Antibody response to Phlebotomus perniciosus saliva in cats naturally exposed to phlebotomine sand flies is positively associated with Leishmania infection.
Antibodies
Cat
Leishmania infantum
Phlebotomus perniciosus
Portugal
Saliva
Journal
Parasites & vectors
ISSN: 1756-3305
Titre abrégé: Parasit Vectors
Pays: England
ID NLM: 101462774
Informations de publication
Date de publication:
26 Mar 2019
26 Mar 2019
Historique:
received:
15
11
2018
accepted:
05
03
2019
entrez:
27
3
2019
pubmed:
27
3
2019
medline:
4
4
2019
Statut:
epublish
Résumé
Zoonotic leishmaniosis, caused by the protozoan Leishmania infantum, is a public and animal health problem in Asia, Central and South America, the Middle East and the Mediterranean Basin. Several phlebotomine sand fly species from the subgenus Larroussius are vectors of L. infantum. Data from dogs living in endemic areas of leishmaniosis advocate the use of antibody response to phlebotomine sand fly saliva as an epidemiological biomarker for monitoring vector exposure. The aim of this study was to analyse the exposure of cats to phlebotomine sand flies using detection of IgG antibodies to Phlebotomus perniciosus saliva. The association between phlebotomine sand fly exposure and the presence of Leishmania infection was also investigated. IgG antibodies to P. perniciosus saliva were detected in 167 (47.7%) out of 350 cats; higher antibody levels were present in sera collected during the period of phlebotomine sand fly seasonal activity (OR = 19.44, 95% CI: 9.84-38.41). Cats of 12-35 months had higher antibody levels than younger ones (OR = 3.56, 95% CI: 1.39-9.16); this difference was also significant with older cats (for 36-95 months-old, OR = 9.43, 95% CI: 3.62-24.48; for older than 95 months, OR = 9.68, 95% CI: 3.92-23.91). Leishmania spp. DNA was detected in the blood of 24 (6.9%) cats, while antibodies to L. infantum were detected in three (0.9%). Only one cat was positive to Leishmania by both techniques. Cats presenting IgG antibodies to P. perniciosus had a significantly higher risk of being positive for Leishmania infection. To our knowledge, this is the first study demonstrating anti-sand fly saliva antibodies in cats. The evaluation of the contact of this animal species with the vector is important to the development of prophylactic measures directed to cats, with the aim of reducing the prevalence of infection in an endemic area. Therefore, studies evaluating whether the use of imidacloprid/flumethrin collars reduces the frequency of P. perniciosus bites in cats are needed. It is also important to evaluate if there is a correlation between the number of phlebotomine sand fly bites and IgG antibody levels.
Sections du résumé
BACKGROUND
BACKGROUND
Zoonotic leishmaniosis, caused by the protozoan Leishmania infantum, is a public and animal health problem in Asia, Central and South America, the Middle East and the Mediterranean Basin. Several phlebotomine sand fly species from the subgenus Larroussius are vectors of L. infantum. Data from dogs living in endemic areas of leishmaniosis advocate the use of antibody response to phlebotomine sand fly saliva as an epidemiological biomarker for monitoring vector exposure. The aim of this study was to analyse the exposure of cats to phlebotomine sand flies using detection of IgG antibodies to Phlebotomus perniciosus saliva. The association between phlebotomine sand fly exposure and the presence of Leishmania infection was also investigated.
RESULTS
RESULTS
IgG antibodies to P. perniciosus saliva were detected in 167 (47.7%) out of 350 cats; higher antibody levels were present in sera collected during the period of phlebotomine sand fly seasonal activity (OR = 19.44, 95% CI: 9.84-38.41). Cats of 12-35 months had higher antibody levels than younger ones (OR = 3.56, 95% CI: 1.39-9.16); this difference was also significant with older cats (for 36-95 months-old, OR = 9.43, 95% CI: 3.62-24.48; for older than 95 months, OR = 9.68, 95% CI: 3.92-23.91). Leishmania spp. DNA was detected in the blood of 24 (6.9%) cats, while antibodies to L. infantum were detected in three (0.9%). Only one cat was positive to Leishmania by both techniques. Cats presenting IgG antibodies to P. perniciosus had a significantly higher risk of being positive for Leishmania infection.
CONCLUSIONS
CONCLUSIONS
To our knowledge, this is the first study demonstrating anti-sand fly saliva antibodies in cats. The evaluation of the contact of this animal species with the vector is important to the development of prophylactic measures directed to cats, with the aim of reducing the prevalence of infection in an endemic area. Therefore, studies evaluating whether the use of imidacloprid/flumethrin collars reduces the frequency of P. perniciosus bites in cats are needed. It is also important to evaluate if there is a correlation between the number of phlebotomine sand fly bites and IgG antibody levels.
Identifiants
pubmed: 30909940
doi: 10.1186/s13071-019-3376-0
pii: 10.1186/s13071-019-3376-0
pmc: PMC6434892
doi:
Substances chimiques
Immunoglobulin G
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
128Subventions
Organisme : Fundação para a Ciência e a Tecnologia
ID : SFRH/BD/116516/2016
Organisme : Fundação para a Ciência e a Tecnologia
ID : IF/01302/2015
Références
Trans R Soc Trop Med Hyg. 2002 Apr;96 Suppl 1:S185-9
pubmed: 12055836
Kidney Int. 2008 Feb;73(3):256-60
pubmed: 17978811
Vector Borne Zoonotic Dis. 2008 Aug;8(4):443-50
pubmed: 18260789
Vector Borne Zoonotic Dis. 2008 Aug;8(4):555-9
pubmed: 18471058
PLoS Negl Trop Dis. 2010 Mar 23;4(3):e638
pubmed: 20351786
Acta Trop. 2010 Dec;116(3):193-9
pubmed: 20696122
Vet Parasitol. 2010 Dec 15;174(3-4):336-40
pubmed: 20869810
J Vector Ecol. 2011 Mar;36 Suppl 1:S1-9
pubmed: 21366760
Trends Parasitol. 2011 Aug;27(8):341-4
pubmed: 21570915
PLoS Negl Trop Dis. 2011 Oct;5(10):e1344
pubmed: 22022626
Vet Parasitol. 2012 Oct 26;189(2-4):189-96
pubmed: 22575278
PLoS One. 2012;7(5):e35671
pubmed: 22693548
Acta Trop. 2013 Mar;125(3):339-48
pubmed: 23262215
Parasit Vectors. 2013 Apr 15;6:99
pubmed: 23587366
Mem Inst Oswaldo Cruz. 2013 Jun;108(4):481-7
pubmed: 23827997
Parasit Vectors. 2014 Mar 24;7:115
pubmed: 24655431
Exp Parasitol. 2014 Dec;147:54-9
pubmed: 25307685
Parasitol Int. 2015 Apr;64(2):154-6
pubmed: 25463307
Parasit Vectors. 2015 Jun 04;8:302
pubmed: 26041555
PLoS Negl Trop Dis. 2015 Jun 25;9(6):e0003855
pubmed: 26111018
PLoS Negl Trop Dis. 2016 Feb 22;10(2):e0004458
pubmed: 26900688
Parasit Vectors. 2016 May 10;9(1):245
pubmed: 27160667
Sci Rep. 2016 Sep 06;6:32619
pubmed: 27595802
Med Vet Entomol. 2017 Mar;31(1):88-93
pubmed: 27718267
JFMS Open Rep. 2015 Jul 01;1(2):2055116915593969
pubmed: 28491373
PLoS Negl Trop Dis. 2017 Jul 13;11(7):e0005600
pubmed: 28704370
Parasit Vectors. 2018 Jan 4;11(1):7
pubmed: 29301571
Front Cell Infect Microbiol. 2018 Jul 26;8:245
pubmed: 30175073
Parasit Vectors. 2018 Oct 11;11(1):545
pubmed: 30309376