Fipronil and (S)-methoprene can lessen the risk of transmission of Bartonella clarridgeiae among cats with exposure to Ctenocephalides felis.

Bartonella clarridgeiae Ctenocephalides felis fipronil and (S)-methoprene transmission vector

Journal

American journal of veterinary research
ISSN: 1943-5681
Titre abrégé: Am J Vet Res
Pays: United States
ID NLM: 0375011

Informations de publication

Date de publication:
09 Jul 2024
Historique:
received: 10 04 2024
accepted: 13 06 2024
medline: 10 7 2024
pubmed: 10 7 2024
entrez: 10 7 2024
Statut: aheadofprint

Résumé

To cohouse cats experimentally infected with Bartonella clarridgeiae (Bc) with naive cats in a flea-free environment or with Ctenocephalides felis, Bartonella henselae (Bh), Mycoplasma haemofelis, and Candidatus Mycoplasma haemominutum to determine which flea could be a vector and to assess whether transmission of the infectious agents could be blocked by fipronil and (S)-methoprene. Specific pathogen-free cats (n = 34). In experiment 1, Bc was inoculated in 1 cat that was housed with 9 naive cats without C felis. In experiment 2, the 2 cats inoculated with Bc were housed with 6 other cats (2 inoculated with Bh, 2 inoculated with M haemofelis, and 2 inoculated with Candidatus M haemominutum) in the center (enclosure 2) of 3 housing enclosures separated by mesh walls that allow passage of fleas but precludes fighting. C felis were placed only on cats in enclosure 2 (5 times). Cats in enclosures 1 (n = 8) and 2 (8) were untreated, and cats in enclosure 3 (8) were administered fipronil and (S)-methoprene. Blood was collected from all cats for PCR assays for the pathogens. None of the cats housed with the cat inoculated with Bc became PCR positive in the absence of C felis. All cats in enclosure 2 became Bc DNA positive. While 2 of 8 cats in enclosure 1 became Bc PCR positive, none of the treated cats in enclosure 3 became infected. The study demonstrated that C felis can be a vector for Bc. The results support the recommendation that flea control products can reduce the risk of transmission of flea-borne pathogens.

Identifiants

pubmed: 38984890
doi: 10.2460/ajvr.24.04.0102
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-6

Auteurs

Jade A Peralta (JA)

Department of Clinical Sciences, Colorado State University, Fort Collins, CO.

Douglas S Carithers (DS)

Boehringer Ingelheim, Duluth, GA.

Frederik Beugnet (F)

Boehringer Ingelheim, Lyon, France.

Michael R Lappin (MR)

Department of Clinical Sciences, Colorado State University, Fort Collins, CO.

Classifications MeSH