Literature DB >> 328787

Isolation and identification of encapsulated strains of Bacteroides fragilis.

D L Kasper, M E Hayes, B G Reinap, F O Craft, A B Onderdonk, B F Polk.   

Abstract

One hundred three clinical isolates of Bacteroides fragilis were identified during a two-year period. Most of these isolates were strains of B. fragilis subspecies fragilis, which constitutes a minor component of the fecal flora in comparison with the other subspecies of B. fragilis. By use of several techniques for demonstration of capsules, it was found that only B. fragilis strains classified as subspecies fragilis were encapsulated. An indirect immunofluorescence assay was developed for identification of clinical isolates possessing capsular material that was immunologically similar to that found in the reference strain of B. fragilis subspecies fragilis. All strains examined that were classified as subspecies fragilis were positive in this assay for the capsular material, whereas strains of the other subspecies were negative. This tests represents a rapid and sensitive means of identifying the most prevalent anaerobic gram-negative bacillus involved in human infections. The capsular polysaccharide of B. fragilis subspecies fragilis is a unique factor associated with the predominant subspecies of B. fragilis isolated from clinical material.

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Year:  1977        PMID: 328787     DOI: 10.1093/infdis/136.1.75

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  26 in total

1.  Promoter orientation of the immunomodulatory Bacteroides fragilis capsular polysaccharide A (PSA) is off in individuals with inflammatory bowel disease (IBD).

Authors:  Lucy E Blandford; Emma L Johnston; Jeremy D Sanderson; William G Wade; Alistair J Lax
Journal:  Gut Microbes       Date:  2019-02-07

Review 2.  Serological responses to antigens of Bacteroidaceae.

Authors:  T Hofstad
Journal:  Microbiol Rev       Date:  1979-03

3.  The pathogenic properties of Fusobacterium and Bacteroides species from wallabies and other sources.

Authors:  G R Smith; J C Oliphant; R Parsons
Journal:  J Hyg (Lond)       Date:  1984-04

4.  Characterization of opsonins for Bacteroides fragilis in immune sera collected from experimentally infected mice.

Authors:  T M Ellis; J T Barrett
Journal:  Infect Immun       Date:  1982-03       Impact factor: 3.441

5.  Immune response to Bacteroides ureolyticus in a patient with brain abscess.

Authors:  M K Lalitha; K V Mathai; G Koshi
Journal:  J Clin Microbiol       Date:  1983-08       Impact factor: 5.948

6.  Evidence for T cell-dependent immunity to Bacteroides fragilis in an intraabdominal abscess model.

Authors:  A B Onderdonk; R B Markham; D F Zaleznik; R L Cisneros; D L Kasper
Journal:  J Clin Invest       Date:  1982-01       Impact factor: 14.808

7.  The distribution of Bacteroides fragilis serotypes amongst clinical strains.

Authors:  K M Elhag; S Tabaqchali
Journal:  J Hyg (Lond)       Date:  1978-08

8.  Relationships between serological groups and deoxyribonucleic acid homology groups in Bacteroides fragilis and related species.

Authors:  J L Babb; C S Cummings
Journal:  J Clin Microbiol       Date:  1981-02       Impact factor: 5.948

9.  Encapsulation of Bacteroides species.

Authors:  J L Babb; C S Cummins
Journal:  Infect Immun       Date:  1978-03       Impact factor: 3.441

10.  Adherence of Bacteroides fragilis in vivo.

Authors:  A B Onderdonk; N E Moon; D L Kasper; J G Bartlett
Journal:  Infect Immun       Date:  1978-03       Impact factor: 3.441

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