Expression of putative virulence factors of Escherichia coli O157:H7 differs in bovine and human infections

被引:49
作者
Rashid, Rebecca A.
Tabata, Tami A.
Oatley, Melissa J.
Besser, Thomas E.
Tarr, Phillip I.
Moseley, Steve L.
机构
[1] Univ Washington, Dept Microbiol, Seattle, WA 98195 USA
[2] Washington State Univ, Dept Vet Microbiol & Pathol, Pullman, WA 99164 USA
[3] Washington State Univ, Sch Med, Pullman, WA 99164 USA
关键词
D O I
10.1128/IAI.00299-06
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Escherichia coli O157:H7 is a commensal organism in cattle, but it is a pathogen in humans. This differential expression of virulence suggests that specific virulence factors are regulated differently in human and bovine hosts. To test this hypothesis, relative real-time reverse transcription-PCR was used to relate the expression of several putative virulence genes (eae espA stx(2) rfbE, ehx4, and iha) to that of the "housekeeping" gene gnd during natural human and experimental bovine infection with E. coli O157:H7. We examined these genes in fecal samples from eight humans and four calves. iha and espA were significantly more expressed in bovine infections. rfbE and ehxA appeared to be more highly expressed in human infections, though these differences did not achieve statistical significance. Our results support the hypothesis that some virulence-associated genes of O157:H7 are differentially expressed in a host-specific manner.
引用
收藏
页码:4142 / 4148
页数:7
相关论文
共 45 条
[1]   Characterization of an RTX toxin from enterohemorrhagic Escherichia coli O157:H7 [J].
Bauer, ME ;
Welch, RA .
INFECTION AND IMMUNITY, 1996, 64 (01) :167-175
[2]   Fractionation of nucleic acids into single-stranded and double-stranded forms [J].
Beld, M ;
Sol, C ;
Goudsmit, J ;
Boom, R .
NUCLEIC ACIDS RESEARCH, 1996, 24 (13) :2618-2619
[3]   Role of the Escherichia coli O157:H7 O side chain in adherence and analysis of an rfb locus [J].
Bilge, SS ;
Vary, JC ;
Dowell, SF ;
Tarr, PI .
INFECTION AND IMMUNITY, 1996, 64 (11) :4795-4801
[4]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[5]   The complete DNA sequence and analysis of the large virulence plasmid of Escherichia coli O157:H7 [J].
Burland, V ;
Shao, Y ;
Perna, NT ;
Plunkett, G ;
Sofia, HJ ;
Blattner, FR .
NUCLEIC ACIDS RESEARCH, 1998, 26 (18) :4196-4204
[6]   INHIBITION OF TRANSLATION INITIATION ON ESCHERICHIA-COLI GND MESSENGER-RNA BY FORMATION OF A LONG-RANGE SECONDARY STRUCTURE INVOLVING THE RIBOSOME BINDING-SITE AND THE INTERNAL COMPLEMENTARY SEQUENCE [J].
CHANG, JHT ;
GREEN, CBR ;
WOLF, RE .
JOURNAL OF BACTERIOLOGY, 1995, 177 (22) :6560-6567
[7]   Haemolysin production by strains of verocytotoxin-producing Escherichia coli [J].
Chart, H ;
Jenkins, C ;
Smith, HR ;
Hedges, D ;
Rowe, B .
MICROBIOLOGY-UK, 1998, 144 :103-107
[8]   Pathogenicity of Escherichia coli O157:H7 in the intestines of neonatal calves [J].
DeanNystrom, EA ;
Bosworth, BT ;
Cray, WC ;
Moon, HW .
INFECTION AND IMMUNITY, 1997, 65 (05) :1842-1848
[9]   Microarray based comparison of two Escherichia coli O157:H7 lineages [J].
Dowd, SE ;
Ishizaki, H .
BMC MICROBIOLOGY, 2006, 6 (1)
[10]   Identification of Escherichia coli O157:H7 genes influencing colonization of the bovine gastrointestinal tract using signature-tagged mutagenesis [J].
Dziva, F ;
van Diemen, PM ;
Stevens, MP ;
Smith, AJ ;
Wallis, TS .
MICROBIOLOGY-SGM, 2004, 150 :3631-3645