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101.
Martin-Laurent F Piutti S Hallet S Wagschal I Philippot L Catroux G Soulas G 《Pest management science》2003,59(3):259-268
We report the development of quantitative competitive (QC) PCR assays for quantifying the 16S, 18S ribosomal and atzC genes in nucleic acids directly extracted from soil. QC-PCR assays were standardised, calibrated and evaluated with an experimental study aiming to evaluate the impact of atrazine application on soil microflora. Comparison of QC-PCR 16S and 18S results with those of soil microbial biomass showed that, following atrazine application, the microbial biomass was not affected and that the amount of 16S rDNA gene representing 'bacteria' increased transitorily, while the amount of 18S rDNA gene representing fungi decreased in soil. In addition, comparison of atzC QC-PCR results with those of atrazine mineralisation revealed that, in response to atrazine treatment, the amount of atzC gene increased transitorily in soil pre-treated with atrazine, suggesting that accelerated atrazine biodegradation in soil could be due to a transient increase in the size of the atrazine mineralising community. 相似文献
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104.
Samartino LE 《Veterinary microbiology》2002,90(1-4):71-80
Brucellosis has been recognized in Argentina since the 19th century. Several studies demonstrated the presence of the disease in most of the domestic species. Actually, the estimate of prevalence is that between 10 and 13% of the farm animals are infected with bovine brucellosis with an individual rate of 4–5%. The annual economical losses have been estimated at US$ 60,000,000. The control of bovine brucellosis began in 1932 and successive resolutions have been issued since then. The current resolution indicates that B. abortus S19 is mandatory in female calves between 3 and 8 months of age. The vaccine strain B. abortus RB51 was provisionally approved but only for cattle older than 10 months of age. The brucellosis control program consists principally of test and slaughter. This methodology has been successful mainly in the dairy farms that have the incentive due to increased pricing because of obtaining a low prevalence of the disease. Brucellosis has been found in porcine, caprine, ovine and canine species. All Brucella species have been found in the country. Human brucellosis is an important disease and a national coordinated diagnostic net has been formed to better control the disease in man. 相似文献
105.
提取鸡病毒性关节炎病毒(AVAV)内蒙古分离株(C-98株)总RNA,参考GenBank中禽呼肠孤病毒(ARV)S1133株S1基因序列设计了2对引物,应用RT—PCR技术扩增了病毒S1基因,将S1基因cDNA克隆到pGEM—T Easy载体后测序。将测定序列拼接后与参考毒株ARV-176、ARV-138、ARV-S1133、MDRV—YJL的S1基因序列进行了比较。结果显示,AVAV C-98分离株的S1基因与强毒株ARV-176株的同源性最高,达99.9%;与MDRV—YJL的同源性为99.3%,与弱毒疫苗株ARV—S1133的同源性也达97.9%;与ARV-138株的同源性最低,为81.2%。表明,AVAVC-98株与参考毒株的差异较小,与疫苗株ARV-S1133有很高的同源性。 相似文献
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107.
斑点叉尾(鮰)嗜麦芽寡养单胞菌的分离鉴定及系统发育分析 总被引:1,自引:0,他引:1
从发生在四川、重庆等省市的斑点叉尾(鮰)急性流行性传染病病鱼的肝脏、肾脏内分离到1株高致病性菌株(CCF00024),人工感染健康鱼表现出与自然病鱼相同的症状,并从中分离获得同种细菌,证实其为斑点叉尾(鮰)急性流行性传染病的病原菌.形态、生理生化检测表明,该菌为非发酵型直杆菌,严格需氧,革兰氏阴性,极生多鞭毛,对除麦芽糖和甘露糖以外的多种糖类不利用产酸,氧化酶阴性,DNA酶、蛋白酶、脲酶、赖氨酸脱羧酶阳性,MR、VP阴性.在以该菌16S rDNA序列(GenBank登录号AY970826)和GenBank及RDP数据库内同源性较高的细菌16S rDNA序列构建的系统发育树中,分离菌CCF00024与嗜麦芽寡养单胞菌(Stenotrophomonas maltophilia)聚在一簇,特别是与S.maltophilia M5-1的同源性最高,序列相似性达99.6%,结合形态和生理生化特点将其鉴定为嗜麦芽寡养单胞菌(Stenotrophomonas maltophilia).药敏试验结果表明,对磺胺甲(口恶)唑、磺胺异(口恶)唑、阿齐霉素、洛美沙星高度敏感,而对新霉素、卡那霉素、氨苄青霉素,头孢唑啉、先锋霉素V和链霉素不敏感. 相似文献
108.
Real‐time polymerase chain reaction (PCR) assays for 11 representative rumen bacterial species were validated. The sensitivity was tested by using the serially diluted target 16S rDNA from respective bacterial species. The recovery of the target DNA and the assay reproducibility were determined using DNA from rumen fluid spiked with different quantities of the target. Minimum detection levels for the target were 10–100 copies in pure culture. The recovery of the added target ranged from 82.4 to 116.6%. The intra‐ and inter‐assay variations of each assay were <9.4 and <12.6%, respectively. Therefore, the real‐time PCR assays evaluated in the present study are considered to be sufficiently reliable for monitoring all 11 bacterial species in the rumen. The assays were then applied to the monitoring of the bacterial species attached to ruminally incubated rice straw. Among the monitored fibrolytic species, Fibrobacter succinogenes was found to be the most dominant, accounting for 2.61% of total bacteria after 24 h incubation. Selenomonas ruminantium and Streptococcus bovis, non‐fibrolytics, were detected on the rice straw at 8.96% and 1.16% of total bacteria, respectively. Such high levels of non‐fibrolytics on the plant fiber suggest a synergistic relationship between fibrolytics and non‐fibrolytics. 相似文献
109.
16S rRNA基因及外膜蛋白基因分析在鸭疫里默氏菌鉴定中的应用 总被引:1,自引:0,他引:1
本实验对鸭疫里默氏菌(包括6个血清型)、大肠杆菌、鼠伤寒沙门氏菌和多杀性巴氏杆菌进行了16S rRNA基因片段的扩增和测序,并将测序结果进行了同源性比较和酶切分析;同时根据标准血清2型鸭疫里默氏菌外膜蛋白的基因序列设计一对引物进行扩增。根据16S rRNA的测序结果及EcoRⅠ和HaeⅢ酶切片段分析,可将鸭疫里默氏菌与其它临床症状易混淆的细菌感染相区别,而外膜蛋白基因序列的特异性也为鸭疫里默氏菌的鉴别诊断提供了一种快速、准确的PCR鉴定方法。 相似文献
110.
为探讨水貂的系统发育关系,对金州水貂的12S rRNA基因进行了克隆测序,序列长度为450 bp。结果表明,金洲水貂的12S rRNA基因与伶釉的同源性为92.48%,与林釉的同源性为91.83%,与北美水貂的同源性为90.99%,与獾的同源性为90.99%。 相似文献