Cargando…

Norovirus Disease Among Children <5 Years in 3 Sub-Saharan African Countries: Findings From the Vaccine Impact on Diarrhea in Africa (VIDA) Study, 2015–2018

BACKGROUND: To address a paucity of data from sub-Saharan Africa, we examined the prevalence, severity, and seasonality of norovirus genogroup II (NVII) among children <5 years old in The Gambia, Kenya, and Mali following rotavirus vaccine introduction. METHODS: Population-based surveillance was...

Descripción completa

Detalles Bibliográficos
Autores principales: Omore, Richard, Powell, Helen, Sow, Samba O, Jahangir Hossain, M, Ogwel, Billy, Doh, Sanogo, Ochieng, John B, Jones, Joquina Chiquita M, Zaman, Syed M A, Awuor, Alex O, Juma, Jane, Kasumba, Irene N, Roose, Anna, Jamka, Leslie P, Nasrin, Dilruba, Liu, Jie, Keita, Adama Mamby, Traoré, Awa, Onwuchekwa, Uma, Badji, Henry, Sarwar, Golam, Antonio, Martin, Sugerman, Ciara E, Mintz, Eric D, Houpt, Eric R, Verani, Jennifer R, Widdowson, Marc-Alain, Tennant, Sharon M, Platts-Mills, James A, Tate, Jacqueline E, Parashar, Umesh D, Kotloff, Karen L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116553/
https://www.ncbi.nlm.nih.gov/pubmed/37074441
http://dx.doi.org/10.1093/cid/ciac967
_version_ 1785028449152270336
author Omore, Richard
Powell, Helen
Sow, Samba O
Jahangir Hossain, M
Ogwel, Billy
Doh, Sanogo
Ochieng, John B
Jones, Joquina Chiquita M
Zaman, Syed M A
Awuor, Alex O
Juma, Jane
Kasumba, Irene N
Roose, Anna
Jamka, Leslie P
Nasrin, Dilruba
Liu, Jie
Keita, Adama Mamby
Traoré, Awa
Onwuchekwa, Uma
Badji, Henry
Sarwar, Golam
Antonio, Martin
Sugerman, Ciara E
Mintz, Eric D
Houpt, Eric R
Verani, Jennifer R
Widdowson, Marc-Alain
Tennant, Sharon M
Platts-Mills, James A
Tate, Jacqueline E
Parashar, Umesh D
Kotloff, Karen L
author_facet Omore, Richard
Powell, Helen
Sow, Samba O
Jahangir Hossain, M
Ogwel, Billy
Doh, Sanogo
Ochieng, John B
Jones, Joquina Chiquita M
Zaman, Syed M A
Awuor, Alex O
Juma, Jane
Kasumba, Irene N
Roose, Anna
Jamka, Leslie P
Nasrin, Dilruba
Liu, Jie
Keita, Adama Mamby
Traoré, Awa
Onwuchekwa, Uma
Badji, Henry
Sarwar, Golam
Antonio, Martin
Sugerman, Ciara E
Mintz, Eric D
Houpt, Eric R
Verani, Jennifer R
Widdowson, Marc-Alain
Tennant, Sharon M
Platts-Mills, James A
Tate, Jacqueline E
Parashar, Umesh D
Kotloff, Karen L
author_sort Omore, Richard
collection PubMed
description BACKGROUND: To address a paucity of data from sub-Saharan Africa, we examined the prevalence, severity, and seasonality of norovirus genogroup II (NVII) among children <5 years old in The Gambia, Kenya, and Mali following rotavirus vaccine introduction. METHODS: Population-based surveillance was conducted to capture medically-attended moderate-to-severe diarrhea (MSD) cases, defined as a child 0–59 months old passing ≥3 loose stools in a 24-hour period with ≥1 of the following: sunken eyes, poor skin turgor, dysentery, intravenous rehydration, or hospitalization within 7 days of diarrhea onset. Diarrhea-free matched controls randomly selected from a censused population were enrolled at home. Stools from cases and controls were tested for enteropathogens, including norovirus and rotavirus, by TaqMan quantitative polymerase chain reaction (PCR) and conventional reverse transcription PCR. We used multiple logistic regression to derive adjusted attributable fractions (AFe) for each pathogen causing MSD, which takes into consideration the prevalence in both cases and controls, for each site and age. A pathogen was considered etiologic if AFe was ≥0.5. In further analyses focusing on the predominant NVII strains, we compared rotavirus and NVII severity using a 20-point modified Vesikari score and examined seasonal fluctuations. RESULTS: From May 2015 to July 2018, we enrolled 4840 MSD cases and 6213 controls. NVI was attributed to only 1 MSD episode. NVII was attributed to 185 (3.8%) of all MSD episodes and was the sole attributable pathogen in 139 (2.9%); peaking (36.0%) at age 6–8 months with majority (61.2%) aged 6–11 months. MSD cases whose episodes were attributed to NVII alone compared with rotavirus alone were younger (median age, 8 vs 12 months, P < .0001) and had less severe illness (median Vesikari severity score, 9 vs 11, P = .0003) but equally likely to be dehydrated. NVII occurred year-round at all study sites. CONCLUSIONS: Infants aged 6–11 months bear the greatest burden of norovirus disease, with NVII predominating. An early infant vaccine schedule and rigorous adherence to guidelines recommended for management of dehydrating diarrhea may offer substantial benefit in these African settings.
format Online
Article
Text
id pubmed-10116553
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-101165532023-04-21 Norovirus Disease Among Children <5 Years in 3 Sub-Saharan African Countries: Findings From the Vaccine Impact on Diarrhea in Africa (VIDA) Study, 2015–2018 Omore, Richard Powell, Helen Sow, Samba O Jahangir Hossain, M Ogwel, Billy Doh, Sanogo Ochieng, John B Jones, Joquina Chiquita M Zaman, Syed M A Awuor, Alex O Juma, Jane Kasumba, Irene N Roose, Anna Jamka, Leslie P Nasrin, Dilruba Liu, Jie Keita, Adama Mamby Traoré, Awa Onwuchekwa, Uma Badji, Henry Sarwar, Golam Antonio, Martin Sugerman, Ciara E Mintz, Eric D Houpt, Eric R Verani, Jennifer R Widdowson, Marc-Alain Tennant, Sharon M Platts-Mills, James A Tate, Jacqueline E Parashar, Umesh D Kotloff, Karen L Clin Infect Dis VIDA Supplement BACKGROUND: To address a paucity of data from sub-Saharan Africa, we examined the prevalence, severity, and seasonality of norovirus genogroup II (NVII) among children <5 years old in The Gambia, Kenya, and Mali following rotavirus vaccine introduction. METHODS: Population-based surveillance was conducted to capture medically-attended moderate-to-severe diarrhea (MSD) cases, defined as a child 0–59 months old passing ≥3 loose stools in a 24-hour period with ≥1 of the following: sunken eyes, poor skin turgor, dysentery, intravenous rehydration, or hospitalization within 7 days of diarrhea onset. Diarrhea-free matched controls randomly selected from a censused population were enrolled at home. Stools from cases and controls were tested for enteropathogens, including norovirus and rotavirus, by TaqMan quantitative polymerase chain reaction (PCR) and conventional reverse transcription PCR. We used multiple logistic regression to derive adjusted attributable fractions (AFe) for each pathogen causing MSD, which takes into consideration the prevalence in both cases and controls, for each site and age. A pathogen was considered etiologic if AFe was ≥0.5. In further analyses focusing on the predominant NVII strains, we compared rotavirus and NVII severity using a 20-point modified Vesikari score and examined seasonal fluctuations. RESULTS: From May 2015 to July 2018, we enrolled 4840 MSD cases and 6213 controls. NVI was attributed to only 1 MSD episode. NVII was attributed to 185 (3.8%) of all MSD episodes and was the sole attributable pathogen in 139 (2.9%); peaking (36.0%) at age 6–8 months with majority (61.2%) aged 6–11 months. MSD cases whose episodes were attributed to NVII alone compared with rotavirus alone were younger (median age, 8 vs 12 months, P < .0001) and had less severe illness (median Vesikari severity score, 9 vs 11, P = .0003) but equally likely to be dehydrated. NVII occurred year-round at all study sites. CONCLUSIONS: Infants aged 6–11 months bear the greatest burden of norovirus disease, with NVII predominating. An early infant vaccine schedule and rigorous adherence to guidelines recommended for management of dehydrating diarrhea may offer substantial benefit in these African settings. Oxford University Press 2023-04-19 /pmc/articles/PMC10116553/ /pubmed/37074441 http://dx.doi.org/10.1093/cid/ciac967 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle VIDA Supplement
Omore, Richard
Powell, Helen
Sow, Samba O
Jahangir Hossain, M
Ogwel, Billy
Doh, Sanogo
Ochieng, John B
Jones, Joquina Chiquita M
Zaman, Syed M A
Awuor, Alex O
Juma, Jane
Kasumba, Irene N
Roose, Anna
Jamka, Leslie P
Nasrin, Dilruba
Liu, Jie
Keita, Adama Mamby
Traoré, Awa
Onwuchekwa, Uma
Badji, Henry
Sarwar, Golam
Antonio, Martin
Sugerman, Ciara E
Mintz, Eric D
Houpt, Eric R
Verani, Jennifer R
Widdowson, Marc-Alain
Tennant, Sharon M
Platts-Mills, James A
Tate, Jacqueline E
Parashar, Umesh D
Kotloff, Karen L
Norovirus Disease Among Children <5 Years in 3 Sub-Saharan African Countries: Findings From the Vaccine Impact on Diarrhea in Africa (VIDA) Study, 2015–2018
title Norovirus Disease Among Children <5 Years in 3 Sub-Saharan African Countries: Findings From the Vaccine Impact on Diarrhea in Africa (VIDA) Study, 2015–2018
title_full Norovirus Disease Among Children <5 Years in 3 Sub-Saharan African Countries: Findings From the Vaccine Impact on Diarrhea in Africa (VIDA) Study, 2015–2018
title_fullStr Norovirus Disease Among Children <5 Years in 3 Sub-Saharan African Countries: Findings From the Vaccine Impact on Diarrhea in Africa (VIDA) Study, 2015–2018
title_full_unstemmed Norovirus Disease Among Children <5 Years in 3 Sub-Saharan African Countries: Findings From the Vaccine Impact on Diarrhea in Africa (VIDA) Study, 2015–2018
title_short Norovirus Disease Among Children <5 Years in 3 Sub-Saharan African Countries: Findings From the Vaccine Impact on Diarrhea in Africa (VIDA) Study, 2015–2018
title_sort norovirus disease among children <5 years in 3 sub-saharan african countries: findings from the vaccine impact on diarrhea in africa (vida) study, 2015–2018
topic VIDA Supplement
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116553/
https://www.ncbi.nlm.nih.gov/pubmed/37074441
http://dx.doi.org/10.1093/cid/ciac967
work_keys_str_mv AT omorerichard norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT powellhelen norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT sowsambao norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT jahangirhossainm norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT ogwelbilly norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT dohsanogo norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT ochiengjohnb norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT jonesjoquinachiquitam norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT zamansyedma norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT awuoralexo norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT jumajane norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT kasumbairenen norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT rooseanna norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT jamkalesliep norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT nasrindilruba norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT liujie norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT keitaadamamamby norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT traoreawa norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT onwuchekwauma norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT badjihenry norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT sarwargolam norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT antoniomartin norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT sugermanciarae norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT mintzericd norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT houptericr norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT veranijenniferr norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT widdowsonmarcalain norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT tennantsharonm norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT plattsmillsjamesa norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT tatejacquelinee norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT parasharumeshd norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018
AT kotloffkarenl norovirusdiseaseamongchildren5yearsin3subsaharanafricancountriesfindingsfromthevaccineimpactondiarrheainafricavidastudy20152018