CAMP factor homologues in Propionibacterium acnes: a new protein family differentially expressed by types I and II

Author:

Valanne Susanna1,McDowell Andrew1,Ramage Gordon1,Tunney Michael M.1,Einarsson Gisli G.1,O'Hagan Seamus1,Wisdom G. Brian2,Fairley Derek3,Bhatia Ajay4,Maisonneuve Jean-Francois4,Lodes Michael4,Persing David H.4,Patrick Sheila1

Affiliation:

1. Department of Microbiology and Immunobiology, School of Medicine, Queen's University, Grosvenor Road, Belfast BT12 6BN, UK

2. School of Biology and Biochemistry, Medical Biology Centre, 97 Lisburn Road, Queen's University, Belfast BT9 7BL, UK

3. QUESTOR Centre, Queen's University, David Keir Building, Stranmillis Road, Belfast BT9 5AG, UK

4. Corixa Corporation, Infectious Disease Institute, Seattle, WA 98104, USA

Abstract

Analysis of the draft genome sequence of the opportunistic pathogenPropionibacterium acnestype strain NCTC 737 (=ATCC 6919) revealed five genes with sequence identity to the co-haemolytic Christie–Atkins–Munch-Peterson (CAMP) factor ofStreptococcus agalactiae. The predicted molecular masses for the expressed proteins ranged from 28 to 30 kDa. The genes were present in each of the three recently identifiedrecA-based phylogenetic groupings ofP. acnes(IA, IB and II), as assessed by PCR amplification. Conserved differences in CAMP factor gene sequences between these three groups were also consistent with their previous phylogenetic designations. All type IA, IB and II isolates were positive for the co-haemolytic reaction on sheep blood agar. Immunoblotting and silver staining of SDS-PAGE gels, however, revealed differential protein expression of CAMP factors amongst the different groups. Type IB and II isolates produced an abundance of CAMP factor 1, detectable by specific antibody labelling and silver staining of SDS-PAGE gels. In contrast, abundant CAMP factor production was lacking in type IA isolates, although larger amounts of CAMP factor 2 were detectable by immunoblotting compared with type II isolates. While the potential role of the abundant CAMP factor 1 in host colonization or virulence remains to be determined, it should be noted that the type strain ofP. acnesused in much of the published literature is a type IA isolate and is, therefore, lacking in this attribute.

Publisher

Microbiology Society

Subject

Microbiology

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