In vitro and In vivo Activity of Cyprodinil and Pyrimethanil on Botrytis cinerea Isolates Resistant to other Botryticides and Selection for Resistance to Pyrimethanil in a Greenhouse Population in Greece

No cross-resistance was observed between pyrimethanil or cyprodinil and the fungicides benomyl, iprodione or carbendazim + diethofencarb. In vitro, both anilinopyrimidine fungicides were effective against strains of Botrytis cinerea resistant to benzimidazoles and/or dicarboximides and against a wild type strain insensitive to diethofencarb (EC₅₀ values ranged between 0.03–0.19 and 0.006–0.054gml^–1 for pyrimethanil and cyprodinil, respectively). Preventive applications of anilinopyrimidines completely protected young cucumber plants and fruits that were inoculated with all strains of B. cinerea. The effectiveness of pyrimethanil against grey mould was studied in greenhouse grown tomatoes in relation to (a) the type of infection and the progress of the disease on different plant parts and (b) the response of the naturally occurring B. cinerea population to the selection pressure caused by eight successive applications of this fungicide. Pyrimethanil effectively controlled grey mould on leaves, fruits and stems but did not significantly reduce the number of dead plants and fruits with 'ghost spot' symptoms. The selection pressure caused by the consecutive applications of pyrimethanil resulted in reduction of its effectiveness on leaves that became apparent after the sixth application. This was correlated with a shift of the B. cinerea population (not previously exposed to anilinopyrimidines) towards reduced sensitivity, probably due to the development of a low level of resistance (R _L = 7.7). Pyrimethanil delayed the onset of the disease but it did not reduce the infection rate.     

Evaluation of treatment and prophylaxis with nitrofurans and comparison with alternative antimicrobial agents in experimental Salmonella enterica Serovar enteritidis infection in chicks

The ability of the nitrofuran antimicrobial agents furazolidone and furaltadone to prevent, reduce or eliminate Salmonella enterica serovar enteritidis PT4 infection in artificially challenged day-old chicks was evaluated. Treating the birds with the nitrofurans failed to eliminate established infections with either furazolidone-resistant (Fz^R) or furazolidone-sensitive (Fz^S) strains. Simultaneous administration of the nitrofurans to day-old chicks challenged with Fz^S failed to prevent infection but reduced colonization significantly (p<0.05) compared to unmedicated controls. No reduction of colonization occurred with Fz^R. Challenging birds with Fz^S and simultaneous dosing with nitrofurans for 1 week, followed by a second week of continued treatment, resulted in an increase in the level of colonization in the second week rather than a decrease. Dosing with the nitrofurans (200 ppm) for 1 week prior to challenge with Fz and continued medication for a further week prevented colonization of the caecum, liver and spleen. However, cessation of dosing at the time of challenge with salmonella resulted in colonization. Chloramphenicol and tetracycline at concentrations of 200 ppm were both independently capable of preventing colonization by salmonella. Sulphadiazine initially reduced colonization but failed to eliminate the infection. Only when furazolidone was combined with chloramphenicol or when sulphadiazine was combined with trimethoprim, and the combined drugs were administered concurrently with the challenge, was colonization prevented.     

猪源致病性沙门氏菌耐药基因的分析

采用平板稀释法，选用氨基糖苷类、四环素类、磺胺类和氯霉素类4大类抗生素的11种药物，对30株猪源致病性沙门氏菌进行了药敏试验，结果有28株菌（93．3％）至少对一种药物有耐药性；对四环素、强力霉素、磺胺甲基异口恶唑、复方新诺明、链霉素、卡那霉索和氯霉素有耐药性的菌株较普遍，在所有菌株中占比例分别为83．3％、80％、80％、76．7％、60％、56．7％和56．7％。设计了25对引物，对耐药基因进行了扩增及序列测定，结果扩增到13种耐药基因，与GenBank中的相应基因有很高的同源性（≥98．1％）。30株猪源致病性沙门氏菌中至少含有一种耐药基因的菌株有28株（93．3％），sul1、aph（3′）-Ⅱa、tetC、Catl、tetA和aadAl耐药基因较为普遍，检出率分别为76．7％、60％、60％、43．3％、40％和36．7％。药敏试验结果与耐药基因检测结果有很高的一致性（≥88％）。     

乳中黄嘌呤氧化还原酶的研究进展

黄嘌呤氧化还原酶属于含钼脱氢酶黄素蛋白家族，是组成乳脂肪球膜的主要蛋白，通过硫酸胺分级沉淀和DEAE-Sepharose柱可从乳脂肪球膜中纯化。XOR作为乳脂肪球膜的膜结合蛋白，在脂肪滴的包裹和分泌中起到重要的结构作用，并且在肠道能够起到一定的抗菌作用。     

干酪乳杆菌LC2W抗菌物质的研究

采用异丙醇抽提的方法，从干酪乳杆菌LC2W（Lb．casei CGMCC NO．0828）细胞中抽提到痢疾志贺氏菌（S．dysenteriae CMCC（B）51387）具有拮抗作用的蛋白类物质。该物质对蛋白酶尤其是胰蛋白酶敏感，对热不敏感。采用SDS—PAGE聚丙稀酰胺凝胶电泳的方法测得抑菌物质的分子量分别为32．1，44．3，87．6kDa。     

动物应用抗菌药的风险及防制对策

食品动物因大量应用抗菌药物产生耐药菌株，对动物和人类健康及生态环境造成危害，为此欧盟对多种促生长抗菌药颁布了禁令，导致了动物治疗用抗菌药的急剧增加及畜牧业经济效益的降低。本文就此展开讨论，强调必须开发新型抗菌药物，合理应用抗菌药，加强抗菌药药效学及药动学研究，健全食源性病原菌耐药性监测系统等。     

种子处理对籽瓜细菌性果斑病防治效果的研究

籽瓜细菌性果斑病(Acidovorax avenae subsp.citrulli)是近年来在新疆出现的一种检疫性病害,种子带菌是该病传播的重要方式之一.通过对市售的带有细菌性果斑病的籽瓜种子进行不同温度及不同药剂的处理,经温室种植测定,计算出各种处理方法对籽瓜果斑病的防治效果.结果显示50℃湿热处理30min;60℃干热处理4h,以及2%的HCl处理20min对防治籽瓜细菌性果斑病种子带菌具有良好的效果,各生产单位可以根据实际情况选择合适的方法,以减轻细菌性果斑病的危害和蔓延.     

中国鲎(Tachypleus tridentatus)基因工程抗菌肽的制备及其抗菌活性

从中国鲎血细胞RT-PCR扩增抗菌肽tachyplesins基因,经改造构建原核和真核表达载体pET-KRN、pPIC9-KRY,并分别在大肠杆菌DE3和毕赤酵母GSll5中诱导表达.用Tris-Tricine SDS-PAGE检测并进一步电洗脱纯化表达产物,经体外生物活性测定表明,表达产物KRN对大肠杆菌、金黄色葡萄球菌、枯草杆菌、伤寒沙门菌的抑菌环为25、22、25、16mm;MIC值为3.57、7.14、3.57、14.28mg/L.表达产物KRY对大肠杆菌、金黄色葡萄球菌、枯草杆菌、伤寒沙门菌和李氏杆菌的抑菌环为26、22、25、18、16mm;MIC值为1.57、3.14、1.57、6.28、6.28mg/L,对水霉的抑菌效果尤其显著,抑菌环达35mm.     

猪尿液中抗菌药物快速筛选拭子法的建立

为防止抗菌药物在动物性食品中的残留,以枯草芽孢杆菌为受试菌,建立一种检测活体动物尿液中抗菌药物残留的快速筛选拭子法,进行宰前活体检疫.添加试验测定猪尿液中5类抗菌药物最低检测限分别为:β-内酰胺类青霉素和氨苄青霉素均为0.05mg/L;氨基糖苷类庆大霉素0.05mg/L、新霉素0.4mg/L;四环素类金霉素0.1mg/L;大环内酯类红霉素0.05mg/L和氟喹诺酮类恩诺沙星0.2mg/L.各抗菌药物添加回收率范围均在64.0%～107.7%,变异系数均小于15%.假阴性结果显示,除青霉素(5%)和氨苄青霉素(4%)出现假阴性外,红霉素、庆大霉素、新霉素、恩诺沙星和金霉素均未出现假阴性.与国外同类试剂盒比较,结果显示两者对10种抗菌药物的检测限一致.     

牛蛙(Rana catesbeiana)蛙皮抗菌肽基因的克隆、测序及其表达

利用RT—PCR的方法从牛蛙皮肤组织中克隆到大小为270bp的片段RCABP，将其克隆到pGEM—T载体，测序获得1个新的碱基序列。将此基因克隆到原核表达载体pQE一80L，获得融合表达质粒pQE一80L／DHFR／ABP，在1％IPTG诱导下进行表达。SDS—PAGE检测表明，重组蛙皮抗菌肽蛋白的表达量占菌体总蛋白的24％，以包涵体形式存在。体外抑菌试验表明，所构建的质粒能在大肠杆菌中表达具有体外抑菌活性的蛙皮抗菌肽，该融合蛋白具有良好的应用前景。