Abundance and distribution of bacteria carrying sltll gene in natural river water

被引:29
作者
Kurokawa, K
Tani, K
Ogawa, M
Nasu, M
机构
[1] Osaka Univ, Grad Sch Pharm, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Geneome Informat Res Ctr, Suita, Osaka 565, Japan
关键词
D O I
10.1046/j.1365-2672.1999.00516.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Direct in situ PCR with HNPP/Fast Red TR was used to enumerate bacteria carrying the sltII gene in river water. By direct in situ PCR with a sltII-specific EVS primer, 10(2)-10(5) cells ml(-1) of bacteria carrying the sltII gene were detected from all sampling sites, except the site nearest to the source of the river, while 10(2)-10(4) cells ml(-1) of Escherichia coli O157:H7 were detected using a direct fluorescent antibody staining method. These results indicate that such bacteria are commonly distributed in natural river water. Direct ii? situ PCR with HNPP/Fast Red TR is a useful tool for detecting cells carrying specific genes, such as verotoxin-producing bacteria in natural environments.
引用
收藏
页码:405 / 410
页数:6
相关论文
共 31 条
  • [1] Swimming-associated haemorrhagic colitis due to Escherichia coli O157:H7 infection: Evidence of prolonged contamination of a fresh water lake
    Ackman, D
    Marks, S
    Mack, P
    Caldwell, M
    Root, T
    Birkhead, G
    [J]. EPIDEMIOLOGY AND INFECTION, 1997, 119 (01) : 1 - 8
  • [2] LEGIONELLA CONTAMINATION OF DENTAL-UNIT WATERS
    ATLAS, RM
    WILLIAMS, JF
    HUNTINGTON, MK
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (04) : 1208 - 1213
  • [3] DETECTION OF COLIFORM BACTERIA IN WATER BY POLYMERASE CHAIN-REACTION AND GENE PROBES
    BEJ, AK
    STEFFAN, RJ
    DICESARE, J
    HAFF, L
    ATLAS, RM
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (02) : 307 - 314
  • [4] In situ reverse transcription, an approach to characterize genetic diversity and activities of prokaryotes
    Chen, F
    Gonzalez, JM
    Dustman, WA
    Moran, MA
    Hodson, RE
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (12) : 4907 - 4913
  • [5] VIABLE BUT NON-CULTURABLE VIBRIO-CHOLERAE AND RELATED PATHOGENS IN THE ENVIRONMENT - IMPLICATIONS FOR RELEASE OF GENETICALLY ENGINEERED MICROORGANISMS
    COLWELL, RR
    BRAYTON, PR
    GRIMES, DJ
    ROSZAK, DB
    HUQ, SA
    PALMER, LM
    [J]. BIO-TECHNOLOGY, 1985, 3 (09): : 817 - 820
  • [6] Analysis of the enterohemorrhagic Escherichia coli O157 DNA region containing lambdoid phage gene p and shiga-like toxin structural genes
    Datz, M
    JanetzkiMittmann, C
    Franke, S
    Gunzer, F
    Schmidt, H
    Karch, H
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (03) : 791 - 797
  • [7] The effect of temperature, pH and medium in a surface adhesion immunofluorescent technique for detection of Listeria monocytogenes
    Duffy, G
    Sheridan, JJ
    [J]. JOURNAL OF APPLIED MICROBIOLOGY, 1997, 83 (01) : 95 - 101
  • [8] RAPID DETECTION OF SALMONELLAE IN POULTRY WITH THE MAGNETIC IMMUNO-POLYMERASE CHAIN-REACTION ASSAY
    FLUIT, AC
    WIDJOJOATMODJO, MN
    BOX, ATA
    TORENSMA, R
    VERHOEF, J
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (05) : 1342 - 1346
  • [9] IN-SITU PCR FOR VISUALIZATION OF MICROSCALE DISTRIBUTION OF SPECIFIC GENES AND GENE-PRODUCTS IN PROKARYOTIC COMMUNITIES
    HODSON, RE
    DUSTMAN, WA
    GARG, RP
    MORAN, MA
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (11) : 4074 - 4082
  • [10] JACKSON MP, 1987, FEMS MICROBIOL LETT, V44, P109, DOI 10.1111/j.1574-6968.1987.tb02252.x