摩西管柄囊霉Funneliformis mosseae对连作大豆分枝期根系AM真菌群落结构的影响

本文研究摩西管柄囊霉Funneliformis mosseae对短期连作3个大豆品种分枝期根系AM真菌群落结构的影响,旨在探索不同大豆品种与AM真菌在连作土壤中的互作效应。通过向黑农44（HN44）、黑农48（HN48）和恳丰16（KF16）3个大豆品种盆栽土壤中接种F. mosseae,对接菌连作0年（未连作对照组）、连作1年、连作2年土壤中的大豆根系,采用Nested-Program Control Register-DGGE技术分析。结果表明,接种F. mosseae后,不同大豆品种根系AM真菌多样性指数和丰度值表现为连作2年的土壤>连作1年的土壤>未连作的土壤;其中,球囊霉属Glomus和F. mosseae为3个大豆品种根系中AM真菌的优势菌群。接种F. mosseae对连作1年、连作2年3个大豆品种根系AM真菌群落结构具有显著影响。     

摩西斗管囊霉改善连作花生根际土壤的微环境

花生(Arachis hypogaea)长期连作导致土壤环境恶化, 严重影响产量和品质。丛枝菌根真菌(AMF)作为有益真菌能够与80%的陆生植物根系形成共生关系, 这种共生体能够改善植物根系微环境, 提高植物对营养物质的吸收和对逆境胁迫的抗性。为了探究AMF对花生连作土壤微环境的影响, 该研究通过对花生连作土壤接种和未接种摩西斗管囊霉(Funneliformis mosseae)试验, 在花生不同生长期检测根际土壤的酶活性、土壤矿物质含量、土壤微生物群落结构和多度的变化情况, 以及对连作花生产量和品质的影响。研究结果表明: 1)摩西斗管囊霉能够显著提高花生根际土壤蔗糖酶、脲酶、碱性磷酸酶和硝酸还原酶的活性; 2)摩西斗管囊霉显著增加花生连作土壤中全氮、全磷、全钾、速效磷和速效钾的含量; 3)摩西斗管囊霉显著降低土壤中有害真菌曲霉菌属(Aspergillus)的多度, 减少镰刀菌属(Fusarium)和赤霉菌属(Gibberella)的多度, 但是没有达到显著水平, 显著增加有益细菌放线菌Gaiella属的多度; 4)摩西斗管囊霉显著提高连作花生的产量, 增加籽仁中蛋白质、油酸和亚油酸的含量。因此, 摩西斗管囊霉能够改善连作花生根际土壤微生态环境, 增强连作土壤对致病菌的抵抗能力, 从而缓解连作障碍对花生根系的危害。     

Prokaryotic diversity in continuous cropping and rotational cropping soybean soil

In spite of the techniques based on the amplification of 16S rRNA genes (16S rDNA) to compare bacterial communities that are now widely in use in microbial ecology, little is known about the composition of the soybean continuous cropping (CC) and rotational cropping (RC) soil microbial community. To address this, we compared the levels of bacterial community diversity in RC and 5-year CC rhizosphere soil samples. We selected 407 clones in RC and 490 clones in CC for restriction fragment length polymorphism analysis. A total of 123 phylotypes were identified among the 16S rDNA clones, while 78 unique and 21 common phylotypes were identified among the CC soil isolates. Analysis of sequences from a subset of the phylotypes showed that at least 11 bacterial divisions were represented in the clone libraries. The phylotype richness, frequency distribution (evenness), and composition of the two clone libraries were investigated using a variety of diversity indices. Although the analysis of diversity indices and LIBSHUFF comparisons revealed that the compared libraries were not significantly different ( P =0.05) between the RC vs. CC soils, some differences could be observed in terms of specific phyla and groups. We concluded that the group variance was not determined immediately by the cropping system's induction, but was a long-term and slow process.     

滁菊连作土壤中尖孢镰刀菌的分离、鉴定及变化特征

采用传统平板培养法及尖孢镰刀菌专性培养基对滁菊连作土壤的真菌和尖孢镰刀菌进行分析测定,结果表明,在滁菊连作条件下,土壤中真菌和尖孢镰刀菌的数量显著增加,平均分别达到8.71×105 cfu/g干土和3.12×104cfu/g干土,各自是对照土壤的2.24倍和5.57倍。土壤中尖孢镰刀菌数量显著增加可能是导致滁菊连作障碍的重要因素。     

A β-lactamase gene of Fusarium oxysporum alters the rhizosphere microbiota of soybean

The rhizosphere is a multitrophic environment, and for soilborne pathogens such as Fusarium oxysporum, microbial competition in the rhizosphere is inevitable before reaching and infecting roots. This study established a tritrophic interaction among the plant growth-promoting rhizobacterium Burkholderia ambifaria, F. oxysporum and Glycine max (soybean) to study the effects of F. oxysporum genes on shaping the soybean microbiota. Although B. ambifaria inhibited mycelial growth and increased bacterial propagation in the presence of F. oxysporum, F. oxysporum still managed to infect soybean in the presence of B. ambifaria. RNA-Seq identified a putative F. oxysporum secretory β-lactamase-coding gene, FOXG_18438 (abbreviated as Fo18438), that is upregulated during soybean infection in the presence of B. ambifaria. The ∆Fo18438 mutants displayed reduced mycelial growth towards B. ambifaria, and the complementation of full Fo18438 and the Fo18438 β-lactamase domain restored mycelial growth. Using the F. oxysporum wild type, ∆Fo18438 mutants and complemented strains with full Fo18438, Fo18438 β-lactamase domain or Fo18438 RTA1-like domain for soil inoculation, 16S rRNA amplicon sequencing revealed that the abundance of a Burkholderia operational taxonomic unit (OTU) was increased in the rhizosphere microbiota infested by the strains with Fo18438 β-lactamase domain. Non-metric multidimensional scaling and PICRUSt2 functional analysis revealed differential abundance for the bacterial β-lactam-related functions when contrasting the genotypes of F. oxysporum. These results indicated that the Fo18438 β-lactamase domain provides F. oxysporum with the advantage of growing into the soybean rhizosphere, where β-lactam antibiosis is involved in microbial competition. Accordingly, this study highlights the capability of an F. oxysporum gene for altering the soybean rhizosphere and taproot microbiota.     

不同大豆连作年限对黑土细菌群落结构的影响

大豆连作导致作物产量下降、病原微生物富集和土壤退化等问题日趋严重。然而,目前关于大豆连作对土壤细菌群落结构组成及多样性分布的影响及发生机制尚不清楚。采用高通量测序技术,对大豆连作(不同年限)和大豆-玉米轮作下的黑土细菌16S rRNA基因进行测序分析。结果表明:轮作5年(CR5)和13年长期连作(CC13)处理显著增加了土壤pH、全氮(TN)、全磷(TP)和速效养分(AN、AP和AK)含量。与短期连作相比,CR5和CC13处理均提高了细菌群落的OTUs数量、PD值、Chao1指数和Shannon指数。聚类分析图谱结果显示细菌群落结构组成受到轮作和连作年限的双重影响,而土壤pH、TN、TP、AN、AP和AK是细菌群落结构发生变化的主要驱动因子(P0.05)。此外,VPA分析发现上述土壤因子中,土壤pH对细菌群落结构变化的贡献度最大。本研究证明大豆长期连作提高了土壤养分含量和细菌群落的丰富度和多样性指数,从分子生物学的角度证实大豆长期连作在一定程度上改善了土壤环境,为大豆连作障碍的研究提供了理论依据。     

添加高粱根茬根际土对连作黄瓜生长和根际微生物的影响

为了分析添加高粱根茬根际土对连作黄瓜生长和根际微生物群落特征的影响,本研究通过盆栽试验,采用荧光定量PCR和高通量测序技术分析土壤细菌和真菌群落组成的差异。试验共设4个处理: CK(不施肥),T₁(单施化肥),T₂(优化施肥),T₃(优化施肥+高粱根茬根际土)。结果表明: 与其他处理相比,T₃处理促进了黄瓜生长发育,提高了土壤中16S rRNA和ITS rRNA基因数量。与T₁处理相比,T₂和T₃处理明显提高了细菌群落的丰富度和多样性,不同处理间真菌群落的丰富度和多样性差异不明显。添加高粱根茬根际土在一定程度上改变了基于门、属水平上的细菌和真菌群落结构。其中,细菌中提高了酸杆菌门和拟杆菌门的丰度,降低了变形菌门、厚壁菌门、硝化螺旋菌门和芽孢杆菌属的丰度;真菌中提高了担子菌门、木霉菌属和假散囊菌属的丰度,降低了镰刀菌属和绿僵菌属的丰度。冗余分析表明,土壤硝态氮和有机质含量分别是影响细菌和真菌群落结构差异的关键因子。添加高粱根茬根际土不仅提高了连作黄瓜土壤微生物数量和细菌多样性,而且增加了有益菌木霉菌属的丰度,降低了致病镰刀菌的丰度和数量,保障了黄瓜存活率,为缓解黄瓜连作障碍提供了一条切实可行的解决途径。     

Effect of dsRNA-containing and dsRNA-free hypovirulent isolates of Fusarium oxysporum on severity of Fusarium seedling disease of soybean in naturally infested soil

In the sandy soils of eastern Virginia, soybean seedlings are colonized by hypovirulent and virulent isolates of Fusarium oxysporum and F. solani. Our objectives were to determine if prior inoculation of soybean seeds with hypovirulent F. oxysporum isolates reduced severity of seedling disease in naturally infested soil, and to determine if there was an association between the presence of dsRNA mycovirus and hypovirulence in isolates of F. oxysporum and F. solani from soybean plants. The presence of dsRNA was not associated with hypovirulence in F. oxysporum since some hypovirulent isolates contained dsRNA while other hypovirulent isolates did not. Furthermore, of six dsRNA-containing F. oxysporum isolates, three were hypovirulent and three were virulent. Four segments of dsRNA, with sizes of 4.0, 3.1, 2.7 and 2.2 kb were detected in extracts of all six F. oxysporum isolates. No hypovirulent or dsRNA-containing of F. solani isolates were found. Prior inoculation of cv. Essex soybean seeds with conidia of dsRNA-free hypovirulent F. oxysporum isolates significantly (P < 0.05) reduced disease severity on cotyledons and hypocotyls, and increased the rate of seedling emergence in field soil, compared to control plants. No significant (P > 0.05) differences were found between dsRNA-containing and dsRNA-free hypovirulent F. oxysporum isolates in their effects on reducing disease severity. Hypovirulent isolates that colonize soybean tissues may play a role in reducing Fusarium seedling disease of soybean in natural soils.     

不同菠萝品种种植对连作蕉园土壤理化性质和可培养微生物数量的影响

【背景】不同作物轮作是克服作物连作障碍的重要措施,香蕉与菠萝轮作能有效缓解香蕉土传枯萎病。【目的】以休耕(CK)、高病蕉园土壤中种植巴西香蕉苗(B)、高病蕉园土壤中种植"巴厘"菠萝苗(B_BP)、高病蕉园土壤中种植"金菠萝"菠萝苗(B_GP)和高病蕉园土壤中种植"台农17号"菠萝苗(B_PP)为对象,研究不同菠萝品种种植对连作蕉园土壤理化性质和可培养尖孢镰刀菌、真菌、细菌和放线菌数量的影响,揭示不同菠萝品种种植在高病蕉园土壤中理化性质差异及微生物分布特征。【方法】采用盆栽试验结合可培养微生物研究方法,探究在高病蕉园土壤种植不同菠萝品种后的土壤理化性质和可培养微生物数量的变化。【结果】与休耕(CK)处理相比,高病蕉园土壤中继续种植巴西香蕉苗(B)处理显著增加土壤中尖孢镰刀菌数量,而种植菠萝品种"金菠萝"和"台农17号"(B_GP和B_PP)处理均能显著降低土壤中可培养尖孢镰刀菌数量,增加细菌和放线菌数量。土壤速效磷、细菌及放线菌数量均与可培养尖孢镰刀菌数量呈显著负相关关系;pH和真菌数量与可培养尖孢镰刀菌数量呈显著正相关关系。主坐标分析(principalco-ordinatesanalysis,PCoA)和多元回归树(multivariate regression trees,MRT)分析结果表明,种植"金菠萝"和"台农17号"菠萝(B_GP和B_PP)处理间的土壤肥力质量相近,并显著区别于其他3个处理。【结论】在高发病香蕉园地,种植菠萝品种"金菠萝"和"台农17号"(B_GP和B_PP)可以显著改善其土壤理化性质和土壤可培养微生物状况,对香蕉连作障碍有较好的缓解作用。     

连作障碍因素对大豆养分吸收和固氮作用的影响

采用分室装置,利用不同孔径的膜研究大豆连作条件下,化感物质、土壤有害生物和大豆胞囊线虫等因素不断累加对植株生长、生物固氮作用和矿质养分吸收和分配的影响。结果表明,随着各因素不断累加,植株的地上部、根系和根瘤干重逐渐降低;除Ca元素外,植株组织的P、K等矿质元素单位含量下降,吸收总量下降,地上部分配的养分比例下降。在化感物质和土壤有害生物因素的基础上接种线虫,对生物固氮和矿质养 分的吸收和分配影响明显。     

新疆绿洲农田不同连作年限棉花根际土壤微生物群落多样性

以南北疆不同连作年限棉花根际土壤为研究对象,采用Biolog技术,并结合传统平板培养法和土壤酶的测定,研究连作对棉花根际土壤微生物群落多样性的影响。Biolog分析结果表明,不同连作年限棉花根际土壤微生物碳源利用和功能多样性差异显著。荒地土壤微生物活性较低;在连作年限较短时(5—10a),根际土壤微生物群落的平均颜色变化率(AWCD)和Shannon指数较高;长期连作(15—20a),则呈明显下降趋势。主成分分析表明,不同连作年限的棉花根际土壤微生物碳源利用特征有明显不同。第一、二组开垦与未开垦土壤分别在PC1和PC2上出现差异,未开垦土壤得分均为负值,开垦土壤均为正值;而正茬与连作多年的棉花土壤在PC1上差异显著。其中在PC1上起分异作用的碳源主要是羧酸类和聚合物类,这两类碳源可能是影响连作棉花根际土壤微生物的主要碳源。可培养微生物数量的测定结果表明,荒地细菌数量最少;在连作年限较低时(5—10a左右),细菌数量呈上升趋势;而长期连作(>15a)后,细菌数量呈现下降趋势。真菌数量在连作多年后(10—15a)也开始增加。放线菌变化趋势不明显。四种土壤酶活性在连作的初中期(5—15a),连作障碍表现明显,土壤酶活性呈下降(过氧化氢酶和磷酸酶)或先升高后下降(脲酶和蔗糖酶)趋势,但随着连作年限的延长(15—20a),这4种土壤酶活性均表现出增高趋势。综上所述,棉花长期连作使棉花根际土壤微生物群落多样性降低,发生连作障碍,进而导致棉花产量降低。     

不同作物轮作对连作高粱生长及其根际土壤环境的影响

以高粱连作5年为对照(CK),研究了高粱连作3年轮作苜蓿(T₁)和葱(T₂),对下茬高粱生长、根际土壤微生物及土壤酶活性的影响.结果表明:与CK相比,轮作改善了高粱地上部的生长;T₁增产16.5%,效果明显.轮作也促进了高粱根系的生长,T₁和T₂处理的高粱总根长是CK的1.3和1.4倍,根总表面积是CK的1.6和1.5倍,根体积是CK的2.2和1.6倍,根系生物量是CK的2.0和1.3倍,T₁促进了根系在10 cm以下土层中的分布.借助Biolog法对穗花期根际土壤微生物群落功能多样性分析表明,T₁和T₂处理根际土壤微生物活性显著高于CK,且Shannon多样性指数分别是CK的1.2和1.1倍;轮作提高了根际土壤蔗糖酶活性.综上,轮作苜蓿比轮作葱更能改善高粱根际土壤环境,提高土壤微生物活性和酶活性,控制高粱连作障碍,提高高粱产量.     

白术连作根际土壤的理化性质及微生物区系变化

对不同种植年限白术(Atractylodes macrocephala Koidz.)根际土壤的部分理化指标、酶活性和微生物区系进行了测定和比较。结果表明:随白术种植年限的增加(0、1和2 a),根际土壤pH值显著下降(P<0.05),根际土壤中有机质和全氮含量呈先升高后降低趋势,速效钾含量则逐渐升高,而有效磷含量和C/N比小幅波动,总体上不同种植年限根际土壤的这些指标差异不显著;根际土壤中有效铁、有效铝和交换性锰含量显著或极显著(P<0.01)增加,且较对照(未种植白术的土壤)分别增加了127.51%、18.38%和106.83%,但有效铅含量变化幅度较小;2年生白术根际土壤中过氧化氢酶、脲酶和蛋白酶活性显著低于对照;2年生白术根际土壤中细菌和放线菌数量及微生物总量较1年生白术根际土壤显著下降,真菌数量则显著上升。结果显示:土壤酸化严重、金属离子大量积累、主要酶活性失调以及微生物区系改变可能是白术连作障碍的潜在原因。     

Molecular detection of Fusarium oxysporum f. sp. niveum and Mycosphaerella melonis in infected plant tissues and soil

We developed two species-specific PCR assays for rapid and accurate detection of the pathogenic fungi Fusarium oxysporum f. sp. niveum and Mycosphaerella melonis in diseased plant tissues and soil. Based on differences in internal transcribed spacer (ITS) sequences of Fusarium spp. and Mycosphaerella spp., two pairs of species-specific primers, Fn-1/Fn-2 and Mn-1/Mn-2, were synthesized. After screening 24 isolates of F. oxysporum f. sp. niveum, 22 isolates of M. melonis, and 72 isolates from the Ascomycota, Basidiomycota, Deuteromycota, and Oomycota, the Fn-1/Fn-2 primers amplified only a single PCR band of approximately 320 bp from F. oxysporum f. sp.niveum, and the Mn-1/Mn-2 primers yielded a PCR product of approximately 420 bp from M. melonis. The detection sensitivity with primers Fn-1/Fn-2 and Mn-1/Mn-2 was 1fg of genomic DNA. Using ITS1/ITS4 as the first-round primers, combined with either Fn-1/Fn-2 and or Mn-1/Mn-2, two nested PCR procedures were developed, and the detection sensitivity increased 1000-fold to 1ag. The detection sensitivity for the soil pathogens was 100-microconidia/g soil. A duplex PCR method, combining primers Fn-1/Fn-2 and Mn-1/Mn-2, was used to detect F. oxysporum f. sp. niveum and M. melonis in plant tissues infected by the pathogens. Real-time fluorescent quantitative PCR assays were developed to detect and monitor the pathogens directly in soil samples. The PCR-based methods developed here could simplify both plant disease diagnosis and pathogen monitoring as well as guide plant disease management.     

连作对浙贝母生长及土壤性质的影响

采用大田试验,分别在浙贝母种植的头茬、二茬及四茬田里进行植物及土壤取样,分析土壤理化性质、微生物区系、关键酶等指标.结果表明:随着连作年数的增加,浙贝母连作土壤中有效氮、有效磷及有效钾的含量显著降低,但有机质含量逐年增加,土壤呈酸化趋势;根区土壤中细菌、放线菌及微生物总量呈线性减少,但真菌数量呈线性增长;重茬根区土壤的脲酶、过氧化氢酶活性显著低于头茬土,但多酚氧化酶及蔗糖酶活性出现增加现象.在连作障碍下,浙贝母叶内膜脂过氧化程度加剧,SOD、POD等抗氧化酶活性降低,地上、地下部生物量以及根长、根表面积均显著降低.说明浙贝母连作障碍是由于土壤营养元素缺乏、根际酸化、微生物区系改变、氧化胁迫加剧等多原因造成的.     

Stability of transformed antagonistic Fusarium oxysporum strains in vitro and in soil microcosms

The stability of a genetically modified strain of Fusarium oxysporum used as antagonist against phytopathogenic formae speciales of F. oxysporum was evaluated both in vitro and in microcosm assays. The Escherichia coli hygromycin B phosphotransferase gene (hph), conferring hygromycin B resistance, was introduced by genetic transformation into a recipient strain marked by benomyl resistance and a dark red pigmentation. Hybridization with the complete plasmid suggested that the integration had generally occurred in a multiple-tandem array at multiple sites. Among nine independent transformants tested, only three of them were mitotically stable after four rounds of vegetative growth with no selective pressure, while six showed various changes in the integration pattern. One transformant had lost the ability to grow in the presence of hygromycin B. In soil microcosms all the transformants maintained the hygromycin B resistant phenotype, but six of them showed rearrangement of transforming DNA. Only one strain (coded T26.40) underwent no obvious rearrangement both after in vitro growth and after recovery from the soil microcosm. The nine transformants were used in three biological control experiments against Fusarium wilt of carnation in comparison to two untransformed reference strains and to the recipient mutant. A high degree of variability in the biocontrol activity was observed throughout the experiments and only transformant T26.40 consistently controlled the incidence of disease. The results are discussed in relation to risk assessment of the release of transgenic antagonistic fungi.     

连作花生田根际土壤优势微生物的分离和鉴定

【目的】从不同连作年限的花生田根际土壤中分离优势微生物并进行鉴定,为研究花生连作后优势微生物的变化奠定基础。【方法】采用土壤稀释分离法从不同连作年限花生根际土壤中分离优势细菌、真菌和放线菌,结合菌株形态特征、培养性状、生理生化特征及16S rDNA序列分析对细菌、放线菌进行鉴定,通过形态特征、培养特征和分子鉴定方法对优势真菌进行鉴定。【结果】从连作花生田根际土壤中分离鉴定出7种优势细菌、7种优势真菌和7种优势放线菌。7种优势细菌分别为Leifsonia xyli、氯酚节杆菌(Arthrobacterchlorophenolicus)、黄色微杆菌(Microbacterium flavescens)、鞘氨醇单胞菌属(Sphingomonas sp.)、巴斯德菌属(Pasteurella sp.)、简单芽孢杆菌(Bacillus simplex)和巨大芽孢杆菌(Bacillus megaterium)。7种优势真菌分别为枝状枝孢菌(Cladosporium cladosporioides)、产紫青霉(Penicillium purpurogenum)、哈茨木霉有性型(Hypocrea lixii)、Exophiala pisciphila、微紫青霉(Penicillium janthinellum)、曲霉(Aspergillus sp.)和大丽轮枝菌(Verticillium dahliae)。7种优势放线菌分别为紫红链霉菌(Streptomyces violaceoruber)、华丽黄链霉菌(Streptomyces flaveus)、Streptomyces panaciterrae、不产色链霉菌(Streptomyces achromogenes)、假浅灰链霉菌(Streptomyces pseudogriseolus)、纤维素链霉菌(Streptomyces cellulosae)和金色链霉菌(Streptomyces aureus)。【结论】本研究是第一次系统的从连作花生根际土中分离鉴定优势微生物,种植花生后根际土壤中优势微生物的种类发生了明显变化,但变化没有规律。     

灵芝连作土壤真菌群落分析

本研究通过Illumina MiSeq平台对邻近野生土壤（GL0）、种植1年（GL1）、2年（GL2）和4年（GL4）的灵芝覆土进行ITS1扩增子测序,分析灵芝连作覆土中真菌群落的变化,为揭示灵芝连作障碍的机理提供理论依据。研究结果表明,12个灵芝土壤样本一共获得349 642条有效序列,经聚类得到2 426个OTU,分别隶属于8门、28纲、64目、127科、233属和449种。在门水平上,随着连作年限的增加,灵芝覆土中真菌的多样性水平逐渐减低,在GL4组中只含有担子菌门（Basidiomycota,占85.03%）、子囊菌门（Ascomycota,占14.77%）和少量被孢霉门（Mortierellomycota,占0.20%）。其中,担子菌门的相对丰度随着连作年限的增加显著增加,子囊菌门的相对丰度显著减少,而被孢霉门的相对丰度无显著性差异。在属水平上,担子菌门灵芝属Ganoderma的相对丰度随着连作年限的增加而极显著增加,子囊菌门仅青霉属Penicillium菌群的相对丰度呈现先减少后增加的趋势,在GL4组中相对于GL0组其相对丰度增加了57.92%,表明青霉属可能是引发该地区灵芝连作障碍的重要菌群,该研究为探索灵芝连作障碍的分子机制和生态防控提供了理论依据。     

低温茬口空闲期土壤强还原消毒对西瓜枯萎病的影响

为探明低温茬口空闲期土壤强还原消毒(RSD)对西瓜枯萎病的防控效果,设置对照(CK)、淹水对照(FCK)、淹水添加2%(w/w)苜蓿粉(AL)、0.25%(w/w)乙酸(AC)以及AL+AC的RSD处理进行西瓜盆栽试验,采用定量PCR和Illumina Miseq等测定真菌、尖孢镰刀菌数量及真菌群落组成,并统计发病率和产量。结果表明: 与CK相比,FCK和各RSD处理均能显著降低尖孢镰刀菌数量及其在真菌中的比例,杀菌效果达86.1%～94.6%;AL、AC以及AL+AC处理显著增加了西瓜产量,降低了枯萎病发病率,且枯萎病防控效果分别为63.2%、73.7%和94.7%,而FCK与CK无显著差异。与CK相比,AL和AC处理显著改变了土壤真菌群落组成,FCK处理对真菌群落无显著影响;RSD处理均显著增加了柄孢壳属、假散囊菌、地丝菌、粪盘菌、韦斯特壳属以及久浩酵母菌等优势属的相对丰度,且其中大部分与尖孢镰刀菌数量及其在真菌中的比例以及发病率呈显著负相关关系。综上,低温茬口空闲期的RSD处理可以通过重塑真菌群落组成有效防控西瓜枯萎病的发生。