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Clinical severity of enteric viruses detected using a quantitative molecular assay compared to conventional assays in the Global Enteric Multicenter Study.
Cates, Jordan; Powell, Helen; Platts-Mills, James; Nasrin, Dilruba; Panchalingam, Sandra; Sow, Samba O; Traore, Awa; Sur, Dipika; Ramamurthy, Thandavarayan; Zaidi, Anita K M; Kabir, Furqan; Faruque, Abu S G; Ahmed, Dilruba; Breiman, Robert F; Omore, Richard; Ochieng, John Benjamin; Hossain, M Jahangir; Antonio, Martin; Mandomando, Inácio; Vubil, Delfino; Nataro, James P; Levine, Myron M; Parashar, Umesh D; Kotloff, Karen L; Tate, Jacqueline E.
Afiliação
  • Cates J; Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Powell H; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Platts-Mills J; Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
  • Nasrin D; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Panchalingam S; Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Sow SO; Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Traore A; Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
  • Sur D; Centre pour le Développement des Vaccins, Bamako, Mali.
  • Ramamurthy T; Centre pour le Développement des Vaccins, Bamako, Mali.
  • Zaidi AKM; National Institute of Cholera and Enteric Diseases, Kolkata, India.
  • Kabir F; National Institute of Cholera and Enteric Diseases, Kolkata, India.
  • Faruque ASG; Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
  • Ahmed D; Department of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
  • Breiman RF; International Centre for Diarrhoeal Disease Research, Mohakhali, Dhaka, Bangladesh.
  • Omore R; International Centre for Diarrhoeal Disease Research, Mohakhali, Dhaka, Bangladesh.
  • Ochieng JB; Department of Global Health, Rollins School of Public Health, Emory University, USA.
  • Hossain MJ; Infectious Diseases and Oncology Research Institute, University of the Witwatersrand, Johannesburg, South Africa.
  • Antonio M; Kenya Medical Research Institute, Centers for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
  • Mandomando I; Kenya Medical Research Institute, Centers for Global Health Research (KEMRI-CGHR), Kisumu, Kenya.
  • Vubil D; Medical Research Council (UK) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
  • Nataro JP; Medical Research Council (UK) Unit The Gambia at the London School of Hygiene and Tropical Medicine, Fajara, The Gambia.
  • Levine MM; Centre for Epidemic Preparedness and Response, London School of Hygiene & Tropical Medicine, London, UK.
  • Parashar UD; Department of Infection Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
  • Kotloff KL; Centro de Investigação em Saúde da Manhiça, Maputo, Mozambique.
  • Tate JE; Centro de Investigação em Saúde da Manhiça, Maputo, Mozambique.
J Infect Dis ; 2024 Apr 18.
Article em En | MEDLINE | ID: mdl-38637321
ABSTRACT

BACKGROUND:

Quantitative molecular assays are increasingly used for detection of enteric viruses.

METHODS:

We compared the clinical severity using modified Vesikari score (mVS) of enteric viruses detected by conventional assays (enzyme immunoassays [EIA] for rotavirus and adenovirus 40/41 and conventional polymerase chain reaction for astrovirus, sapovirus, and norovirus) and a quantitative molecular assay (TaqMan Array Card [TAC]) among children aged 0-59 months in the Global Enteric Multicenter Study. For rotavirus and adenovirus 40/41, we compared severity between EIA-positive and TAC-positive cases assigned etiologies using different cycle threshold (CT) cutoffs.

RESULTS:

Using conventional assays, the median (interquartile range) mVS was 10 (8, 11) for rotavirus, 9 (7, 11) for adenovirus 40/41, 8 (6, 10) for astrovirus, sapovirus, and norovirus GII, and 7 (6, 9) for norovirus GI. Compared to rotavirus EIA-positive cases, the median mVS was 2 and 3 points lower for EIA-negative/TAC-positive cases with CT<32.6 and 32.6≤CT<35, respectively (p-value<.0001). Adenovirus 40/41 EIA-positive and EIA-negative/TAC-positive cases were similar, regardless of CT cutoff.

CONCLUSIONS:

Quantitative molecular assays compared to conventional assays, such as EIA, may influence severity of identified cases, especially for rotavirus. Cutoffs to assign etiology for quantitative assays should be considered in the design and interpretation of enteric virus studies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Infect Dis Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Infect Dis Ano de publicação: 2024 Tipo de documento: Article