Home LiteratureArticle Details
PMID: 3132368 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Role of intestinal anaerobic bacteria in colonization resistance.

Wells CL, Maddaus MA, Jechorek RP, Simmons RL

Abstract

The purpose of this study was to clarify the role of the intestinal anaerobe bacteria in colonization resistance. Germfree mice were associated with Escherichia coli C25 and either (a) no other species; (b) enterococcus; (c) Escherichia coli M14 and Proteus mirabilis, or (d) Bacteroides fragilis and Bacteroides vulgatus. All species colonized the cecum in high numbers, but only enterococcus significantly limited the translocation of Escherichia coli C25 to mesenteric lymph nodes. However, the overall translocation rates were similar in all groups and ranged from 60% to 100%, due to translocation of other intestinal flora in addition to Escherichia coli C25. Conventionally reared mice were given either streptomycin, bacitracin/streptomycin or metronidazole which selectively eliminated facultative gram-negative bacteria, nearly all bacterial species or strictly anaerobic bacteria respectively. Only metronidazole significantly increased the rates of translocation of normal intestinal bacteria into mesenteric lymph nodes. Cohort groups of mice were then orally inoculated with drug resistant Escherichia coli C25, which actively colonized the cecum of all drug treated mice and translocated to the mesenteric lymph nodes of approximately half the streptomycin and metronidazole treated mice and nearly all the bacitracin/streptomycin treated mice. These results indicate that anaerobic bacteria play a pivotal role in limiting the translocation of normal intestinal bacteria, but that other bacterial groups also have a role in preventing the intestinal colonization and translocation of potential pathogens.

MeSH Terms
Animals Antibiosis Bacitracin/pharmacology Bacteria, Anaerobic/drug effects,growth & development Bacteroides/drug effects,growth & development Bacteroides fragilis/drug effects,growth & development Cecum/microbiology Drug Resistance, Microbial Escherichia coli/drug effects,growth & development,physiology Female Germ-Free Life Intestines/microbiology Lymph Nodes/microbiology Male Mesentery Metronidazole/pharmacology Mice Mice, Inbred BALB C Proteus mirabilis/drug effects,growth & development Streptomycin/pharmacology
Chemicals
Bacitracin Metronidazole Streptomycin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wells C L
Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis 55455.
Maddaus M A
Jechorek R P
Simmons R L
References (15)
15 references, click to expand
  1. Colonization resistance of the digestive tract and the spread of bacteria to the lymphatic organs in mice.
    J Hyg (Lond). 1972 Jun;70(2):335-42 PMID: 4626276
  2. Relationship between cecal population levels of indigenous bacteria and translocation to the mesenteric lymph nodes.
    Infect Immun. 1983 Mar;39(3):1252-9 PMID: 6341234
  3. Prevention of infection by trimethoprim-sulfamethoxazole plus amphotericin B in patients with acute nonlymphocytic leukaemia.
    Ann Intern Med. 1981 Nov;95(5):555-9 PMID: 6794406
  4. Colonization resistance of the digestive tract of mice during systemic antibiotic treatment.
    J Hyg (Lond). 1972 Dec;70(4):605-10 PMID: 4567309
  5. Translocation of certain indigenous bacteria from the gastrointestinal tract to the mesenteric lymph nodes and other organs in a gnotobiotic mouse model.
    Infect Immun. 1979 Feb;23(2):403-11 PMID: 154474
  6. Promotion by burn stress of the translocation of bacteria from the gastrointestinal tracts of mice.
    Arch Surg. 1984 Feb;119(2):166-72 PMID: 6230067
  7. Ecology of Candida albicans gut colonization: inhibition of Candida adhesion, colonization, and dissemination from the gastrointestinal tract by bacterial antagonism.
    Infect Immun. 1985 Sep;49(3):654-63 PMID: 3897061
  8. Colonization resistance of the digestive tract in conventional and antibiotic-treated mice.
    J Hyg (Lond). 1971 Sep;69(3):405-11 PMID: 4999450
  9. Trimethoprim-sulfamethoxazole in the prevention of infection in neutropenic patients. EORTC International Antimicrobial Therapy Project Group.
    J Infect Dis. 1984 Sep;150(3):372-9 PMID: 6384377
  10. Promotion of the translocation of enteric bacteria from the gastrointestinal tracts of mice by oral treatment with penicillin, clindamycin, or metronidazole.
    Infect Immun. 1981 Sep;33(3):854-61 PMID: 6456996
  11. Role of the macrophage in the translocation of intestinal bacteria.
    Arch Surg. 1987 Jan;122(1):48-53 PMID: 3541854
  12. Selective suppression of alimentary tract microbial flora as prophylaxis during granulocytopenia.
    Antimicrob Agents Chemother. 1981 Nov;20(5):620-4 PMID: 6275778
  13. Protective role of intestinal flora against infection with Pseudomonas aeruginosa in mice: influence of antibiotics on colonization resistance.
    Infect Immun. 1985 Jan;47(1):118-22 PMID: 2856912
  14. Selective antimicrobial modulation as prophylaxis against infection during granulocytopenia: trimethoprim-sulfamethoxazole vs. nalidixic acid.
    J Infect Dis. 1983 Apr;147(4):624-34 PMID: 6842003
  15. Selective antimicrobial modulation of human microbial flora: infection prevention in patients with decreased host defense mechanisms by selective elimination of potentially pathogenic bacteria.
    J Infect Dis. 1981 May;143(5):644-54 PMID: 7017019
Article Info
Journal
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology
Abbr.
Eur J Clin Microbiol Infect Dis
ISSN
0934-9723
Published
1988-02-00
Pages
107-13
Language
English
Region
Germany
NLM ID
8804297
Subset
IM
Grants
NIAID NIH HHS · AI23484 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com