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[抗Bt和敏感棉铃虫中肠细菌群落的比较]

[Comparison of midgut bacterial community between Bt-resistant and sensitive Helicoverpa armigera].

作者信息

Jiang Weiyu, Liang Gemei, Lin Yi, Shu Changlong, Song Fuping, Zhang Jie

机构信息

College of Chemical Engineering, Huaqiao University, Xiamen 361021, China.

出版信息

Wei Sheng Wu Xue Bao. 2010 Jun;50(6):828-34.

Abstract

OBJECTIVE

To investigate the midgut bacterial community of sensitive and resistant Helicoverpa armigera for the emergence of resistance to Bacillus thuringiensis.

METHODS

Two culture-independent techniques (16S rDNA library and DGGE) were introduced. The genomic DNA of midgut bacteria was extracted. The full length gene of 16S rDNA was amplified by PCR and then cloned. The 16S rDNA library was analyzed with Alu I and Sac I. The V3 region of 16S rDNA was amplified by PCR. The intrapopulation variation and variation between resistant and sensitive Helicoverpa armigera were assayed by DGGE.

RESULTS

Analysis of 16S rDNA library showed similar patterns of midgut bacterial structure and diversity in terms of the dominant bacteria, but the inferior bacteria were significant different. The resistant population harbored abundant phylotypes belonging to uncultured bacterium (56.4%), Enterococcus gallinarum (17.0%) and Enterococcus casseliflavus (17.0%). For the sensitive population, the dominant bacteria were uncultured bacterium (60.2%), Enterococcus casseliflavus (14.7%) and Enterococcus gallinarum (19.3%). The divergence of midgut bacteria community between resistant and sensitive populations detected by 16S rDNA library analysis was verified by PCR with specific primers, and the result showed that all those inferior bacteria presented in both varieties. DGGE profile revealed that the similarity of the two varieties was 92.3%.

CONCLUSION

The midgut bacterial community of resistant and sensitive H. armigera was similar, which had no direct effect on Bt-resistance of H. armigera.

摘要

目的

研究对苏云金芽孢杆菌产生抗性的敏感和抗性棉铃虫的中肠细菌群落,以探究抗性产生的原因。

方法

引入两种非培养技术(16S rDNA文库和变性梯度凝胶电泳,DGGE)。提取中肠细菌的基因组DNA。通过PCR扩增16S rDNA的全长基因,然后进行克隆。用Alu I和Sac I分析16S rDNA文库。通过PCR扩增16S rDNA的V3区域。用DGGE分析抗性和敏感棉铃虫种群内的变异以及两者之间的变异。

结果

16S rDNA文库分析表明,就优势细菌而言,中肠细菌结构和多样性的模式相似,但劣势细菌有显著差异。抗性种群中含有丰富的未培养细菌(56.4%)、鹑鸡肠球菌(17.0%)和格氏肠球菌(17.0%)的系统发育型。对于敏感种群,优势细菌是未培养细菌(60.2%)、格氏肠球菌(14.7%)和鹑鸡肠球菌(19.3%)。通过16S rDNA文库分析检测到的抗性和敏感种群之间中肠细菌群落的差异,经特异性引物PCR验证,结果表明所有这些劣势细菌在两个品种中均有出现。DGGE图谱显示两个品种的相似性为92.3%。

结论

抗性和敏感棉铃虫的中肠细菌群落相似,对棉铃虫的Bt抗性没有直接影响。

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