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RESUMEN: La tripanosomiasis bovina es una enfermedad hemoparasitaria transmitida en Latinoamérica principalmente por moscas picadoras de la familia Tabanidae. El objetivo del estudio fue evaluar la infección por Trypanosoma vivax y Trypanosoma evansi en ganadería bovina especializada en producción de leche en una hacienda y sus potenciales vectores. Se realizó un estudio parasitológico y entomológico directo por técnicas de microscopia y reacción en cadena de la polimerasa (PCR) con dos marcadores moleculares para diferenciar especies de Trypanosoma en muestras de sangre de bovinos y moscas. La frecuencia de infección por Trypanosoma vivax y Trypanosoma evansi en bovinos fue de 3,6 y 0%, respectivamente. La caracterización de vectores muestra a Haematobia irritans como la mosca más frecuente en la zona de estudio (97,1%), seguida de Stomoxys calcitrans (2,8%). No se identificaron tabánidos. Se encontró T. vivax y T. evansi en probóscide y toráx-abdomen de las moscas picadoras Haematobia irritans y Stomoxys calcitrans, lo que representa un comportamiento epizoótico atípico al que sucede en países de Suramérica. Por su alta densidad poblacional, se sugiere la mosca Haematobia irritans como el principal potencial vector. ABSTRACT: Bovine trypanosomiasis is a hemoparasitic disease transmitted in Latin America mainly by biting flies of the family Tabanidae. The study aimed to evaluate infection by Trypanosoma vivax and Trypanosoma evansi in cattle specialized in milk production on a farm and their potential vectors. A direct parasitological and entomological study was performed using microscopy techniques and polymerase chain reaction (PCR) with two molecular markers to differentiate Trypanosoma species in blood samples of cattle and flies. Infection frequency with Trypanosoma vivax and Trypanosoma evansi in cattle was 3.6 and 0%, respectively. Characterization of vectors shows Haematobia irritans as the most frequent fly in the study area (97.1%), followed by Stomoxys calcitrans (2.8%). No horseflies were identified. T. vivax and T. evansi were found in proboscis and thorax-abdomen of biting flies Haematobia irritans and Stomoxys calcitrans, representing an epizootic behavior, atypical in South American countries. Due to its high population density, it is suggested that the Haematobia irritans fly is the main potential vector. RESUMO: A tripanossomíase bovina é uma doença causada por hemoparasitas e transmitida na América Latina principalmente por moscas picadoras da família Tabanidae. O objetivo do estudo foi avaliar a infecção por Trypanosoma vivax e Trypanosoma evansi em gado bovino especializada em produção de leite em uma fazenda e seus potenciais vectores. Se realizou um estudo parasitológico e entomológico direto por técnicas de microscopia e reação em cadeia da polimerase (PCR) com dois marcadores moleculares para diferenciar espécies de Typanosoma em amostras de sangue de bovinos e moscas. A frequência de infecção por Trypanosoma vivax e Trypanosoma evansi em bovinos foi de 3,6 e 0%, respectivamente. A caracterização de vetores mostra a Haematobia irritans como a mosca mais frequente na zona de estudo (97,1%), seguida de Stomoxys calcitrans (2,8%). Não se identificaram tabanídeos. Se encontrou T. vivax e T. evansi em proboscídea e tórax-abdômen das moscas picadoras Haematobia irritans e Stomoxys calcitrans, o que representa um comportamento epizoótico atípico ao que sucede em países da América do Sul. Por sua alta densidade populacional, se sugere a mosca Haematobia irritans como o principal potencial vetor. COL0021461

IEPL; International audience; It has been previously shown that the long-term inhibition of milking-induced prolactin (PRL) release by quinagolide (QN), a dopamine agonist, reduces milk yield in dairy cows. To further demonstrate that PRL is galactopoietic in cows, we performed a short-term experiment that used PRL injections to restore the release of PRL at milking in QN-treated cows. Nine Holstein cows were assigned to treatments during three 5-d periods in a 3 × 3 Latin square design: 1) QN: twice-daily i.m. injections of 1 mg of QN; 2) QN-PRL: twice-daily i.m. injections of 1 mg of QN and twice-daily (at milking time) i.v. injections of PRL (2 µg/kg body weight); and 3) control: twice-daily injections of the vehicles. Mammary epithelial cells (MEC) were purified from milk so that their viability could be assessed, and mammary biopsies were harvested for immunohistological analyses of cell proliferation using PCNA and STAT5 staining. In both milk-purified MEC and mammary tissue, the mRNA levels of milk proteins and BAX were determined using real-time reverse-transcription PCR. Daily QN injections reduced milking-induced PRL release. The area under the PRL curve was similar in the control and PRL injection treatments, but the shape was different. The QN treatment decreased milk, lactose, protein, and casein production. Injections of PRL did not restore milk yield but tended to increase milk protein yield. In mammary tissue, the percentage of STAT5-positive cells was reduced during QN but not during QN-PRL in comparison with the control treatment. The percentage of PCNA-positive cells was greater during QN-PRL injections than during the control or QN treatment and tended to be lower during QN than during the control treatment. In milk-purified MEC, κ-casein and α-lactalbumin mRNA levels were lower during QN than during the control treatment, but during QN-PRL, they were not different from the control treatment. In mammary tissue, the BAX mRNA level was lower during QN-PRL than during QN. The number of MEC exfoliated into milk was increased by QN injections but tended to be decreased by PRL injections. Injections of PRL also increased the viability of MEC harvested from milk. Although PRL injections at milking could not reverse the effect of QN treatment on milk production, their effects on cell survival and exfoliation and on gene expression suggest that the effect of QN treatment on the mammary gland is due to QN's inhibition of PRL secretion.

High-quality colostrum is an important factor influencing neonatal calf health, and quality assessment is essential to obtain good health results. This research evaluated the effects of the calf’s sex, the parity of the cow and the hour of colostrum harvest after parity on the fat, nonfat solids, protein and Ig contents in Holstein colostrum for cows under high grazing conditions in the tropics. The effects of the calf’s sex and parity on somatic cell count (SCC) at the first milking postpartum were determined. A comparison was made between a laboratory method and a farm method for the estimation of the fat and protein content of colostrum. Thirty-three cows were sampled in the study. The calf’s sex was shown to have an effect on the amount of colostrum, on the concentration of fat, and on the amount of milk produced by lactating Holstein cows; all were higher in cows that gave birth to a female calf. Colostrum protein decreased after the first hour postpartum, and the Ig concentration had a tendency to decrease after 4 h. The cows that had parity 1–2 had lower Ig concentrations and total production of Igs, and higher SCC at the first milking postpartum. Ekomilk was a reliable method to measure the colostrum fat on the farm. COL0009556