PhD

Twenty-five isolates from ducks and one from fowl were characterized as P. multocida using standard bacteriological procedures. A reference chicken strain (LKO) obtained from IVRI was used for comparison. All the avian isolates were found to be pathogenic for mice. Variation in fermentation patterns of dulcitol, mannitol, sorbitol and trehalose allowed the 27 isolates to be grouped into ten biovars. Two biotypes P. multocida subsp. septica, and P. multocida subsp. multocida were observed among the avian examined. All the isolates were uniformly sensitive to enrofloxacin, chloramphenicol and pefloxacin. Eight isolates from ducks and one from fowl have been serotyped as A:1. A species-specific PCR assay was used to confirm the identity of the isolates. Performing PCR on template DNA prepared from blood smears was found to be an extremely rapid method of diagnosis for pasteurella.
No polymorphism within the KMT1 gene could be demonstrated by restriction analysis of PM-PCR product with Hae III. Restriction endonucleases analysis of genomic DNA of all the avian isolates with Hpa II and Hha I revealed three profiles each. The fowl isolates had a profile that was common to majority of the duck isolates.
Eighty-eight per cent of the isolates carried plasmids. Two plasmid profiles were observed among the isolates examined. All the avian isolates showed a single REP-PCR profile indicating a high level of homogeneity among them.
The outer membrane protein profiles of all the avian isolates were similar. Two protein fractions with molecular weights of 37.15 and 26.36 kDa were identified as the major OMPs by SDS-PAGE.

A 37.15-kDa protein was identified the major antigenic fraction of OMPs of avian isolates as of P. multocida by Western blotting. Two other proteins with a molecular mass of 31.33 and 26.36 kDa were also found to be antigenic using this technique.
The OmpH gene of all the avian isolates as well serotypes A:3 and B:2 were amplified using primers designed based on published OmpH gene sequence of a chicken isolate of P. multocida. The amplified product digested with restriction endonucleases Dra I and Hinf I generated four and three fragments respectively. The similarity of the profiles for all the avian isolates of P. multocida, suggested a high degree of homogeneity amongst the amplified region.
Restriction analysis of the OmpH-PCR products of serotypes A:1, A:3 and B:2 with Dra I generated profiles which were distinct from each other for the three serotypes. This technique can be helpful for differentiation of various serotypes of P. multocida. Studies on the OmpH gene(s) of inactivated fowl cholera vaccine revealed similarity with the amplified region of the local duck isolate of P. multocida. Since this gene codes for the major antigenic fraction of P. multocida the vaccine can be expected to confer immunity to ducks in Kerala against pasteurellosis.
The sequence the OmpH-PCR product has been submitted to the GenBank and has been assigned the accession No AY606823. The sequence showed 98 per cent identity with P. multocida strain X-73 (serotype A:1) outer membrane protein (OmpH) gene.