Development and validation of 2 probe-hybridization quantitative PCR assays for rapid detection of a pathogenic Coxiellaspecies in captive psittacines

Autor: Flanders, Alison J., Speer, Brian, Reavill, Drury R., Roberts, John F., Childress, April L., Atlas, Alvin, Wellehan, James F. X.
Zdroj: Journal of Veterinary Diagnostic Investigation; May 2020, Vol. 32 Issue: 3 p423-428, 6p
Abstrakt: Avian coxiellosis is an emerging cause of morbidity and mortality among captive psittacines, and the utility of a rapid detection test using easily obtained samples is paramount in a clinical setting. New sequences were obtained from 3 genes: groEL, dnaK, and rpoB. We developed probe-hybridization quantitative PCR (qPCR) assays using groELand dnaKgenes. Samples, including splenic aspirates, liver aspirates, whole blood, and choanal, conjunctival, and cloacal swabs, were collected from 4 psittacine species including 3 blue-and-gold macaws (Ara ararauna), 2 scarlet-chested parrots (Neophema splendida), 1 Timneh African grey parrot (Psittacus timneh), and 1 yellow-naped Amazon parrot (Amazona auropalliata). Retrospective review of postmortem findings from 3 of these psittacines included splenomegaly, hepatitis, and/or transmission electron microscopy confirmation consistent with previous reports of avian coxiellosis. There was 100% agreement between these assays and consensus PCR with sequencing. A Wilcoxon rank-sum test found a strong correlation between groELand dnaKcycle threshold values (p< 0.001), validating these assays for detection of this avian Coxiellasp.
Databáze: Supplemental Index