Genetic diversity and molecular evolution of human adenovirus serotype 41 strains circulating in Beijing, China, during 2010–2019

Human adenovirus serotype 41 (HAdV-F41) is an important pathogen that causes diarrhea in children. However, the data on its molecular genetic characteristics and evolutionary history are still neither comprehensive nor sufficient. Four capsid protein genes from 58 HAdV-F41-positive specimens taken f...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Infection, genetics and evolution genetics and evolution, 2021-11, Vol.95, p.105056-105056, Article 105056
Hauptverfasser: Liu, Liying, Qian, Yuan, Jia, Liping, Dong, Huijin, Deng, Li, Huang, Hui, Zhao, Linqing, Zhu, Runan
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 105056
container_issue
container_start_page 105056
container_title Infection, genetics and evolution
container_volume 95
creator Liu, Liying
Qian, Yuan
Jia, Liping
Dong, Huijin
Deng, Li
Huang, Hui
Zhao, Linqing
Zhu, Runan
description Human adenovirus serotype 41 (HAdV-F41) is an important pathogen that causes diarrhea in children. However, the data on its molecular genetic characteristics and evolutionary history are still neither comprehensive nor sufficient. Four capsid protein genes from 58 HAdV-F41-positive specimens taken from diarrheal children in Beijing during 2010–2019 were amplified and analyzed. Variant amino acids in the hexon gene (18 sites) and short fiber gene (4 sites) clustered these strains into two clades and four subclades. The deletion of 15 amino acids found in the gene seemed to have little effect on the genomic strain cluster same as to penton gene. The HAdV-F41 strains had high diversity, as assessed from the intraspecific recombination of hexon, short fiber and long fiber. The molecular evolutionary rate of HAdV-F41's concatenated genes was 4.07 × 10−5 substitutions/site/year, and it diverged from the most recent common ancestor in 1720. Apart from in the penton gene, positive selection codons were predicted in the other three genes, which may play a synergistic role in the evolution of HAdV-F41. These results provide new insights for understanding the characteristics of infectivity and developing vectors and vaccine vehicles for HAdV-F41. •High diversity in the HAdV-41 strains circulating in Beijing.•Amino acid substitutions were mainly located on the hexon and short fiber genes.•Two types of the 15 amino acid deletions displayed in the shaft of long fiber.•The molecular evolutionary rate of HAdV-41 was 4.07 × 10−5 substitutions/site/year.•HAdV-41 diverged from the most recent common ancestor in 1720.
doi_str_mv 10.1016/j.meegid.2021.105056
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2569378875</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1567134821003543</els_id><sourcerecordid>2569378875</sourcerecordid><originalsourceid>FETCH-LOGICAL-c428t-c77ad1534b19341bf5f48c9c1fa3f2f1799a7902c7b5e40b3c6cd6554c7bd63c3</originalsourceid><addsrcrecordid>eNp9kM9u1DAQxiMEon_gDRDykUN38d84uSDBqhSkSlzas-XYk3ZWib3Yzkp7Q-oj8IY8CVlly5HTjGa-bz7Nr6reMbpmlNUft-sR4AH9mlPO5pGiqn5RnTNV65XmSr889UzI5qy6yHlLKdOUN6-rMyFlw2jNzqunGwhQ0BGPe0gZy4HY4MkYB3DTYBOBfRymgjGQ2JPHabSBWA8h7jFNmWRIsRx2QCQjuSSLIROH6WgtGB4IBvIFcDu3V2TziMFeET-l44ZTRv_8-j2X9k31qrdDhrenelndf72-23xb3f64-b75fLtykjdl5bS2nikhO9YKybpe9bJxrWO9FT3vmW5bq1vKne4USNoJVztfKyXnga-FE5fVh-XuLsWfE-RiRswOhsEGiFM2XNWt0E2j1SyVi9SlmHOC3uwSjjYdDKPmiN9szYLfHPGbBf9se39KmLoR_D_TM-9Z8GkRwPznHiGZ7BCCA48JXDE-4v8T_gLFDZkd</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2569378875</pqid></control><display><type>article</type><title>Genetic diversity and molecular evolution of human adenovirus serotype 41 strains circulating in Beijing, China, during 2010–2019</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Liu, Liying ; Qian, Yuan ; Jia, Liping ; Dong, Huijin ; Deng, Li ; Huang, Hui ; Zhao, Linqing ; Zhu, Runan</creator><creatorcontrib>Liu, Liying ; Qian, Yuan ; Jia, Liping ; Dong, Huijin ; Deng, Li ; Huang, Hui ; Zhao, Linqing ; Zhu, Runan</creatorcontrib><description>Human adenovirus serotype 41 (HAdV-F41) is an important pathogen that causes diarrhea in children. However, the data on its molecular genetic characteristics and evolutionary history are still neither comprehensive nor sufficient. Four capsid protein genes from 58 HAdV-F41-positive specimens taken from diarrheal children in Beijing during 2010–2019 were amplified and analyzed. Variant amino acids in the hexon gene (18 sites) and short fiber gene (4 sites) clustered these strains into two clades and four subclades. The deletion of 15 amino acids found in the gene seemed to have little effect on the genomic strain cluster same as to penton gene. The HAdV-F41 strains had high diversity, as assessed from the intraspecific recombination of hexon, short fiber and long fiber. The molecular evolutionary rate of HAdV-F41's concatenated genes was 4.07 × 10−5 substitutions/site/year, and it diverged from the most recent common ancestor in 1720. Apart from in the penton gene, positive selection codons were predicted in the other three genes, which may play a synergistic role in the evolution of HAdV-F41. These results provide new insights for understanding the characteristics of infectivity and developing vectors and vaccine vehicles for HAdV-F41. •High diversity in the HAdV-41 strains circulating in Beijing.•Amino acid substitutions were mainly located on the hexon and short fiber genes.•Two types of the 15 amino acid deletions displayed in the shaft of long fiber.•The molecular evolutionary rate of HAdV-41 was 4.07 × 10−5 substitutions/site/year.•HAdV-41 diverged from the most recent common ancestor in 1720.</description><identifier>ISSN: 1567-1348</identifier><identifier>EISSN: 1567-7257</identifier><identifier>DOI: 10.1016/j.meegid.2021.105056</identifier><identifier>PMID: 34481061</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adenovirus Infections, Human - virology ; Adenoviruses, Human - genetics ; Amino Acid Sequence ; Beijing ; Capsid Proteins - chemistry ; Capsid Proteins - genetics ; Capsid Proteins - metabolism ; Children ; Diarrhea ; Evolution, Molecular ; Genetic diversity ; Genetic Variation ; Human adenovirus serotype 41 ; Humans ; Molecular revolution ; Sequence Alignment ; Serogroup</subject><ispartof>Infection, genetics and evolution, 2021-11, Vol.95, p.105056-105056, Article 105056</ispartof><rights>2021 Elsevier B.V.</rights><rights>Copyright © 2021 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-c77ad1534b19341bf5f48c9c1fa3f2f1799a7902c7b5e40b3c6cd6554c7bd63c3</citedby><cites>FETCH-LOGICAL-c428t-c77ad1534b19341bf5f48c9c1fa3f2f1799a7902c7b5e40b3c6cd6554c7bd63c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.meegid.2021.105056$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34481061$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Liying</creatorcontrib><creatorcontrib>Qian, Yuan</creatorcontrib><creatorcontrib>Jia, Liping</creatorcontrib><creatorcontrib>Dong, Huijin</creatorcontrib><creatorcontrib>Deng, Li</creatorcontrib><creatorcontrib>Huang, Hui</creatorcontrib><creatorcontrib>Zhao, Linqing</creatorcontrib><creatorcontrib>Zhu, Runan</creatorcontrib><title>Genetic diversity and molecular evolution of human adenovirus serotype 41 strains circulating in Beijing, China, during 2010–2019</title><title>Infection, genetics and evolution</title><addtitle>Infect Genet Evol</addtitle><description>Human adenovirus serotype 41 (HAdV-F41) is an important pathogen that causes diarrhea in children. However, the data on its molecular genetic characteristics and evolutionary history are still neither comprehensive nor sufficient. Four capsid protein genes from 58 HAdV-F41-positive specimens taken from diarrheal children in Beijing during 2010–2019 were amplified and analyzed. Variant amino acids in the hexon gene (18 sites) and short fiber gene (4 sites) clustered these strains into two clades and four subclades. The deletion of 15 amino acids found in the gene seemed to have little effect on the genomic strain cluster same as to penton gene. The HAdV-F41 strains had high diversity, as assessed from the intraspecific recombination of hexon, short fiber and long fiber. The molecular evolutionary rate of HAdV-F41's concatenated genes was 4.07 × 10−5 substitutions/site/year, and it diverged from the most recent common ancestor in 1720. Apart from in the penton gene, positive selection codons were predicted in the other three genes, which may play a synergistic role in the evolution of HAdV-F41. These results provide new insights for understanding the characteristics of infectivity and developing vectors and vaccine vehicles for HAdV-F41. •High diversity in the HAdV-41 strains circulating in Beijing.•Amino acid substitutions were mainly located on the hexon and short fiber genes.•Two types of the 15 amino acid deletions displayed in the shaft of long fiber.•The molecular evolutionary rate of HAdV-41 was 4.07 × 10−5 substitutions/site/year.•HAdV-41 diverged from the most recent common ancestor in 1720.</description><subject>Adenovirus Infections, Human - virology</subject><subject>Adenoviruses, Human - genetics</subject><subject>Amino Acid Sequence</subject><subject>Beijing</subject><subject>Capsid Proteins - chemistry</subject><subject>Capsid Proteins - genetics</subject><subject>Capsid Proteins - metabolism</subject><subject>Children</subject><subject>Diarrhea</subject><subject>Evolution, Molecular</subject><subject>Genetic diversity</subject><subject>Genetic Variation</subject><subject>Human adenovirus serotype 41</subject><subject>Humans</subject><subject>Molecular revolution</subject><subject>Sequence Alignment</subject><subject>Serogroup</subject><issn>1567-1348</issn><issn>1567-7257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM9u1DAQxiMEon_gDRDykUN38d84uSDBqhSkSlzas-XYk3ZWib3Yzkp7Q-oj8IY8CVlly5HTjGa-bz7Nr6reMbpmlNUft-sR4AH9mlPO5pGiqn5RnTNV65XmSr889UzI5qy6yHlLKdOUN6-rMyFlw2jNzqunGwhQ0BGPe0gZy4HY4MkYB3DTYBOBfRymgjGQ2JPHabSBWA8h7jFNmWRIsRx2QCQjuSSLIROH6WgtGB4IBvIFcDu3V2TziMFeET-l44ZTRv_8-j2X9k31qrdDhrenelndf72-23xb3f64-b75fLtykjdl5bS2nikhO9YKybpe9bJxrWO9FT3vmW5bq1vKne4USNoJVztfKyXnga-FE5fVh-XuLsWfE-RiRswOhsEGiFM2XNWt0E2j1SyVi9SlmHOC3uwSjjYdDKPmiN9szYLfHPGbBf9se39KmLoR_D_TM-9Z8GkRwPznHiGZ7BCCA48JXDE-4v8T_gLFDZkd</recordid><startdate>202111</startdate><enddate>202111</enddate><creator>Liu, Liying</creator><creator>Qian, Yuan</creator><creator>Jia, Liping</creator><creator>Dong, Huijin</creator><creator>Deng, Li</creator><creator>Huang, Hui</creator><creator>Zhao, Linqing</creator><creator>Zhu, Runan</creator><general>Elsevier B.V</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></search><sort><creationdate>202111</creationdate><title>Genetic diversity and molecular evolution of human adenovirus serotype 41 strains circulating in Beijing, China, during 2010–2019</title><author>Liu, Liying ; Qian, Yuan ; Jia, Liping ; Dong, Huijin ; Deng, Li ; Huang, Hui ; Zhao, Linqing ; Zhu, Runan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-c77ad1534b19341bf5f48c9c1fa3f2f1799a7902c7b5e40b3c6cd6554c7bd63c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenovirus Infections, Human - virology</topic><topic>Adenoviruses, Human - genetics</topic><topic>Amino Acid Sequence</topic><topic>Beijing</topic><topic>Capsid Proteins - chemistry</topic><topic>Capsid Proteins - genetics</topic><topic>Capsid Proteins - metabolism</topic><topic>Children</topic><topic>Diarrhea</topic><topic>Evolution, Molecular</topic><topic>Genetic diversity</topic><topic>Genetic Variation</topic><topic>Human adenovirus serotype 41</topic><topic>Humans</topic><topic>Molecular revolution</topic><topic>Sequence Alignment</topic><topic>Serogroup</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Liying</creatorcontrib><creatorcontrib>Qian, Yuan</creatorcontrib><creatorcontrib>Jia, Liping</creatorcontrib><creatorcontrib>Dong, Huijin</creatorcontrib><creatorcontrib>Deng, Li</creatorcontrib><creatorcontrib>Huang, Hui</creatorcontrib><creatorcontrib>Zhao, Linqing</creatorcontrib><creatorcontrib>Zhu, Runan</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><jtitle>Infection, genetics and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Liying</au><au>Qian, Yuan</au><au>Jia, Liping</au><au>Dong, Huijin</au><au>Deng, Li</au><au>Huang, Hui</au><au>Zhao, Linqing</au><au>Zhu, Runan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic diversity and molecular evolution of human adenovirus serotype 41 strains circulating in Beijing, China, during 2010–2019</atitle><jtitle>Infection, genetics and evolution</jtitle><addtitle>Infect Genet Evol</addtitle><date>2021-11</date><risdate>2021</risdate><volume>95</volume><spage>105056</spage><epage>105056</epage><pages>105056-105056</pages><artnum>105056</artnum><issn>1567-1348</issn><eissn>1567-7257</eissn><abstract>Human adenovirus serotype 41 (HAdV-F41) is an important pathogen that causes diarrhea in children. However, the data on its molecular genetic characteristics and evolutionary history are still neither comprehensive nor sufficient. Four capsid protein genes from 58 HAdV-F41-positive specimens taken from diarrheal children in Beijing during 2010–2019 were amplified and analyzed. Variant amino acids in the hexon gene (18 sites) and short fiber gene (4 sites) clustered these strains into two clades and four subclades. The deletion of 15 amino acids found in the gene seemed to have little effect on the genomic strain cluster same as to penton gene. The HAdV-F41 strains had high diversity, as assessed from the intraspecific recombination of hexon, short fiber and long fiber. The molecular evolutionary rate of HAdV-F41's concatenated genes was 4.07 × 10−5 substitutions/site/year, and it diverged from the most recent common ancestor in 1720. Apart from in the penton gene, positive selection codons were predicted in the other three genes, which may play a synergistic role in the evolution of HAdV-F41. These results provide new insights for understanding the characteristics of infectivity and developing vectors and vaccine vehicles for HAdV-F41. •High diversity in the HAdV-41 strains circulating in Beijing.•Amino acid substitutions were mainly located on the hexon and short fiber genes.•Two types of the 15 amino acid deletions displayed in the shaft of long fiber.•The molecular evolutionary rate of HAdV-41 was 4.07 × 10−5 substitutions/site/year.•HAdV-41 diverged from the most recent common ancestor in 1720.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>34481061</pmid><doi>10.1016/j.meegid.2021.105056</doi><tpages>1</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1567-1348
ispartof Infection, genetics and evolution, 2021-11, Vol.95, p.105056-105056, Article 105056
issn 1567-1348
1567-7257
language eng
recordid cdi_proquest_miscellaneous_2569378875
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Adenovirus Infections, Human - virology
Adenoviruses, Human - genetics
Amino Acid Sequence
Beijing
Capsid Proteins - chemistry
Capsid Proteins - genetics
Capsid Proteins - metabolism
Children
Diarrhea
Evolution, Molecular
Genetic diversity
Genetic Variation
Human adenovirus serotype 41
Humans
Molecular revolution
Sequence Alignment
Serogroup
title Genetic diversity and molecular evolution of human adenovirus serotype 41 strains circulating in Beijing, China, during 2010–2019
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T14%3A12%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genetic%20diversity%20and%20molecular%20evolution%20of%20human%20adenovirus%20serotype%2041%20strains%20circulating%20in%20Beijing,%20China,%20during%202010%E2%80%932019&rft.jtitle=Infection,%20genetics%20and%20evolution&rft.au=Liu,%20Liying&rft.date=2021-11&rft.volume=95&rft.spage=105056&rft.epage=105056&rft.pages=105056-105056&rft.artnum=105056&rft.issn=1567-1348&rft.eissn=1567-7257&rft_id=info:doi/10.1016/j.meegid.2021.105056&rft_dat=%3Cproquest_cross%3E2569378875%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2569378875&rft_id=info:pmid/34481061&rft_els_id=S1567134821003543&rfr_iscdi=true