Molecular detection of parapoxvirus in Ixodidae ticks collected from cattle in Corsica, France.


Journal

Veterinary medicine and science
ISSN: 2053-1095
Titre abrégé: Vet Med Sci
Pays: England
ID NLM: 101678837

Informations de publication

Date de publication:
03 2022
Historique:
pubmed: 30 1 2022
medline: 22 4 2022
entrez: 29 1 2022
Statut: ppublish

Résumé

Several viruses belonging to the family Poxviridae can cause infections in humans and animals. In Corsica, livestock farming (sheep, goats, pigs, and cattle) is mainly mixed, leading to important interactions between livestock, wildlife, and human populations. This could facilitate the circulation of zoonotic diseases, and makes Corsica a good example for studies of tick-borne diseases. To gain understanding on the circulation of poxviruses in Corsica, we investigated their presence in tick species collected from cattle, sheep, horses, and wild boar, and characterized them through molecular techniques. Ticks were tested using specific primers targeting conserved regions of sequences corresponding to two genera: parapoxvirus and orthopoxvirus. A total of 3555 ticks were collected from 1549 different animals (687 cattle, 538 horses, 106 sheep, and 218 wild boars). They were tested for the presence of parapoxvirus DNA on one hand and orthopoxvirus DNA on the other hand using Pangeneric real-time TaqMan assays. Orthopoxvirus DNA was detected in none of the 3555 ticks. Parapoxvirus DNA was detected in 6.6% (36/544) of ticks collected from 23 cows from 20 farms. The remaining 3011 ticks collected from horses, wild boars, and sheep were negative. The infection rate in cow ticks was 8.0% (12/148) in 2018 and 6.0% (24/396) in 2019 (p = 0.57). Parapoxvirus DNA was detected in 8.5% (5/59) of Hyalomma scupense pools, 8.2% (15/183) of Hyalomma marginatum pools, and 6.7% (16/240) of Rhipicephalus bursa pools (p = 0.73). We successfully amplified and sequenced 19.4% (7/36) of the positive samples which all corresponded to pseudocowpox virus. Obviously, further studies are needed to investigate the zoonotic potential of pseudocowpox virus and its importance for animals and public health.

Sections du résumé

BACKGROUND
Several viruses belonging to the family Poxviridae can cause infections in humans and animals. In Corsica, livestock farming (sheep, goats, pigs, and cattle) is mainly mixed, leading to important interactions between livestock, wildlife, and human populations. This could facilitate the circulation of zoonotic diseases, and makes Corsica a good example for studies of tick-borne diseases.
OBJECTIVES
To gain understanding on the circulation of poxviruses in Corsica, we investigated their presence in tick species collected from cattle, sheep, horses, and wild boar, and characterized them through molecular techniques.
METHODS
Ticks were tested using specific primers targeting conserved regions of sequences corresponding to two genera: parapoxvirus and orthopoxvirus.
RESULTS
A total of 3555 ticks were collected from 1549 different animals (687 cattle, 538 horses, 106 sheep, and 218 wild boars). They were tested for the presence of parapoxvirus DNA on one hand and orthopoxvirus DNA on the other hand using Pangeneric real-time TaqMan assays. Orthopoxvirus DNA was detected in none of the 3555 ticks. Parapoxvirus DNA was detected in 6.6% (36/544) of ticks collected from 23 cows from 20 farms. The remaining 3011 ticks collected from horses, wild boars, and sheep were negative. The infection rate in cow ticks was 8.0% (12/148) in 2018 and 6.0% (24/396) in 2019 (p = 0.57). Parapoxvirus DNA was detected in 8.5% (5/59) of Hyalomma scupense pools, 8.2% (15/183) of Hyalomma marginatum pools, and 6.7% (16/240) of Rhipicephalus bursa pools (p = 0.73). We successfully amplified and sequenced 19.4% (7/36) of the positive samples which all corresponded to pseudocowpox virus.
CONCLUSIONS
Obviously, further studies are needed to investigate the zoonotic potential of pseudocowpox virus and its importance for animals and public health.

Identifiants

pubmed: 35092189
doi: 10.1002/vms3.700
pmc: PMC8959304
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

907-916

Informations de copyright

© 2022 The Authors. Veterinary Medicine and Science published by John Wiley & Sons Ltd.

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Auteurs

Vincent Cicculli (V)

Laboratoire de Virologie, Université de Corse-Inserm, Corte, France.
Unité Des Virus Emergents (UVE: Aix Marseille Université, IRD 190, Inserm 1207, IHU Méditerranée Infection), Marseille, France.

Nazli Ayhan (N)

Unité Des Virus Emergents (UVE: Aix Marseille Université, IRD 190, Inserm 1207, IHU Méditerranée Infection), Marseille, France.

Léa Luciani (L)

Unité Des Virus Emergents (UVE: Aix Marseille Université, IRD 190, Inserm 1207, IHU Méditerranée Infection), Marseille, France.

Laura Pezzi (L)

Unité Des Virus Emergents (UVE: Aix Marseille Université, IRD 190, Inserm 1207, IHU Méditerranée Infection), Marseille, France.

Apolline Maitre (A)

Laboratoire de Virologie, Université de Corse-Inserm, Corte, France.

Dorine Decarreaux (D)

Laboratoire de Virologie, Université de Corse-Inserm, Corte, France.

Xavier de Lamballerie (X)

Unité Des Virus Emergents (UVE: Aix Marseille Université, IRD 190, Inserm 1207, IHU Méditerranée Infection), Marseille, France.

Jean-Christophe Paoli (JC)

UR045 Laboratoire de Recherches sur le Développement de l'Élevage, Institut National de la Recherche pour l'Agriculture, l'Alimentation et l'Environnement, Corte, France.

Laurence Vial (L)

UMR CIRAD-INRA ASTRE (Animal, Health, Territories, Risks and Ecosystems) Department BIOS, Campus International de Baillarguet, Montpellier, France.

Remi Charrel (R)

Unité Des Virus Emergents (UVE: Aix Marseille Université, IRD 190, Inserm 1207, IHU Méditerranée Infection), Marseille, France.

Alessandra Falchi (A)

Laboratoire de Virologie, Université de Corse-Inserm, Corte, France.

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Classifications MeSH