Folacin and cyanocobalamin in relation to naturalTrypanosoma evansi Infection in buffaloes

Summary The haematological values of haemoglobin (Hb), packed cell volume (PCV) and vitamin levels of folacin (folic acid), cyanocobalamin (vitamin B₁₂) of buffaloes, in a surra endemic area of Eastern Haryana, India, were determined. Surra-positive buffaloes had significantly low levels of Hb, PCV, folic acid and vitamin B₁₂. These low levels of folic acid and vitamin B₁₂ may have enhanced the clinical signs of chronic trypanosomosis, caused byTrypanosoma evansi.

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Folacina Y Cianocobalamina En Relacion Con La Infeccion Natural De Bufalos ConTrypanosoma Evansi

Resumen Se determinaron los valores hematológicos de hemoglobina (Hb), volumen corpuscular celular (PCV) y los niveles vitamínicos de ácido fólico y cianocobalamina (vitamina B₁₂) de búfalos, en un área endémica de surra en Haryana Oriental, India. Los búfalos positivos a surra tuvieron niveles bajos de Hb, PCV, ácido fólico y vitamina B₁₂. Los niveles bajos de ácido fólico y cianocobalamina, pudieron haber exacerbado los sintomas clinicos de tripanosomiasis crónica, causada porTrypanosoma evansi.

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Folacine Et Cyanocobalamine En Relation Avec La Trypanosomose ATrypanosoma Evansi Chez Des Buffles

Résumé Les valeurs hématologiques de l'hémoglobine (Hb), l'hématocrite (PCV) et les taux de la folacine (acide folique) et de la cyanocobalamine (vitamine B₁₂) chez des buffles ont été déterminés dans une région de l'Est Haryana, Inde, où sévit le surra à l'état endémique. Les buffles positifs vis-à-vis du surra présentaient des taux significativement faibles de Hb, PCV, d'acide folique et de vitamine B₁₂. Les taux peu élevés de ces deux derniers éléments peuvent renforcer les siqnes cliniques de la trypanosomose chronique, due àT. evansi.

     

Epidemiology of ovine helminthiasis in Haryana,India

Tracer lambs were used to study the pasture contamination with infective stages of helminth parasites during one annual cycle in a subtropical climate. Post-mortem worm counts indicated that low infections with Haemonchus contortus occurred throughout the year except in June. However, twenty five or more H. contortus per lamb were recorded in January, April, May and August. Trichostrongylus colubriformis infection was detected throughout the year and 150 or more worms per lamb were recorded during January to May and in August. Anoplocephalids were recorded from the lambs throughout the year but had no seasonal pattern. Low infections with Oesophagostomum columbianum and Trichuris ovis were observed. The faecal egg counts from the permanent flock with whom the tracer lambs were grazed revealed heavy to mild worm burdens throughout the year. Coproculture indicated that H. contortus predominated from the second fortnight of May to December except in the second fortnight of July. Infection with T. colubriformis was more severe from January to the first fortnight of May and in the second fortnight of July. Negligible infections with O. columbianum, Bunostomum trigonocephalum, Gaigeria pachyscelis and Dictyocaulus filaria were also observed. Biohythergraphs prepared for H. contortus and T. colubriformis showed differences between observed and expected results. It is suggested that for realistic biohythergraphs related parameters in addition to rainfall and temperature should also be considered.     

Available Moisture in Relation to Water-stable Aggregates of Two Forest Soils

Available moisture release characteristics for two well aggregated clayey forest soils of West Bengal (INDIA) were determined with respect to different-sized water-stable aggregates. In situ determination of higher range of available moisture differed appreciably from classic 1/3 bar moisture retention, for the soils. Release of moisture at lower tensions (0.33 > bar) were mainly governed by the inter-aggregate pore size distribution while that at higher tension chiefly attributed to the texture of aggregates i.e. the intra-aggregate pore size distribution. The difference in moisture releasing capacity particularly in the range 0.33—15.0 bar amongst different sized aggregates, was due mainly to varying amount of clay and organic carbon in different-sized aggregates.     

Effect of bovine horn cancer serum on E-rosetting capacity of peripheral blood lymphocytes from normal unaffected animals

The effect of serum from horn cancer affected bullocks and cows on E-rosetting capacity of peripheral blood lymphocytes (PBL) from unaffected control animals was examined. The E-rosette counts were made using 2-aminoethyl isothiouronium bromide (AET) treated sheep red blood cells. A significant decrease in the percentage of EAET rosette forming cells was noticed when PBL were incubated with 50 per cent serum from animals affected with horn cancer. However, no such effect was noticed when PBL were treated with 50 per cent serum from unaffected control animals. A linear relationship was observed between percentage of EAET rosette forming cells of animals affected with horn cancer and E-rosette inhibitory activity of the corresponding serum on PBL from control animals.     

Potentiation of malathion by other insecticides against Musca domestica

Twenty-seven insecticides, including organochlorine, organophosphorus compounds and carbamates were tried for potentiation of the toxic effect of malathion. Carbaryl, diazinon, fenthion, gamma-BHC, parathion and tetrachlorvinphos potentiated the action of malathion. Fourteen insecticides gave additive effects while seven proved antagonistic. Insecticides which showed potentiation, were further tested by mixing with malathion in the ratios of 1:9, 3:7, 5:5, 7:3 and 9:1. All the five combinations in the six mixtures gave potentiating effects. Maximum potentiation of 17.6 times was observed in 1:9 combination of malathion and gamma-BHC. The proportions in which the insecticides were mixed had a pronounced effect on the toxic effect of malathion.     

Romifidine-ketamine anaesthesia in atropine and triflupromazine pre-medicated buffalo calves

The study was conducted on 10 buffalo calves with a weight of 98.5 +/- 3.9 kg and age 9.7 +/- 1.3 months. Ten trials of two treatments were carried out using a randomized block design. Atropine at the dose of 0.02 mg/kg bodyweight was administered in both the groups. The animals of group I received romifidine at the dose of 10 microg/kg i.v., 10 min after atropine administration, whereas, animals of group II received triflupromazine at the dose of 0.3 mg/kg i.m. and 10 min later romifidine at the dose of 10 microg/kg i.v. immediately followed by ketamine at the dose of 5 mg/kg i.v. The onset of action of romifidine in group I occurred within 2 min and the animals remained under mild sedation for 31 +/- 4.8 min. In group II, the triflupromazine-romifidine-ketamine combination induced anaesthesia for 14 +/- 2.3 min. Hypothermia, significant bradycardia and respiratory depression was noticed in both groups at different time intervals.     

Association mapping for pre-harvest sprouting tolerance in common wheat (Triticum aestivum L.)

Association mapping was undertaken in common wheat to identify markers associated with pre-harvest sprouting tolerance (PHST). For this purpose, a population of 242 wheat genotypes and 250 SSR markers were used. The population used consisted of diverse germplasm, which carried sufficient phenotypic variation for PHS for conducting association mapping. The population was found to be structured and stratified into 15 sub-populations; the tolerant and moderately tolerant wheat genotypes were distributed in all the sub-populations. This feature of the population along with other information on population structure was used in association mapping using both the available models, the general linear model (GLM) and the mixed linear model (MLM); hopefully, this minimized the rate of false positives. As many as 30 markers were found to be associated with PHST, 26 markers with GLM and 17 markers with MLM; 13 markers were detected using both the approaches. Only eight SSR markers associated with QTL for PHST were such, which were located within the marker intervals that were earlier reported to carry QTLs for PHST. The remaining 22 markers that were found to be associated with PHST could not be associated with any of the genomic regions known to carry QTLs for PHST, which are known to occur on all the 42 chromosome arms of wheat genome.