Evolving viral and serological stages of Zika virus RNA-positive blood donors and estimation of incidence of infection during the 2016 Puerto Rican Zika epidemic: an observational cohort study.


Journal

The Lancet. Infectious diseases
ISSN: 1474-4457
Titre abrégé: Lancet Infect Dis
Pays: United States
ID NLM: 101130150

Informations de publication

Date de publication:
12 2020
Historique:
received: 10 04 2019
revised: 31 08 2019
accepted: 14 11 2019
pubmed: 17 7 2020
medline: 7 1 2021
entrez: 17 7 2020
Statut: ppublish

Résumé

Puerto Rico began screening blood donations for Zika virus RNA with nucleic acid amplification tests (NAATs) on April 3, 2016, because of an emerging Zika virus outbreak. We followed up positive donors to assess the dynamics of viral and serological markers during the early stages of Zika virus infection and update the estimate of infection incidence in the Puerto Rican population during the outbreak. Blood donations from volunteer donors in Puerto Rico were screened for the presence of Zika virus RNA using the cobas Zika NAAT. Positive donations were further tested to confirm infection, estimate viral load, and identify Zika virus-specific IgM antibodies. Individuals with positive blood donations were invited to attend follow-up visits. Donations with confirmed infection (defined as detection of Zika virus RNA or IgM on additional testing of index or follow-up samples) were assessed for stage of infection according to Zika virus RNA detectability in simulated minipools, viral load, and Zika virus IgM status. A three-step process was used to estimate the mean duration of NAAT reactivity of Zika virus in human plasma from individuals identified pre-seroconversion with at least one follow up visit and to update the 2016 incidence estimate of Zika virus infection. Between April 3 and Dec 31, 2016, 53 112 blood donations were screened for Zika virus, of which 351 tested positive, 339 had confirmed infections, and 319 could be staged. Compared with IgM-positive index donations (n=110), IgM-negative index donations (n=209) had higher mean viral loads (1·1 × 10 Characterisation of early Zika virus infection has implications for blood safety because infectivity of blood donations and utility of screening methods likely correlate with viral load and serological stage of infection. Our findings also have implications for diagnostic testing, public health surveillance, and epidemiology, and we estimate that around 21% of the Puerto Rican population was infected during the 2016 outbreak. Biomedical Advanced Research and Development Authority, National Heart, Lung, and Blood Institute.

Sections du résumé

BACKGROUND
Puerto Rico began screening blood donations for Zika virus RNA with nucleic acid amplification tests (NAATs) on April 3, 2016, because of an emerging Zika virus outbreak. We followed up positive donors to assess the dynamics of viral and serological markers during the early stages of Zika virus infection and update the estimate of infection incidence in the Puerto Rican population during the outbreak.
METHODS
Blood donations from volunteer donors in Puerto Rico were screened for the presence of Zika virus RNA using the cobas Zika NAAT. Positive donations were further tested to confirm infection, estimate viral load, and identify Zika virus-specific IgM antibodies. Individuals with positive blood donations were invited to attend follow-up visits. Donations with confirmed infection (defined as detection of Zika virus RNA or IgM on additional testing of index or follow-up samples) were assessed for stage of infection according to Zika virus RNA detectability in simulated minipools, viral load, and Zika virus IgM status. A three-step process was used to estimate the mean duration of NAAT reactivity of Zika virus in human plasma from individuals identified pre-seroconversion with at least one follow up visit and to update the 2016 incidence estimate of Zika virus infection.
FINDINGS
Between April 3 and Dec 31, 2016, 53 112 blood donations were screened for Zika virus, of which 351 tested positive, 339 had confirmed infections, and 319 could be staged. Compared with IgM-positive index donations (n=110), IgM-negative index donations (n=209) had higher mean viral loads (1·1 × 10
INTERPRETATION
Characterisation of early Zika virus infection has implications for blood safety because infectivity of blood donations and utility of screening methods likely correlate with viral load and serological stage of infection. Our findings also have implications for diagnostic testing, public health surveillance, and epidemiology, and we estimate that around 21% of the Puerto Rican population was infected during the 2016 outbreak.
FUNDING
Biomedical Advanced Research and Development Authority, National Heart, Lung, and Blood Institute.

Identifiants

pubmed: 32673594
pii: S1473-3099(19)30706-6
doi: 10.1016/S1473-3099(19)30706-6
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Immunoglobulin G 0
Immunoglobulin M 0
RNA, Viral 0

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1437-1445

Subventions

Organisme : Intramural CDC HHS
ID : CC999999
Pays : United States
Organisme : WHI NIH HHS
ID : HHSN268201100001C
Pays : United States
Organisme : NHLBI NIH HHS
ID : HHSN268201100001I
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

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Auteurs

Phillip C Williamson (PC)

Creative Testing Solutions, Tempe, AZ, USA. Electronic address: pwilliamson@mycts.org.

Brad J Biggerstaff (BJ)

Centers for Disease Control and Prevention, Fort Collins, CO, USA.

Graham Simmons (G)

Vitalant Research Institute, San Francisco, CA, USA.

Mars Stone (M)

Vitalant Research Institute, San Francisco, CA, USA.

Val Winkelman (V)

Creative Testing Solutions, Tempe, AZ, USA.

Gerardo Latoni (G)

Banco de Sangre Servicios Mutuos, Guaynabo, PR, USA.

Jose Alsina (J)

Banco de Sangre Servicios Mutuos, Guaynabo, PR, USA.

Sonia Bakkour (S)

Vitalant Research Institute, San Francisco, CA, USA.

Christina Newman (C)

Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI, USA.

Lisa L Pate (LL)

Roche Molecular Systems, Pleasanton, CA, USA.

Susan A Galel (SA)

Roche Molecular Systems, Pleasanton, CA, USA.

Steven Kleinman (S)

Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.

Michael P Busch (MP)

Vitalant Research Institute, San Francisco, CA, USA.

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Classifications MeSH