期刊文献+

肝移植患者肠道双歧杆菌的生态结构

Molecular ecological structure of intestinal Bifidobacterium spp in liver-transplanted patients
原文传递
导出
摘要 目的探讨肝移植患者肠道双歧杆菌属细菌种群分子生态结构变化特点。方法采用荧光定量PCR技术分析健康人27例、肝硬化患者51例及肝移植后患者113例粪便双歧杆菌在属及种水平上的定性和定量变化。结果与健康人比较,肝移植及肝硬化患者肠道双歧杆菌总量、肠道假小链双歧杆菌或小链双歧杆菌组细菌及青春型双歧杆菌显著减少均P〈0.01;肝移植患者肠道长双歧杆菌显著增多(P〈0.01)。肝移植患者肠道假小链双歧杆菌或小链双歧杆菌、青春型双歧杆菌、短型双歧杆菌检出率显著低于健康人群均P〈0.01。肝移植组患者肠道双歧杆菌多样性显著低于健康人群(Х^2=20.1,P〈0.01)。结论肝移植及肝硬化患者肠道双歧杆菌种群生态结构均存在显著异常,尤以假小链双歧杆菌或小链双歧杆菌组及青春型双歧杆菌的数量及检出率降低最为显著,肝移植组患者肠道双歧杆菌多样性显著低于健康人群。 Objective To investigate the ecological structure of intestinal Bifidobacterium spp in liver-transplanted patients from the molecular ecological view. Methods Intestinal Bifidobacterium spp from all subjects(including 27 healthy volunteers, 51 patients with hepatic cirrhosis and 113 liver-transplanted patients) were quantified by real-time PCR using 16S rRNA gene-targeted genus and species specific primers. Results Total 16S rRNA gene copy numbers(per gram of wet weight of feces) of Bifidobacteria (P 〈0. 01, P 〈 0.01, respectively), Bifidobacteriurn catenulaturn group (including Bi f idobacteriurn catenulaturn and Bi f idobacteriurn pseudocatnulaturn ) ( P 〈0. 01, P 0.01, respectively) and Bifidobacterium adolescentis (P 〈0. 01, P 〈 0.01, respectively) were lowered markedly in patients with cirrhosis or liver transplantation. The counts of Bifidobacteriurn longum in cirrhotic patients were markedly increased compared to that in healthy volunteers (P 〈 0.01). The detection rates of faecal Bifidobacteriurn catenulaturn group (P 〈 0.01), Bifidobacteriurn ado- lescentis (P 〈0. 01) and Bifidobacteriurn breve (P 〈0. 01) in liver-transplanted patients were significantly lower than those in healthy volunteers, respectively. The distribution diversity of Bifidobacteriurn species in patients with liver transplantation was remarkably less than that in healthy volunteers (Х^2= 20.1, P 〈 0.01). Conclusions The obviously abnormal structure of Bifidobacterium communities is observed in liver-transplanted patients and cirrhotic patients. Both the counts and the detection rates of Bifidobacterium catenulatum group and Bifidobacterium adolescentis are decreased significantly. These results may provide theoretical bases for administration of some Bifidobacterium probiotics in patients with both liver transplantation and cirrhosis.
出处 《中华传染病杂志》 CAS CSCD 北大核心 2007年第1期9-14,共6页 Chinese Journal of Infectious Diseases
基金 科技部“973”项目资助(2003CB515506) 浙江省医药卫生优秀青年科技人才专项科研基金项目(2003QN005) 浙江省科技厅重点项目(2006C23017)
关键词 肝移植 肝硬化 双歧杆菌 Liver transplantation Cirrhosis Bifidobacterium
  • 相关文献

参考文献9

  • 1Rayes N, Seehofer D, Theruvath T, et al. Supply of pre- and probiotics reduces bacterial infection rates after liver transplantation-a randomized, double-blind trial. Am J Transplant, 2005, 5:125-130.
  • 2Rayes N, Seehofer D, Hansen S, et al. Early enteral supply of lactobacillus and fiber versus selective bowel decontamination: a controlled trial in liver transplant recipients. Transplantation, 2002, 74 : 123-127.
  • 3Leahy SC, Higgins DG, Fitzgerald GF, et al. Getting better with bifidobacteria. J Appl Microbiol, 2005, 98:1303 1315.
  • 4Matsuki T, Watanabe K, Fujimoto J, et al. Quantitative PCR with 16S rRNA-gene-targeted species-specific primers for analysis of human intestinal bifidobacteria. Appl Environ Microbiol, 2004, 70:167-173.
  • 5Matsuki T, Watanabe K, Tanaka R. Genus-and speciesspecific PCR primers for the detection and identification of bifidobacteria. Curr Issues Intest Microbiol, 2003, 4:61-69.
  • 6Malinen E, Kassinen A, Rinttila T, et al. Comparison of real-time PCR with SYBR Green 1 or 5'-nuclease assays and dot-blot hybridization with rDNA-targeted oligonucleotide probes in quantification of selected faecal bacteria. Microbiology, 2003, 149:269-277.
  • 7Satokari RM, Vaughan EE, Akkermans AD, et al. Bifidobacterial diversity in human feces detected by genus-specific PCR and denaturing gradient gel electrophoresis. Appl Environ Microbiol, 2001, 67:504-513.
  • 8庞小燕,张宝让,魏桂芳,赵立平.应用TGGE技术分析人肠道中双歧杆菌的组成[J].微生物学报,2005,45(5):738-743. 被引量:10
  • 9Klijn A, Mercenier A, Arigoni F. Lessons from the genomes of bifidobacteria. FEMS Microbiol Rev, 2005, 29:491-509.

二级参考文献30

  • 1许本发,王艳萍,陈莹.耐氧双歧杆菌的分离和鉴定[J].微生物学报,1994,34(1):9-13. 被引量:22
  • 2Satokari R M,Vaughan E E,Akkermans A,et al.Bifidobacterial diversity in human feces detected by genus-specific PCR and denaturing gradient gel electrophoresis.Appl Environ Microbiol,2001,67(2):504-513.
  • 3Matsuki T,Watanabe K,Tanaka R,et al.Distribution of bifidobacterial species in human intestinal microflora examined with 16S rRNA-gene-targeted species-specific primers.Appl Envir Microbiol,1999,65(10):4506-4512.
  • 4Langendijk P,Schut F,Jansen G J,et al.Quantitative fluorescence in situ hybridization of Bifidobacterium spp.with genus-specific 16S rRNA-targeted probes and its application in fecal samples.Appl Environ Microbiol,1995,61(8):3069-3075.
  • 5Wei G,Pan L,Du H,et al.ERIC-PCR fingerprinting-based community DNA hybridization to pinpoint genome-specific fragments as molecular markers to identify and track populations common to healthy human guts.J Microbiol Methods,2004,59(1):91-108.
  • 6Wang R F,Cao W W,Cerniglia C E.PCR detection and quantitation of predominant anaerobic bacteria in human and animal fecal samples.Appl Environ Microbiol,1996,62(4):1242-1247.
  • 7Di Cello F,Bevivino A,Chiarini L,et al.Biodiversity of a Burkholderia cepacia population isolated from the maize rhizosphere at different plant growth stages.Appl Environ Microbiol,1997,63(11):4485-4493.
  • 8Favier C F,Vaughan E E,De Vos W M,et al.Molecular monitoring of succession of bacterial communities in human neonates.Appl Environ Microbiol,2002,68(1):219-226.
  • 9Suau A,Bonnet R,Sutren M,et al.Direct analysis of genes encoding 16S rRNA from complex communities reveals many novel molecular species within the human gut.Appl Environ Microbiol,1999,65(11):4799-4807.
  • 10Sekiguchi H,Watanabe M,Nakahara T,et al.Succession of bacterial community structure along the Changjiang river determined by denaturing gradient gel electrophoresis and clone library analysis.Appl Environ Microbiol,2002,68(10):5142-5150.

共引文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部