Multiphasic analysis of xanthomonads causing bacterial spot disease on tomato and pepper in the Caribbean and Central America: Evidence for common lineages within and between countries

Citation
H. Bouzar et al., Multiphasic analysis of xanthomonads causing bacterial spot disease on tomato and pepper in the Caribbean and Central America: Evidence for common lineages within and between countries, PHYTOPATHOL, 89(4), 1999, pp. 328-335
Citations number
44
Categorie Soggetti
Plant Sciences
Journal title
PHYTOPATHOLOGY
ISSN journal
0031949X → ACNP
Volume
89
Issue
4
Year of publication
1999
Pages
328 - 335
Database
ISI
SICI code
0031-949X(199904)89:4<328:MAOXCB>2.0.ZU;2-P
Abstract
Four hundred thirty-three xanthomonad strains isolated fi om tomato or pepp er plants from 32 different fields in four Caribbean and Central American c ountries were screened for the ability to hydrolyze starch and sodium polyp ectate and for resistance to copper and streptomycin. Of these, 95 represen tative strains were further characterized by various phnetic tests, and 63 of these strains were then analyzed by genomic fingerprinting. Most of the strains (>90%) were tolerant to copper. However, there was much more variab ility in sensitivity to streptomycin. All strains in Guadeloupe and 93% of the strains in Barbados were sensitive to streptomycin. The majority of str ains were typical Xanthomonas campestris pv. vesicatoria group A strains. i n Barbados, however, a unique group of strains was identified that was sero logically similar to group A strains but was amylolytic. These strains were designated Al. The occurrence of X. campestris pv. vesicatoria group B str ains in Central America was found to be limited to two fields in Costa Pica and one in Guatemala. No group B strains were identified in the Caribbean, in contrast to common occurrence in the central United States and in South America. T3 strains were not found in this study, despite the recent incre ase of such strains in Florida and Mexico. Unique strains from Costa Rica b elonging to the X. gardneri group were identified. Little linkage was found among phenotypic and rep-polymerase chain reaction (rep-PCR) genomic finge rprinting profiles of the pathogens except at the species/pathovar level; s trains displaying virtually identical fingerprint profiles were found to co rrespond to distinct races and vice versa. The rep-PCR genomic fingerprinti ng analyses suggest that certain lineages may have evolved or predominated in specific regions or specific countries.