对增强辣椒疫霉菌抗性的研究

病原物诱导型启动子能精确控制抗病基因在侵染位点的表达,是抗病基因工程的有效工具。prp1-1是来自马铃薯谷胱甘肽巯基转移酶基因启动子的一个273bp的片段,能够快速准确地启动被侵染位点抗病基因的表达;Rs-AFP2是具有对致病性丝状真菌的广谱抗性。该研究构建prp1-1调控Rs-AFP2基因表达的载体,经农杆菌介导转化法导入辣椒。逆转录PCR检测发现,转基因辣椒只在受到疫霉菌孢子侵染时,才由prp1-1启动Rs-AFP2基因的转录。用疫霉菌孢子灌根接种转基因辣椒T1代植株,35株T1代辣椒中有29株表现出明显的疫霉菌抗性。另将23株T1代辣椒种于人工气候箱,发现其形态和发育特征与相同条件下的非转基因植株无明显区别。研究表明,prp1-1调控Rs-AFP2的诱导表达达到了增强辣椒疫霉菌抗性的目的,而且避免了负面效应的发生。     

抗甲霜灵辣椒疫霉菌的环境适合度

摘要:【目的】研究抗甲霜灵辣椒疫霉菌的环境适合度,对于评估甲霜灵防治辣椒疫霉的抗药性风险具有重要意义。【方法】以室内药剂驯化的抗甲霜灵辣椒疫霉菌株Pc2-3为研究对象,分析比较其与原始敏感菌株Pc2的主要生物学特性、生长竞争力、致病力及土壤适合度等环境适合度指标。【结果】Pc2-3孢子囊产生量(3 d后)、孢子囊释放率(24 h后)和游动孢子萌发率(8 h后)分别是Pc2的0.44、0.09和0.54倍。Pc2-3可生长温度和pH范围及最适生长温度与Pc2基本一致,但菌丝生长速率低于Pc2。竞争力测定显示,在胡萝卜(CA)平板培养条件下,Pc2-3生长极显著弱于Pc2。盆栽致病试验显示,Pc2-3对辣椒植株的致病率为14.3%,明显低于Pc2(88.6%)。两者等量混合后接种,辣椒植株的发病率为75.7%,接近单独接种Pc2时的发病率,且所有病株分离出的辣椒疫霉菌均为甲霜灵敏感型。分别将Pc2-3和Pc2游动孢子加入自然土壤培养20 d后,实时定量PCR检测显示Pc2-3数量是Pc2的0.28倍,当土壤中含有300 mg/kg干土的甲霜灵,则前者为后者的0.42倍。此外,2个菌株最适存活土壤温度和湿度基本一致,当土壤温度和湿度利于辣椒疫霉存活时,Pc2-3土壤适合度显著低于Pc2,不利于辣椒疫霉存活时,Pc2-3土壤适合度略低于Pc2。【结论】抗甲霜灵菌株Pc2-3环境适合度弱于原始敏感菌株Pc2。     

接种木霉菌对黄瓜幼苗生长和根际土壤AM真菌侵染的影响

在盆栽试验中分别接种3株长枝木霉菌株Trichoderma longibrachiatum MF-1、MF-2和MF-3,以不接种木霉菌处理作为对照,研究木霉菌接种对土著AM真菌和黄瓜幼苗生长的影响。结果表明,菌株MF-1和MF-2显著提高了AM真菌侵染率和根外菌丝密度,与对照相比,AM真菌侵染率分别提高了26.85%和54.66%,根外菌丝密度分别是对照的3.94和3.76倍。接种菌株MF-2使植株地上部生物量显著提高了39.07%。菌株MF-3显著提高土壤pH和土壤有效磷含量。Pearson相关分析发现,添加木霉菌后,AM真菌侵染率与根外菌丝密度和孢子密度均呈显著正相关关系,土壤pH与植株地上部生物量和土壤有效磷含量均呈显著正相关关系。研究表明,3株长枝木霉与土著AM真菌的联合作用效果有明显差异,菌株MF-1和MF-2显著促进AM真菌生长,菌株MF-2更有利于黄瓜幼苗生长,而菌株MF-3主要改善土壤pH和有效磷含量。将几种木霉菌复合应用,有助于达到联合促生和改善土壤环境的综合效果。     

疫霉侵染下辣椒幼苗消减文库的构建与初步分析

为了分离和鉴定辣椒中疫霉诱导基因,以高抗疫霉病辣椒品种L11为材料,以接种辣椒疫霉菌的幼嫩叶片为处理（tester）,以未接种自然生长的幼嫩叶片为对照(driver),利用抑制性消减杂交技术(suppression subtractive hybridization,SSH)构建了疫霉侵染下辣椒幼苗的消减文库。从消减文库中随机挑取30个阳性克隆,提取质粒进行PCR鉴定,显示插入片段大小大部分集中在200～1 000 bp之间,文库质量良好。随机挑取40个克隆进行测序,共获得35个有效EST序列。经Blastx分析表明：有30个EST与GenBank中其他序列有同源性,5个EST为未知功能序列。已知功能的EST序列分别编码NAC转录因子、丝氨酸/苏氨酸蛋白激酶、P450单加氧酶、叶绿素a/b结合蛋白、谷胱甘肽转移酶、几丁质酶等,这些蛋白涉及抗病信号传递、抗氧化作用、转录调控及光合作用等多种生理过程。本研究为抗病基因克隆和系统研究疫霉侵染下辣椒基因的表达奠定了重要的理论基础。     

铁皮石斛疫病及其病原菌

铁皮石斛疫病2001年发现在浙江义乌栽培田间,是由疫霉菌引起的。在田间,疫霉菌侵染茎基部,引起当年移植苗根腐、植株枯萎和死亡,但侵染2-3年植株幼嫩顶部仅引起项枯症状。通过对病原菌形态学、交配型的观察,以及核糖体DNA ITS序列分析,侵染铁皮石斛的5个分离菌株被鉴定为烟草疫霉菌Phytophthora nicotianae。致病性试验表明,铁皮石斛是烟草疫霉菌的寄主。     

铁皮石斛疫病及其病原菌

铁皮石斛疫病2001年发现在浙江义乌栽培田间,是由疫霉菌引起的。在田间,疫霉菌侵染茎基部,引起当年移植苗根腐、植株枯萎和死亡,但侵染2-3年植株幼嫩顶部仅引起顶枯症状。通过对病原菌形态学、交配型的观察,以及核糖体DNAITS序列分析,侵染铁皮石斛的5个分离菌株被鉴定为烟草疫霉菌Phytophthora nicotianae。致病性试验表明,铁皮石斛是烟草疫霉菌的寄主。     

银杏内生细菌的分离鉴定及抑菌活性初探

【目的】从银杏(Ginkgo biloba)茎叶中分离鉴定内生细菌, 测定其体外抑菌活性及对辣椒果疫病的防治效果。【方法】采用平板对峙法筛选出对辣椒疫霉菌(Phytophthora capsici)有拮抗作用的内生细菌, 并用平板对扣法测定其中一株防治效果较好的内生细菌产生的挥发性物质对辣椒疫霉菌生长的影响。通过生防菌液和病原菌孢子悬浮液喷雾接种辣椒果测定该菌株对辣椒果疫病的防治效果。基于形态特征、生理生化特性、16S rDNA和gyrA基因序列同源性分析鉴定该生防菌株。【结果】从银杏的茎和叶中分离获得9株内生细菌。平板对峙生长试验结果表明, 菌株W5对供试的辣椒疫霉菌、稻瘟病菌(Pyricularia grisea)、水稻纹枯菌(Rhizoctonia solani)、黄瓜枯萎病菌(Fusarium oxysporum)、荔枝霜疫霉菌(Peronophythora litchi)、荔枝酸腐菌(Geotrichum candidum)均有抑制作用, 其中对辣椒疫霉菌、稻瘟病菌和荔枝霜疫霉菌的抑菌效果显著, 抑菌率分别为88.9%、86.3%和90.2%。其产生的挥发性物质能明显抑制辣椒疫霉菌菌丝的生长。对辣椒采后果疫病的防治效果表明, 先喷雾接种W5菌悬液24 h后再接种辣椒疫霉病菌孢子悬浮液的防治效果最好, 可将辣椒果的保鲜期延长2?3 d。该菌株被鉴定为解淀粉芽胞杆菌(Bacillus amyloliquefaciens)。【结论】获得了一株对植物病原菌物有良好防治效果的银杏内生解淀粉芽胞杆菌W5, 对辣椒采后果疫病及其他病原真菌的防治具有潜在应用价值。     

贵州地区木霉菌分离鉴定及对辣椒疫霉的拮抗作用

【背景】辣椒疫霉是一种毁灭性的土传病害,当前主要使用化学合成杀菌剂防治,但容易导致环境污染和食品安全等问题。【目的】筛选可拮抗辣椒疫霉的候选菌株,探究分离菌株拮抗辣椒疫霉的生理生化作用机制。【方法】综合应用形态学、核糖体RNA (rRNA)基因非转录区ITS序列相似性方法鉴定分离菌株,通过对峙实验筛选抑菌效果较高的拮抗菌株,基于比色法测定分离菌株发酵液粗提物对辣椒疫霉菌丝脂质过氧化、纤维素酶、β-葡萄糖苷酶(β-GC)和多聚半乳糖醛酸酶(PG)活性的影响。【结果】从腐木和土壤样品中分离得到11株木霉,分属于绿色木霉(Trichodermavirens)、哈茨木霉(Trichoderma harzianum)、钩状木霉(Trichoderma hamatum)和棘孢木霉(Trichoderma asperellum) 4个种。11株木霉对辣椒疫霉均有一定的抑制作用,抑制率达到90%以上的菌株包括:绿色木霉Tv-1(92.68%)、Tv-2 (95.12%),哈茨木霉Thz-2 (92.68%),钩状木霉Tha-1 (90.24%)。以4株高效木霉的发酵液粗提物处理辣椒疫霉菌丝5 d后,因脂质过氧化产生的丙二醛含量显著增加,分别达到1.20、1.48、2.69和3.16 nmol/g,显著高于对照处理的0.77 nmol/g;与对照组相比,β-GC、PG酶活性显著下降,分别降低了12.28%-64.91%、7.2%-15.5%;同时纤维素酶活性呈上升趋势,最显著组为2.647 U/mL,相对于对照组增加了0.831U/mL。【结论】分离得到4株明显抑制辣椒疫霉菌生长的高效木霉菌,主要通过破坏细胞壁结构、降低致病因子酶活力和增强脂质过氧化等方式起拮抗作用,可为辣椒疫病的生物防治提供理论依据和技术支持。     

木霉对辣椒疫霉菌抑制作用的超微结构与细胞化学

哈茨木霉菌株NF9和TC3对辣椒疫霉病菌具有强烈的抑制作用。超微结构与细胞化学研究表明,木霉菌丝能够缠绕并寄生疫霉菌菌丝,且重寄生作用主要发生在培养基内的菌丝上。但在绝大多数情况下,木霉菌可直接水解和破坏疫霉菌菌丝,说明木霉抑菌作用的主要机制是直接向外分泌水解酶分解疫霉的细胞壁及细胞质,而不是重寄生作用。不同培养基对木霉的重寄生作用有重要影响,减少培养基中葡萄糖含量可以增强木霉的重寄生作用和抑菌效果。此外,在菌落生长后期,疫霉的新生菌丝均可侵染自身的老菌丝。     

卡特兰与丝核菌共培养体系的建立及卡特兰菌根显微结构的研究*

用3个分离自野生卡特兰的丝核菌菌株接种卡特兰组培幼苗,对幼苗生长有不同程度的促进作用,处理苗的鲜重增长率(%)分别是67.5、67.3和62.4,而不接菌的对照仅为49.5,其中KW214菌株处理苗与对照差异达显著水平(α=0.05)。接菌处理后植株的N、P、K含量没有明显增加。在三个接菌处理苗的营养根中均分离获得了原接种真菌,并观察了接种KW214菌株的卡特兰营养根。真菌先侵入根被组织,经通道细胞最后侵染皮层组织细胞,并通过菌丝穿越细胞壁不断地向内延伸扩展。菌丝在皮层组织细胞内形成大量着色较深形状不规则的菌丝结等兰科菌根典型结构,菌丝结在皮层组织中分布不均,多出现在靠外侧的几层皮层细胞内,在被侵染的细胞中,菌丝结常出现在细胞核附近。菌丝结、针状晶体和细胞核在形态和着色反应上有明显区别。菌丝结和细胞核常常相互靠近。从生物量增长、显微结构、重分离接种菌株等三个方面获得的证据表明,已成功建立了卡特兰组培幼苗和丝核菌KW214的共培养体系。     

拮抗辣椒疫霉菌海洋细菌菌株SH-27的筛选鉴定及其防病促生作用

【背景】由辣椒疫霉引起的辣椒疫病是全球辣椒生产中一种毁灭性的病害。近年来生物防治因其具有对环境友好、对人畜安全的特性而倍受关注。【目的】筛选对辣椒具有防病促生作用的海洋细菌菌株SH-27并鉴定其分类地位。【方法】采用稀释分离法和平板对峙法筛选拮抗辣椒疫霉菌的海洋细菌菌株,以发酵液灌根法测定海洋细菌SH-27菌株对辣椒盆栽的防病促生作用;通过形态特征、生理生化测试及多基因序列分析对海洋细菌SH-27菌株进行鉴定。【结果】从分离的142株海洋细菌中筛选获得11株对辣椒疫霉菌具有较强抑制作用的细菌菌株,其中以来自珊瑚的SH-27菌株的抑菌作用最强、抑菌谱广;室内盆栽试验结果表明,SH-27菌株发酵液处理后的辣椒植株根长、株高、茎粗、鲜重、干重均显著高于对照处理。SH-27菌株发酵液灌根处理后,对辣椒疫病4、6和9 d的防效分别为70.81%、66.55%和48.20%。经形态特征、生理生化测试及16S rRNA、gyrA基因序列分析,鉴定SH-27菌株为解淀粉芽孢杆菌(Bacillus amyloliquefaciens)。【结论】海洋细菌SH-27菌株对辣椒具有较好的防病促生效果,具有开发为微生物农药及菌肥的潜力。     

Isolation and Identification of Bacillus amyloliquefaciens IBFCBF‐1 with Potential for Biological Control of Phytophthora Blight and Growth Promotion of Pepper

In this study, 76 bacterial strains were isolated from the rhizosphere soil of pepper. Of these, 23 bacterial isolates capable of inhibiting Phytophthora capsici growth were selected. Among the antagonistic bacteria, one strain, IBFCBF‐1 showed the strongest antagonistic activity, and was identified as Bacillus amyloliquefaciens based on the results of 16S rRNA gene sequence analysis, physiological and biochemical testing, and morphological characteristics. When tested with a dual‐culture method and with laboratory greenhouse studies, the strain IBFCBF‐1 was found to be a potential biocontrol agent for controlling the plant pathogen, P. capsici. Moreover, it showed high efficiency and broad‐spectrum antifungal properties in vitro. Under greenhouse conditions, IBFCBF‐1 could significantly promote the growth of pepper seedlings, and was able to solubilize phosphate, and produce indole acetic acid (IAA) and ammonia. This study clearly demonstrated that IBFCBF‐1 is a potential candidate exhibiting phytophthora blight‐suppressive and plant growth‐promoting effects on pepper.     

Effect of tissue wounding and time of soil inoculation on pepper root rot development

Five-week-old pepper plants with wounds created on stems and roots were transplanted to soils having inoculum of Phytophthora capsici incorporated for different lengths of time. Disease severity (39.99%) on root trimmed seedlings was not significantly different (P ≤ 0.05) from the severity (36.24%) obtained on stem lacerated seedlings. The wound treatments did not result in significantly different rates of lesion extension per day; stem lacerated seedling had the fastest, 1.99 mm/day lesion extension rate, followed by 1.90 and 1.89 mm/day extension rates obtained on root trimmed and unwounded treatments, respectively. However, time of soil inoculation had significant effect on severity; root trimmed and stem lacerated treatments had 46.3% and 39.8% severities, respectively. Tissue wounding × time of soil inoculation interaction did not have significant effect on disease severity; stem lacerated seedlings transplanted to 1-day and 3-day inoculated soils gave highest severity (49.9%), followed by seedlings inoculated at the time of transplantation. Root trimmed seedlings inoculated at the time of transplantation had highest severity (61.1%), while the lowest severity was obtained on seedlings transplanted to 5-day inoculated soil.     

Treatment of Paenibacillus illinoisensis suppresses the activities of antioxidative enzymes in pepper roots caused by Phytophthora capsici infection

Summary The activity of antioxidative enzymes after inoculation of pepper (Capsicum annuum L. Chungok) with a pathogen, Phytophthora capsici (P), the causal agent of Phytophtora blight and dual inoculation of pathogen and an antagonist, Paenibacillus illinoisensis KJA-424 (P+A), were measured and compared with that of non-inoculated (C) roots. Root mortality was significantly reduced by about 84% in P+A treatment compared with P treatment alone. When compared to the non-inoculated (C) roots, malondialdehyde (MDA) concentration gradually decreased by 52.4% in 7 days only in P-treated roots and hydrogen peroxide (H₂O₂) was not significantly affected by the treatment for 5 days but significantly decreased in the P+A-treated roots at day 7. P-treatment continuously induced peroxidase (POD) and superoxide dismutase (SOD), resulting in significant increases of 36.7% and 27.7% at day 7, respectively, compared to the control. In P+A-treated roots, the activities of POD and SOD also increased for 5 days but returned to the control level at day 7. Catalase activity fluctuated but again increased over the 7-day period following P+A inoculation. These results indicate that an antagonist P. illinoisensis KJA-424 alleviated root mortality and suppressed the elevated activities of POD and SOD in the root of pepper plant root caused by P.␣capsici infection.     

Occurrence of symptomless source of Piper yellow mottle virus in black pepper (Piper nigrum L.) varieties and a wild Piper species

Symptomless nature of Piper yellow mottle virus (PYMoV) infection in three varieties of black pepper (Piper nigrum) (Panniyur 1, Panniyur 5 and Panchami) and a wild species of Piper (Piper colubrinum) was confirmed by polymerase chain reaction (PCR) using PYMoV specific primers. The virus could be transmitted from these PYMoV-infected symptomless plants onto symptom producing black pepper cv. Karimunda through mealybug vector, Ferrisia virgata and by graft transmission. About 20–50% seedlings showed typical symptoms of the PYMoV at 30 days after mealybug inoculations while it was 75–94% at 90 days after inoculation. PCR test of the inoculated seedlings confirmed the presence of PYMoV in 50–64%, 76–100% and 80–100% of plants in 30, 60 and 90 days after inoculation, respectively. Similarly, 50–66%, 91–100% and 100% of graft-transmitted plants showed typical symptoms of the disease at 30, 60 and 90 days after grafting. PCR test of the graft-transmitted plants showed 100% PYMoV infection at 60 days after grafting. The results clearly demonstrated the existence of PYMoV-infected symptomless plants that can act as source for secondary spread of the virus in the field.     

高温处理防治黄瓜霜霉病的生理生化机制

以黄瓜感病品种‘长春密刺’为试材,通过室内盆栽试验研究高温对已感染霜霉病菌的黄瓜幼苗生理生化特征的影响.结果显示:(1)在黄瓜幼苗接种霜霉菌后8h,用45℃高温处理90min防治效果最明显.(2)与只接种霜霉病菌的黄瓜幼苗相比,接种霜霉菌后进行高温处理可显著提高叶片叶绿素含量,降低丙二醛含量;与对照相比,接种霜霉菌后进行高温处理可显著提高叶片几丁质酶活性,Western blotting验证了几丁质酶的活性变化.(3)SDS-PAGE结果表明,霜霉菌侵染可诱导一种28kD蛋白表达,高温处理后28kD蛋白的表达量降低.研究结果表明高温处理可能在杀死病原菌的同时,还诱导黄瓜幼苗对霜霉病产生了部分抗性.     

Comparative effects of Glomus mosseae and P fertilizer on foliar mineral composition of Acacia senegal seedlings inoculated with Rhizobium

Summary A factorial experiment with two controlled factors was conducted in the greenhouse with Acacia Senegal seedlings. The substrate was a degraded sandy soil (Dior soil) poor in available P (11 ppm — Olsen). The first controlled factor was soil sterilization, with two levels: (A) sterilized soil; (B) non-sterilized soil. The second factor was fertilization, with six levels: (1) uninoculated control; (2) inoculation with Rhizobium (ORS 1007); (3) inoculation with Glomus mosseae; (4) double inoculation with ORS 1007 and G. mosseae; (5) inoculation with ORS 1007 and 30 ppm phosphorus per plant; (6) inoculation with ORS 1007 and 60 ppm phosphours. The combination of the two factors and their levels led to 12 different plant treatments (A1–A6 and B1–B6). Compared to the control B1, the B5 and B6 treatments containing phosphorus increased: nodule dry weight about 7 times ; leaf dry weight about 4 times ; total N, P and Mg 4–5 times; total K and Ca 3–4 times. The mycorrhizal inoculation had the same positive effect on plant growth and mineral composition but with lower values. Plants inoculated with Rhizobium alone gave the lowest results. The A1 treatment gave lower values than B1. Foliar mineral contents varied within a narrow range (20–30%).     

Colonization of root tissues and protection against Fusarium wilt of rye (Secale cereale) by nonpathogenic rhizosphere strains of Fusarium culmorum

Colonization of rye (Secale cereale) tissues by nonpathogenic rhizosphere Fusarium culmorum isolates DEMFc2 and DEMFc5 and a pathogenic strain DEMFc37, and their effect on plant fresh weight were studied in pot experiments. Both rhizosphere isolates colonized the epidermis and the cortex but were not found in vessels, while the pathogen colonized all three layers of root cells. The numbers of pathogen CFU isolated from plant tissues were much higher than those of the rhizosphere isolates in spite of the same number of macroconidia used as inoculum (1 × 10⁵ g⁻¹ of soil). Inoculation of seedlings with DEMFc2 resulted in a 20% increase, with DEMFc5 in more than a 20% reduction, and with DEMFc37 in a 38% reduction of shoot fresh weight of 14-day-old plants. Pre-colonization of plants with (either of) the rhizosphere isolates and subsequent inoculation with the pathogen resulted in plant weights the same as those observed in plants inoculated with the rhizosphere strain alone. The disease severity index for shoots of plants pre-colonized with DEMFc2 was reduced from class 4 (86% diseased plants) observed for plants inoculated with the pathogen alone to class 2 (average of 8% diseased plants) when pre-treated with the rhizosphere strain. The CFU number of the pathogen isolated from the interior of roots of plants pre-colonized with the rhizosphere isolates was as low as 10% of the number isolated from plants inoculated with the pathogen alone. A study of in vitro interactions between the rhizosphere isolates and the pathogen suggests that changes in plant colonization by the pathogen and its effect on fresh weight of plants pre-colonized with the rhizosphere isolates were not connected with inhibition of its growth by a direct action of the rhizosphere isolates. The results suggest that strain DEMFc2 can be considered as a potential biocontrol agent.