研究简报

棘球蚴病患者肠道菌群差异性分析

  • 曹得萍 ,
  • 毋德芳 ,
  • 庞明泉 ,
  • 彭小红 ,
  • 李大宇 ,
  • 樊海宁
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  • 1.桂林医学院基础医学院人体寄生虫学教研室,广西桂林 541199
    2.青海省包虫病重点实验室,西宁 810001
    3.青海大学附属医院肝胆胰外科,西宁 810000
曹得萍(1970-),女,博士,教授,从事人体寄生虫学教学和包虫病分子生物学研究,Email:qhmccdp@163.com
* 樊海宁(1970-),男,硕士,主任医师,从事肝胆胰疾病外科治疗和包虫病临床研究。Email:fanhaining@medmail.com.cn

收稿日期: 2022-04-14

  修回日期: 2022-10-09

  网络出版日期: 2023-02-22

基金资助

国家自然科学基金(NSFC 8196057);青海省科技厅项目(2019-SF-131)

Difference analysis of the gut microbiome in patients with echinococcosis

  • CAO Deping ,
  • WU Defang ,
  • PANG Mingquan ,
  • PENG Xiaohong ,
  • LI Dayu ,
  • FAN Haining
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  • 1. Department of Human Parasitology, Basic Medical College, Guilin Medical University, Guilin 541199, Guangxi, China
    2. Qinghai Research Key Laboratory for Echinococcosis, Xining 810001, China
    3. Department of Hepatopancreatobiliary Surgery, Affiliated Hospital of Qinghai University, Xining 810000, China

Received date: 2022-04-14

  Revised date: 2022-10-09

  Online published: 2023-02-22

Supported by

National Natural Science Foundation of China(NSFC 8196057);Qinghai Science and Technology Department Project(2019-SF-131)

摘要

2020年10—12月在青海大学附属医院肝胆外科收集13例棘球蚴患者(其中7例多房棘球蚴病、6例细粒棘球蚴病,为感染组)与13例护理患者健康家属(为对照组)的粪样。提取粪样DNA并测定浓度,逆转录合成cDNA文库,利用宏基因组二代测序平台进行测序。用线性判别分析统计棘球蚴病患者与健康对照组之间肠道菌群的差异性。结果显示,棘球蚴病患者与健康对照组肠道菌群属于厚壁菌门、拟杆菌群门、变形菌门及放线菌门等。多房棘球蚴组相对丰度较高的细菌是另枝菌、拟杆菌,细粒棘球蚴组相对丰度较高的细菌是另枝菌、史氏甲烷短杆菌、前庭链球菌。健康对照组相对丰度较高的细菌是粪拟杆菌、青春双歧杆菌、琥珀酸考拉杆菌。其中另枝菌和粪拟杆菌是差异较大的细菌。本研究中的差异菌群或许可成为棘球蚴病肠道微生物标志菌,值得进一步研究。

本文引用格式

曹得萍 , 毋德芳 , 庞明泉 , 彭小红 , 李大宇 , 樊海宁 . 棘球蚴病患者肠道菌群差异性分析[J]. 中国寄生虫学与寄生虫病杂志, 2023 , 41(1) : 103 -107 . DOI: 10.12140/j.issn.1000-7423.2023.01.016

Abstract

Fecal samples of 13 patients (7 patients with alveolar echinococcosis, 6 patients with cystic echinococcosis as infected group) and 13 healthy family members caring for patients (as control group) were collected in the Department of Hepatobiliary Surgery of Qinghai University Affiliated Hospital from October to December in 2020. The fecal DNA was extracted and the concentration was determined, and the cDNA library was synthesized by reverse transcription, and then sequenced using the metagenomic next generation sequencing. The metagenome second-generation sequencing was used to observe the changes of intestinal flora. Linear discriminant analysis was used to analyse the differences in intestinal flora between echinococcosis patients and healthy controls. The results revealed that the flora with higher relative abundance in the alveolar echinococcosis group were Alistipes onderdonkii, Bacteroides dorei, A. finegoldii, and the flora with higher relative abundance in the cystic echinococcosis group were A. shahii, Methanobrevibacter smithii, Streptococcus vestibularis. In the healthy individuals group, there were high relative abundance of B. caccae, Bifidobacterium adolescentis, Phascolarctobacterium succinatutens. Among them, A. onderdonkii, A. shahii and B. caccae are more meaningful flora. The differential flora in this study may be the intestinal microbial marker of echinococcosis, which deserves further to study.

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