Development of an amplicon-based sequencing approach in response to the global emergence of mpox

Detalhes bibliográficos
Autor(a) principal: Chen, Nicholas F.G.
Data de Publicação: 2023
Outros Autores: Chaguza, Chrispin, Gagne, Luc, Doucette, Matthew, Smole, Sandra, Buzby, Erika, Hall, Joshua, Ash, Stephanie, Harrington, Rachel, Cofsky, Seana, Clancy, Selina, Kapsak, Curtis J., Sevinsky, Joel, Libuit, Kevin, Park, Daniel J., Hemarajata, Peera, Garrigues, Jacob M., Green, Nicole M., Sierra-Patev, Sean, Carpenter-Azevedo, Kristin, Huard, Richard C., Pearson, Claire, Incekara, Kutluhan, Nishimura, Christina, Huang, Jian Ping, Gagnon, Emily, Reever, Ethan, Razeq, Jafar, Muyombwe, Anthony, Borges, Vítor, Ferreira, Rita, Sobral, Daniel, Duarte, Silvia, Santos, Daniela, Vieira, Luís, Gomes, João Paulo, Aquino, Carly, Savino, Isabella M., Felton, Karinda, Bajwa, Moneeb, Hayward, Nyjil, Miller, Holly, Naumann, Allison, Allman, Ria, Greer, Neel, Fall, Amary, Mostafa, Heba H., McHugh, Martin P., Maloney, Daniel M., Dewar, Rebecca, Kenicer, Juliet, Parker, Abby, Mathers, Katharine, Wild, Jonathan, Cotton, Seb, Templeton, Kate E., Churchwell, George, Lee, Philip A., Pedrosa, Maria, McGruder, Brenna, Schmedes, Sarah, Plumb, Matthew R., Wang, Xiong, Barcellos, Regina Bones, Godinho, Fernanda M.S., Salvato, Richard Steiner, Ceniseros, Aimee, Breban, Mallery I., Grubaugh, Nathan D., Gallagher, Glen R., Vogels, Chantal B.F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.18/8955
Resumo: The 2022 multicountry mpox outbreak concurrent with the ongoing Coronavirus Disease 2019 (COVID-19) pandemic further highlighted the need for genomic surveillance and rapid pathogen whole-genome sequencing. While metagenomic sequencing approaches have been used to sequence many of the early mpox infections, these methods are resource intensive and require samples with high viral DNA concentrations. Given the atypical clinical presentation of cases associated with the outbreak and uncertainty regarding viral load across both the course of infection and anatomical body sites, there was an urgent need for a more sensitive and broadly applicable sequencing approach. Highly multiplexed amplicon-based sequencing (PrimalSeq) was initially developed for sequencing of Zika virus, and later adapted as the main sequencing approach for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Here, we used PrimalScheme to develop a primer scheme for human monkeypox virus that can be used with many sequencing and bioinformatics pipelines implemented in public health laboratories during the COVID-19 pandemic. We sequenced clinical specimens that tested presumptively positive for human monkeypox virus with amplicon-based and metagenomic sequencing approaches. We found notably higher genome coverage across the virus genome, with minimal amplicon drop-outs, in using the amplicon-based sequencing approach, particularly in higher PCR cycle threshold (Ct) (lower DNA titer) samples. Further testing demonstrated that Ct value correlated with the number of sequencing reads and influenced the percent genome coverage. To maximize genome coverage when resources are limited, we recommend selecting samples with a PCR Ct below 31 Ct and generating 1 million sequencing reads per sample. To support national and international public health genomic surveillance efforts, we sent out primer pool aliquots to 10 laboratories across the United States, United Kingdom, Brazil, and Portugal. These public health laboratories successfully implemented the human monkeypox virus primer scheme in various amplicon sequencing workflows and with different sample types across a range of Ct values. Thus, we show that amplicon-based sequencing can provide a rapidly deployable, cost-effective, and flexible approach to pathogen whole-genome sequencing in response to newly emerging pathogens. Importantly, through the implementation of our primer scheme into existing SARS-CoV-2 workflows and across a range of sample types and sequencing platforms, we further demonstrate the potential of this approach for rapid outbreak response.
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spelling Development of an amplicon-based sequencing approach in response to the global emergence of mpoxMpoxMpox OutbreakMonkeypox VirusGenomic SurveillanceWhole-genome SequencingOutbreak ResponseGlobal EmergencePandemicsInfecções EmergentesThe 2022 multicountry mpox outbreak concurrent with the ongoing Coronavirus Disease 2019 (COVID-19) pandemic further highlighted the need for genomic surveillance and rapid pathogen whole-genome sequencing. While metagenomic sequencing approaches have been used to sequence many of the early mpox infections, these methods are resource intensive and require samples with high viral DNA concentrations. Given the atypical clinical presentation of cases associated with the outbreak and uncertainty regarding viral load across both the course of infection and anatomical body sites, there was an urgent need for a more sensitive and broadly applicable sequencing approach. Highly multiplexed amplicon-based sequencing (PrimalSeq) was initially developed for sequencing of Zika virus, and later adapted as the main sequencing approach for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Here, we used PrimalScheme to develop a primer scheme for human monkeypox virus that can be used with many sequencing and bioinformatics pipelines implemented in public health laboratories during the COVID-19 pandemic. We sequenced clinical specimens that tested presumptively positive for human monkeypox virus with amplicon-based and metagenomic sequencing approaches. We found notably higher genome coverage across the virus genome, with minimal amplicon drop-outs, in using the amplicon-based sequencing approach, particularly in higher PCR cycle threshold (Ct) (lower DNA titer) samples. Further testing demonstrated that Ct value correlated with the number of sequencing reads and influenced the percent genome coverage. To maximize genome coverage when resources are limited, we recommend selecting samples with a PCR Ct below 31 Ct and generating 1 million sequencing reads per sample. To support national and international public health genomic surveillance efforts, we sent out primer pool aliquots to 10 laboratories across the United States, United Kingdom, Brazil, and Portugal. These public health laboratories successfully implemented the human monkeypox virus primer scheme in various amplicon sequencing workflows and with different sample types across a range of Ct values. Thus, we show that amplicon-based sequencing can provide a rapidly deployable, cost-effective, and flexible approach to pathogen whole-genome sequencing in response to newly emerging pathogens. Importantly, through the implementation of our primer scheme into existing SARS-CoV-2 workflows and across a range of sample types and sequencing platforms, we further demonstrate the potential of this approach for rapid outbreak response.This publication was made possible by CTSA Grant Number UL1 TR001863 from the National Center for Advancing Translational Science (NCATS), a component of the National Institutes of Health (NIH) awarded to CBFV. INSA was partially funded by the HERA project (Grant/ 2021/PHF/23776) supported by the European Commission through the European Centre for Disease Control (to VB).Public Library of ScienceRepositório Científico do Instituto Nacional de SaúdeChen, Nicholas F.G.Chaguza, ChrispinGagne, LucDoucette, MatthewSmole, SandraBuzby, ErikaHall, JoshuaAsh, StephanieHarrington, RachelCofsky, SeanaClancy, SelinaKapsak, Curtis J.Sevinsky, JoelLibuit, KevinPark, Daniel J.Hemarajata, PeeraGarrigues, Jacob M.Green, Nicole M.Sierra-Patev, SeanCarpenter-Azevedo, KristinHuard, Richard C.Pearson, ClaireIncekara, KutluhanNishimura, ChristinaHuang, Jian PingGagnon, EmilyReever, EthanRazeq, JafarMuyombwe, AnthonyBorges, VítorFerreira, RitaSobral, DanielDuarte, SilviaSantos, DanielaVieira, LuísGomes, João PauloAquino, CarlySavino, Isabella M.Felton, KarindaBajwa, MoneebHayward, NyjilMiller, HollyNaumann, AllisonAllman, RiaGreer, NeelFall, AmaryMostafa, Heba H.McHugh, Martin P.Maloney, Daniel M.Dewar, RebeccaKenicer, JulietParker, AbbyMathers, KatharineWild, JonathanCotton, SebTempleton, Kate E.Churchwell, GeorgeLee, Philip A.Pedrosa, MariaMcGruder, BrennaSchmedes, SarahPlumb, Matthew R.Wang, XiongBarcellos, Regina BonesGodinho, Fernanda M.S.Salvato, Richard SteinerCeniseros, AimeeBreban, Mallery I.Grubaugh, Nathan D.Gallagher, Glen R.Vogels, Chantal B.F.2024-01-23T11:54:36Z2023-06-132023-06-13T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.18/8955engPLoS Biol. 2023 Jun 13;21(6):e3002151. doi: 10.1371/journal.pbio.3002151. eCollection 2023 Jun1544-917310.1371/journal.pbio.3002151info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-01-27T01:31:55Zoai:repositorio.insa.pt:10400.18/8955Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T01:57:59.620135Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Development of an amplicon-based sequencing approach in response to the global emergence of mpox
title Development of an amplicon-based sequencing approach in response to the global emergence of mpox
spellingShingle Development of an amplicon-based sequencing approach in response to the global emergence of mpox
Chen, Nicholas F.G.
Mpox
Mpox Outbreak
Monkeypox Virus
Genomic Surveillance
Whole-genome Sequencing
Outbreak Response
Global Emergence
Pandemics
Infecções Emergentes
title_short Development of an amplicon-based sequencing approach in response to the global emergence of mpox
title_full Development of an amplicon-based sequencing approach in response to the global emergence of mpox
title_fullStr Development of an amplicon-based sequencing approach in response to the global emergence of mpox
title_full_unstemmed Development of an amplicon-based sequencing approach in response to the global emergence of mpox
title_sort Development of an amplicon-based sequencing approach in response to the global emergence of mpox
author Chen, Nicholas F.G.
author_facet Chen, Nicholas F.G.
Chaguza, Chrispin
Gagne, Luc
Doucette, Matthew
Smole, Sandra
Buzby, Erika
Hall, Joshua
Ash, Stephanie
Harrington, Rachel
Cofsky, Seana
Clancy, Selina
Kapsak, Curtis J.
Sevinsky, Joel
Libuit, Kevin
Park, Daniel J.
Hemarajata, Peera
Garrigues, Jacob M.
Green, Nicole M.
Sierra-Patev, Sean
Carpenter-Azevedo, Kristin
Huard, Richard C.
Pearson, Claire
Incekara, Kutluhan
Nishimura, Christina
Huang, Jian Ping
Gagnon, Emily
Reever, Ethan
Razeq, Jafar
Muyombwe, Anthony
Borges, Vítor
Ferreira, Rita
Sobral, Daniel
Duarte, Silvia
Santos, Daniela
Vieira, Luís
Gomes, João Paulo
Aquino, Carly
Savino, Isabella M.
Felton, Karinda
Bajwa, Moneeb
Hayward, Nyjil
Miller, Holly
Naumann, Allison
Allman, Ria
Greer, Neel
Fall, Amary
Mostafa, Heba H.
McHugh, Martin P.
Maloney, Daniel M.
Dewar, Rebecca
Kenicer, Juliet
Parker, Abby
Mathers, Katharine
Wild, Jonathan
Cotton, Seb
Templeton, Kate E.
Churchwell, George
Lee, Philip A.
Pedrosa, Maria
McGruder, Brenna
Schmedes, Sarah
Plumb, Matthew R.
Wang, Xiong
Barcellos, Regina Bones
Godinho, Fernanda M.S.
Salvato, Richard Steiner
Ceniseros, Aimee
Breban, Mallery I.
Grubaugh, Nathan D.
Gallagher, Glen R.
Vogels, Chantal B.F.
author_role author
author2 Chaguza, Chrispin
Gagne, Luc
Doucette, Matthew
Smole, Sandra
Buzby, Erika
Hall, Joshua
Ash, Stephanie
Harrington, Rachel
Cofsky, Seana
Clancy, Selina
Kapsak, Curtis J.
Sevinsky, Joel
Libuit, Kevin
Park, Daniel J.
Hemarajata, Peera
Garrigues, Jacob M.
Green, Nicole M.
Sierra-Patev, Sean
Carpenter-Azevedo, Kristin
Huard, Richard C.
Pearson, Claire
Incekara, Kutluhan
Nishimura, Christina
Huang, Jian Ping
Gagnon, Emily
Reever, Ethan
Razeq, Jafar
Muyombwe, Anthony
Borges, Vítor
Ferreira, Rita
Sobral, Daniel
Duarte, Silvia
Santos, Daniela
Vieira, Luís
Gomes, João Paulo
Aquino, Carly
Savino, Isabella M.
Felton, Karinda
Bajwa, Moneeb
Hayward, Nyjil
Miller, Holly
Naumann, Allison
Allman, Ria
Greer, Neel
Fall, Amary
Mostafa, Heba H.
McHugh, Martin P.
Maloney, Daniel M.
Dewar, Rebecca
Kenicer, Juliet
Parker, Abby
Mathers, Katharine
Wild, Jonathan
Cotton, Seb
Templeton, Kate E.
Churchwell, George
Lee, Philip A.
Pedrosa, Maria
McGruder, Brenna
Schmedes, Sarah
Plumb, Matthew R.
Wang, Xiong
Barcellos, Regina Bones
Godinho, Fernanda M.S.
Salvato, Richard Steiner
Ceniseros, Aimee
Breban, Mallery I.
Grubaugh, Nathan D.
Gallagher, Glen R.
Vogels, Chantal B.F.
author2_role author
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dc.contributor.none.fl_str_mv Repositório Científico do Instituto Nacional de Saúde
dc.contributor.author.fl_str_mv Chen, Nicholas F.G.
Chaguza, Chrispin
Gagne, Luc
Doucette, Matthew
Smole, Sandra
Buzby, Erika
Hall, Joshua
Ash, Stephanie
Harrington, Rachel
Cofsky, Seana
Clancy, Selina
Kapsak, Curtis J.
Sevinsky, Joel
Libuit, Kevin
Park, Daniel J.
Hemarajata, Peera
Garrigues, Jacob M.
Green, Nicole M.
Sierra-Patev, Sean
Carpenter-Azevedo, Kristin
Huard, Richard C.
Pearson, Claire
Incekara, Kutluhan
Nishimura, Christina
Huang, Jian Ping
Gagnon, Emily
Reever, Ethan
Razeq, Jafar
Muyombwe, Anthony
Borges, Vítor
Ferreira, Rita
Sobral, Daniel
Duarte, Silvia
Santos, Daniela
Vieira, Luís
Gomes, João Paulo
Aquino, Carly
Savino, Isabella M.
Felton, Karinda
Bajwa, Moneeb
Hayward, Nyjil
Miller, Holly
Naumann, Allison
Allman, Ria
Greer, Neel
Fall, Amary
Mostafa, Heba H.
McHugh, Martin P.
Maloney, Daniel M.
Dewar, Rebecca
Kenicer, Juliet
Parker, Abby
Mathers, Katharine
Wild, Jonathan
Cotton, Seb
Templeton, Kate E.
Churchwell, George
Lee, Philip A.
Pedrosa, Maria
McGruder, Brenna
Schmedes, Sarah
Plumb, Matthew R.
Wang, Xiong
Barcellos, Regina Bones
Godinho, Fernanda M.S.
Salvato, Richard Steiner
Ceniseros, Aimee
Breban, Mallery I.
Grubaugh, Nathan D.
Gallagher, Glen R.
Vogels, Chantal B.F.
dc.subject.por.fl_str_mv Mpox
Mpox Outbreak
Monkeypox Virus
Genomic Surveillance
Whole-genome Sequencing
Outbreak Response
Global Emergence
Pandemics
Infecções Emergentes
topic Mpox
Mpox Outbreak
Monkeypox Virus
Genomic Surveillance
Whole-genome Sequencing
Outbreak Response
Global Emergence
Pandemics
Infecções Emergentes
description The 2022 multicountry mpox outbreak concurrent with the ongoing Coronavirus Disease 2019 (COVID-19) pandemic further highlighted the need for genomic surveillance and rapid pathogen whole-genome sequencing. While metagenomic sequencing approaches have been used to sequence many of the early mpox infections, these methods are resource intensive and require samples with high viral DNA concentrations. Given the atypical clinical presentation of cases associated with the outbreak and uncertainty regarding viral load across both the course of infection and anatomical body sites, there was an urgent need for a more sensitive and broadly applicable sequencing approach. Highly multiplexed amplicon-based sequencing (PrimalSeq) was initially developed for sequencing of Zika virus, and later adapted as the main sequencing approach for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). Here, we used PrimalScheme to develop a primer scheme for human monkeypox virus that can be used with many sequencing and bioinformatics pipelines implemented in public health laboratories during the COVID-19 pandemic. We sequenced clinical specimens that tested presumptively positive for human monkeypox virus with amplicon-based and metagenomic sequencing approaches. We found notably higher genome coverage across the virus genome, with minimal amplicon drop-outs, in using the amplicon-based sequencing approach, particularly in higher PCR cycle threshold (Ct) (lower DNA titer) samples. Further testing demonstrated that Ct value correlated with the number of sequencing reads and influenced the percent genome coverage. To maximize genome coverage when resources are limited, we recommend selecting samples with a PCR Ct below 31 Ct and generating 1 million sequencing reads per sample. To support national and international public health genomic surveillance efforts, we sent out primer pool aliquots to 10 laboratories across the United States, United Kingdom, Brazil, and Portugal. These public health laboratories successfully implemented the human monkeypox virus primer scheme in various amplicon sequencing workflows and with different sample types across a range of Ct values. Thus, we show that amplicon-based sequencing can provide a rapidly deployable, cost-effective, and flexible approach to pathogen whole-genome sequencing in response to newly emerging pathogens. Importantly, through the implementation of our primer scheme into existing SARS-CoV-2 workflows and across a range of sample types and sequencing platforms, we further demonstrate the potential of this approach for rapid outbreak response.
publishDate 2023
dc.date.none.fl_str_mv 2023-06-13
2023-06-13T00:00:00Z
2024-01-23T11:54:36Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.18/8955
url http://hdl.handle.net/10400.18/8955
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv PLoS Biol. 2023 Jun 13;21(6):e3002151. doi: 10.1371/journal.pbio.3002151. eCollection 2023 Jun
1544-9173
10.1371/journal.pbio.3002151
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Public Library of Science
publisher.none.fl_str_mv Public Library of Science
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