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Effect of oral administration of cyclosporine on Toxoplasma gondii infection status of cats
2015
Lappin, Michael R. | VanLare, Karen A. | Seewald, Wolfgang | Roycroft, Linda M. | Scorza, Andrea V. | King, Stephen | Roberts, Elizabeth S.
OBJECTIVE To evaluate whether anti-inflammatory doses of cyclosporine activate Toxoplasma gondii in chronically infected cats or potentiate infection in cats exposed for the first time. ANIMALS 30 T gondii–negative cats. PROCEDURES Cats were assigned to 1 of 3 groups (10 cats/group). Group 1 (control) cats were administered a placebo for 126 days; group 2 cats were administered a placebo for 84 days, followed by cyclosporine at 7.5 mg/kg/d, PO, for 42 days; and group 3 cats were administered cyclosporine at 7.5 mg/kg/d, PO, for 126 days. Cats were orally inoculated with T gondii on day 42. Results for fecal flotations, PCR assays, and histologic examinations and IgM and IgG titers were analyzed. Cyclosporine concentrations were measured on selected days. RESULTS All cats were infected by T gondii and developed signs of self-limiting gastrointestinal tract infection. Group 3 had the highest incidence and severity of CNS and pulmonary histopathologic findings typical of toxoplasmosis. One cat in group 3 died of systemic toxoplasmosis; that cat had a cyclosporine concentration of 1,690 ng/mL. Group 2 cats infected with T gondii before cyclosporine administration did not have repeated oocyst shedding. Group 3 cats shed fewer oocysts for a shorter time than did control cats of group 1. CONCLUSIONS AND CLINICAL RELEVANCE Oral administration of cyclosporine in accordance with the protocol for this study did not potentiate the enteroepithelial phase of T gondii infection. Cats with high cyclosporine blood concentrations at the time of primary T gondii infection may be at risk of developing systemic toxoplasmosis.
اظهر المزيد [+] اقل [-]Prevalence of internal parasites in beef cows in the United States: Results of the National Animal Health Monitoring System’s (NAHMS) beef study, 2007‐2008
2015
Stromberg, Bert E. | Gasbarre, Louis C. | Ballweber, Lora R. | Dargatz, David A. | Rodriguez, Judith M. | Kopral, Christine A. | Zarlenga, Dante S.
During the United States Department of Agriculture (USDA) National Animal Health Monitoring System’s (NAHMS) 2007‐2008 beef study, 567 producers from 24 US States were offered the opportunity to collect fecal samples from weaned beef calves and have them evaluated for the presence of parasite eggs (Phase 1). Participating producers were provided with instructions and materials for sample collection. Up to 20 fresh fecal samples were collected from each of the 99 participating operations. Fresh fecal samples were submitted to one of 3 randomly assigned laboratories for evaluation. Upon arrival at the laboratories, all samples were processed for the enumeration of strongyle, Nematodirus, and Trichuris eggs using the modified Wisconsin technique. The presence or absence of coccidian oocysts and tapeworm eggs was also noted. In submissions where the strongyle eggs per gram exceeded 30, aliquots from 2 to 6 animals were pooled for DNA extraction. Extracted DNA was subjected to genus level polymerase chain reaction (PCR) identification for the presence of Ostertagia, Cooperia, Haemonchus, Oesophagostomum, and Trichostrongylus. In this study, 85.6% of the samples had strongyle type, Nematodirus, and Trichuris eggs. Among the samples evaluated, 91% had Cooperia, 79% Ostertagia, 53% Haemonchus, 38% Oesophagostomum, 18% Nematodirus, 7% Trichuris, and 3% Trichostrongylus. The prevalence of coccidia and tapeworm eggs was 59.9% and 13.7%, respectively.
اظهر المزيد [+] اقل [-]Effectiveness of current anthelmintic treatment programs on reducing fecal egg counts in United States cow-calf operations
2015
Gasbarre, Louis C. | Ballweber, Lora R. | Stromberg, Bert E. | Dargatz, David A. | Rodriguez, Judy M. | Kopral, Christine A. | Zarlenga, Dante S.
During the United States Department of Agriculture (USDA) National Animal Health Monitoring System’s (NAHMS) 2007‐2008 beef study, producers from 24 states were offered the opportunity to evaluate their animals for internal parasites and for overall responses to treatment with anthelmintics. A lapse of 45 d was required between initial sampling and any previous treatments. Choice of anthelmintic (oral benzimidazoles, and both injectable and pour-on endectocides) was at the discretion of the producer so as not to alter the local control programs. Fresh fecal samples were collected from 20 animals, or from the entire group if less than 20, then randomly assigned to 1 of 3 participating laboratories for examination. Analyses consisted of double centrifugation flotation followed by enumeration of strongyle, Nematodirus, and Trichuris eggs (the presence of coccidian oocysts and tapeworm eggs was also noted). Where strongyle eggs per gram (epg) exceeded 30, aliquots from 2 to 6 animals were pooled for egg isolation and polymerase chain reaction (PCR) analysis for the presence of Ostertagia, Cooperia, Haemonchus, Oesophagostomum, and Trichostrongylus. Results from 72 producers (19 States) indicated that fecal egg count reductions were < 90% in 1/3 of the operations. All operations exhibiting less than a 90% reduction had used pour-on macrocyclic lactones as the anthelmintic treatment. While some of these less than expected reductions could have been the result of improper drug application, PCR analyses of the parasite populations surviving treatment, coupled with follow-up studies at a limited number of sites, indicated that less than expected reductions were most likely due to anthelmintic resistance in Cooperia spp. and possibly Haemonchus spp.
اظهر المزيد [+] اقل [-]Mcmaster method of worm egg count from faecal samples of goats: a comparison of single and double chamber enumeration of worm eggs
2015
Chandrawathani P. | Premaalatha B. | Jamnah O. | Priscilla F. X. | Erwanas A. I. | Lily Rozita M. H. | Jackie P. | Josephin S. J. A. L.
Many parasitology laboratories practiced the McMaster technique as a method in obtaining the quantitative diagnosis of Strongyle eggs burden in farm animals especially ruminants. The McMaster technique also play a crucial role in faecal egg count reduction test (FECRT) for anthelmintic resistance identification. Some laboratoriesrecommend two-chamber counting method while some recommend single chamber counting method. This study focuses on the comparison between single and double counting in McMaster technique fordetection of Strongyle egg count. In this study, it is shown that there is no significant difference between both methods basedon the p-value obtained which is p>0.05 from 127 fresh goat faecal samples. The techniques practised during the study follow the standard established technique. Single chamber counting is suitable for a large number of faecal samples from big herds because it is faster, less laborious and produces sensitive and reliable results in Strongyle egg count. As more commercial farms are set up, there is a need to conduct a fast and efficient test to help farmers evaluate their livestock worm burden.
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