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Identification and cloning of the gene encoding BmpC: an outer-membrane lipoprotein associated with Brachyspira pilosicoli membrane vesicles

¹ School of Veterinary Science, The University of Queensland, St Lucia, Queensland, Australia
² Bacterial Pathogenesis Research Group, Department of Microbiology, Monash University, Victoria, Australia
³ Bacterial Diseases of Livestock Research, National Animal Disease Center, Ames, IA, USA
⁴ Microscopy Services, National Animal Disease Center, Ames, IA, USA
⁵ Pre-Harvest Food Safety Research, National Animal Disease Center, Ames, IA, USA
⁶ Veterinary Medical Research Institute, Iowa State University, Ames, IA, USA

Correspondence
Darren J. Trott
d.trott{at}mailbox.uq.edu.au

The intestinal spirochaete Brachyspira pilosicoli causes colitis in a wide variety of host species. Little is known about the structure or protein constituents of the B. pilosicoli outer membrane (OM). To identify surface-exposed proteins in this species, membrane vesicles were isolated from B. pilosicoli strain 95-1000 cells by osmotic lysis in dH₂O followed by isopycnic centrifugation in sucrose density gradients. The membrane vesicles were separated into a high-density fraction (HDMV; =1·18 g cm^–3) and a low-density fraction (LDMV; =1·12 g cm^–3). Both fractions were free of flagella and soluble protein contamination. LDMV contained predominantly OM markers (lipo-oligosaccharide and a 29 kDa B. pilosicoli OM protein) and was used as a source of antigens to produce mAbs. Five B. pilosicoli-specific mAbs reacting with proteins with molecular masses of 23, 24, 35, 61 and 79 kDa were characterized. The 23 kDa protein was only partially soluble in Triton X-114, whereas the 24 and 35 kDa proteins were enriched in the detergent phase, implying that they were integral membrane proteins or lipoproteins. All three proteins were localized to the B. pilosicoli OM by immunogold labelling using specific mAbs. The gene encoding the abundant, surface-exposed 23 kDa protein was identified by screening a B. pilosicoli 95-1000 genome library with the mAb and was expressed in Escherichia coli. Sequence analysis showed that it encoded a unique lipoprotein, designated BmpC. Recombinant BmpC partitioned predominantly in the OM fraction of E. coli strain SOLR. The mAb to BmpC was used to screen a collection of 13 genetically heterogeneous strains of B. pilosicoli isolated from five different host species. Interestingly, only strain 95-1000 was reactive with the mAb, indicating that either the surface-exposed epitope on BmpC is variable between strains or that the protein is restricted in its distribution within B. pilosicoli.

The GenBank accession numbers for the sequences reported in this paper are AY363613, AY363614 and AY376355.

This article has been cited by other articles:

				D. J. Hampson, T. La, B. Adler, and D. J. Trott Proposed revisions to the nomenclature for Brachyspira membrane proteins and lipoproteins Microbiology, January 1, 2006; 152(1): 1 - 2. [Full Text] [PDF]