorcontrib><creatorcontrib>Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN (United States)</creatorcontrib><title>Deletion of E184L, a Putative DIVA Target from the Pandemic Strain of African Swine Fever Virus, Produces a Reduction in Virulence and Protection against Virulent Challenge</title><title>Journal of virology</title><addtitle>J Virol</addtitle><addtitle>J Virol</addtitle><description>African swine fever (ASF) is currently causing a major pandemic affecting the swine industry and protein availability from Central Europe to East and South Asia. No commercial vaccines are available, making disease control dependent on the elimination of affected animals. Here, we show that the deletion of the African swine fever virus (ASFV) E184L gene from the highly virulent ASFV Georgia 2010 (ASFV-G) isolate produces a reduction in virus virulence during the infection in swine. Of domestic pigs intramuscularly inoculated with a recombinant virus lacking the E184L gene (ASFV-G-ΔE184L), 40% experienced a significantly (5 days) delayed presentation of clinical disease and, overall, had a 60% rate of survival compared to animals inoculated with the virulent parental ASFV-G. Importantly, all animals surviving ASFV-G-ΔE184L infection developed a strong antibody response and were protected when challenged with ASFV-G. As expected, a pool of sera from ASFV-G-ΔE184L-inoculated animals lacked any detectable antibody response to peptides partially representing the E184L protein, while sera from animals inoculated with an efficacious vaccine candidate, ASFV-G-ΔMGF, strongly recognize the same set of peptides. These results support the potential use of the E184L deletion for the development of vaccines able to differentiate infected from vaccinated animals (DIVA). Therefore, it is shown here that the E184L gene is a novel ASFV determinant of virulence that can potentially be used to increase safety in preexisting vaccine candidates, as well as to provide them with DIVA capabilities. To our knowledge, E184L is the first ASFV gene product experimentally shown to be a functional DIVA antigenic marker. No commercial vaccines are available to prevent African swine fever (ASF). The ASF pandemic caused by the ASF virus Georgia 2010 (ASFV-G) strain is seriously affecting pork production in a contiguous geographical area from Central Europe to East Asia. The only effective experimental vaccines are viruses attenuated by deleting ASFV genes associated with virus virulence. Therefore, identification of such genes is of critical importance for vaccine development. Here, we report the discovery of a novel determinant of ASFV virulence, the E184L gene. Deletion of the E184L gene from the ASFV-G genome (ASFV-G-ΔE184L) produced a reduction in virus virulence, and importantly, animals surviving infection with ASFV-G-ΔE184L were protected from developing ASF after challenge with the virulent parental virus ASFV-G. Importantly, the virus protein encoded by E184L is highly immunogenic, making a virus lacking this gene a vaccine candidate that allows the differentiation of infected from vaccinated animals (DIVA). Here, we show that unlike what is observed in animals inoculated with the vaccine candidate ASFV-G-ΔMGF, ASFV-G-ΔE184L-inoculated animals do not mount a E184L-specific antibody response, indicating the feasibility of using the E184L deletion as the antigenic marker for the development of a DIVA vaccine in ASFV.</description><subject>African swine fever</subject><subject>African Swine Fever - diagnosis</subject><subject>African Swine Fever - virology</subject><subject>African Swine Fever Virus - classification</subject><subject>African Swine Fever Virus - genetics</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>ASF</subject><subject>ASFV</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Body Temperature</subject><subject>Conserved Sequence</subject><subject>DIVA</subject><subject>E184L</subject><subject>Gene Expression Regulation, Viral</subject><subject>Host-Pathogen Interactions</subject><subject>Macrophages - immunology</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - virology</subject><subject>Pathogenesis and Immunity</subject><subject>Phylogeny</subject><subject>Sequence Deletion</subject><subject>Swine</subject><subject>Viral Proteins - chemistry</subject><subject>Viral Proteins - genetics</subject><subject>Viral Proteins - metabolism</subject><subject>Viremia</subject><subject>Virology</subject><subject>Virulence</subject><subject>Virulence Factors - chemistry</subject><subject>Virulence Factors - genetics</subject><subject>Virulence Factors - metabolism</subject><subject>Virus Replication</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1ktFv0zAQxiMEYmXwxjOyeAKpGbZjN8nLpKrboKgSFRsVb9bFubSeknjYThH_E38kTrtN8MCTT7rvfnef9SXJa0bPGOPFh8-b5RllgpUpZ0-SCaNlkUrJxNNkQinnqcyK7yfJC-9vaZSJmXienGRiNivynE-S3xfYYjC2J7Yhl6wQqykBsh4CBLNHcrHczMkNuC0G0jjbkbBDsoa-xs5och0cmMPkvHFGQ0-uf5oeyRXu0ZGNcYOfkrWz9aDRR-xXjNVhWZwa2y32GknEjaqAxx5sI9SHB0Egix20sdjiy-RZA63HV_fvafLt6vJm8Sldffm4XMxXKQghQypLJnQOtKwqkbGMgQakJa8AasoFw4zVfFZCI7WkFCQrIcrrnCOreFXmLDtNzo_cu6HqsNbxCAetunOmA_dLWTDq305vdmpr96rIpeAsj4C3R4D1wSivTfS207bvo0XFyiLL5Ljl3f0WZ38M6IPqjNfYttCjHbzishA0wmYjb3qUame9d9g83sKoGlOgYgrUIQWKj-T3Rzn4jqtbO7g-ftf_tG_-9voIfohI9gdyhbsb</recordid><startdate>20220112</startdate><enddate>20220112</enddate><creator>Ramirez-Medina, Elizabeth</creator><creator>Vuono, Elizabeth</creator><creator>Rai, Ayushi</creator><creator>Pruitt, Sarah</creator><creator>Espinoza, Nallely</creator><creator>Velazquez-Salinas, Lauro</creator><creator>Pina-Pedrero, Sonia</creator><creator>Zhu, James</creator><creator>Rodriguez, Fernando</creator><creator>Borca, Manuel V</creator><creator>Gladue, Douglas P</creator><general>American Society for Microbiology</general><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>7X8</scope><scope>OIOZB</scope><scope>OTOTI</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7894-0233</orcidid><orcidid>https://orcid.org/0000000278940233</orcidid></search><sort><creationdate>20220112</creationdate><title>Deletion of E184L, a Putative DIVA Target from the Pandemic Strain of African Swine Fever Virus, Produces a Reduction in Virulence and Protection against Virulent Challenge</title><author>Ramirez-Medina, Elizabeth ; Vuono, Elizabeth ; Rai, Ayushi ; Pruitt, Sarah ; Espinoza, Nallely ; Velazquez-Salinas, Lauro ; Pina-Pedrero, Sonia ; Zhu, James ; Rodriguez, Fernando ; Borca, Manuel V ; Gladue, Douglas P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a445t-5914c7a09bb43131acae092baad0241e31d269af5c500a519a4c7d72e1b2b9713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>African swine fever</topic><topic>African Swine Fever - diagnosis</topic><topic>African Swine Fever - virology</topic><topic>African Swine Fever Virus - classification</topic><topic>African Swine Fever Virus - genetics</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>ASF</topic><topic>ASFV</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Body Temperature</topic><topic>Conserved Sequence</topic><topic>DIVA</topic><topic>E184L</topic><topic>Gene Expression Regulation, Viral</topic><topic>Host-Pathogen Interactions</topic><topic>Macrophages - immunology</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - virology</topic><topic>Pathogenesis and Immunity</topic><topic>Phylogeny</topic><topic>Sequence Deletion</topic><topic>Swine</topic><topic>Viral Proteins - chemistry</topic><topic>Viral Proteins - genetics</topic><topic>Viral Proteins - metabolism</topic><topic>Viremia</topic><topic>Virology</topic><topic>Virulence</topic><topic>Virulence Factors - chemistry</topic><topic>Virulence Factors - genetics</topic><topic>Virulence Factors - metabolism</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramirez-Medina, Elizabeth</creatorcontrib><creatorcontrib>Vuono, Elizabeth</creatorcontrib><creatorcontrib>Rai, Ayushi</creatorcontrib><creatorcontrib>Pruitt, Sarah</creatorcontrib><creatorcontrib>Espinoza, Nallely</creatorcontrib><creatorcontrib>Velazquez-Salinas, Lauro</creatorcontrib><creatorcontrib>Pina-Pedrero, Sonia</creatorcontrib><creatorcontrib>Zhu, James</creatorcontrib><creatorcontrib>Rodriguez, Fernando</creatorcontrib><creatorcontrib>Borca, Manuel V</creatorcontrib><creatorcontrib>Gladue, Douglas P</creatorcontrib><creatorcontrib>Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN (United States)</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramirez-Medina, Elizabeth</au><au>Vuono, Elizabeth</au><au>Rai, Ayushi</au><au>Pruitt, Sarah</au><au>Espinoza, Nallely</au><au>Velazquez-Salinas, Lauro</au><au>Pina-Pedrero, Sonia</au><au>Zhu, James</au><au>Rodriguez, Fernando</au><au>Borca, Manuel V</au><au>Gladue, Douglas P</au><au>Heise, Mark T</au><au>Heise, Mark T.</au><aucorp>Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Deletion of E184L, a Putative DIVA Target from the Pandemic Strain of African Swine Fever Virus, Produces a Reduction in Virulence and Protection against Virulent Challenge</atitle><jtitle>Journal of virology</jtitle><stitle>J Virol</stitle><addtitle>J Virol</addtitle><date>2022-01-12</date><risdate>2022</risdate><volume>96</volume><issue>1</issue><spage>e0141921</spage><epage>e0141921</epage><pages>e0141921-e0141921</pages><issn>0022-538X</issn><eissn>1098-5514</eissn><abstract>African swine fever (ASF) is currently causing a major pandemic affecting the swine industry and protein availability from Central Europe to East and South Asia. No commercial vaccines are available, making disease control dependent on the elimination of affected animals. Here, we show that the deletion of the African swine fever virus (ASFV) E184L gene from the highly virulent ASFV Georgia 2010 (ASFV-G) isolate produces a reduction in virus virulence during the infection in swine. Of domestic pigs intramuscularly inoculated with a recombinant virus lacking the E184L gene (ASFV-G-ΔE184L), 40% experienced a significantly (5 days) delayed presentation of clinical disease and, overall, had a 60% rate of survival compared to animals inoculated with the virulent parental ASFV-G. Importantly, all animals surviving ASFV-G-ΔE184L infection developed a strong antibody response and were protected when challenged with ASFV-G. As expected, a pool of sera from ASFV-G-ΔE184L-inoculated animals lacked any detectable antibody response to peptides partially representing the E184L protein, while sera from animals inoculated with an efficacious vaccine candidate, ASFV-G-ΔMGF, strongly recognize the same set of peptides. These results support the potential use of the E184L deletion for the development of vaccines able to differentiate infected from vaccinated animals (DIVA). Therefore, it is shown here that the E184L gene is a novel ASFV determinant of virulence that can potentially be used to increase safety in preexisting vaccine candidates, as well as to provide them with DIVA capabilities. To our knowledge, E184L is the first ASFV gene product experimentally shown to be a functional DIVA antigenic marker. No commercial vaccines are available to prevent African swine fever (ASF). The ASF pandemic caused by the ASF virus Georgia 2010 (ASFV-G) strain is seriously affecting pork production in a contiguous geographical area from Central Europe to East Asia. The only effective experimental vaccines are viruses attenuated by deleting ASFV genes associated with virus virulence. Therefore, identification of such genes is of critical importance for vaccine development. Here, we report the discovery of a novel determinant of ASFV virulence, the E184L gene. Deletion of the E184L gene from the ASFV-G genome (ASFV-G-ΔE184L) produced a reduction in virus virulence, and importantly, animals surviving infection with ASFV-G-ΔE184L were protected from developing ASF after challenge with the virulent parental virus ASFV-G. Importantly, the virus protein encoded by E184L is highly immunogenic, making a virus lacking this gene a vaccine candidate that allows the differentiation of infected from vaccinated animals (DIVA). Here, we show that unlike what is observed in animals inoculated with the vaccine candidate ASFV-G-ΔMGF, ASFV-G-ΔE184L-inoculated animals do not mount a E184L-specific antibody response, indicating the feasibility of using the E184L deletion as the antigenic marker for the development of a DIVA vaccine in ASFV.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>34668772</pmid><doi>10.1128/JVI.01419-21</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-7894-0233</orcidid><orcidid>https://orcid.org/0000000278940233</orcidid><oa>free_for_read</oa></addata></record>
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subjects African swine fever
African Swine Fever - diagnosis
African Swine Fever - virology
African Swine Fever Virus - classification
African Swine Fever Virus - genetics
Amino Acid Sequence
Animals
ASF
ASFV
BASIC BIOLOGICAL SCIENCES
Body Temperature
Conserved Sequence
DIVA
E184L
Gene Expression Regulation, Viral
Host-Pathogen Interactions
Macrophages - immunology
Macrophages - metabolism
Macrophages - virology
Pathogenesis and Immunity
Phylogeny
Sequence Deletion
Swine
Viral Proteins - chemistry
Viral Proteins - genetics
Viral Proteins - metabolism
Viremia
Virology
Virulence
Virulence Factors - chemistry
Virulence Factors - genetics
Virulence Factors - metabolism
Virus Replication
title Deletion of E184L, a Putative DIVA Target from the Pandemic Strain of African Swine Fever Virus, Produces a Reduction in Virulence and Protection against Virulent Challenge
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