INVESTIGADORES
CAMPERO Lucia Maria
congresos y reuniones científicas
Título:
ASSOCIATION OF NEOSPORA CANINUM INFECTION WITH LATE EMBRYO LOSSES IN GRAZING DAIRY COW
Autor/es:
QUINTERO RODRIGUEZ, L.E.; CAMPERO, L.M.; MORÉ, G.; DOMINGUEZ, G.; DE LA SOTA, L.; VENTURINI, M.C.; MADOZ, L.V.; GIULIODORI, M.J.
Reunión:
Simposio; International Ruminant Reproduction Symposium.; 2018
Resumen:
Introduction: The fertility of high-producing lactating dairy cows has decreased during the last decades. Pregnancy losses in dairy cows are an important aspect of infertility leading to poor economic performance. Late embryo losses (LEL) are assumed to be of multifactorial origin, being N. caninum infection one potential cause. Objective: The objective of this study was to evaluate the association of N. caninum infection with LEL in grazing dairy cows. Material and Methods: A case-control study was carried out in a commercial dairy herd (32°49´ S, 62°52´ W, Argentina) where Holstein cows (n=92) were enrolled. Pregnancy was diagnosed by ultrasonography at 30-44 days post-insemination. Lack of heart beats, identification of membrane detachment, disorganization or echoic floating structures including embryo remnants were used as indicative of LEL (CASE). Cows with positive pregnancy diagnosis on the same date of each case were considered as control (CON) and the ratio of case-control was 1. For each case animal, the conceptus was sampled (day 0) with an insemination pistol attached to a 10 mL syringe and transported refrigerated at 4°C in a 1.5 ml tube. Cows were bled on days 0 and 30 for serological studies. Blood samples were refrigerated at 4°C and transported to the laboratory within 24 h, centrifuged and sera were stored at -20°C until analysis. Sera were tested by indirect fluorescent antibody test (IFAT) for the detection of antibodies against N. caninum using a cut-off titer of 1:200 and processed to final titer. The DNA from conceptus from seropositive cows, was extracted using a commercial kit according manufacturer's recommendations. The DNA samples were analyzed by PCR with the specific primer pair Np6+/Np21+ for N. caninum. Chi squared test was used to detect differences between groups and P