Single-step RT-PCR assay for dual genotyping of GI and GII norovirus strains
•We validated genogroup-specific one-step conventional RT-PCR assays (PC assays) for sequence-based dual typing of GI and GII norovirus strains.•The PC assays use a combination of oligonucleotide primers that target a genomic region spanning the 3’-end of ORF1 and 5’end of ORF2 of GI and GII norovir...
Gespeichert in:
Veröffentlicht in: | Journal of clinical virology 2021-01, Vol.134, p.104689-104689, Article 104689 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 104689 |
---|---|
container_issue | |
container_start_page | 104689 |
container_title | Journal of clinical virology |
container_volume | 134 |
creator | Chhabra, Preeti Browne, Hannah Huynh, Thalia Diez-Valcarce, Marta Barclay, Leslie Kosek, Margaret N. Ahmed, Tahmeed Lopez, Maria Renee Pan, Chao-Yang Vinjé, Jan |
description | •We validated genogroup-specific one-step conventional RT-PCR assays (PC assays) for sequence-based dual typing of GI and GII norovirus strains.•The PC assays use a combination of oligonucleotide primers that target a genomic region spanning the 3’-end of ORF1 and 5’end of ORF2 of GI and GII noroviruses.•The PC assays are sensitive (5 to 50 copies/rx) and detect all currently identified norovirus P-types and capsid genotypes from different geographic regions.•The PC assays have been successfully implemented by CaliciNet USA and CaliciNet China.
Noroviruses are the major cause of acute gastroenteritis (AGE) in people of all ages globally. Standardized genotyping is key for outbreak investigations and surveillance networks.
Here we describe the validation of a one-step conventional RT-PCR assay for sequence-based dual typing of GI and GII noroviruses.
This polymerase (P) and capsid (C) dual typing assay uses a combination of previously published oligonucleotide primers amplifying a genomic region spanning the 3'-end of ORF1 and 5'end of ORF2 resulting in a 579 bp product for GI and 570 bp product for GII viruses.
The limit of detection of the assay ranged from 5 to 50 copies of viral RNA per reaction for GI and GII. To validate the assay, we tested 2,663 noroviruspositive stool samples from outbreaks and sporadic cases of AGE in Bangladesh, Guatemala, Peru, and USA collected between 2010–2019, of which 2,392 (90 %) were genotyped successfully. Most of the known genotypes infecting humans (GI (n = 9) and GII (n = 23)) and P types (GI (n = 15), GII, (n = 20)) could be detected. The remaining 270 samples had low viral load (Ct > 30) by real-time RT-PCR. A panel of 166 samples positive for other enteric viruses (rotavirus, astrovirus, sapovirus, adenovirus type 40/41) tested negative.
The use of broadly reactive genotyping assays greatly strengthens exchange of standardized genotype data globally to monitor trends in genotype diversity which is important for both the development of vaccines and to measure their impact. |
doi_str_mv | 10.1016/j.jcv.2020.104689 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7816162</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1386653220304315</els_id><sourcerecordid>2466293152</sourcerecordid><originalsourceid>FETCH-LOGICAL-c517t-1a8bf62fff92af2dbdeae40f798faa5b74f5f5a479343264f0f37835fdaaa5643</originalsourceid><addsrcrecordid>eNp9kU9rGzEQxUVoSdIkH6CXomMv6-i_dikUimkTgyElcc5C3h25MmvJlXYN_vaVsRuSS04jMb_3ZpiH0GdKJpRQdbuerNvdhBF2-AtVN2foktaaV7JR-kN581pVSnJ2gT7lvCaESi70ObrgnClSFJdo_uTDqocqD7DFj4vq9_QR25ztHruYcDfaHq8gxGG_LRyODt_NsA1dKTMcYoo7n8aM85CsD_kafXS2z3Bzqlfo-dfPxfS-mj_czaY_5lUrqR4qauulU8w51zDrWLfswIIgTje1s1YutXDSSSt0w0VZVDjiuK65dJ0tbSX4Ffp-9N2Oyw10LYQyvzfb5Dc27U203rztBP_HrOLO6Joqqlgx-HoySPHvCHkwG59b6HsbII7ZMKEUaziVB5Qe0TbFnBO4lzGUmEMKZm1KCuaQgjmmUDRfXu_3ovh_9gJ8OwJQrrTzkExuPYQWOp-gHUwX_Tv2_wCjuZiu</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2466293152</pqid></control><display><type>article</type><title>Single-step RT-PCR assay for dual genotyping of GI and GII norovirus strains</title><source>Elsevier ScienceDirect Journals</source><creator>Chhabra, Preeti ; Browne, Hannah ; Huynh, Thalia ; Diez-Valcarce, Marta ; Barclay, Leslie ; Kosek, Margaret N. ; Ahmed, Tahmeed ; Lopez, Maria Renee ; Pan, Chao-Yang ; Vinjé, Jan</creator><creatorcontrib>Chhabra, Preeti ; Browne, Hannah ; Huynh, Thalia ; Diez-Valcarce, Marta ; Barclay, Leslie ; Kosek, Margaret N. ; Ahmed, Tahmeed ; Lopez, Maria Renee ; Pan, Chao-Yang ; Vinjé, Jan</creatorcontrib><description>•We validated genogroup-specific one-step conventional RT-PCR assays (PC assays) for sequence-based dual typing of GI and GII norovirus strains.•The PC assays use a combination of oligonucleotide primers that target a genomic region spanning the 3’-end of ORF1 and 5’end of ORF2 of GI and GII noroviruses.•The PC assays are sensitive (5 to 50 copies/rx) and detect all currently identified norovirus P-types and capsid genotypes from different geographic regions.•The PC assays have been successfully implemented by CaliciNet USA and CaliciNet China.
Noroviruses are the major cause of acute gastroenteritis (AGE) in people of all ages globally. Standardized genotyping is key for outbreak investigations and surveillance networks.
Here we describe the validation of a one-step conventional RT-PCR assay for sequence-based dual typing of GI and GII noroviruses.
This polymerase (P) and capsid (C) dual typing assay uses a combination of previously published oligonucleotide primers amplifying a genomic region spanning the 3'-end of ORF1 and 5'end of ORF2 resulting in a 579 bp product for GI and 570 bp product for GII viruses.
The limit of detection of the assay ranged from 5 to 50 copies of viral RNA per reaction for GI and GII. To validate the assay, we tested 2,663 noroviruspositive stool samples from outbreaks and sporadic cases of AGE in Bangladesh, Guatemala, Peru, and USA collected between 2010–2019, of which 2,392 (90 %) were genotyped successfully. Most of the known genotypes infecting humans (GI (n = 9) and GII (n = 23)) and P types (GI (n = 15), GII, (n = 20)) could be detected. The remaining 270 samples had low viral load (Ct > 30) by real-time RT-PCR. A panel of 166 samples positive for other enteric viruses (rotavirus, astrovirus, sapovirus, adenovirus type 40/41) tested negative.
The use of broadly reactive genotyping assays greatly strengthens exchange of standardized genotype data globally to monitor trends in genotype diversity which is important for both the development of vaccines and to measure their impact.</description><identifier>ISSN: 1386-6532</identifier><identifier>EISSN: 1873-5967</identifier><identifier>DOI: 10.1016/j.jcv.2020.104689</identifier><identifier>PMID: 33260046</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Gastroenteritis ; Norovirus ; RT-PCR ; Short Communication</subject><ispartof>Journal of clinical virology, 2021-01, Vol.134, p.104689-104689, Article 104689</ispartof><rights>2020</rights><rights>Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c517t-1a8bf62fff92af2dbdeae40f798faa5b74f5f5a479343264f0f37835fdaaa5643</citedby><cites>FETCH-LOGICAL-c517t-1a8bf62fff92af2dbdeae40f798faa5b74f5f5a479343264f0f37835fdaaa5643</cites><orcidid>0000-0001-6227-8057 ; 0000-0002-4607-7439</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1386653220304315$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33260046$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chhabra, Preeti</creatorcontrib><creatorcontrib>Browne, Hannah</creatorcontrib><creatorcontrib>Huynh, Thalia</creatorcontrib><creatorcontrib>Diez-Valcarce, Marta</creatorcontrib><creatorcontrib>Barclay, Leslie</creatorcontrib><creatorcontrib>Kosek, Margaret N.</creatorcontrib><creatorcontrib>Ahmed, Tahmeed</creatorcontrib><creatorcontrib>Lopez, Maria Renee</creatorcontrib><creatorcontrib>Pan, Chao-Yang</creatorcontrib><creatorcontrib>Vinjé, Jan</creatorcontrib><title>Single-step RT-PCR assay for dual genotyping of GI and GII norovirus strains</title><title>Journal of clinical virology</title><addtitle>J Clin Virol</addtitle><description>•We validated genogroup-specific one-step conventional RT-PCR assays (PC assays) for sequence-based dual typing of GI and GII norovirus strains.•The PC assays use a combination of oligonucleotide primers that target a genomic region spanning the 3’-end of ORF1 and 5’end of ORF2 of GI and GII noroviruses.•The PC assays are sensitive (5 to 50 copies/rx) and detect all currently identified norovirus P-types and capsid genotypes from different geographic regions.•The PC assays have been successfully implemented by CaliciNet USA and CaliciNet China.
Noroviruses are the major cause of acute gastroenteritis (AGE) in people of all ages globally. Standardized genotyping is key for outbreak investigations and surveillance networks.
Here we describe the validation of a one-step conventional RT-PCR assay for sequence-based dual typing of GI and GII noroviruses.
This polymerase (P) and capsid (C) dual typing assay uses a combination of previously published oligonucleotide primers amplifying a genomic region spanning the 3'-end of ORF1 and 5'end of ORF2 resulting in a 579 bp product for GI and 570 bp product for GII viruses.
The limit of detection of the assay ranged from 5 to 50 copies of viral RNA per reaction for GI and GII. To validate the assay, we tested 2,663 noroviruspositive stool samples from outbreaks and sporadic cases of AGE in Bangladesh, Guatemala, Peru, and USA collected between 2010–2019, of which 2,392 (90 %) were genotyped successfully. Most of the known genotypes infecting humans (GI (n = 9) and GII (n = 23)) and P types (GI (n = 15), GII, (n = 20)) could be detected. The remaining 270 samples had low viral load (Ct > 30) by real-time RT-PCR. A panel of 166 samples positive for other enteric viruses (rotavirus, astrovirus, sapovirus, adenovirus type 40/41) tested negative.
The use of broadly reactive genotyping assays greatly strengthens exchange of standardized genotype data globally to monitor trends in genotype diversity which is important for both the development of vaccines and to measure their impact.</description><subject>Gastroenteritis</subject><subject>Norovirus</subject><subject>RT-PCR</subject><subject>Short Communication</subject><issn>1386-6532</issn><issn>1873-5967</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kU9rGzEQxUVoSdIkH6CXomMv6-i_dikUimkTgyElcc5C3h25MmvJlXYN_vaVsRuSS04jMb_3ZpiH0GdKJpRQdbuerNvdhBF2-AtVN2foktaaV7JR-kN581pVSnJ2gT7lvCaESi70ObrgnClSFJdo_uTDqocqD7DFj4vq9_QR25ztHruYcDfaHq8gxGG_LRyODt_NsA1dKTMcYoo7n8aM85CsD_kafXS2z3Bzqlfo-dfPxfS-mj_czaY_5lUrqR4qauulU8w51zDrWLfswIIgTje1s1YutXDSSSt0w0VZVDjiuK65dJ0tbSX4Ffp-9N2Oyw10LYQyvzfb5Dc27U203rztBP_HrOLO6Joqqlgx-HoySPHvCHkwG59b6HsbII7ZMKEUaziVB5Qe0TbFnBO4lzGUmEMKZm1KCuaQgjmmUDRfXu_3ovh_9gJ8OwJQrrTzkExuPYQWOp-gHUwX_Tv2_wCjuZiu</recordid><startdate>202101</startdate><enddate>202101</enddate><creator>Chhabra, Preeti</creator><creator>Browne, Hannah</creator><creator>Huynh, Thalia</creator><creator>Diez-Valcarce, Marta</creator><creator>Barclay, Leslie</creator><creator>Kosek, Margaret N.</creator><creator>Ahmed, Tahmeed</creator><creator>Lopez, Maria Renee</creator><creator>Pan, Chao-Yang</creator><creator>Vinjé, Jan</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6227-8057</orcidid><orcidid>https://orcid.org/0000-0002-4607-7439</orcidid></search><sort><creationdate>202101</creationdate><title>Single-step RT-PCR assay for dual genotyping of GI and GII norovirus strains</title><author>Chhabra, Preeti ; Browne, Hannah ; Huynh, Thalia ; Diez-Valcarce, Marta ; Barclay, Leslie ; Kosek, Margaret N. ; Ahmed, Tahmeed ; Lopez, Maria Renee ; Pan, Chao-Yang ; Vinjé, Jan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c517t-1a8bf62fff92af2dbdeae40f798faa5b74f5f5a479343264f0f37835fdaaa5643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Gastroenteritis</topic><topic>Norovirus</topic><topic>RT-PCR</topic><topic>Short Communication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chhabra, Preeti</creatorcontrib><creatorcontrib>Browne, Hannah</creatorcontrib><creatorcontrib>Huynh, Thalia</creatorcontrib><creatorcontrib>Diez-Valcarce, Marta</creatorcontrib><creatorcontrib>Barclay, Leslie</creatorcontrib><creatorcontrib>Kosek, Margaret N.</creatorcontrib><creatorcontrib>Ahmed, Tahmeed</creatorcontrib><creatorcontrib>Lopez, Maria Renee</creatorcontrib><creatorcontrib>Pan, Chao-Yang</creatorcontrib><creatorcontrib>Vinjé, Jan</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chhabra, Preeti</au><au>Browne, Hannah</au><au>Huynh, Thalia</au><au>Diez-Valcarce, Marta</au><au>Barclay, Leslie</au><au>Kosek, Margaret N.</au><au>Ahmed, Tahmeed</au><au>Lopez, Maria Renee</au><au>Pan, Chao-Yang</au><au>Vinjé, Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-step RT-PCR assay for dual genotyping of GI and GII norovirus strains</atitle><jtitle>Journal of clinical virology</jtitle><addtitle>J Clin Virol</addtitle><date>2021-01</date><risdate>2021</risdate><volume>134</volume><spage>104689</spage><epage>104689</epage><pages>104689-104689</pages><artnum>104689</artnum><issn>1386-6532</issn><eissn>1873-5967</eissn><abstract>•We validated genogroup-specific one-step conventional RT-PCR assays (PC assays) for sequence-based dual typing of GI and GII norovirus strains.•The PC assays use a combination of oligonucleotide primers that target a genomic region spanning the 3’-end of ORF1 and 5’end of ORF2 of GI and GII noroviruses.•The PC assays are sensitive (5 to 50 copies/rx) and detect all currently identified norovirus P-types and capsid genotypes from different geographic regions.•The PC assays have been successfully implemented by CaliciNet USA and CaliciNet China.
Noroviruses are the major cause of acute gastroenteritis (AGE) in people of all ages globally. Standardized genotyping is key for outbreak investigations and surveillance networks.
Here we describe the validation of a one-step conventional RT-PCR assay for sequence-based dual typing of GI and GII noroviruses.
This polymerase (P) and capsid (C) dual typing assay uses a combination of previously published oligonucleotide primers amplifying a genomic region spanning the 3'-end of ORF1 and 5'end of ORF2 resulting in a 579 bp product for GI and 570 bp product for GII viruses.
The limit of detection of the assay ranged from 5 to 50 copies of viral RNA per reaction for GI and GII. To validate the assay, we tested 2,663 noroviruspositive stool samples from outbreaks and sporadic cases of AGE in Bangladesh, Guatemala, Peru, and USA collected between 2010–2019, of which 2,392 (90 %) were genotyped successfully. Most of the known genotypes infecting humans (GI (n = 9) and GII (n = 23)) and P types (GI (n = 15), GII, (n = 20)) could be detected. The remaining 270 samples had low viral load (Ct > 30) by real-time RT-PCR. A panel of 166 samples positive for other enteric viruses (rotavirus, astrovirus, sapovirus, adenovirus type 40/41) tested negative.
The use of broadly reactive genotyping assays greatly strengthens exchange of standardized genotype data globally to monitor trends in genotype diversity which is important for both the development of vaccines and to measure their impact.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>33260046</pmid><doi>10.1016/j.jcv.2020.104689</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-6227-8057</orcidid><orcidid>https://orcid.org/0000-0002-4607-7439</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1386-6532 |
ispartof | Journal of clinical virology, 2021-01, Vol.134, p.104689-104689, Article 104689 |
issn | 1386-6532 1873-5967 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7816162 |
source | Elsevier ScienceDirect Journals |
subjects | Gastroenteritis Norovirus RT-PCR Short Communication |
title | Single-step RT-PCR assay for dual genotyping of GI and GII norovirus strains |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T10%3A56%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Single-step%20RT-PCR%20assay%20for%20dual%20genotyping%20of%20GI%20and%20GII%20norovirus%20strains&rft.jtitle=Journal%20of%20clinical%20virology&rft.au=Chhabra,%20Preeti&rft.date=2021-01&rft.volume=134&rft.spage=104689&rft.epage=104689&rft.pages=104689-104689&rft.artnum=104689&rft.issn=1386-6532&rft.eissn=1873-5967&rft_id=info:doi/10.1016/j.jcv.2020.104689&rft_dat=%3Cproquest_pubme%3E2466293152%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2466293152&rft_id=info:pmid/33260046&rft_els_id=S1386653220304315&rfr_iscdi=true |