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Peru Gopal BISWAS Yuma OHARI Uday Kumar MOHANTA Tadashi ITAGAKI 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2021,83(4):666
We analyzed the nuclear ribosomal internal transcribed spacer (ITS) 1 and ITS2 sequences for Bangladesh isolates of Ascaridia galli, and we determined that the sequences were unreliable as molecular markers for distinguishing A. galli from other Ascaridia species, because the sequences showed high identity with that of A. columbae. However, the ITS1 sequences were available for designing PCR primers distinguishable between Ascaridia galli and Heterakis spp. Bangladesh isolates of A. galli constituted a monophyletic clade along with other geographical isolates in the cytochrome c oxidase subunit I (COI) phylogenetic tree, however, we could not clarify the phylogenetic relationships between A. galli and other Ascaridia spp., because their available sequences in GenBank were very few. The developed PCR method using DNA from A. galli and Heterakis spp. eggs would enable differential diagnosis of the individual infections in the future. 相似文献
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Christian Pillonel 《Pest management science》1995,43(2):107-113
Experiments with intact cells and submitochondrial fractions of Pythium aphanidermatum (Edson) Fitz. indicated an interference of benzimidazole-N-sulfonamides with the NADH- or succinate-driven electron transport system between cytochromes b and c. Comparison with Ustilago maydis (DC) Corda and Botrytis cinerea Pers. ex Fr. revealed that this effect is Oomycetes specific. The molecular interaction between benzimidazole-N-sulfonamides and the mitochondrial cytochrome b/c1 complex from P. aphanidermatum has been investigated. Binding assays with [14C]52232 RP (dimefluazole) indicated a time- and dose-dependent labelling of two proteins. The molecular mass of one labelled protein and the competition of the binding with antimycin A suggest that benzimidazole-N-sulfonamides interact with the Q1-centre of cytochrome b. Furthermore, experiments with doubly labelled [3H][14C]CGA 323103 revealed a possible irreversible inactivation of the b/c1 complex leading to covalent linkage of the dimethylsulfonamoyl moiety to the target site. 相似文献
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Gunner Hi Srensen 《Acta veterinaria Scandinavica》1980,21(3):438
The growth and the toxin (i.e. hemolysin) producing capacity of Corynebacterium pyogenes were studied in monocultures and in co-cultures with 1 or more of the organisms frequently accompanying it in summer mastitis in cattle (Peptococcus indolicus, Stuart-Schwan cocci, Bacteroides melaninogenicus subsp. levii, Fusobacterium necrophorum and Streptococcus dysgalactiae) or with organisms seldom associated with summer mastitis (Streptococcus uberis, Streptococcus agalactiae, non-toxic staphylococci and Escherichia coli).Pc. indolicus, and to some extent also Stuart-Schwan cocci, stimulated the growth as well as the hemolysin producing capacity of Gb. pyogenes (Table 1) while Str. dysgalactiae, Str. uberis, Str. agalactiae, E. coli and the majority of the staphylococci reduced these activities. Most F. necrophorum strains stimulated the growth, but not the hemolytic activity. With B. melaninogenicus the results were inconclusive.The effect of Pc. indolicus appeared to be associated with the production of a filterable factor (Tables 2 and 3).Mouse toxicity and hemolytic activity of culture filtrates were closely correlated (Table 4). 相似文献
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细胞色素C在生物医学方面的研究进展 总被引:1,自引:0,他引:1
综合论述了细胞色素C的研究简史和结构性质,探讨了细胞色素C与细胞线粒体呼吸链、生物进化细胞凋亡的关系,并对细胞色素C的应用前景作了展望。 相似文献
7.
用不同剂量的口蹄疫灭活疫苗免疫3组雌性BALB/c小鼠,同时设空白对照组,每组8只。免疫后每7d采血一次,用液相阻断ELISA(LPB-ELISA)检测血清抗体水平;第28d用800LD50同源强毒攻击,攻毒后36h,每组随机选取3只BALB/c小鼠,采全血,分别用每只BALg/c小鼠全血注射12只乳鼠,每组共注射36只乳鼠,以乳鼠试验判定BALB/c小鼠的病毒血症和攻毒保护情况。结果表明,免疫组BALB/c小鼠均可产生特异性抗体,保护率分别为75.0%、63.9%、36.1%;对照组小鼠血清抗体为阴性。提示,BALB/c小鼠可以用来评价口蹄疫灭活疫苗的免疫效力。 相似文献
8.
梁丽娟 《农业环境科学学报》2007,(1)
从建立科学合理的藏书体系、图书馆现代化建设、开架借阅、加强合作、提高馆员业务 能力和加强读者信息素质教育等方面论述了中等专业学校图书馆的发展路向。
相似文献9.
The use of COLD‐PCR,DHPLC and GeneScanning for the highly sensitive detection of c‐KIT somatic mutations in canine mast cell tumours 下载免费PDF全文
The conventional polymerase chain reaction (PCR)/sequencing methods may be poorly suited for the detection of somatic mutations in canine mast cell tumour (MCT) samples owing to limited sensitivity. This study was aimed at establishing novel and more sensitive methods, assessing their limit of detection and comparing their sensitivity with conventional methods.Two different ‘driver’ somatic mutations of c‐KIT, together with the wild‐type counterparts, were cloned in plasmids to prepare standard samples with known concentrations of mutated alleles in a background of wild‐type alleles; the plasmids standards were assayed using either conventional or novel, highly sensitive technique. Conventional PCR/sequencing showed a sensitivity of 50–20%. Conversely, all the novel methods obtained higher sensitivities allowed reaching as low as 2.5–1.2% of the mutated DNA.The study demonstrates that early conventional methods could likely have underestimated the prevalence of KIT mutations of MCTs, therefore affecting the assessment of their relevance in prognosis and tyrosine kinase inhibitor (TKI) treatment effectiveness. 相似文献
10.
The value of molecular expression of KIT and KIT ligand analysed using real‐time polymerase chain reaction and immunohistochemistry as a prognostic indicator for canine cutaneous mast cell tumours 下载免费PDF全文
T. A. Costa Casagrande L. M. de Oliveira Barros H. Fukumasu B. Cogliati L. M. Chaible M. L. Z. Dagli J. M. Matera 《Veterinary and comparative oncology》2015,13(1):1-10
This study investigated the correlation between KIT gene expression determined by immunohistochemistry and real‐time polymerase chain reaction (RT‐PCR) and the rate of tumour recurrence and tumour‐related deaths in dogs affected with mast cell tumour (MCT). Kaplan–Meier curves were constructed to compare tumour recurrence and tumour‐related death between patients. The log‐rank test was used to check for significant differences between curves. KIT‐I, KIT‐II and KIT‐III staining patterns were observed in 9 (11.11%), 50 (61.73%) and 22 (27.16%) tumours, respectively. Tumour recurrence rates and tumour‐related deaths were not associated with KIT staining patterns (P = 0278, P > 0.05), KIT (P = 0.289, P > 0.05) or KIT ligand (P = 0.106, P > 0.05) gene expression. Despite the lack of association between KIT staining pattern and patient survival time, the results suggest a correlation between aberrant KIT localization and increased proliferative activity of MCTs. RT‐PCR seems to be a sensible method for quantitative detection of KIT gene expression in canine MCT, although expressions levels are not correlated with prognosis. 相似文献