Serum protein electrophoretogram profile detected in apparently healthy cats infected with Leishmania infantum - Short communication.
Leishmania infantum
PCR
agarose gel electrophoresis
cat
serology
Journal
Acta veterinaria Hungarica
ISSN: 0236-6290
Titre abrégé: Acta Vet Hung
Pays: Hungary
ID NLM: 8406376
Informations de publication
Date de publication:
28 Feb 2022
28 Feb 2022
Historique:
received:
04
08
2021
accepted:
15
12
2021
entrez:
8
3
2022
pubmed:
9
3
2022
medline:
9
3
2022
Statut:
aheadofprint
Résumé
The information about the clinical features of Leishmania infantum infection in cats is scarce. In this study, we evaluated the serum protein electrophoresis of samples from 19 infected but apparently healthy cats. To detect L. infantum infection, two serological tests, i.e. western blot (WB) and enzyme-linked immunosorbent assay (ELISA) as well as quantitative polymerase chain reaction (qPCR) on the blood samples were performed. Eventual infection by several selected bacterial and viral pathogens was also tested. All but one of the cats were found positive with WB. The WB-negative cat was positive by ELISA only. From the 18 WB-positive cats, only three were positive also by ELISA and eight with qPCR, including the only animal which was positive in all the three tests. No concomitant infections were detected in any of the cats. The main alteration of the proteinogram was characterised by an increase of the α-2 fraction. In the five cats with hypergammaglobulinaemia, the pattern detected was polyclonal. None of the cats were seropositive to any other pathogens tested. The presence of polyclonal gammopathy and elevation of the α-2 fraction could suggest the presence of active infection. In contrast, the only detection of an increase of the α-2 fraction alone with the presence of positive serological result could be associated by immune response activation against L. infantum.
Identifiants
pubmed: 35258480
doi: 10.1556/004.2021.00055
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM