稻曲病菌致病机制研究进展

 稻曲病是一种水稻穗部病害,在世界各水稻主产区均有发生,已成为世界性病害,在我国也属于水稻主要病害之一。稻曲病的发生严重影响水稻产量和稻米品质。研究其病原菌致病机制,对找寻防治药物的特异性靶标具有重要作用,可为抗病分子育种提供新的思路,为稻曲病菌防治药剂研发提供新的靶标。本文综述了稻曲病菌侵染过程、致病相关基因功能研究、水稻响应稻曲病菌侵染等方面的研究进展,提出进一步研究的策略。现有研究表明,稻曲病菌能成功侵染水稻孕穗期雄蕊的花丝引起发病。病原菌可通过抑制多个水稻免疫途径实现成功侵染;还可模仿胚珠受精激活水稻灌浆、糖代谢等途径为稻曲球的形成提供营养物质;全基因组测序完成和基因编辑技术在基因敲除中的成功应用,为稻曲病菌功能基因研究提供了很好的基础。稻曲病菌独特的侵染过程和营养利用机制是未来研究的重要方向。     

Y-S-Y12发酵液和生物质热解液混配对辣椒炭疽病的防治及作用机理

为探究解淀粉芽孢杆菌Y-S-Y12拮抗菌发酵液和生物质热解液混配对辣椒炭疽病的协同防病作用及其作用机理，对不同浓度生物质热解液、拮抗细菌Y-S-Y12菌株的发酵浓缩液及其混配溶液对辣椒炭疽病的抑菌作用进行检测，计算出毒力方程，根据EC50值将两种溶液进行混配，求得最佳配比。通过活体试验检测Y-S-Y12菌株对辣椒炭疽病果实的防治效果，测定叶片超氧化物歧化酶（superoxide dismutase，SOD)、过氧化物酶（peroxidase，POD）和过氧化氢酶（hydrogen peroxidase，CAT）活性，并探究各药剂对辣椒炭疽病病菌菌丝的细胞膜通透性、生理代谢和菌丝形态的影响。结果显示，Y-S-Y12菌株发酵浓缩液和生物质热解液以1∶9混配具有明显的协同增效作用;混配的防效显著高于单剂，防效达到79.62%，进一步说明混配具有增效作用。混剂处理的辣椒炭疽病菌菌丝中的几丁质酶活性、β-1,3-葡聚糖酶活性和蛋白酶活性显著高于对照和单剂处理，处理后菌体的保护屏障被打破，使培养液的电导率、外渗液中蛋白质和核酸含量上升。混剂处理的辣椒叶片中SOD、POD、CAT酶活性显著高于对照和单剂处理，说明辣椒植株抗病性增强。综上，Y-S-Y12菌株发酵液和生物质热解液混配对辣椒炭疽病有协同防病作用，可能是因为Y-S-Y12菌株具有破坏辣椒炭疽病菌菌丝和诱导辣椒植株抗病性作用。研究为辣椒炭疽病无公害防治提供理论依据。     

油茶内生拮抗细菌的筛选、鉴定及防效

为筛选出对油茶炭疽菌有拮抗效果的生防菌株，以油茶健康叶为对象，平板对峙法筛选，利用形态和生理生化特征以及16S rDNA基因和gyrA基因序列对菌株进行鉴定，测定其抑菌活性，并将该菌株与枯草芽胞杆菌Y13复配进行林间防效试验。结果表明，对油茶炭疽病菌拮抗作用效果较强的内生菌株为HBMC—B05；菌落为乳白色，不透明，边缘不整齐，中间有凸起；分子鉴定结果显示菌株HBMC—B05为贝莱斯芽胞杆菌Bacillus velezensis，其对果生炭疽菌Collectotrichum fructicola，抑菌率可达到81.31%，对另外3种油茶炭疽病病原菌抑菌率可达到70%以上，对其他4种致病菌也有抑制作用；复合菌剂对油茶病害的田间防治效果达到59%以上。该菌株的抑菌具有广谱性，可为油茶病害的生物防治扩充菌种资源，具有广泛的应用前景。     

植物内生肠杆菌对狗牙根耐盐性的调控研究

以从海滨雀稗中分离得到的内生肠杆菌为材料，采用种子萌发与盆栽试验两种方式研究植物内生细菌对狗牙根耐盐性的影响。通过对狗牙根种子和幼苗接种单一内生细菌和混合内生细菌，并测定种子发芽率、苗长、根长、生物量等生长指标与叶绿素含量、相对含水量、相对电导率和叶片中钠离子、钾离子的含量综合评价植物内生细菌对狗牙根耐盐能力的调控。结果表明，在150 mmol·L^-1盐胁迫下处理14 d后，接种混合菌液B3014比接种单一菌液B30更能提升狗牙根种子的萌发率、对盐胁迫下胚根及胚芽长度的增长也较显著（P<0.05）。在成坪期，与空白对照相比，接种内生细菌可以提升200 mmol·L^-1盐胁迫下狗牙根的成坪质量，增加地上、地下生物量的积累、苗长与根长生长量，并提升植株叶绿素含量与叶片相对含水量，降低细胞膜破损程度。在接种内生细菌处理中，接种混合菌液B3014可以使狗牙根在盐胁迫下受到的损伤显著低于（P<0.05）接种单一菌液B30。与此同时，接种混合菌液B3014对狗牙根叶片中钠离子含量降低程度高于接种单一菌液B30，同样，接种混合菌液B3014也能更好地积累盐胁迫下狗牙根叶片内钾离子含量，增加盐胁迫下狗牙根的耐盐能力。因此，接种混合菌液B3014对盐胁迫下狗牙根种子的萌发和成坪后的耐盐能力的提升高于接种单一菌液B30。探讨植物内生细菌对狗牙根耐盐能力的调控，为提高草坪草在盐碱环境中的应用提供了新思路。     

硫化细菌的分离及对碱土pH的影响

通过对样品的富集，利用选择培养进行化能自养硫化细菌的分离；以大庆本地碱土作为实验材料，通过硫化细菌及辅料的添加，利用pH计测定碱土pH值变化。分离获得了硫化细菌lh-1，利用该菌株改良碱土以添加0.27% 硫粉混合硫化细菌效果最为明显，经过两个半月的改良，pH可从10.53降到8.23。     

一株耐铝甜瓜枯萎病拮抗细菌的分离鉴定及其耐铝特性研究

从甜瓜根际酸性土壤中分离筛选到1株耐铝甜瓜枯萎病拮抗菌，命名为A2。根据表型、生理生化特征和16S rRNA基因序列相似性分析，将其鉴定为Pseudomonas sp.。菌株A2对甜瓜枯萎病病原菌的相对防效为68.3%，且拮抗能力具有遗传稳定性。相比AlCl3处理，菌株A2对Al2(SO4)3表现出了更好的耐受性，最高可耐受50mmol/L Al3+。在含有A13+的S-LB培养基中，菌株最适生长温度为30 ℃；培养基初始pH值的降低会加剧A13+对菌株A2的毒害作用。研究结果可为含活性铝的酸性土壤中甜瓜枯萎病的生物防治提供优良菌株资源和理论基础。     

Effect of dietary GroBiotic®‐A supplementation as a prebiotic on the intestinal microflora,growth performance,haemato‐serological parameters,survival rate and body composition in juvenile beluga (Huso huso Linnaeus, 1754)

The objectives of the present study were to investigate of GroBiotic^®‐A (GBA) on growth, autochthonous intestinal microbiota and haemato‐serological parameters of beluga juvenile. A total of 180 fish (40.82 ± 5.81 g) were fed diets containing graded levels of GBA (0, 5, 10 and 20 g kg^?1 diet) for 8 weeks. No significantly differences in body composition, total viable aerobic bacteria, mean cell volume, mean cell haemoglobin, mean cell haemoglobin concentration, neutrophils, eosinophils, monocytes, albumin, glucose, triglyceride, cholesterol, alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase and lactate dehydrogenase were detected between treatment groups. The fish fed on 10 and 20 g kg^?1 GBA significantly showed higher lactic acid bacteria, final weight, body weight increases, weight gain and lower feed conversion ratio compared with the control and 5 g kg^?1 groups. The group fed 20 g kg^?1 GBA showed a highly significant difference in condition factor, survival rate, final length, total red and white blood cells, lymphocytes, haematocrit, haemoglobin, total protein, total immunoglobulin and lysozyme activity. The specific growth rate of the treatment groups was significantly elevated compared with the control groups. These results indicated that GBA at level 20 g kg^?1 improved growth, welfare and survival of beluga juvenile.     

外源溶磷菌对不同土壤条件下大豆生长特性的影响

为了明确溶磷菌在多种土壤中的应用效果,探讨了两株溶磷菌对黑土及盐碱土种植大豆的促生效应。采用盆栽试验分析了不同处理对大豆光合作用、渗透调节物质含量、生物量、氮磷吸收及产量的影响。结果表明:加菌处理可增加植株Pn,显著降低R6、R8两时期叶片可溶性蛋白、可溶性糖及游离氨基酸含量,增加R2~R8时期大豆株高和根干重,混合土壤中加菌处理也可提高植株地上部分氮、磷及植株全磷、全氮含量。添加wj1和混合菌处理的植株干重优于添加wj3的处理。黑土加混合菌可显著提高大豆R2期叶片WUE,增加V3、R2和R8这3个时期大豆地上、地下部分氮、磷及植株全氮、全磷的含量。黑土加wj1与混合土壤加菌处理的大豆株荚数、总粒数、单株粒重及百粒重均高于未加菌处理。添加外源溶磷菌,对黑土及盐碱土栽培大豆均有不同程度的促生效果,能明显增强大豆在混合盐碱土壤中的适应性,增加植株生物量、氮磷吸收量和产量,且混合菌处理对大豆的促生效应优于wj1及wj3单一菌株处理。     

A bacterium with close genetic identity to Pseudomonas mandelii associated with spring fish kills in wild bluegill Lepomis macrochirus Rafinesque and pumpkinseed sunfish Lepomis gibbosus (Linnaeus)

Pseudomonas fluorescens are known bacterial pathogens in fish. The P. fluorescens group contains at least nine different bacterial species, although species from fish have rarely been differentiated. Two isolated fish kills affecting wild bluegills, Lepomis macrochirus Rafinesque, and pumpkinseed sunfish, Lepomis gibbosus (Linnaeus), occurred in the spring of 2015 during cool water temperatures (12.5°C–15.5°C). Disease signs included severe bacteraemia with rare gross external signs. Pure bacterial cultures isolated from kidneys of all affected fish were identified as P. fluorescens using the API 20NE system, while no bacteria were isolated from asymptomatic fish. To further identify the species of bacterium within the P. fluorescens complex, genetic analysis of the 16S rRNA, rpoD and gyrB genes was conducted. DNA sequences of bacterial isolates from both mortality events were identical and had close identity (≥99.7%) to Pseudomonas mandelii. Although likely widespread in the aquatic environment, this is the first report of a bacterium closely resembling P. mandelii infecting and causing disease in fish. The bacterium grew at temperatures between 5°C and 30°C, but not at 37°C. It is possible that infections in fish were a result of immunosuppression associated with spring conditions combined with the psychrotrophic nature of the bacterium.