Crislaine Soares Oliveira, Juliane Rafaele Alves Barros, Viviane Siqueira Lima Silva, Paula Rose de Almeida Ribeiro, Francislene Angelotti, Paulo Ivan Fernandes-Júnior
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引用次数: 0
Abstract
Future climatic scenario predictions indicate a substantial temperature increase, reducing crop production worldwide and demanding the development of adaptations in agriculture. This study aimed to assess the impact of high temperatures and amendments with Bacillus on nodulating bradyrhizobia. Two cowpea genotypes were evaluated at low (min = 20.0°C, max = 33.0°C) and high-temperature regimes (min = 24.8 C, max = 37.8°C). Plants were also inoculated with Bacillus sp. ESA 402, a plant growth-promoting bacterium. The molecular diversity of the bradyrhizobia isolated from cowpea nodules and plant growth was assessed. High temperatures reduced nodulation of the BRS Itaim cowpea genotype. One hundred and eighty-six were genotyped, clustering the collection into 45 groups. The high temperatures reduced the number of groups, but this negative influence was diminished by Bacillus inoculation. Alpha diversity showed little impact on the experimental interactions. However, this influence was evident for all factors and the interaction of the three factors when beta diversity was assessed. 16S rRNA and constitutive gene sequences identified all strains as Bradyrhizobium spp. mainly within the B. japonicum supercluster. Cowpea-Bradyrhizobium association diversity is multifactorial under different temperature regimes, as is the presence or absence of the plant-growth-promoting bacteria Bacillus sp. ESA 402.
对未来气候情景的预测表明,气温将大幅上升,这将导致全球农作物减产,并要求发展适应气候变化的农业。本研究旨在评估高温和芽孢杆菌改性对慢生根瘤菌结瘤的影响。两种豇豆基因型分别在低温(最低20.0°C,最高33.0°C)和高温(最低24.8°C,最高37.8°C)条件下进行评估。植物也接种了芽孢杆菌sp. ESA 402,一种促进植物生长的细菌。从豇豆根瘤和植株生长中分离得到的慢生根瘤菌的分子多样性进行了评价。高温降低了BRS Itaim豇豆基因型的结瘤。对186个样本进行基因分型,分为45组。高温使菌群数量减少,但接种芽孢杆菌后,这种负面影响减弱。α多样性对实验相互作用影响不大。然而,当评估β多样性时,这种影响对所有因素和三个因素的相互作用都很明显。16S rRNA和组成基因序列鉴定所有菌株均为缓生根瘤菌属,主要分布在日本芽孢杆菌超簇内。在不同的温度条件下,豇豆-缓生根瘤菌的关联多样性是多因子的,促进植物生长的细菌芽孢杆菌sp. ESA 402的存在与否也是如此。
期刊介绍:
The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions.
Papers published deal with:
microbial interactions (pathogenic, mutualistic, environmental),
ecology,
physiology,
genetics and cell biology/development,
new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications)
novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).