ABSTRACT
ABSTRACT: The prevalence of trypanosomiasis in sheep is of worldwide concern. It is a hemoparasitic disease caused by the protozoan Trypanosoma (T) spp., andthe biological cycle of transmission involves susceptible hosts and certain hematophagous flies, such as Tabanids and Stomoxys. The objective of this study was to determine the presence of Trypanosomasp. in sheep (Ovisaries). Through an applied, descriptive-prospective-cross-sectional qualitative study conducted between October 1, 2018, and January 29, 2019, blood samples extracted from the jugular vein were analyzed by the blood smear method using 2 Romanowsky staining techniques (Giemsa and Diff-Quick). Animals studied were between ages of 3 and 10 years, coming from 3 farms in the city of Colimes (Ecuador). Of 100 sampled and processed animals, 2 (2%) were positive for Trypanosoma sp., constituting the first report of this hemoparasite in sheep in Ecuador, and 1 case of Babesia spp. (1%) and 4 cases of Anaplasma marginale (4%) were also identified. However, none of these cases presented symptomatology of any hemotropic-parasitic disease. Subsequently, the positive animals were dewormed.The presence of these parasites wasconfirmedat the study site and,thus, could become a serious animal health problem.
RESUMO: A tripanossomíase em ovelhas é uma hemoparasitose globalmente prevalente causada pelo protozoário chamado Trypanosoma (T) sp. O ciclo de vida de transmissão envolve hospedeiros suscetíveis e alguns dípteros hematófagos como Tabanids e Stomoxys. O objetivo destetrabalho foi determinar a presença de Trypanosoma sp. em ovelhas (Ovisaries). Através de um estudo aplicado, com abordagem qualitativa, do tipo descritivo prospectivo-transversal, realizado entre o dia primeiro de outubro de 2018 e 29 de janeiro de 2019, foram analisadas amostras de sangue extraídas da veía jugular pelo método do esfregaço de sangue, utilizando duas técnicas de coloração Romanowski (Giensa e Diff-Quick). Os animais estudados tinham entre três e dez anos de idade, de três fazendas no municipio de Colimes (Equador). Dos 100 animais amostrados e processados, dois casos (2%) foram positivos para Trypanosoma sp., constituindo o primeiro relato deste hemoparasita em ovelhas no Equador. Além disso, um caso de Babesia sp. (1%) e quatro casos de Anaplasma marginale (4%); entretanto, em nenhum desses casos houve sintomas de qualquer doença hemotropicoparasitária. Animais positivos foram posteriormente desparasitados. A presença desses parasitas foi confirmada no local do estudo e, portanto, pode se tornar um sério problema de saúde animal.
ABSTRACT
Background: Current Leishman staining technique for staining thin blood films for differential leukocyte count is too time consuming to meet emergency needs in hospitalized patients with infectious and other deadly diseases. This study aimed at discovering optimal phenol: Leishman powder ratio appropriate for modified Leishman stain and finding an optimized staining reaction and facilitating rapid cellular analysis of blood without alteration in quantity and quality. Methodology: Leishman stain was modified using phenol crystals and liquefied phenol. Various ratios of phenol and Leishman powder were experimented in absolute methanol. Fixing and staining times of staining process were manipulated to develop new staining procedures that gave optimal staining reaction on thin blood films prepared within two hours of receipt. Results were presented as photomicrographs of stained slides. Results: 30mg and 50mg of phenol crystals or 30μL and 50μL of liquefied phenol were required to give 1:5 and 1:3 phenol: Leishman powder ratios respectively. Two modified Leishman staining techniques were developed. The first fixed thin blood films for 25 seconds and stained for 50 seconds while the second technique fixed slides for 1 minute Original Research Article RRRreResearch…….. Article British Journal of Medicine & Medical Research, 4(27): 4591-4606, 2014 4592 and stained for 3 minutes. Photomicrographs of thin blood films showed excellent staining results that compared well with the conventional technique. Conclusion: Unlike the conventional method which requires a total of 10-12 minutes, to complete the staining process, modified Leishman staining techniques require only 75.0 seconds and 4.0 minutes! Batches of blood films can be stained within a short time thus facilitating rapid diagnosis and treatment of patients.