Rahim Sorouri
1*, Ali Ramazani
2, Ali Karami
3, Reza Ranjbar
3, Edward C. Guy
41 Department of Microbiology, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran
2 Zanjan Pharmaceutical Biotechnology Research Center, Zanjan University of Medical Sciences, Zanjan, Iran
3 Molecular Biology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
4 Toxoplasma Reference Laboratory (TRL), Singleton Hospital, Swansea, Wales, UK
Abstract
Introduction: Lyme disease is an infectious disease caused by the by spiral-shaped bacterium Borrelia burgdorferi. We investigated the presence and prevalence of Borrelia species in ticks from southern England.
Methods:
One hundred fifty-five ticks (103 adult ticks and 52 nymphal ticks)
were collected from animal carcases. The midguts were removed and
cultured in Barbour/Stoenner/Kelly II (BSK-II) and
Barbour/Stoenner/Kelly F (BSK-F) media, examined by IF, dark-field
microscopy, and nested PCR.
Results:
From a total 155 cultured ticks, two showed evidence of spirochetes and
denoted as SO-1 and SO-2 strains. The availability of these two
isolates enabled their antigenic characterization with SDS-PAGE and
western blotting and comparison with two standard isolates. These
studies identified six protein antigens with molecular weights of 18,
30, 39, 47, 60 and 88 kDa with particular promise for detecting specific
immune responses to B. burgdorferi infection including Lyme
disease. We also investigated the effect of repeated subculture on the
antigenic pattern of UK isolate of B. burgdorferi.
Conclusion:
As a result of this study, antigenic differences have been seen between
the UK isolates and the foreign isolates used as laboratory standards.