四种杀菌剂对小麦根病病原菌的室内药效试验

室内药效试验表明：麦根宁1号、敌力脱对小麦根腐病菌的生长均有良好的抑制作用。麦根宁Ⅰ号稀释300倍时，平均抑菌圈直径最大；敌力脱稀释800倍时，平均抑菌圈直径最大。同时，麦根宁Ⅰ号、敌力脱Ⅱ号，粉锈宁对小麦全蚀病菌生长也有明显的抑制作用。粉锈宁，麦根宁Ⅰ，Ⅱ号在稀释10000倍时，抑菌率均达100％；敌力脱在稀释15000倍时，平均抑菌率仍达89．7％。     

人工培植羊体羊黄的研究

本试验以外科手术方法在北京农户所养绵羊胆囊内放人异物网核和注入致黄菌(SEBF8,50亿/ml),诱发羊黄,均获成功.其间,对术前术后血清胆红质、胆固醇、谷草转氨酶和GROS反应等项进行测定.结果表明:上述各项指标在术后8天内与术前比,均有降低,差异显著,但以后逐渐恢复正常.而体重、临床表现,以及饲养指标本出现异常.预示着,人工培植羊体羊黄可行.同时,本试验还为进一步提高人工培植羊黄的产黄量,提供了参考数据.     

鸡舍环境耐药细菌气溶胶及其向环境传播的研究

通过对舍内粪便、空气和舍外环境(10、50、100m)中的空气分离到的细菌鉴定，包括细菌DNA分子生物学检测及药物敏感实验以及细菌含量统计学分析，证明三者之间存在着内在联系；舍内环境微生物气溶胶包括耐药细菌通过舍内外气体交换排往鸡舍周围环境，舍周边环境在一定范围内受到生物污染。研究显示，在粪便、舍内空气、舍外环境10、50、100m空气中分离的金黄色葡萄球菌和链球菌80％以上对氯霉素(CMP)和对苯唑青霉素(OXA)耐药；粪便和舍内外环境空气中的80％以上的大肠杆菌和沙门氏菌对氨苄青霉素(AMP）、氯霉素(CMP)、头孢唑啉(CFZ)均为抑制。证明该鸡舍曾经使用过这些药物治疗或作为添加剂在饲料中添加，鸡群产生了耐药细菌菌株，并向环境传播。测量数据统计结果指出，十里河鸡场鸡舍内环境空气中的大肠杆菌、沙门氏菌、金黄色葡萄球菌和链球菌与舍外环境中相应菌群含量比较差异显著或极显著(P＜0．05或P＜0．01)，但舍外10、50、100m之间的相应菌群比较差异不显著(P＞0．05)，这说明鸡舍内环境细菌气溶胶含量产生多，含量高，菌源强度大；另一方面，反应了鸡舍内环境微生物气溶胶包括耐药细菌能向舍外环境扩散，位舍外环境在一定的范围内受到动物源性生物污染，影响范围大于100m。通过对鸡舍环境微生物气溶胶来源的探讨发现，粪便中的大肠杆菌、沙门氏菌、金黄色葡萄球菌和链球菌与舍内空气相应菌群数量关系比较，呈现正相关(r=0.99)。这从一个侧面揭示了粪便可能是微生物气溶胶的主要来源。     

马铃薯品种抗软腐病测定条件的研究

用全薯块吸头刺伤接种法测定时,较理想的测定条件为:每接种点接种0.1ml浓度为10~2～10~5CFU/ml菌悬液,随后在21±5℃～31±5℃(依所用菌株而定)下保持2～3天,以接种点腐烂斑的最大直径作记载标准。用新鲜薯片法测定时,除接种浓度为10~2～10~3CFU/ml,保持时间为1～2天及以侵染限值作评价标准外,其余条件和全薯块吸头刺伤接种法相同。当用皮孔浸渍法接种时,薯块在10_6CFU/ml菌悬液中浸5分钟,然后使薯块表面保持连续水膜,3～5天后测量薯块表面腐烂面积。上述3种方法都必须有20个以上重复,并使用大小一致、无伤无病的成熟薯块。     

亚麻细菌病发生及防治技术研究

从亚麻细菌病的发生、发展、危害及病原茵特性到病害综合防治，进行了系统研究，明确了该病的发生与品种抗性、耕作栽培等诸方面的关系，为病害防治提供了理论依据；明确了种子带茵是该病害主要侵染源和传播途径，同时建立综合防病体系。     

兔舍内气载需氧菌和气载葡萄球菌的检测

本研究采用A ndersen-6级空气微生物样品收集器,选用血-葡萄糖-琼脂培养基为采样介质,对两个不同种兔舍环境空气中需氧菌总数和葡萄球菌总数进行了检测,并对葡萄球菌的菌群组成进行了分析。结果表明,两个兔舍内需氧菌含量分别为1.73~85.8×103CFU/m3、2.71~9.66×103CFU/m3空气,葡萄球菌含量分别为0.94~7.84×103CFU/m3、1.02~6.54×103CFU/m3空气。兔舍空气中葡萄球菌主要包括金黄色葡萄球菌、腐生葡萄球菌、表皮葡萄球菌、科氏葡萄球菌、头状葡萄球菌和马胃葡萄球菌,其中金黄色葡萄球菌的含量占葡萄球菌总数的26.3%~29.6%,其次是腐生葡萄球菌和表皮葡萄球菌。另外,还对需氧菌和金黄色葡萄球菌在A ndersen-6级收集器不同层级上的分布情况进行了统计分析,结果表明,约有56.4%的需氧菌和49%金黄色葡萄球菌分布在3~6层上,空气动力学直径(A erody-nam ic d iam eter,D ae)在6~0.2μm,它们能进入人、畜的气管、支气管,甚至细支气管,对饲养员和动物的呼吸道构成严重危害。     

Physiological Races and Vegetative Compatibility Groups of Fusarium oxysporum f. sp. lactucae Isolated from Crisphead Lettuce in Japan

One hundred and sixteen isolates of Fusarium oxysporum f. sp. lactucae obtained from 85 fields in three crisphead lettuce-producing areas in Nagano Prefecture, Japan were typed for races using differential cultivars Patriot, Banchu Red Fire and Costa Rica No. 4. They were also grouped into vegetative compatibility groups (VCGs) using complementation tests with nitrate non-utilizing (nit) mutants. Two California strains reported as F. oxysporum f. sp. lactucum, a type culture of F. oxysporum f. sp. lactucae, and 28 avirulent isolates of F. oxysporum obtained from crisphead lettuce were included for comparison. Among Nagano isolates, 66 isolates were identified as race 1, and 50 as race 2. Race 1 strains derived from Shiojiri and Komoro cities and race 2 from Kawakami village and Komoro city. All isolates of race 2 were biotin auxotrophs, and the race could be distinguished based on its requirement for biotin on minimal nitrate agar medium (MM). Pathogenic isolates were classified into two VCGs and three heterokaryon self-incompatible isolates. Strong correlations were found between race and VCG. All the race 1 strains were assigned to VCG 1 except self-incompatible isolates, and all the race 2 strains to VCG 2. The 28 avirulent isolates of F. oxysporum were incompatible with VCG 1 and VCG 2. California strains was vegetatively compatible with VCG 1, and they were assigned to race 1. Based on vegetative compatibility, these two races of F. oxysporum f. sp. lactucae may be genetically distinct, and F. oxysporum f. sp. lactucae race 1 is identical to F. oxysporum f. sp. lactucum. Received 7 May 2002/ Accepted in revised form 6 September 2002     

Development of Stem-base Pathogens on Different Cultivars of Winter Wheat Determined by Quantitative PCR

The progress of development of stem-base pathogens in crops of second winter wheat was plotted in nine experiments in three years. The amount of each pathogen present was determined by quantitative PCR. Where Tapesia yallundae was present in quantifiable amounts, it usually developed earlier than the other eyespot pathogen, T. acuformis. Both species were usually present in greater amounts on cultivars which are more susceptible to eyespot. The sharp eyespot pathogen, Rhizoctonia cerealis, developed more erratically than either of the Tapesia spp. and there were no consistent effects on different cultivars. Fusarium spp., the cause of brown foot rot, were rarely present in quantifiable amounts, but Microdochium nivale was usually present as one or both of the varieties nivale and majus. Late-season (after anthesis) decreases in M. nivale suggest that any brown foot rot symptoms attributable to this fungus would have fully developed earlier. Cultivar differences in amounts of M. nivale were most clear in stems during internode extension and when relatively large amounts of DNA were present. Such differences approximately reflected eyespot susceptibility, cv. Soissons containing most and cv. Lynx containing least DNA. The results emphasise the difficulty in relating diagnoses, by quantitative PCR or other means, at early growth stages when decisions to apply fungicides against stem-base disease are made, to later disease severity.