GENETIC AND PLASMID DIVERSITY WITHIN NATURAL-POPULATIONS OF PSEUDOMONAS-SYRINGAE WITH VARIOUS EXPOSURES TO COPPER AND STREPTOMYCIN BACTERICIDES

Citation
Gw. Sundin et al., GENETIC AND PLASMID DIVERSITY WITHIN NATURAL-POPULATIONS OF PSEUDOMONAS-SYRINGAE WITH VARIOUS EXPOSURES TO COPPER AND STREPTOMYCIN BACTERICIDES, Applied and environmental microbiology, 60(12), 1994, pp. 4421-4431
Citations number
69
Categorie Soggetti
Microbiology,"Biothechnology & Applied Migrobiology
ISSN journal
00992240
Volume
60
Issue
12
Year of publication
1994
Pages
4421 - 4431
Database
ISI
SICI code
0099-2240(1994)60:12<4421:GAPDWN>2.0.ZU;2-W
Abstract
We examined the genetic and plasmid diversity within natural populatio ns of Pseudomonas syringae isolated from three ornamental pear nurseri es in eastern Oklahoma. The bactericide spray regimen differed at each nursery; copper and streptomycin, only copper, and no bactericides we re applied at nurseries I, II and III, respectively. Resistance to cop per (Cu-r) and resistance to streptomycin (Sm-r were determined for 1, 938 isolates of P. syringae; isolates from nurseries I and II were gen erally Cu-r Sm-s; whereas most isolates from nursery III were Cu-s Sm- s. The plasmid profiles of 362 isolates were determined, and six, one, seven, and four plasmid profiles were obtained for Cu-r Sm-r, Cu-r Sm -r, and Cu-s Sm-s isolates, respectively. All Sm-r plasmids contained sequences homologous to the strA and strB Sm-r genes from broad-host-r ange plasmid RSF1010 and were associated with Sm-r transposon Tn5393. Plasmids were placed into two groups on the basis of hybridization to the oriV and par sequences from pOSU900, a cryptic plasmid in P. syrin gae pv. syringae. A total of 100 randomly chosen P. syringae isolates from nurseries I and III were analyzed for genetic diversity by using the arbitrarily primed PCR (AP-PCR) technique. An analysis of chromoso mal genotypes by AP-PCR revealed a high degree of genetic diversity am ong the isolates, and the results of this analysis indicated that the isolates could be clustered into two distinct groups. The plasmid prof iles were specific to isolates belonging to particular AP-PCR groups. Within each AP-PCR group, identical plasmid profiles were produced by isolates that had different chromosomal genotypes, implying that plasm id transfer has played an important role in the dissemination of Cu-r and Sm-r within the populations studied.