
Distribution of streptomycin resistance and biosynthesis genes in streptomycetes recovered from different soil sites
Author(s) -
Tolba Sahar,
Egan Sharon,
Kallifidas Dimitris,
Wellington Elizabeth M.H.
Publication year - 2002
Publication title -
fems microbiology ecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.377
H-Index - 155
eISSN - 1574-6941
pISSN - 0168-6496
DOI - 10.1111/j.1574-6941.2002.tb01017.x
Subject(s) - streptomycin , biology , streptomyces griseus , streptomyces , 16s ribosomal rna , microbiology and biotechnology , streptomycetaceae , gene , botany , bacteria , genetics , antibiotics , actinomycetales
Streptomycin resistant streptomycetes were isolated from four diverse sites. Two sites in Germany were sampled and included an agricultural experimental plot of apple trees which had a history of streptomycin application (AR) and a control site without antibiotic application (CR). Two sites in the UK were sampled; a pastureland site which had sewage injection (DW) and an agricultural site (CW). The actinomycete counts indicated a high proportion of streptomycin resistant isolates in the CW soil. Streptomycetes were identified by partial sequencing of the 16S rDNA. PCR product of the hypervariable γ region of 16S rDNA allowed analysis by denaturing gradient gel electrophoresis to assess the diversity within the isolates. The streptomycin and sewage sludge treated sites showed decreased diversity within streptomycete populations. Isolates were screened for the streptomycin resistance gene, strA , and flanking biosynthesis gene, strB 1. Distribution of these genes indicated the prevalence of str genes in the streptomycin treated soil. Evidence of horizontal gene transfer was recorded in isolates identified as Streptomyces platensis recovered from CR and AR sites which had acquired a streptomycin resistance gene homologous to that found in Streptomyces griseus . Members of the latter species were the most abundant streptomycin resistant streptomycetes isolated from all soils.