Iwm. Tenaya et al., PREPARATION OF DIAGNOSTIC POLYCLONAL AND MONOCLONAL-ANTIBODIES AGAINST OUTER ENVELOPE PROTEINS OF SERPULINA-PILOSICOLI, Journal of Medical Microbiology, 47(4), 1998, pp. 317-324
The purpose of this study was to prepare specific sera for use in the
rapid detection and identification of the intestinal spirochaete Serpu
lina pilosicoli. In Western blot analysis, with pig antiserum which wa
s raised against whole cells of S. pilosicoli and absorbed with outer
envelope protein extracts from S. hyodysenteriae and S. innocens, a pr
ominent protein with M-r of c. 72 kDa was consistently identified in o
uter envelope preparations of S. pilosicoli strains. Immunogold labell
ing demonstrated that this was located on the outer surface of intact
S. pilosicoli cells. Two monoclonal antibodies (MAbs), designated C12
and M96, were raised against the protein. Although C12 reacted with a
protein band of c. 72 kDa, this was also present in preparations from
strains of other Serpulina spp. examined. MAb M96 reacted with an 80-k
Da protein which was present only in preparations made from strains of
S. pilosicoli. This was used in Western blot analysis and in an immun
odot-blot assay with outer envelope extracts to specifically identify
S. pilosicoli strains isolated from man, pigs, dogs and poultry. An in
direct immunofluorescence test with MAb M96 also was used to detect an
d identify whole S. pilosicoli cells. Therefore, both the cross-absorb
ed antiserum and MAb M96 are potentially useful reagents for the detec
tion and identification of S. pilosicoli.