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자료유형
학술저널
저자정보
Wei Zhao (Sichuan Agricultural University) Ziwei Ren (Sichuan Agricultural University) Yan Luo (Sichuan Agricultural University) Jianguo Cheng (Sichuan Institute of Musk Deer Breeding) Jie Wang (Sichuan Agricultural University China) Yin Wang (Sichuan Agricultural University) Zexiao Yang (Sichuan Agricultural University) Xueping Yao (Sichuan Agricultural University) Zhijun Zhong (Sichuan Agricultural University) Wei Yang (Sichuan Agricultural University) Xi Wu (Sichuan Agricultural University)
저널정보
한국유전학회 Genes & Genomics Genes & Genomics Vol.43 No.1
발행연도
2021.1
수록면
43 - 53 (11page)

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Background The forest musk deer (FMD, Moschus berezovskii) is an threatened species in China. Bacterial pneumonia was found to seriously restrict the development of FMD captive breeding. Historical evidence has demonstrated the relationship between immune system and intestinal Lactobacillus in FMD. Objective We sought to elucidate the differences in the gut microbiota of healthy and bacterial pneumonia FMD. Methods The bacterial pneumonia FMD was demonstrated by bacterial and pathological diagnosis, and the gut microbiome of healthy and bacterial pneumonia FMD was sequenced and analysed. Results There are three pathogens (Pseudomonas aeruginosa, Streptococcus equinus and Trueperella pyogenes) isolated from the bacterial pneumonia FMD individuals. Compared with the healthy group, the abundance of Firmicutes and Proteobacteria in the pneumonia group was changed, and a high level of Proteobacteria was found in the pneumonia group. In addition, a higher abundance of Acinetobacter (p = 0.01) was observed in the population of the pneumonia group compared with the healthy group. Several potentially harmful bacteria and disease-related KEGG subsystems were only found in the gut of the bacterial pneumonia group. Analysis of KEGG revealed that many genes related to type IV secretion system, type IV pilus, lipopolysaccharide export system, HTH-type transcriptional regulator/antitoxin MqsA, and ArsR family transcriptional regulator were significantly enriched in the metagenome of the bacterial pneumonia FMD. Conclusion Our results demonstrated that the gut microbiome was significantly altered in the bacterial pneumonia group. Overall, our research improves the understanding of the potential role of the gut microbiota in the FMD bacterial pneumonia.

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