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91.
Summary Humoral antibody responses in cattle or rabbits infected with virulent rinderpest virus or lapinised rinderpest virus respectively were assessed. Rinderpest specific antibodies could be first detected 6 days post-infection. No correlation could be established between antibody response and the course of the disease in infected animals during the early stages of infection. The animals with fatal infection either did not respond or had a transient antibody response. A gradual increase in antibody titre from 7 days post-infection was observed in animals which ultimately recovered.
Respuesta De Anticuerpos Humorales En Animales Infectados Con Virus Virulento De Rinderpest
Resumen Se llevó a cabo un estudio tendiente a captar la respuesta de anticuerpos humorales en bovinos o conejos infectados con virus virulento de rinderpest o virus lapinizado de rinderpest, respectivamente. Los anticuerpos específicos de rinderpest fueron detectados a partir de los 6 días despues de la inoculación. No se pudo establecer correlación entre la respuesta de anticuerpos y el curso de la enfermedad en animales infectados, durante los estadíos iniciales de la enfermedad. Los animales con infecciones fatales o no respondieron o tuvieron una respuesta humoral débil. Los animales que se recuperaron presentaron un alza progresiva en el nivel de anticuerpos desde los 7 días después de la infección.
Response Immunitaire Humorale Chez Des Animaux Infectes Par Le Virus De La Peste Bovine
Résumé Les réponses immunitaires de bovines ou lapins infectés respectivement par le virus de la peste bovine virulent ou lapinisé ont été évaluées. Des anticorps spécifiques contre la peste bovine ont pu être décelés 6 jours après l'infection. Aucune corrélation n'a pu être établie entre la réponse immunitaire et l'évolution de la maladie chez les animaux durant les premiers stades de l'infection. Les animaux n'ayant pas survécu soit n'ont pas développé une réponse immunitaire soit l'on présentée mais de façon transitoire. Une augmentation graduelle de taux d'anticorps à partir du 7e jour après l'infection a été observée chez les animaux qui ont fini par guérir.相似文献
92.
Antisperm antibodies in repeat‐breeding cows: Frequency,detection and validation of threshold levels employing sperm immobilization,sperm agglutination and immunoperoxidase assay 下载免费PDF全文
SK Srivastava S Shinde SK Singh S Mehrotra MR Verma AK Singh S Nandi N Srivastava SK Singh TK Goswami SK Bhure H Kumar SK Ghosh 《Reproduction in domestic animals》2017,52(2):195-202
Antisperm antibodies have been found in repeat‐breeding(RB) cows, and those causing agglutination and/or immobilization of sperm are considered to be closely related to unexplained infertility. However, a standard protocol for identifying antisperm antibodies (ASA) in cattle is not validated. Therefore, an investigation was undertaken to evaluate sperm immobilization (SIT), sperm agglutination (SAT) and immunoperoxidase (IPT)assays for detection of ASA in serum and their respective threshold levels for confirmation. Animals (heifers, normally breeding, repeat‐breeding and pregnant animals) that were free from IBR, brucellosis and uterine infections (screened by clinical examination) were included in the study. Sperm agglutinating, sperm immobilizing and antisperm antibodies evaluated by respective assay were significantly higher (p < .05) in RB cows compared to other groups. The SIT assay was able to identify 61% of RB caused by ASA, more than those employing SAT and IPT. Furthermore, a dilution rate of 1:5 and 1:80 (confirms 59.0 and 57.0% RB+ve)were sufficient to diagnose ASA by SAT and IPT, respectively. Results indicate the presence of __12.6% clumped spermatozoa and __ 2.6%(cut‐off value) peroxidase‐positive spermatozoa at 1:5 and 1:80 dilutions diagnosed with SAT and IPT, respectively, may be considered as repeaters arising out of ASA. Furthermore, study also showed the presence of lower incidence of ASA positivity in other groups of animals (heifer<normal breeder<pregnant animals) compared to repeaters. Study results show that although IPT is more specific and accurate but SAT and SIT are comparatively simple and cost‐effective assays suitable for detecting ASA under field conditions and thus can be recommended for screening of repeaters. 相似文献
93.
Biodiversity of arbuscular mycorrhizal (AM) colonization and AM fungal spores were studied in the roots and rhizosphere soils of Acacia catechu (L.f). Wild., A. mangium Willd, Anthocephala cadamba Miq., Artocarpus chaplasha Roxb., Chickrassia tabularis A. Juss., Swietenia macrophylla King., Tectona grandis L. from plantations; Albizia procera (Roxb.) Benth., A. falcataria L., Alstonia scholaris (L.) R. Br., Aphanamixis polystachya (Wall.) Parker., Hydnocarpus kurzii (King.) Warb., Heynea trijuga Roxb., Lagerstroemia speciosa (L.) Pers., Messua ferrea Linn., Podocarpus nerifolia Don., Swintonia floribunda Griff., Syzygium fruticosum (Roxb.) DC., S. grandis (Wt.) Wal. from forest and nursery seedlings of A. polystachya, A. chaplasha, Gmelina arborea Roxb. and S. cuminii (L.) Skeels from Hazarikhil forest, Chittagong of Bangladesh. Roots were stained in aniline blue and rhizosphere soils were assessed by wet sieving and decanting methods. The range of AM colonization varied significantly from 10%-73% in the plantations samples. Maximum colonization was observed in A. mangium (73%) and minimum colonization was observed in C. tabularis (10%). Vesicular colonization was recorded 15%-67% in five plantation tree species. The highest was in A. cadamba (67%) and the lowest was in T. grandis; A. chaplasha and C. tabularis showed no vesicular colonization. Arbuscular colonization was recorded 12%-60% in four plantation tree species. The highest was in A. mangium (60%) and the lowest was in A. cadamba. Roots of Artocarpus chaplasha, C. tabularis and T. grandis showed no arbuscular colonization. Among 12 forest tree species, nine tree species showed AM colonization. The highest was in A. falcataria (62%) and the lowest was in S. fruticosum (10%). Significant variation in vesicular colonization was recorded in seven forest tree species. The highest was in H. trijuga (52%) and the lowest was in L. speciosa (18%). Hydnocarpus kurzii, M. ferrea, P. nerifolia S. fruticosum and S. grandis showed no vesicular colonization. Arbuscular colonization was recorded in seven forest tree species. The highest was in A. falcataria (60%) and the lowest was in A. procera (10%). All the nursery seedlings showed AM colonization and the range was 10%-73%. Vesicules were recorded in G. arborea (40%) and S. cumini (40%). Arbuscular colonization was recorded in G. arborea (100%) and S. cumini (100%). Spore population was recorded 77-432/100 g dry soils, 80-276/100 g dry soils, and 75-153/100g dry soils in plantation, forest and nursery, respectively. Glomus and Acaulospora were dominant genera among the six AM fungi recorded. Significantly positive correlation was observed between AM colonization and AM fungal spore population in Hazarikhil plantation tree species, forest tree species and nursery tree seedlings. The present study showed the biodiversity of root colonization and AM fungi are active in nutrient cycling, survivals and seedling establishment of the plants in the Hazarikhil forest, plantation and nursery. 相似文献
94.
95.
M H Kaplan A Dhar T R Brown R S Sundick 《Veterinary immunology and immunopathology》1992,34(1-2):63-79
Current assays for chicken interleukin-2 (IL-2) utilize mitogen-activated lymphocytes. However, very high inter-assay variability and sporadic high background proliferation limit their usefulness. In view of the above, several Marek's disease virus (MDV)-transformed T-cell lines (which grow well in a serum-supplemented medium) were tested for a response to chicken IL-2 when grown in serum-free media. Five of six lines examined showed a dose-dependent proliferative response to chicken T-cell conditioned media. One line, MDCC-CU14, was chosen for further studies. In addition to the tumor cells' dose-dependent responses to semi-purified chicken IL-2, they expressed T-cell activation antigens on the cell surface. Furthermore, the level of surface expression was enhanced on cells provided IL-2. Co-incubation of the tumor cells with monoclonal antibody INN-CH-16 (specific for an antigen on the surface of activated T-cells) and IL-2 resulted in a modulation of lymphokine-induced proliferation. Together, these data suggest that signalling mechanisms in MDV T-cell tumors are intact and that these lines can be used as an assay for chicken T-cell lymphokines. Furthermore, they provide an interesting model for the study of avian and mammalian T-cell transformation. Implications for the study of Marek's disease are also discussed. 相似文献
96.
A number of 2-aryl- and 2-aryloxymethyl-5-aryl-7H-1,3,4-thiadiazolo[3,2-a][1,3,5]triazine-7-thiones have been synthesised and their fungitoxicities determined in vitro against Aspergillus niger and Fusarium oxysporum. Two alternative routes for synthesis of the title compounds are described. Some of the compounds had activities comparable with that of the commercial fungicide mancozeb. Structure/activity relationships for the compounds are discussed. 相似文献
97.
98.
Comparison of in vitro and in vivo fertilizing potential of buffalo bull semen frozen in egg yolk‐, soya bean lecithin‐ and liposome‐based extenders 下载免费PDF全文
AK Singh A Kumar M Honparkhe S Kaur H Kaur SPS Ghuman PS Brar 《Reproduction in domestic animals》2018,53(1):195-202
The objective of this study was to compare different extenders for post‐thaw in vitro sperm function and in vivo fertility of buffalo semen. Accordingly, sperm of 30 ejaculates extended in egg yolk (TRIS with 20% egg yolk; EY), two soya lecithin‐based (SL‐1; AndroMed® and SL‐2; Bioxcell®) and a liposome‐based extender (LS; OptiXcell®) were tested. The post‐thaw semen was evaluated for computer‐assisted sperm analysis (CASA), sperm viability, membrane and acrosome integrity, DNA integrity and acrosome reaction and first service pregnancy rate (FSPR) in a fixed‐time artificial insemination programme. Total motility and VCL were the only CASA‐based parameters that exhibited significantly higher (p < .05) percentage in LS among these extenders. Post‐thaw percentage of acrosome integrity (55.9 ± 1.4, 58.1 ± 2.0, 55.8 ± 2.0, 56.6 ± 2.3) and DNA integrity (68.8 ± 2.0, 69.2 ± 2.3, 71.3 ± 2.1, 69.1 ± 2.1) did not differ (p > .05) in EY, SL‐1, SL‐2 and LS extender, respectively. However, a variable response in terms of efficacy of different extenders for sperm viability and plasma membrane integrity was observed. Assessment of inducibility of acrosome reaction showed significant differences between extenders (51.9 ± 2.1, 44.3 ± 2.4, 46.1 ± 2.3 and 58.1 ± 3.1%, respectively, for EY, SL‐1, SL‐2 and LS). Furthermore, field trials revealed significantly higher (p < .05) FSPR of LS‐extended semen as compared to that for EY, SL‐1 and SL‐2 extender (46.3%, 41.2%, 31.2% and 29.7%, respectively). It is concluded that the liposome‐based extender is more effective than egg yolk‐ and soya lecithin‐based extenders and may be used for cryopreservation of buffalo semen in the future. 相似文献
99.
R Singh GS Sengar U Singh R Deb V Junghare S Hazra S Kumar S Tyagi AK Das TV Raja A Kumar 《Reproduction in domestic animals》2018,53(3):588-608
Male infertility is one of the prime concerns of dairy cattle production. The study was designed to find out differentially expressed proteins in categorized crossbred (Holstein Friesian × Sahiwal) bull semen to serve as potential biomarkers for male infertility. Frozen crossbred bull semen with satisfactory phenotypic records were defined as “good” and “poor” based on their fertility rates. A total of 1,547 proteins were detected in bull spermatozoa using liquid chromatography–mass spectrometer (LC‐MS/MS) analysis. Results revealed that 558 (36.1%) and 653 (42.2%) proteins were expressed to good and poor quality bull spermatozoa, respectively. A total of 336 proteins (21.7%) were reported to be unique for both good and poor quality bull semen, and among the common proteins, 224 (66.7%) and 112 (33.3%) were up‐ and downregulated in good and poor quality categorized bull semen, respectively. Gene Ontology analysis of global proteomes identified different signalling pathways, and most of them were related to cellular motility, immune systems as well as cellular metabolisms. The distinctive presence of some of the proteins may provide an insight into the molecular mechanistic role played by these proteins in crossbred bull infertility. 相似文献
100.
Luis Fernando Aranguren Caro Hung N. Mai Linda Nunan Joshua Lin Brenda Noble Arun K. Dhar 《Journal of fish diseases》2020,43(4):403-411
White spot syndrome virus has been a threat to the global shrimp industry since it was discovered in Taiwan in 1992. Thus, shrimp-producing countries have launched regulations to prevent import of WSSV-infected commodity shrimp from endemic areas. Recently, cooked shrimp that is infected with WSSV tested positive by PCR. However, there is no study to determine the infectivity of WSSV in cooked shrimp that tested positive by PCR. In the present study, WSSV-infected shrimp were cooked at boiling temperature for different times including 0, 1, 3, 5, 10 and 30 min. Upon exposure to boiling temperature, WSSV-infected shrimp were fed to SPF shrimp (Litopenaeus vannamei). The result showed experimentally challenged shrimp from 0-min treatment (positive control) indeed got infected with WSSV. However, experimentally challenged shrimp that were fed tissues boiled at 1, 3, 5, 10 and 30 min were not infected with WSSV. Mortality data showed that only the positive control (0-min) treatment displayed high mortality, whereas no mortality was observed in any other treatment category. These findings suggest that cooking shrimp at boiling temperature for at least 1 min might prevent any potential spread of WSSV from endemic countries to other geographical areas where WSSV has not yet been reported. 相似文献