寡雄腐霉发酵液对烤烟生长的影响及对烟草黑胫病的防治作用

为了探索对烟草黑胫病高效、稳定的生防制剂,利用寡雄腐霉工程菌株制备发酵液,采用温室盆栽试验研究该发酵液对烟苗生长的影响和对烟草黑胫病的防治作用。寡雄腐霉发酵液可提高正常烟苗生物量达22.6%,促进烟苗氮、磷、钾吸收;带病烟苗的发病率和病情指数分别降低了61.6%和64.2%,相对防治效果达64.2%;施用发酵液明显降低带病烟苗的细胞膜透性和丙二醛含量,提高烟叶多酚氧化酶、超氧化物歧化酶和苯丙氨酸解氨酶活性。说明寡雄腐霉发酵液可诱导烟株的防御作用,并提高其抗病能力和促生作用。     

链霉菌Sa-21对烟草黑胫病的防效及抑菌作用研究

烟草疫霉引起的烟草黑胫病,是烟草生产上的重要病害之一。为了明确链霉菌Sa-21防治烟草黑胫病的应用潜力,用盆栽试验测定了链霉菌Sa-21的生防效果,并用生长速率法等手段探讨了链霉菌Sa-21对烟草疫霉的抑菌作用。盆栽试验表明,链霉菌Sa-21菌株发酵液对苗期和成株期烟草黑胫病有较好的控制效果,最高防效可达98.39%。菌株Sa-21粗浸膏对烟草疫霉菌丝生长的抑菌中浓度为56.1 μg/mL,50 μg/mL的粗浸膏处理后可以降低50%的菌丝生物量。菌株Sa-21粗浸膏对烟草疫霉孢子囊的产生、游动孢子释放、休止孢萌发以及细胞膜透性均有抑制作用,100 μg/mL的粗浸膏基本能够完全抑制孢子囊的产生,并且对游动孢子释放的抑制率达50%以上;粗浸膏浓度为150 μg/mL时,对休止孢萌发的抑制率达94.35%;随着粗浸膏浓度增加,菌丝细胞膜的透性也会加大。研究结果表明,链霉菌Sa-21代谢物对烟草疫霉的生长繁殖产生抑制作用,并为链霉菌Sa-21生防菌剂的开发及其对烟草黑胫病的防治提供了理论依据。     

烟草疫霉拮抗细菌B44R-1的筛选及其生防效果

为获得烟草疫霉Phytophthora nicotiana的优良拮抗菌,从烟草根际土壤和根系中分离对烟草疫霉具有较好拮抗作用的菌群,并从中筛选具有较强抑菌效果的拮抗菌株。通过形态学、生理生化试验、16S rDNA基因测序分析鉴定拮抗菌株种属,评价其防病效果及对烟草的促生作用。结果表明,从烟草根际土壤和根系分离得到拮抗菌群39个,并从中筛选得到拮抗效果较好的菌株B44R-1,初步鉴定其为皮特不动杆菌Acinetobater pittii。菌株B44R-1对烟草黑胫病的防效达到55.37%,对烟株根系生长发育影响明显,烟株鲜重、干重、株高、茎围、叶数和最大叶面积相比对照均有提高。本研究筛选获得对烟草黑胫病菌的拮抗菌不动杆菌,对烟草黑胫病防治效果和促生作用显著,具有较好的生防潜力。     

荧光假单胞菌拮抗菌株对烟草疫霉的抑菌机制及控病效果

为探讨烟草根际生防细菌对烟草疫霉Phytophthora nicotianae的抑菌机制,从重庆地区连作烟田健康烟株根际土壤分离获得5株荧光假单胞菌Pseudomonas fluorescens拮抗菌株。通过平板对峙及代谢产物抑菌试验筛选对烟草疫霉具有高效拮抗作用的菌株,其中,P-72-10菌株抑菌效果最强,抑菌带半径达13.0 mm,相对抑制率为68.57%,且该菌株代谢产物对烟草疫霉菌丝生长有明显的抑制作用,相对抑制率达25.39%～46.03%;显微观察发现该菌株可引起烟草疫霉菌丝的分支增多,菌丝顶端膨大呈畸形,多数菌丝中间或顶端细胞的细胞壁加厚、原生质浓缩和产生类似厚壁孢子的细胞。在温室盆栽条件下P-72-10菌株对烟草黑胫病也表现出良好的控病效果,对抗病和感病品种的相对防效分别为53.57%和66.37%。     

拮抗微生物菌剂对烟草黑胫病的防治效果

采用土根本、恩格兰、三炬耕多邦和中农绿康4种微生物菌剂,在黑胫病发生具有代表性的区域河南南阳进行试验,检验4种菌剂对烟草黑胫病的实际控制效果及对烟草生长的影响,并筛选出有效的微生物菌剂。结果表明,施用4种微生物菌剂均可提早烟草生育期,但促生效果好的菌剂烟叶成熟时间较晚。其中,施用三炬、土根本、中农绿康菌剂可以提前烟株的生育期,比对照处理提前2~3 d。三炬耕多邦微生物菌剂处理的叶面积及叶面积系数优于其他处理;中农绿康菌剂可促进烟株根系生长。施用菌剂处理的烟株较对照处理黑胫病发展较慢,其中,恩格兰菌剂对黑胫病有较好的控制效果,而三炬菌剂控制效果较差。     

拮抗细菌B8对烟草黑胫病菌的抑制作用及其菌株鉴定

从烟草根际土壤中分离到对烟草黑胫病菌及其它植物病原菌具有抑制作用的菌株B8,平板对峙培养抑菌带内菌丝畸形、原生质凝集或外渗。其发酵原液和发酵液的无菌滤液均能抑制烟草黑胫病菌和蜡状芽孢杆菌;离体叶片接种法测定其发酵液对烟草黑胫病的防效,结果表明预防作用达100%。室内盆栽试验表明B8菌株发酵液对烟草黑胫病的预防作用可达78.1%,优于治疗作用。该菌菌体杆状,芽孢侧生、椭圆形,经形态学、生理生化性状和16S rDNA序列测定,将其鉴定为侧孢短芽孢杆菌。     

拮抗真菌HTC的鉴定及其对辣椒疫病的生物防治潜力

为明确拮抗真菌HTC对辣椒疫霉Phytophthora capsici的拮抗机制,采用平板对峙、形态学鉴定和18S rDNA序列比对分析等方法对菌株HTC进行了鉴定,并研究其发酵液与抗生物质粗提液对辣椒疫霉不同发育阶段的影响。经鉴定,菌株HTC为金色毛壳菌Chaetomium aureum。在平皿对峙试验中,菌株HTC的红色分泌物能抑制辣椒疫霉菌丝的生长,抑制率为59.1%,后期HTC菌丝可缠绕并降解辣椒疫霉菌丝。发酵液与抗生物质粗提液对辣椒疫霉不同发育阶段均有抑制作用,发酵液对辣椒疫霉菌丝生长的抑制率高达97.58%,对辣椒疫病的防治效果均高于70%。浇灌发酵液后,可提高辣椒苗的苯丙氨酸解氨酶、过氧化物酶、多酚氧化酶的活性,并明显促进辣椒苗生长,鲜重和干重增加32.27%和18.09%。研究表明,金色毛壳菌菌株HTC是一株具有开发潜力的生防菌株。     

烟草尖孢镰刀菌拮抗真菌的筛选鉴定及促生作用研究

为获得烟草镰刀菌根腐病拮抗真菌菌株,试验以河南省豫中烟区烟草根际土壤为试材,以主要致病菌尖孢镰刀菌Fusarium oxysporum为主要靶标,采用稀释涂布平板法分离获得土壤真菌371株,平板对峙培养法测定获得1株具有明显抑制效果的拮抗菌株,利用形态学和分子生物学的方法将其鉴定为棘孢木霉Trichoderma asperellum Tr-0111。抑制效果测定表明,该菌株对尖孢镰刀菌的抑制率最高可达93.13%,对根串珠霉菌、拟茎点霉、链格孢菌等其他8种烟草病原菌均具有较强的抑制效果。促生作用测定结果表明,菌株发酵液使烟草种子萌发率提高5.34%,烟苗根长增长率为62.39%,对盆栽烟草的最大叶面积和地上部鲜重也具有显著的促生效果。为进一步相关机理的研究和生防菌剂的研制奠定了基础。     

多粘类芽胞杆菌LB-9的诱变及抑菌防病效果研究

为获得对烟草疫霉菌生防效果更佳的拮抗菌株，对多粘类芽胞杆菌LB-9进行基因诱变。利用原生质体电转化法，构建了菌株LB-9的Tn-5转座插入突变体库，获得约2000个转化子，通过平板对峙法筛选出对烟草疫霉菌拮抗能力增强且效果稳定的突变菌株3个，其中编号为A13的突变菌株对烟草疫霉菌的抑制效果达到80%以上，与原始菌株LB-9的抑菌率相比提高了20%以上。采用室内盆栽接种法研究了正突变菌株A13对烟草黑胫病的防控效果，并利用实时荧光定量PCR法初步分析了其诱导烟株体内抗病相关基因的表达。结果表明，正突变菌株A13处理烟株7 d后，对烟草黑胫病的防效高于原始菌株LB-9，防效可达80%以上，同时可诱导烟株体内不同信号通路中抗性相关基因的上调表达。本研究为多粘类芽胞杆菌插入诱变育种方法研究提供了理论支撑，对烟草黑胫病的生物防治具有重要意义。     

几丁寡糖对烟草黑胫病的控制效应及其机制

在室内条件下,采用菌丝生长速率法测定了几丁寡糖对烟草黑胫病菌的抑制作用,继而在温室盆栽和人工接种条件下,分别测定几丁寡糖、木霉、几丁质、几丁寡糖+木霉、几丁寡糖+木霉+几丁质等5种处理对烟草黑胫病的防治效果。结果表明,几丁寡糖在离体条件下对烟草黑胫病菌菌丝生长无抑制作用,但在盆栽试验中对烟草黑胫病具有显著防治效果。5种处理中,几丁寡糖单独处理对烟草黑胫病的防治效果最高,为57.81%,其次为几丁寡糖+木霉+几丁质和几丁寡糖+木霉处理,分别为53.49%和52.49%。在温室条件下对烟草植株施用几丁寡糖及人工接种黑胫病菌后10天内,几丁寡糖能显著提高烟草体内的SOD、POD、PPO和几丁质酶活性,且活性峰值分别比对照提高96.30%、136.36%、10.34%和9.10%。     

Evaluating diverse systems of tobacco genetic resistance to Phytophthora nicotianae in Yunnan,China

Black shank, caused by the soilborne pathogen Phytophthora nicotianae, is one of the most devastating diseases affecting tobacco production in China. The most effective strategy for reducing economic loss from this pathogen is development and use of resistant tobacco varieties. Multiple sources and systems of resistance have been developed in the Western Hemisphere; however, populations of P. nicotianae are variable around the world, including the predominance of different races. Different P. nicotianae isolates may react differently on tobacco plants with different systems of resistance, a possibility that could complicate the breeding of cultivars with resistance that is effective in different tobacco production regions worldwide. The objective of this research was to evaluate an array of tobacco germplasm possessing different systems of genetic resistance to black shank disease in tobacco-growing regions of Yunnan, China. Resistance types included simply inherited resistance mechanisms introgressed from wild Nicotiana relatives and polygenic partial resistance systems of N. tabacum origin. The loci of Wz exhibited high level resistance to black shank in the five diverse disease environments in Yunnan, China. K326 Php/−Wz/− genotype and Beinhart 1000 exhibited the greatest levels of resistance in both 2015 and 2016. Field observed results for 13 tobacco genotypes were highly correlated with those tested in growth chamber evaluation. These findings suggest that both Wz− and Beinhart 1000-mediated resistance have important commercial value in flue-cured tobacco breeding programmes in China. Cultivars developed for black shank resistance in China may also have utility in other tobacco-growing areas.     

烟草黑胫病拮抗根际芽胞杆菌FB-16的筛选鉴定及其抑菌活性

为获得对烟草黑胫病有较强生防效果的拮抗细菌,从健康烟草根际采集30份土壤样品,分离纯化得到347株细菌,经病原真菌定向筛选后得到1株对烟草黑胫病菌等病原真菌拮抗活性较好的细菌FB-16,其对烟草黑胫病菌的抑菌带宽为23mm。采用菌丝生长速率法、作用机制试验、温室防病试验测定FB-16的抑菌作用,并通过形态学特征、生理生化特征及16S rDNA序列分析对菌株进行鉴定。结果显示,菌株FB-16发酵液对烟草黑胫病菌菌丝生长抑制率为95.96%;其代谢产物对烟草黑胫病菌菌丝有致畸作用;菌株FB-16为解淀粉芽胞杆菌Bacillus amyloliauefaciens(Gen-Bank登录号为JN245982);饱和度25%硫酸铵获得的抑菌物质对烟草黑胫病菌的抑菌活性较高,抑菌圈直径达42.00 mm;FB-16活性产物处理的烟草植株在接种烟草黑胫病菌7天后的防治效果为69.96%。表明菌株FB-16在烟草黑胫病生物防治中具有潜在的利用价值。     

烟草黑胫病菌培养特性的研究

研究了云南烟草黑胫病菌在不同培养基、不同温度的生长情况及不同菌龄与不同诱导时间孢子囊的产生数量。结果表明,菌株在8种供试培养基中,以燕麦培养基和选择性培养基上菌落生长最好,其次为胡萝卜培养基,在番茄汁和马铃薯培养基上生长最差。同一菌株在不同培养基上产孢量不同、产生的孢子囊大小亦有所不同。05P226菌株在玉米培养基上产孢量最高;05P55菌株在燕麦培养基上产孢量最高,在番茄汁培养基上产生的孢子囊最大,而05P62菌株在燕麦培养基上产孢量最高,在烟叶汁培养基上产生的孢子囊最大。在30℃菌丝生长速率最高,其次为28℃,以35℃生长最差。供试3个菌株间生长差异显著,以05P226生长最好,05P55菌株次之,05P62生长最差。05P226、05P55菌株皆以培养14d、诱导72h产孢量最高,最适宜试验中产孢培养。     

Pathogenicity and RAPD analysis of Phytophthora nicotianae pathogenic to pepper in Tunisia

Nine isolates of Phtophthora nicotianae were isolated from infected pepper plants. Their pathogenicity was studied in Capsicum annuum in comparison with P. nicotianae isolates from tomato and tobacco. The pathogenicity test showed that pepper isolates of P. nicotianae are adapted to their host. Banding patterns obtained by RAPD analysis with six oligonucleotide primers revealed polymorphism that grouped the isolates independently of the plant host. The polygenic dendrogram showed that pepper isolates were more similar to tomato isolates than to tobacco isolates. The RAPD bands of 1300 and 1500 bp, detected with primers OPD-01 and OPD-10, respectively, appeared specific to the most pathogenic pepper isolates. The OPK-08-1950 seems specific to the isolates of P. nicotianae from tomato. These results suggest that host specified might occur in P. nicotianae and that may be due to interspecific hybridization events resulting in novel pathogenic behavior.     

Molecular and Pathogenicity Characteristics of Phytophthora nicotianae Responsible for Root Necrosis and Wilting of Pepper (Capsicum annuum L.) in Tunisia

Isolates of Phytophthora from pepper, produced in Tunisia, were characterised according to molecular and pathogenicity criteria. Polymerase chain reaction amplification of the ITS1 region in the ribosomal DNA resulted in different sized fragments. The pepper isolates and P. nicotianae yielded a fragment of 310bp that distinguished it from P. capsici with a fragment of 270bp. The ribosomal RNA gene amplicons of both internal transcribed spacers and the 5.8 S of the pepper Phytophthora and P. nicotianae were digested with 8 endonucleases. The patterns generated, with the 2 enzymes that cut, were identical for both taxa. This molecular analysis corroborated the morphological and biological characteristics and suggests strongly that the isolates of Phytophthora from pepper belong to the species P. nicotianae. Inoculation of pepper, tomato, eggplant and tobacco plants with the isolates of P. nicotianae from pepper showed they were highly pathogenic on pepper but not on tobacco, while their pathogenicity was weak on tomato and eggplant and was associated with atypical symptoms not observed in the field. These pathogenicity tests suggest that pepper isolates of P. nicotianae are particularly adapted to their host and may thus constitute a forma specialis of P. nicotianae.     

Phytophthora root rot of sweet pepper

Phytophthora capsici proved to be the causal agent of a root and crown rot of sweet pepper in the Netherlands.P. capsici was pathogenic on sweet pepper, tomato and sometimes on eggplant but not on tobacco Xanthi. Of these test plants only tomato was infected byP. nicotianae.No different symptoms in plants infected with eitherP. capsici orP. nicotianae were found. Dipping the roots of tomato and sweet pepper plants in a suspension ofP. capsici resulted in a more severe attack than pouring the suspension on the stem base.Resistance in tomato toP. nicotianae did not include resistance toP. capsici. A method to distinguishP. capsici fromP. nicotianae after isolation from soil is described. Both species were able to infect green fruits of tomato and sweet pepper.p. capsici survived in moist soil in the absence of a host for at least 15 months.Samenvatting Phytophthora capsici bleek de oorzaak te zijn van een voet-en wortelrot in paprika op twee bedrijven in 1977 in Nederland.P. capsici was pathogeen op paprika, tomaat en soms op aubergine maar niet op tabak Xanthi.P. nicotianae tastte van deze toetsplanten alleen tomaat aan. Verschillen in symptomen tussenP. nicotianae enP. capsici werden bij tomaat niet waargenomen.Het dompelen van de wortels in eenP. capsici suspensie gaf een ernstiger aantasting dan het begieten van de wortelhals met deze suspensie.Resistentie in tomaat tegenP. nicotianae bleek geen resistentie tegenP. capsici in te houden. P. capsici kan in grond worden aangetoond door groene paprikavruchten als vangsubstraat te gebruiken.P. capsici enP. nicotianae kunnen beide zowel vruchten van tomaat als paprika aantasten. P. capsici overleefde een periode van 15 maan den in vochtige grond waarop geen waardplant werd geteeld.     

<Emphasis Type="Italic">Pythium</Emphasis> and <Emphasis Type="Italic">Phytophthora</Emphasis> species associated with root and stem rots of kalanchoe

Pythium and Phytophthora species were isolated from kalanchoe plants with root and stem rots. Phytophthora isolates were identified as Phytophthora nicotianae on the basis of morphological characteristics and restriction fragment length polymorphism (RFLP) analysis of the rDNA-internal transcribed spacer regions. Similarly, the Pythium isolates were identified as Pythium myriotylum and Pythium helicoides. In pathogenicity tests, isolates of the three species caused root and stem rots. Disease severity caused by the Pythium spp. and Ph. nicotianae was the greatest at 35°–40°C and 30°–40°C, respectively. Ph. nicotianae induced stem rot at two different relative humidities (60% and >95%) at 30°C. P. myriotylum and P. helicoides caused root and stem rots at high humidity (>95%), but only root rot at low humidity (60%).     

Acquired resistance triggered by elicitins in tobacco and other plants

Elicitins are a family of proteins excreted byPhytophthora spp. They exhibit high sequence homology but large net charge differences. They induce necrosis in tobacco plants which then become resistant to the tobacco pathogenPhytophthora parasitica var.nicotianae. In stem-treated plants, resistance was not restricted to the site of elicitin application, but could be demonstrated by petiole inoculation at all levels on the stem. Resistance was already maximum after two days and lasted for at least two weeks. It was effective not only towardsP. p. var.nicotianae infection, but also against the unrelated pathogenSclerotinia sclerotiorum. In contrast to dichloroisonicotinic acid, an artificial inducer of systemic acquired resistance, which was increasingly effective with doses ranging from 0.25 to 5mole per plant, the basic elicitin cryptogein exhibited a threshold effect, inducing near total resistance and extensive leaf necrosis above 0.1 nmole per plant. Between 1 and 5 nmole, acidic elicitins (capsicein and parasiticein) protected tobacco plants with hardly any necrotic symptom. Elicitins exhibited similar effects in various tobacco cultivars andNicotiana species, although with quantitative differences, but induced neither necrosis nor protection in other SolanaceÆ (tomato, petunia and pepper). Among 24 additional species tested belonging to 18 botanical families, only some BrassicaceÆ, noticeably rape, exhibited symptoms in response to elicitins, in a cultivar-specific manner. Elicitins appear to be natural specific triggers for systemic acquired resistance and provide a tool for unraveling the mechanisms leading to its establishment.Abbreviations AR acquired resistance - HR hypersensitive response - INA 2,6-dichloroisonicotinic acid - Ppn Phytophthora parasitica var.nicotianae - SAR systemic acquired resistance     

烟草黑胫病拮抗菌的筛选、鉴定及发酵条件优化

为获得对烟草黑胫病（tobacco black shank）具有较好拮抗作用的菌株,从食腐昆虫美洲大蠊Periplaneta americana肠道分离纯化得到1株对烟草黑胫病具有较强抑制作用的D5-8菌株,拟进一步明确该菌株的分类地位,优化其发酵条件并测定其对烟草黑胫病的防治效果。利用形态特征、生理生化特性观察及16S rRNA基因序列分析对D5-8菌株进行鉴定;以细菌发酵液OD₆₀₀值及对病原菌的抑制率为指标,对其发酵培养基和发酵条件进行单因素试验及正交试验;通过室内盆栽试验,明确菌株D5-8对烟草黑胫病的防治效果。结果表明,经平板对峙试验发现菌株D5-8对烟草寄生疫霉的抑制率达66.80%;通过形态特征和生理生化特征初步确定菌株D5-8为芽胞杆菌属Bacillus,结合16S rRNA基因序列分析鉴定菌株D5-8为特基拉芽胞杆菌Bacillus tequilensis;其最适培养基：牛肉浸膏8 g,酵母浸粉5 g,麦芽糖10 g,蒸馏水1000 mL;最佳的发酵条件为温度28℃、初始pH 6、转速210 r/min、装液量30 mL、接种量2%、培养时间60 h、光照时间4 h;盆栽试验结果表明,发酵条件优化后D5-8发酵液（10⁸cfu/mL）对烟草黑胫病的保护防效和治疗防效可达66.89%和53.72%,均高于原始发酵液的61.84%和51.83%。研究结果为特基拉芽胞杆菌D5-8生防菌剂的开发及其对烟草黑胫病的防治应用提供了理论依据。