Toward better monitoring of human noroviruses and F-specific RNA bacteriophages in aquatic environments using bivalve mollusks and passive samplers: A case study.


Journal

Water research
ISSN: 1879-2448
Titre abrégé: Water Res
Pays: England
ID NLM: 0105072

Informations de publication

Date de publication:
01 Sep 2023
Historique:
received: 05 06 2023
revised: 12 07 2023
accepted: 13 07 2023
medline: 7 9 2023
pubmed: 8 8 2023
entrez: 7 8 2023
Statut: ppublish

Résumé

Monitoring pathogenic enteric viruses in continental and marine water bodies is essential to control the viral contamination of human populations. Human Noroviruses (NoV) are the main enteric viruses present in surface waters and foodstuff. In a context of global change, it is currently a challenge to improve the management of viral pollutions in aquatic environments and thereby limit the contamination of vulnerable water bodies or foodstuffs. The aim of this study is to evaluate the potential of specific accumulation systems for improving the detection of NoV in water bodies, compared to direct water analyses. Passive samplers (Zetapor filters) and three species of bivalve molluscan shellfish (BMS) (Dreissena polymorpha, Mytilus edulis and Crassostreas gigas) were used as accumulation systems to determine their performance in monitoring continental and marine waters for viruses. F-specific RNA bacteriophages (FRNAPH) were also analyzed since they are described as indicators of NoV hazard in many studies. During a one-year study in a specific area frequently affected by fecal pollution, twelve campaigns of exposure of passive samplers and BMS in continental and coastal waters were conducted. Using suitable methods, NoV (genome) and FRNAPH (infectious and genome) were detected in these accumulation systems and in water at the same time points to determine the frequency of detection but also to gain a better understanding of viral pollution in this area. The reliability of FRNAPH as a NoV indicator was also investigated. Our results clearly showed that BMS were significantly better than passive samplers and direct water analyses for monitoring NoV and FRNAPH contamination in water bodies. A dilution of viral pollution between the continental and the coastal area was observed and can be explained by the distance from the source of the pollution. Viral pollution is clearly greater during the winter period, and stakeholders should take this into consideration in their attempts to limit the contamination of food and water. A significant correlation was once again shown between NoV and FRNAPH genomes in BMS, confirming the reliability of FRNAPH as a NoV indicator. Moreover, a strong correlation was observed between NoV genomes and infectious FRNAPH, suggesting recent viral pollution since infectious particles had not been inactivated at sufficient levels in the environment. More generally, this study shows the value of using BMS as an active method for improving knowledge on the behavior of viral contamination in water bodies, the ranking of the contamination sources, and the vulnerability of downstream water bodies.

Identifiants

pubmed: 37549447
pii: S0043-1354(23)00793-5
doi: 10.1016/j.watres.2023.120357
pii:
doi:

Substances chimiques

Water 059QF0KO0R

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

120357

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Nicolas Boudaud reports financial support was provided by Conseil Régional de Normandie. Nicolas Boudaud reports financial support was provided by Conseils Départementaux du Calvados et de la Manche. Nicolas Boudaud reports financial support was provided by Actia VIROcontrol Joint Technological Unit.

Auteurs

Julie Do Nascimento (J)

Université de Reims Champagne-Ardenne, UMR-I 02 SEBIO, F-51687 Reims, France.

Marion Bichet (M)

Actalia, Food Safety Department, F-50000 Saint-Lô, France; LCPME, UMR 7564, CNRS, Université de Lorraine, F-54000 Nancy, France.

Julie Challant (J)

LCPME, UMR 7564, CNRS, Université de Lorraine, F-54000 Nancy, France.

Julie Loutreul (J)

Actalia, Food Safety Department, F-50000 Saint-Lô, France.

Stéphanie Petinay (S)

Synergie Mer et Littoral, F-50560 Blainville, France.

Delphine Perrotte (D)

LABEO Manche, Virology Department, F-50000 Saint-Lô, France.

Véronica Roman (V)

LCPME, UMR 7564, CNRS, Université de Lorraine, F-54000 Nancy, France.

Elodie Cauvin (E)

LABEO Manche, Virology Department, F-50000 Saint-Lô, France.

Maëlle Robin (M)

Actalia, Food Safety Department, F-50000 Saint-Lô, France.

Mélissa Palos Ladeiro (MP)

Université de Reims Champagne-Ardenne, UMR-I 02 SEBIO, F-51687 Reims, France.

Stéphanie La Carbona (S)

Actalia, Food Safety Department, F-50000 Saint-Lô, France.

Jean-Louis Blin (JL)

Synergie Mer et Littoral, F-50560 Blainville, France.

Christophe Gantzer (C)

LCPME, UMR 7564, CNRS, Université de Lorraine, F-54000 Nancy, France.

Alain Geffard (A)

Université de Reims Champagne-Ardenne, UMR-I 02 SEBIO, F-51687 Reims, France.

Isabelle Bertrand (I)

LCPME, UMR 7564, CNRS, Université de Lorraine, F-54000 Nancy, France.

Nicolas Boudaud (N)

Actalia, Food Safety Department, F-50000 Saint-Lô, France. Electronic address: n.boudaud@actalia.eu.

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