枸杞炭疽病生防菌株筛选、生物功能测定及防治效果

为研发对枸杞炭疽病有良好防治效果的生防制剂,利用枸杞炭疽病菌Colletotrichum acutatum对实验室已分离保存的芽胞杆菌菌株进行室内筛选,并对拮抗效果较好的菌株进行形态学和分子生物学鉴定、病原菌孢子萌发抑制试验、生物学功能测定、稳定性测定、抑菌谱测定以及室内离体防治效果试验和田间防治效果试验。结果表明,菌株F3A对枸杞炭疽病菌有较好的拮抗作用,对枸杞炭疽病菌菌丝的抑制率为62.13%;结合形态学特征、16S rDNA以及gyrA基因序列分析,将菌株F3A鉴定为贝莱斯芽胞杆菌Bacillus velezensis;菌株F3A具有溶解有机磷和无机磷的能力,在含色氨酸和不含色氨酸的金氏培养液中产吲哚乙酸量分别为5.76 mg/L和5.74 mg/L;菌株F3A产蛋白酶和葡聚糖酶的活性较高;菌株F3A连续培养20代后,对枸杞炭疽病菌的抑制率为61.21%,该菌对棉花枯萎病菌Fusarium oxysporum f.sp.vesinfectum、番茄早疫病菌Alternaria solani、黄瓜枯萎病菌F.oxysporum f.sp.cucumerinum、番茄灰霉病菌Botrytis cinerea、番茄叶霉病菌Cladosporium fulvum、茄子菌核病菌Sclerotinia sclerotiorum和黄芪根腐病菌F.solani的抑制率分别为40.71%、53.58%、32.00%、53.00%、79.27%、71.13%和66.08%;菌株F3A发酵液的保护作用明显优于治疗作用,菌株F3A发酵液1倍稀释液室内预防效果为90.32%;喷施菌株F3A发酵液1倍稀释液3 d和7 d后的田间防治效果分别为78.26%和63.19%。表明菌株F3A有作为开发枸杞炭疽病生物农药的潜力。     

基于DNA条形码的红翅大小蠹和黄杉大小蠹分子鉴定

外来有害生物的快速准确鉴定有助于提高口岸检疫效率。红翅大小蠹(Dendroctonus rufipennis)和黄杉大小蠹(D. pseudotsugae)作为大小蠹属的非中国种是我国口岸原木检疫中频繁截获的检疫性有害昆虫。本研究以mtDNA COI基因5′端和3′端序列为标记对红翅大小蠹与黄杉大小蠹的11个样本开展分子鉴定有效性评价。结果显示,当以COI基因5′端和3′端为靶标时,两种大小蠹间的平均遗传距离分别为0.181和0.144,是种内遗传距离的60.3和48倍,且种内、种间遗传距离间无重叠现象,在系统发育树上都能聚为独立的分支,表明mtDNA COI基因5′端和3′端序列均可有效区分红翅大小蠹与黄杉大小蠹。     

松阳县古松树的松材线虫病现状调查与分析

古松树是历史的见证,是文化的承载,其保护工作具有重要意义,但因松材线虫的传播侵染,其生存状况不容乐观。本研究以松阳古松树为对象,基于分子检测技术,对其松材线虫病现状进行了调查与分析。结果表明,有12个乡镇近60%的古松树均已感病,疫情较为严重,需及时开展抗病保护工作。     

花生荚果发育及其调控研究进展

花生是重要的油料与经济作物,在农业种植业结构调整中发挥重要作用。荚果是花生的收获器官,深入 研究花生荚果发育及其调控,可以为高产育种提供理论依据。本文从花生荚果发育过程和内外限制因素的调控作 用,并结合激素、营养元素、遗传学研究以及DNA、RNA等分子调控机制,综述了近年来花生荚果发育相关的研究进 展,为后续研究提供参考。     

四川地区猕猴桃病毒1的RT-PCR检测及外壳蛋白基因序列分析

为了明确近期新西兰报道的侵染猕猴桃的新病毒——猕猴桃病毒1（Actinidia virus 1,AcV-1）在四川地区猕猴桃上的发生情况及其分子特性,采用RT-PCR对来自四川6个地区疑似感染病毒的90份猕猴桃主栽品种‘红阳’和‘金果’的叶片样品进行检测。结果表明,22份样品为AcV-1阳性,检出率为24.4%。将获得的5个AcV-1分离物和已报道的新西兰分离物K75的外壳蛋白（coat protein,CP）基因序列进行比对,结果表明,分离物间核苷酸序列和氨基酸序列的相似性分别为84.8% ~ 97.1%和89.7% ~ 99.6%,其中除邛崃分离物HYH5与新西兰分离物K75的核苷酸序列相似性较高（97.1%）外,其余4个分离物均低于91%。系统进化分析结果显示,这些分离物主要聚集在3个分支上,分离物HYH5与新西兰分离物K75位于同一分支,其余分离物位于另外2个分支。     

番茄褪绿病毒(tomato chlorosis virus)的新寄主:水茄(Solanum torvum Swartz)

Tomato chlorosis virus (ToCV) is a plant virus that is mainly propagated by Bemisia tabaci in a semi-persistent and non-circulative manner.It has a wide range of host plants,and has been reported in many countries,causing serious economic losses in vegetable production.In 2019,we investigated about 10 fields,one ha each in Shouguang,Shandong province (China),and in each field we observed symptoms of interveinal chlorosis on lower leaves of the Solanum torvum Swartz,and a large number of B.tabaci gathered on the back of its leaves.To determine the presence of ToCV,total RNA of S.torvum was extracted followed by RT-PCR.The 1 074 (GenBank accessions number MN545620) and 466 bp (GenBank accessions number MN545621) fragments were gel purified and sequenced.The sequences shared 99.44% and 99.57% similarity with ToCV reference sequence tomato chlorosis virus segment RNA1 (AY903447) and RNA2 (AY903448).The results of insect transmission test confirmed that ToCV can spread from S. torvum to tomato.This study confirms S.torvum as a newly reported host of ToCV.     

An efficient method to produce segregating populations in quinoa (Chenopodium quinoa)

Quinoa offers a promising alternative for staple food, considering its outstanding nutritional value and tolerance to abiotic stresses. To develop breeding programmes in quinoa, a reliable crossing method for increasing the genetic variation is required. In the following study, we aimed to develop segregating populations in quinoa. We tested the efficiency of three different crossing methods (hand emasculation, warm water emasculation and no emasculation). Moreover we developed a two-stage selection strategy based on morphological traits and molecular markers for the selection of hybrid plants. We reported hand emasculation to be the most efficient crossing method, followed by warm water emasculation and no emasculation. Our results demonstrated that crosses in quinoa can be successfully performed, despite its complicated flower structure and high self-pollination rate. Additionally, we developed 30 segregating populations from crosses between accessions of different origins with varying phylogenetic relationship, which offers a promising perspective for quinoa breeding programmes in the future.     

利用广亲和基因S5-n的功能标记鉴定特殊配组类型杂交种纯度研究

“粳不育系/广亲和恢复系”配组方式在浙江省得到了越来越多的应用。广亲和基因S5-n的功能标记可快速检测种子纯度。为验证水稻广亲和基因S5-n功能标记鉴定粳不育系/广亲和恢复系配组方式杂种一代的效果,我们分别将长粳1A和6个恢复系获得的F₁代进行大田统计和分子标记鉴定,结果显示,由于广亲和基因S5-n分子标记不能特异性检测出串粉形成的异形株,导致其鉴定结果较大田统计鉴定结果高1.0~2.0百分点。未来还需要进一步优化广亲和基因分子标记技术的特异性,进而提高分子检测的准确性,这将有助于杂交稻的安全生产。