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Tatiene R. M. Silva Flvia N. L. Barros Michele Bahia Francisco D. Sampaio Junior Sidney S. F. Santos Larissa S. Inoue Thamirys S. Gonalves Laerzio Chiesorin Neto Diogo C. L. O. Faria Camila Tochetto Gisele M. R. Viana Frederico O. B. Monteiro Gustavo Ges-Cavalcante Alessandra Scofield 《Zoonoses and public health》2019,66(7):798-804
The Brazilian Amazon is endemic for malaria and natural infections by Plasmodium spp. have been detected in Neotropical primates. Despite the diversity of primate species in the region, studies on infections by these agents are limited. The aim of the present study was to investigate the frequency of infection by Plasmodium vivax and P. falciparum in free‐born primates that were kept in captivity, in the western Amazon, Brazil. Blood samples were collected from 98 Neotropical primates. Detection of P. vivax and P. falciparum DNA was performed using a semi‐nested PCR, and the amplified products were sequenced. Plasmodium spp. DNA was detected in 6.12% (6/98) of the primates. P. vivax, and P. falciparum DNA was detected in 2.04% (2/98) and 4.08% (4/98) of these mammals, respectively. Sequencing and phylogenetic analysis confirmed the results obtained from the semi‐nested PCR. The presence of infected non‐human primates (NHP) can be auxiliary in the maintenance of P. falciparum and P. vivax and may have implications for the malaria surveillance and control in the Brazilian Amazon. It is necessary to structure an efficient surveillance system for the aetiological agents of malaria that infect NHP and humans to reduce the risk of Plasmodium spp. introduction into new areas, to protect all susceptible species. 相似文献
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Ednara Ronise Lima de Araújo Luis André Luz Barbas Carlos Massatoshi Ishikawa Danielle de Carla Dias Fábio Rosa Sussel Hélcio Luis de Almeida Marques Leonardo Tachibana 《Aquaculture International》2018,26(1):85-97
This study evaluated the use of the prebiotic Active-MOS® (mannanoligosaccharides—Biorigin®) and two probiotics: PAS-TR® (Bacillus subtilis and Bacillus cereus var. toyoi—Imeve®) and Bioplus 2BC® (1.6 × 1010 UFC g?1 de Bacillus subtilis and 1.6 × 1010 UFC g?1 Bacillus licheniformis—Christian Hansen®) tested separately and together, in the diet of Nile tilapia post-larvae during the sex reversal phase. The experiment was conducted in two stages: (i) a total of 2160 3-day-old post-larvae (PL) (10.39 ± 0.85 mm and 12.28 ± 3.15 mg) were used and distributed in 24 tanks of 40 L each (3.0 PL L?1). Growth performance, chemical analysis of carcass, bacterial recovery, and histomorphometry of intestinal villi were evaluated; (ii) 240 tilapia (4.28 ± 0.19 cm and 1.19 ± 0.09 g) from the previous experiment were used and stocked at 10 PL per aquarium. The parameters evaluated were survival and relative protection level after bacterial challenge against Aeromonas hydrophila. Six treatments with four replications in a completely randomized design were used for both experimental stages. Additives in the diet of tilapia post-larvae did not determine significant differences in growth, survival, microbiological, or histomorphometric parameters in this study. Nevertheless, after the experimental infection, advantages on the use of the additives were observed in terms of higher relative protection levels (38.10%) and relative percent survival in fish receiving Active-MOS® + Bioplus 2BC®. Therefore, we recommend the use of synbiotic (Active-MOS® + Bioplus 2BC®) in the farming of Nile tilapia PL with recurrent outbreaks of bacterial diseases during the sex reversal phase. 相似文献
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Dienifer V. Sutil Cláudio R.S. Mattoso Julieta Volpato Nádia C. Weinert Ádson Costa Rozyanne R. Antunes Thiago R. Muller Suzane L. Beier Ronise Tochetto Felipe Comassetto Mere E. Saito 《Veterinary anaesthesia and analgesia》2017,44(4):746-754
Objective
To evaluate the onset and duration of hematological changes and the use of Doppler ultrasound (spleen) in dogs sedated with acepromazine or xylazine.Study design
Clinical study.Animals
A total of 24 mixed breed dogs aged 1–4 years and weighing 15–25 kg.Methods
Dogs were randomly distributed into two groups: acepromazine group (AG) which were administered acepromazine (0.05 mg kg?1) intramuscularly and xylazine group (XG) administered xylazine (0.5 mg kg?1) intramuscularly. Sonographic evaluations (morphologic and hemodynamic splenic vascularization) and hematologic tests were performed before drug administration (baseline) and 5, 15, 30, 60, 120, 240, 360, 480 and 720 minutes after drug administration.Results
A significant reduction occurred in erythrogram variables in AG at 15–720 minutes corresponding with a significant enlargement of the spleen. In XG, a significant reduction was observed in the erythrogram variables at 30–60 minutes without a significant enlargement of the spleen. Hilar diameter did not change over time in either group. Flow alterations were found only in the splenic artery in AG, with a decreased final diastolic velocity observed at 60–120 minutes.Conclusions
Administration of acepromazine resulted in decreased red blood cell count, hemoglobin, packed cell volume and an increased diameter of the spleen. Xylazine administration resulted in similar hematologic changes but of smaller magnitude and duration and without splenic changes. The absence of significant changes in the Doppler flow parameters of the splenic artery and vein and the hilar diameter suggests that the splenomegaly that was observed in AG was not due to splenic vasodilation. No splenic sequestration occurred after xylazine administration.Clinical relevance
The results indicate that acepromazine decreases the erythrocyte concentrations by splenic erythrocyte sequestration and concomitant splenomegaly. Xylazine can cause slight hematologic changes, but without splenic changes. 相似文献
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