6 个不同品种荔枝果肉内生细菌群落多样性的高通量测序分析

【目的】内生菌在植物生长发育中发挥重要作用,分析不同品种荔枝果肉内生细菌群落结构及多样性,挖掘和利用潜在荔枝内生菌种资源,为进一步研究荔枝与内生菌互作关系提供参考依据。【方法】以 6 个不同品种荔枝的果肉组织为材料,PCR 扩增 16S rDNA 的 V3~V4 区,利用 MiSeq 高通量测序技术分析果肉组织内生细菌在门、科、属和种分类水平上的群落组成及优势菌群,结合 Alpha 多样性分析评估内生细菌群落多样性。【结果】对 6 个品种荔枝果肉内生细菌 16S rDNA 的 V3~V4 区进行扩增,共获得 2 139 086 条序列,其平均长度为 376 bp。不同品种荔枝果肉内生细菌群落在相对丰度和多样性上无显著差异。在门分类水平,变形菌门为主要优势细菌门类,其次为放线菌门。在科、属和种分类水平上,不同品种荔枝内生菌群落结构相似,但相对丰度占比不同。差异菌群分析结果显示,假单胞菌属（Pseudomonas）、果胶杆菌属（Pectobacterium）、苍白杆菌属（Ochrobactrum）和迪基氏菌属（Dickeya) 在优良品种‘鹅蛋荔’‘糯米糍’和‘观音绿’中显著富集,根瘤菌属（Bradyrhizobium）和变形菌属（Snodgrassella）只在‘鹅蛋荔’中富集。根据菌群相对丰度进行聚类分析,‘观音绿’‘糯米糍’和‘鹅蛋荔’的相似性更高。Alpha 多样性分析结果表明,6 种荔枝果肉内生菌群仅在丰度和多样性上存在差异,但未达到显著水平。【结论】该研究首次分析了 6 个不同品种荔枝果肉内生细菌的群落结构,并在优良荔枝品种中发现特有的微 生物类群富集现象,可为后续提升荔枝品质、开发利用内生菌提供理论依据和重要参考。     

铺地木蓝对肇庆地区柑橘园土壤养分及细菌群落的影响

【目的】探究铺地木蓝在柑橘果园种植 1 年后对杂草、0~20 cm 土层土壤养分含量和土壤细菌多样性的影响。【方法】设置自然生草（CK1）、土壤覆盖遮草布（PD1）、土壤覆盖银黑地膜 + 种植铺地木蓝（PD2）、种植铺地木蓝（PD3）4 个处理,1 年后调查杂草种类、测定土壤理化性质（pH、有机质、全氮、碱解氮、全磷、速效磷、全钾和速效钾）和土壤细菌群落情况。【结果】 PD2 处理土壤全氮（0.86 mg/g）、全磷（0.78 g/kg）、速效磷（23.84 mg/kg ）、全钾（11.91 g/kg）、有机质（34.82 g/kg）含量最高;PD2 处理土壤全氮和碱解氮含量比 PD1处理的分别增加了 0.37、27.43 mg/kg,PD1 处理土壤全磷含量最低（0.41 g/kg）,PD3 处理速效磷（10.67 mg/kg）和有机质（25.99 g/kg）含量最低;PD1~PD3 处理的土壤全钾含量均大于 CK1 处理,速效钾含量则相反;杂草调查结果表明 PD1、PD2 处理均可很好地抑制杂草的生长。与 CK1 相比,PD1~PD3 处理均可降低土壤细菌群落多样性,但不影响细菌群落分布均匀性。PD2 和 PD3 处理的土壤细菌群落结构和丰度较相似,表现为变形菌门（Proteobacteria）相对丰度降低,绿弯菌门（Chloroflexi）、酸杆菌门（Acidobacteria）、浮霉菌门（Planctomycetes）、罗库菌门（Rokubacteria）、芽单胞菌门（Gemmatimonadetes）等有益细菌的相对丰度增加;其中 PD2 处理的优势菌属为 MND1（3.47%）、Sh765B-TzT-35（4.37%）,PD3 处理的优势菌属为 MND1（4.29%）。从 PD1 处理土壤中检测到视为土壤环境恶化的标志类群异常球菌 - 栖热菌门（5.10%）。【结论】柑橘果园行间道覆盖地膜后再种植铺地木蓝的综合表现最好,可以增加土壤养分和土壤中有益细菌群落的相对丰度。     

植物染色体重排在作物遗传改良中的应用研究进展

染色体重排是一种可能导致DNA片段丢失、重复、易位和倒位的机制,从而改变基因组结构,为创造新的变异性状提供可能。植物染色体重排事件的准确鉴定有助于更深入地理解植物基因组的结构、功能及它们在植物演化和作物育种中的作用。该文深入探讨了植物染色体重排的基本概念,介绍了植物染色体重排的自然发生和人工诱导的技术方法,阐述了植物染色体重排的细胞生物学、分子遗传学和高通量测序鉴定方法。同时,系统总结了植物染色体重排技术在作物遗传育种中的应用,结合具体实践,着重强调了染色体重排技术在提高农作物的遗传多样性、改良农作物的重要性状、增强农作物的环境适应性等方面极具优越性。然而,目前染色体重排的发生概率较低,技术上仍存在挑战,需要更多精准的工具和策略来实现染色体片段的精准定位和重排。通过全面了解染色体重排及其相关技术,研究人员和育种家可以更好地利用植物基因组,为全球粮食安全和环境可持续发展提供创新解决方案。相关研究不仅为深入认识植物基因组提供新途径,也为未来创新作物育种奠定坚实基础。通过挖掘植物基因组的多样性和可塑性,染色体重排技术有望为培育高产、优质、多抗的农作物新品种提供更多可能性,对解决全球日益严峻的...     

基于 RAD-seq 的菜心 InDel 标记开发及应用

【目的】开发多态性丰富的的InDel分子标记,为菜心育种提供研究基础。【方法】以Chiifu-401-42的基因组序列为模板,利用4份菜心材料的RAD-seq重测序数据,在全基因组范围内鉴定InDel位点。利用生物信息学方法筛选4份菜心材料间具有潜在多态性的InDel位点,挑选分布于10条染色体的80个InDel位点设计引物,对55份菜心种质材料进行遗传多样评价。【结果】通过与参考基因组序列比对,在4份菜心材料的重测序数据中共鉴定出84 510个InDel位点,其中插入/缺失长度大于5 bp的3 609个InDel位点在4份菜心材料间具有潜在多态性。挑选80个InDel位点进行PCR扩增验证,58个（72.5%）在4份测序样品中具有多态性,在55份菜心种质材料中检测到133个等位位点,多态性信息含量（PIC）为0.263～0.618,平均值为0.443。基于InDel标记的检测结果可知,55份菜心种质的遗传相似系数在0.366～0.756,平均值为0.570;在遗传相似系数为0.564时55份菜心种质被分为4个类群,但各类群间的耐热性没有明显差异。【结论】本研究开发的InDel标记具有...     

长春市广场树木生长状况与园林植物多样性相关关系的研究

对长春市广场树木生长状况和园林植物多样性之间的关系研究表明:广场树木生长状况的数量化值与用Shannon-Wiener指数表示的园林植物多样性之间有良好的相关关系,相关方程为:G=1.972 2 2.667 86Ht-0.644 7Ht2,相关系数R=0.908 57,估计可靠性P=99.9%。     

施氮量对番茄根际土壤细菌群落及氮转化功能的影响

为探究施氮量对番茄根际土壤细菌群落组成、结构和氮转化功能的影响,以设施番茄根际土壤为研究对象,通过盆栽试验,设置不施氮处理(CK,0 kg·hm^-2)、低氮处理(L,115 kg·hm^-2)、中氮处理(M,225 kg·hm^-2)和高氮处理(H,450 kg·hm^-2),采用高通量测序技术与FAPROTAX(Functional annotation of prokaryotic taxa)功能预测相结合的方法进行研究。结果表明,放线菌门(Actinobacteria)为主要优势细菌门,相对丰度为35.99%～40.06%,与CK处理相比,M处理放线菌门(Actinobacteria)的相对丰度显著提高,而H处理放线菌门的相对丰度显著降低。M处理的根际土壤细菌群落中,有益细菌属Gaiella、Geminicoccus、红杆菌属(Solirubrobacter)、节杆菌属(Arthrobacter)的比例高于其他处理。施氮量变化未对根际土壤细菌群落的α-多样性产生显著影响,但显著改变了氮转化功能类群的...     

北京八达岭植物群落多样性特征分析

根据34个样地的调查资料,分析了该地区森林植物群落物种多样性的特征:群落内各层物种丰富度指数的大小为草本层>灌木层>乔木层;多样性指数的大小为乔木层<灌木层和草本层。灌木层与草本层的多样性指数随林分郁闭度变化而变化,在林分郁闭度为25%的侧柏黄栌混交林中,灌木层的多样性指数和丰富度指数小于草本层;在郁闭度53%的杂木林中,灌木层和草本层的多样性指数接近;在郁闭度53%以上的各个群落内,草本层的多样性指数和丰富度指数基本上都大于灌木层。人工林中的物种多样性变化多样,明显低于天然林,林分层次单一,更新不良,缺乏灌木层和地被植物,生态系统很不稳定。     

Multilocus sequence typing analysis of Italian Xanthomonas campestris pv. campestris strains suggests the evolution of local endemic populations of the pathogen and does not correlate with race distribution

Xanthomonas campestris pv. campestris (Xcc) is the causal agent of black rot in Brassicaceae. It is widespread in Italy and severe outbreaks occur under conditions that favour disease development. In this study a multilocus sequence typing approach (MLST) based on the partial sequence of seven loci was applied to a selection of strains representative of the main areas of cultivation and hosts. The aim was to investigate whether the long tradition of brassica crops in Italy has influenced the evolution of different Xcc populations. All loci were polymorphic; 14 allelic profiles were identified of which 13 were unique to Italian strains. Based on the seven loci, the most common genotype within the Italian Xcc strains (AP1) was also the most representative genotype found in worldwide Xcc strains. This genotype was included in a new clonal complex in addition to three other clonal complexes already identified in Xcc populations. The phylogenetic reconstruction using a concatenated dataset of four conserved protein-coding genes, dnaK, fuyA, gyrB and rpoD, showed that the Italian strains belonged to two genetic groups. Physiological races were also investigated for the first time in Italy. The race structure of Xcc was determined by inoculating eight differential Brassica lines belonging to five species and showed that, in Italy, race 4 is the most widespread, followed by races 1 and 6. No correlation was found between allelic profiles, host of isolation, geographical origin and races, although a prevalent race was identified within the same clonal complex.     

Genetic diversity and aggressiveness of Calonectria pteridis in Eucalyptus spp.

Calonectria leaf blight, caused by Calonectria pteridis, is currently one of the main foliar diseases in eucalypt plantations in Brazil. In warm and high rainfall regions, the disease can be a limiting factor for eucalypt production when planting susceptible genotypes. The most effective method for controlling this disease in the field is the use of resistant genotypes, which requires knowledge of the genetic variability and aggressiveness of the pathogen population for effective deployment of plant resistance. This work evaluated the genetic diversity and aggressiveness of C. pteridis populations obtained from infected eucalypt plants in Monte Dourado (Pará state) and Imperatriz (Maranhão state), Brazil. To study the genetic diversity, 16 ISSR primers were tested, five of which amplified polymorphic, reproducible and informative bands. Thirty-one closely related genotypes were identified from 84 isolates studied, indicating that the population has a low genetic diversity. The aggressiveness of seven isolates, selected according to geographic origin and their clustering in the ISSR-based dendogram, was determined by inoculation of a hybrid Eucalyptus grandis × E. urophylla clone under controlled conditions. Disease severity was assessed by both measuring the percentage of plant defoliation and assigning a score according to a diagrammatic scale of symptoms. A high correlation between the two evaluation methods was observed, which revealed significant differences in aggressiveness among the isolates. The diagrammatic scale is recommended for disease evaluation because results are obtained much faster, before the occurrence of severe defoliation. No correlation between clustering in the ISSR-based phylogenetic analysis and aggressiveness was observed.     

Cryptic species and population genetic structure of Plasmopara viticola in São Paulo State,Brazil

Downy mildew (Plasmopara viticola) is one of the most important diseases in grape-growing areas worldwide, including Brazil. To examine pathogen population biology and structure, P. viticola was sampled during the 2015/16 growing season from 516 lesions on nine grape cultivars in 11 locations in subtropical areas of São Paulo State, Brazil. For identification of cryptic species, a subsample of 130 isolates was subjected to cleaved amplified polymorphic sequence (CAPS) analysis, and for 91 of these isolates the ITS1 region was sequenced. These analyses suggest that the population of P. viticola in São Paulo State consists of a single cryptic species, P. viticola clade aestivalis. Seven microsatellite markers were used to determine the genetic structure of all 516 P. viticola isolates, identifying 23 alleles and 55 multilocus genotypes (MLGs). Among these MLGs, 34.5% were clonal and represented 93% of the isolates sampled. Four dominant genotypes were present in at least five different locations, corresponding to 65.7% of the isolates sampled. Genotypic diversity (Ĝ = 0.21–0.89) and clonal fraction (0.58–0.96) varied among locations (populations). Most populations showed significant deviation from Hardy–Weinberg expectations; in addition, excess of heterozygosity was verified for many loci. However, principal coordinate analysis revealed no clusters among locations and no significant isolation by distance was found, suggesting high levels of migration. The results indicate that downy mildew epidemics result from multiple clonal infections caused by a few genotypes of P. viticola, and reproduction of P. viticola in São Paulo State is predominantly asexual.