Influenza A Virus Coinfection through Transmission Can Support High Levels of Reassortment

The reassortment of gene segments between influenza viruses increases genomic diversity and plays an important role in viral evolution. We have shown previously that this process is highly efficient within a coinfected cell and, given synchronous coinfection at moderate or high doses, can give rise...

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Veröffentlicht in:Journal of virology 2015-08, Vol.89 (16), p.8453-8461
Hauptverfasser: Tao, Hui, Li, Lian, White, Maria C, Steel, John, Lowen, Anice C
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creator Tao, Hui
Li, Lian
White, Maria C
Steel, John
Lowen, Anice C
description The reassortment of gene segments between influenza viruses increases genomic diversity and plays an important role in viral evolution. We have shown previously that this process is highly efficient within a coinfected cell and, given synchronous coinfection at moderate or high doses, can give rise to ~60 to 70% of progeny shed from an animal host. Conversely, reassortment in vivo can be rendered undetectable by lowering viral doses or extending the time between infections. One might also predict that seeding of transmitted viruses into different sites within the target tissue could limit subsequent reassortment. Given the potential for stochastic factors to restrict reassortment during natural infection, we sought to determine its efficiency in a host coinfected through transmission. Two scenarios were tested in a guinea pig model, using influenza A/Panama/2007/99 (H3N2) virus (wt) and a silently mutated variant (var) thereof as parental virus strains. In the first, coinfection was achieved by exposing a naive guinea pig to two cagemates, one infected with wt and the other with var virus. When such exposure led to coinfection, robust reassortment was typically seen, with 50 to 100% of isolates carrying reassortant genomes at one or more time points. In the second scenario, naive guinea pigs were exposed to a cagemate that had been coinoculated with wt and var viruses. Here, reassortment occurred in the coinoculated donor host, multiple variants were transmitted, and reassortants were prevalent in the recipient host. Together, these results demonstrate the immense potential for reassortment to generate viral diversity in nature. Influenza viruses evolve rapidly under selection due to the generation of viral diversity through two mechanisms. The first is the introduction of random errors into the genome by the viral polymerase, which occurs with a frequency of approximately 10(-5) errors/nucleotide replicated. The second is reassortment, or the exchange of gene segments between viruses. Reassortment is known to occur readily under well-controlled laboratory conditions, but its frequency in nature is not clear. Here, we tested the hypothesis that reassortment efficiency following coinfection through transmission would be reduced compared to that seen with coinoculation. Contrary to this hypothesis, our results indicate that coinfection achieved through transmission supports high levels of reassortment. These results suggest that reassortment is not exquisite
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Two scenarios were tested in a guinea pig model, using influenza A/Panama/2007/99 (H3N2) virus (wt) and a silently mutated variant (var) thereof as parental virus strains. In the first, coinfection was achieved by exposing a naive guinea pig to two cagemates, one infected with wt and the other with var virus. When such exposure led to coinfection, robust reassortment was typically seen, with 50 to 100% of isolates carrying reassortant genomes at one or more time points. In the second scenario, naive guinea pigs were exposed to a cagemate that had been coinoculated with wt and var viruses. Here, reassortment occurred in the coinoculated donor host, multiple variants were transmitted, and reassortants were prevalent in the recipient host. Together, these results demonstrate the immense potential for reassortment to generate viral diversity in nature. Influenza viruses evolve rapidly under selection due to the generation of viral diversity through two mechanisms. The first is the introduction of random errors into the genome by the viral polymerase, which occurs with a frequency of approximately 10(-5) errors/nucleotide replicated. The second is reassortment, or the exchange of gene segments between viruses. Reassortment is known to occur readily under well-controlled laboratory conditions, but its frequency in nature is not clear. Here, we tested the hypothesis that reassortment efficiency following coinfection through transmission would be reduced compared to that seen with coinoculation. Contrary to this hypothesis, our results indicate that coinfection achieved through transmission supports high levels of reassortment. 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S.</contributor><creatorcontrib>Tao, Hui</creatorcontrib><creatorcontrib>Li, Lian</creatorcontrib><creatorcontrib>White, Maria C</creatorcontrib><creatorcontrib>Steel, John</creatorcontrib><creatorcontrib>Lowen, Anice C</creatorcontrib><title>Influenza A Virus Coinfection through Transmission Can Support High Levels of Reassortment</title><title>Journal of virology</title><addtitle>J Virol</addtitle><description>The reassortment of gene segments between influenza viruses increases genomic diversity and plays an important role in viral evolution. We have shown previously that this process is highly efficient within a coinfected cell and, given synchronous coinfection at moderate or high doses, can give rise to ~60 to 70% of progeny shed from an animal host. Conversely, reassortment in vivo can be rendered undetectable by lowering viral doses or extending the time between infections. 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Here, reassortment occurred in the coinoculated donor host, multiple variants were transmitted, and reassortants were prevalent in the recipient host. Together, these results demonstrate the immense potential for reassortment to generate viral diversity in nature. Influenza viruses evolve rapidly under selection due to the generation of viral diversity through two mechanisms. The first is the introduction of random errors into the genome by the viral polymerase, which occurs with a frequency of approximately 10(-5) errors/nucleotide replicated. The second is reassortment, or the exchange of gene segments between viruses. Reassortment is known to occur readily under well-controlled laboratory conditions, but its frequency in nature is not clear. Here, we tested the hypothesis that reassortment efficiency following coinfection through transmission would be reduced compared to that seen with coinoculation. Contrary to this hypothesis, our results indicate that coinfection achieved through transmission supports high levels of reassortment. These results suggest that reassortment is not exquisitely sensitive to stochastic effects associated with transmission and likely occurs in nature whenever a host is infected productively with more than one influenza A virus.</description><subject>Animals</subject><subject>Coinfection - transmission</subject><subject>Dogs</subject><subject>Genetic Diversity and Evolution</subject><subject>Genetic Variation</subject><subject>Genotype</subject><subject>Guinea Pigs</subject><subject>Influenza A virus</subject><subject>Influenza A Virus, H3N2 Subtype - genetics</subject><subject>Influenza A Virus, H3N2 Subtype - physiology</subject><subject>Madin Darby Canine Kidney Cells</subject><subject>Orthomyxoviridae Infections - transmission</subject><subject>Reassortant Viruses - genetics</subject><subject>Stochastic Processes</subject><issn>0022-538X</issn><issn>1098-5514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUlLBDEQhYMoOi43z5KjB1tT2bpzEWRwGRkQ3BAvIdOdOC09yZh0D-ivt8cNPXkqqPrqVT0eQrtADgFocXR5PzokAJJmIFbQAIgqMiGAr6IBIZRmghUPG2gzpWdCgHPJ19EGlYT3u2KAHkfeNZ31bwaf4Ps6dgkPQ-2dLds6eNxOY-iepvg2Gp9mdUrL5tB4fNPN5yG2-KLup2O7sE3CweFra1Lq-zPr22205kyT7M5X3UJ3Z6e3w4tsfHU-Gp6Ms5JL0ma8yN2EQy5JzikvragIOCbUpJJSGVFMLDFWQSEJywVnlSlAmorl0pGKOQdsCx1_6s67ycxWZX86mkbPYz0z8VUHU-u_E19P9VNYaC4op3QpsP8lEMNLZ1Ore6elbRrjbeiShpwokFwo-T8qVcEUMK569OATLWNIKVr38xEQvUxO98npj-Q0iB7f--3iB_6Oir0Di7SUfA</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Tao, Hui</creator><creator>Li, Lian</creator><creator>White, Maria C</creator><creator>Steel, John</creator><creator>Lowen, Anice C</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>7U9</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20150801</creationdate><title>Influenza A Virus Coinfection through Transmission Can Support High Levels of Reassortment</title><author>Tao, Hui ; Li, Lian ; White, Maria C ; Steel, John ; Lowen, Anice C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-487fb417607424ce5d01f359bd669a58be0ae9186037543da816ad376f0d3ff13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Coinfection - transmission</topic><topic>Dogs</topic><topic>Genetic Diversity and Evolution</topic><topic>Genetic Variation</topic><topic>Genotype</topic><topic>Guinea Pigs</topic><topic>Influenza A virus</topic><topic>Influenza A Virus, H3N2 Subtype - genetics</topic><topic>Influenza A Virus, H3N2 Subtype - physiology</topic><topic>Madin Darby Canine Kidney Cells</topic><topic>Orthomyxoviridae Infections - transmission</topic><topic>Reassortant Viruses - genetics</topic><topic>Stochastic Processes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tao, Hui</creatorcontrib><creatorcontrib>Li, Lian</creatorcontrib><creatorcontrib>White, Maria C</creatorcontrib><creatorcontrib>Steel, John</creatorcontrib><creatorcontrib>Lowen, Anice C</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>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</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>Tao, Hui</au><au>Li, Lian</au><au>White, Maria C</au><au>Steel, John</au><au>Lowen, Anice C</au><au>Dermody, T. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influenza A Virus Coinfection through Transmission Can Support High Levels of Reassortment</atitle><jtitle>Journal of virology</jtitle><addtitle>J Virol</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>89</volume><issue>16</issue><spage>8453</spage><epage>8461</epage><pages>8453-8461</pages><issn>0022-538X</issn><eissn>1098-5514</eissn><abstract>The reassortment of gene segments between influenza viruses increases genomic diversity and plays an important role in viral evolution. We have shown previously that this process is highly efficient within a coinfected cell and, given synchronous coinfection at moderate or high doses, can give rise to ~60 to 70% of progeny shed from an animal host. Conversely, reassortment in vivo can be rendered undetectable by lowering viral doses or extending the time between infections. One might also predict that seeding of transmitted viruses into different sites within the target tissue could limit subsequent reassortment. Given the potential for stochastic factors to restrict reassortment during natural infection, we sought to determine its efficiency in a host coinfected through transmission. Two scenarios were tested in a guinea pig model, using influenza A/Panama/2007/99 (H3N2) virus (wt) and a silently mutated variant (var) thereof as parental virus strains. In the first, coinfection was achieved by exposing a naive guinea pig to two cagemates, one infected with wt and the other with var virus. When such exposure led to coinfection, robust reassortment was typically seen, with 50 to 100% of isolates carrying reassortant genomes at one or more time points. In the second scenario, naive guinea pigs were exposed to a cagemate that had been coinoculated with wt and var viruses. Here, reassortment occurred in the coinoculated donor host, multiple variants were transmitted, and reassortants were prevalent in the recipient host. Together, these results demonstrate the immense potential for reassortment to generate viral diversity in nature. Influenza viruses evolve rapidly under selection due to the generation of viral diversity through two mechanisms. The first is the introduction of random errors into the genome by the viral polymerase, which occurs with a frequency of approximately 10(-5) errors/nucleotide replicated. The second is reassortment, or the exchange of gene segments between viruses. Reassortment is known to occur readily under well-controlled laboratory conditions, but its frequency in nature is not clear. Here, we tested the hypothesis that reassortment efficiency following coinfection through transmission would be reduced compared to that seen with coinoculation. Contrary to this hypothesis, our results indicate that coinfection achieved through transmission supports high levels of reassortment. These results suggest that reassortment is not exquisitely sensitive to stochastic effects associated with transmission and likely occurs in nature whenever a host is infected productively with more than one influenza A virus.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>26041285</pmid><doi>10.1128/JVI.01162-15</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Animals
Coinfection - transmission
Dogs
Genetic Diversity and Evolution
Genetic Variation
Genotype
Guinea Pigs
Influenza A virus
Influenza A Virus, H3N2 Subtype - genetics
Influenza A Virus, H3N2 Subtype - physiology
Madin Darby Canine Kidney Cells
Orthomyxoviridae Infections - transmission
Reassortant Viruses - genetics
Stochastic Processes
title Influenza A Virus Coinfection through Transmission Can Support High Levels of Reassortment
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