The Journal of Allergy and Clinical Immunology
Volume 121, Issue 1 , Pages 135-140, January 2008

Bifidobacterium pseudocatenulatum is associated with atopic eczema: A nested case-control study investigating the fecal microbiota of infants

  • Claudia Gore, MD, PhD

      Affiliations

    • North West Lung Research Center, Wythenshawe Hospital, Manchester, United Kingdom
  • ,
  • Karen Munro, NZCS

      Affiliations

    • Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand
  • ,
  • Christophe Lay, PhD

      Affiliations

    • Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand
  • ,
  • Rodrigo Bibiloni, PhD

      Affiliations

    • Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand
  • ,
  • Julie Morris, MSc

      Affiliations

    • North West Lung Research Center, Wythenshawe Hospital, Manchester, United Kingdom
  • ,
  • Ashley Woodcock, MD

      Affiliations

    • North West Lung Research Center, Wythenshawe Hospital, Manchester, United Kingdom
  • ,
  • Adnan Custovic, MD, PhD

      Affiliations

    • North West Lung Research Center, Wythenshawe Hospital, Manchester, United Kingdom
  • ,
  • Gerald W. Tannock, PhD

      Affiliations

    • Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand
    • Corresponding Author InformationReprint requests: Gerald W. Tannock, PhD, Department of Microbiology and Immunology, University of Otago, PO Box 56, Dunedin, New Zealand.

Received 1 July 2007; received in revised form 22 July 2007; accepted 26 July 2007. published online 27 September 2007.

Background

Exposure to specific bacterial bowel commensals may increase/reduce the risk of atopic diseases.

Objective

To compare fecal bacterial communities of young infants with/without eczema.

Methods

Nested case-control study. Infants age 3 to 6 months with eczema (cases, n = 37) and without (controls, n = 24) were matched for sex, age, feeding (breast/bottle/mixed/solids), ethnicity. Information was collected on maternal/infant antibiotic exposure, feeding, gastrointestinal symptoms, family history of allergy. Eczema severity scoring was used (Severity Scoring of Atopic Dermatitis index). Samples were taken for determination of allergen-specific serum IgE (cases) and urinary/fecal eosinophilic protein X. Gastrointestinal permeability was measured. The compositions of fecal bacterial communities were analyzed (culture-independent, nucleic acid–based analyses).

Results

There was no difference in overall profiles of fecal bacterial communities between cases and controls. Family history of allergy increased likelihood of bifidobacteria detection (history, 86%; no history, 56%; P = .047); breast-fed infants were more likely to harbor Bifidobacterium bifidum (odds ratio, 5.19; 95% CI, 1.47-18.36; P = .01). Bifidobacterium pseudocatenulatum was detected more commonly in feces of non–breast-fed children (odds ratio, 5.6; 95% CI, 1.3-24.3; P = .02) and children with eczema (eczema, 26%; no eczema, 4%; P = .04). There were no significant associations between clinical measurements and detection of B pseudocatenulatum.

Conclusion

Presence of B pseudocatenulatum in feces was associated with eczema and with exclusive formula-feeding; B bifidum was associated with breast-feeding.

Key words: Eczema, atopic dermatitis, atopy, allergy, gastrointestinal, microbiota, microflora, bifidobacteria, fecal bacterial community

Abbreviations used: Cy5, Indodicarbocyanine, EPX, Eosinophilic protein X, F-EPX, Fecal eosinophilic protein X, OR, Odds ratio, SCORAD, Severity Scoring of Atopic Dermatitis, TTGE, Temporal temperature gel electrophoresis, U-EPX, Urinary eosinophilic protein X

 

 The probiotic intervention study as part of which infants with atopic eczema were recruited was supported by Nestec Ltd.

 Disclosure of potential conflict of interest: A. Woodcock has received grant support from Nestle. A. Custovic has received grant support from Asthma UK, Moulton Charitable Trust, MRC, and GlaxoSmithKline and is on the speakers' bureau for GlaxoSmithKline, AstraZeneca, UCB Pharma, ALK, and Phadia. The rest of the authors have declared that they have no conflict of interest.

PII: S0091-6749(07)01530-8

doi:10.1016/j.jaci.2007.07.061

The Journal of Allergy and Clinical Immunology
Volume 121, Issue 1 , Pages 135-140, January 2008