A 16S rRNA gene oligonucleotide probe for identification of Bacillus thuringiensis isolates from sheep fleece

被引:20
作者
Akhurst, RJ
Lyness, EW
Zhang, QY
Cooper, DJ
Pinnock, DE
机构
[1] UNIV ADELAIDE, WAITE AGR RES INST, DEPT CROP PROTECT, GLEN OSMOND, SA 5064, AUSTRALIA
[2] ADELAIDE WOMENS & CHILDRENS HOSP, DEPT MICROBIOL, ADELAIDE, SA 5006, AUSTRALIA
关键词
D O I
10.1006/jipa.1996.4610
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
Larvae of the Australian sheep blowfly Lucilia cuprina are susceptible to some strains of Bacillus thuringiensis, including some isolates from sheep fleeces from South Australia and Western Australia. Larvicidal strains of B. thuringiensis include var. thuringiensis, tolworthi, darmstadiensis, morrisoni, and toumanoffi. As part of an ecological study, a large number of B. thuringiensis fleece isolates from untreated sheep and sheep previously treated with larvicidal B. thuringiensis were screened for larvicidal activity. A ribotyping method to distinguish larvicidal B. thuringiensis jetted (sprayed) onto sheep from the natural B. thuringiensis flora of the fleece was developed. A cloned fragment of the 16S rRNA gene used as a probe for B. thuringiensis DNA digested with restriction endonucleases enables separation of B. thuringiensis serovars and separation within the serovars thuringiensis, tolworthi, and kurstaki. The 16S gene probe method is useful for distinguishing between reisolates of larvicidal B. thuringiensis jetted onto sheep and the background B. thuringiensis population present prior to jetting. (C) 1997 Academic Press.
引用
收藏
页码:24 / 30
页数:7
相关论文
共 16 条
[1]   COMBINATION OF 16S RIBOSOMAL-RNA-TARGETED OLIGONUCLEOTIDE PROBES WITH FLOW-CYTOMETRY FOR ANALYZING MIXED MICROBIAL-POPULATIONS [J].
AMANN, RI ;
BINDER, BJ ;
OLSON, RJ ;
CHISHOLM, SW ;
DEVEREUX, R ;
STAHL, DA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (06) :1919-1925
[2]   A STAPHYLOCOCCUS-AUREUS-SPECIFIC OLIGONUCLEOTIDE PROBE DERIVED FROM 16S RIBOSOMAL-RNA GENE-SEQUENCES [J].
BENTLEY, RW ;
HARLAND, NM ;
LEIGH, JA ;
COLLINS, MD .
LETTERS IN APPLIED MICROBIOLOGY, 1993, 16 (04) :203-206
[3]  
COOPER DJ, 1985, 4TH P AUSTR C GRASSL, P236
[4]  
DEBARJAC H, 1990, ENTOMOPHAGA, V35, P233, DOI 10.1007/BF02374798
[5]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[6]  
FENCHEL T, 1992, ARCH MICROBIOL, V158, P394
[7]  
HOFTE H, 1989, MICROBIOL REV, V53, P242
[8]   IDENTIFICATION OF BETA-EXOTOXIN PRODUCTION, PLASMIDS ENCODING BETA-EXOTOXIN, AND A NEW EXOTOXIN IN BACILLUS-THURINGIENSIS BY USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
LEVINSON, BL ;
KASYAN, KJ ;
CHIU, SS ;
CURRIER, TC ;
GONZALEZ, JM .
JOURNAL OF BACTERIOLOGY, 1990, 172 (06) :3172-3179
[9]   MICROBIAL ECOLOGY OF SHEEP FLEECE [J].
LYNESS, EW ;
PINNOCK, DE ;
COOPER, DJ .
AGRICULTURE ECOSYSTEMS & ENVIRONMENT, 1994, 49 (01) :103-112
[10]  
Maniatis T., 1982, MOL CLONING