Genetic Diversity and Pathogenic Potential of Attaching and Effacing Escherichia coli O26:H11 Strains Recovered from Bovine Feces in the United States

被引:16
作者
Ison, Sarah A. [1 ]
Delannoy, Sabine [2 ]
Bugarel, Marie [1 ]
Nightingale, Kendra K. [1 ]
Webb, Hattie E. [1 ]
Renter, David G. [3 ]
Nagaraja, Tiruvoor G. [3 ]
Loneragan, Guy H. [1 ]
Fach, Patrick [2 ]
机构
[1] Texas Tech Univ, Dept Anim & Food Sci, Lubbock, TX 79409 USA
[2] French Agcy Food Environm & Occupat Hlth & Safety, Food Safety Lab, Platform IdentyPath, Maisons Alfort, France
[3] Kansas State Univ, Dept Diagnost Med Pathobiol, Manhattan, KS 66506 USA
基金
美国食品与农业研究所;
关键词
HEMOLYTIC-UREMIC SYNDROME; HUMANS; CATTLE; PREVALENCE; O157; IDENTIFICATION; INFECTIONS; SEROTYPES; VARIANTS; CHILDREN;
D O I
10.1128/AEM.00397-15
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
Escherichia coli O26 has been identified as the most common non-O157 Shiga toxin-producing E. coli (STEC) serogroup to cause human illnesses in the United States and has been implicated in outbreaks around the world. E. coli has high genomic plasticity, which facilitates the loss or acquisition of virulence genes. Attaching and effacing E. coli (AEEC) O26 strains have frequently been isolated from bovine feces, and there is a need to better characterize the relatedness of these strains to defined molecular pathotypes and to describe the extent of their genetic diversity. High-throughput real-time PCR was used to screen 178 E. coli O26 isolates from a single U.S. cattle feedlot, collected from May to July 2011, for the presence or absence of 25 O26 serogroup-specific and virulence-associated markers. The selected markers were capable of distinguishing these strains into molecularly defined groups (yielding 18 unique marker combinations). Analysis of the clustered regularly interspaced short palindromic repeat 1 (CRISPR1) and CRISPR2a loci further discriminated isolates into 24 CRISPR types. The combination of molecular markers and CRISPR typing provided 20.8% diversity. The recent CRISPR PCR target SP_O26-E, which was previously identified only in stx(2)-positive O26:H11 human clinical strains, was identified in 96.4% (161/167 [95% confidence interval, 99.2 to 93.6%]) of the stx-negative AEEC O26: H11 bovine fecal strains. This supports that these stx-negative strains may have previously contained a prophage carrying stx or could acquire this prophage, thus possibly giving them the potential to become pathogenic to humans. These results show that investigation of specific genetic markers may further elucidate our understanding of the genetic diversity of AEEC O26 strains in bovine feces.
引用
收藏
页码:3671 / 3678
页数:8
相关论文
共 53 条
[1]   Genomic diversity of pathogenic Escherichia coli of the EHEC 2 clonal complex [J].
Abu-Ali, Galeb S. ;
Lacher, David W. ;
Wick, Lukas M. ;
Qi, Weihong ;
Whittam, Thomas S. .
BMC GENOMICS, 2009, 10
[2]  
Allerberger Franz, 2003, International Journal of Infectious Diseases, V7, P42, DOI 10.1016/S1201-9712(03)90041-5
[3]   Putative Adhesins of Enteropathogenic and Enterohemorrhagic Escherichia coli of Serogroup O26 Isolated from Humans and Cattle [J].
Bardiau, Marjorie ;
Labrozzo, Sabrina ;
Mainil, Jacques G. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2009, 47 (07) :2090-2096
[4]   Molecular profiling and phenotype analysis of Escherichia coli O26:H11 and O26:NM:: Secular and geographic consistency of enterohemorrhagic and enteropathogenic isolates [J].
Bielaszewska, M ;
Zhang, WL ;
Tarr, PI ;
Sonntag, AK ;
Karch, H .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (08) :4225-4228
[5]   Shiga toxin-negative attaching and effacing Escherichia coli:: Distinct clinical associations with bacterial phylogeny and virulence traits and inferred in-host pathogen evolution [J].
Bielaszewska, Martina ;
Middendorf, Barbara ;
Koeck, Robin ;
Friedrich, Alexander W. ;
Fruth, Angelika ;
Karch, Helge ;
Schmidt, M. Alexander ;
Mellmann, Alexander .
CLINICAL INFECTIOUS DISEASES, 2008, 47 (02) :208-217
[6]   Aspects of genome plasticity in pathogenic Escherichia coli [J].
Bielaszewska, Martina ;
Dobrindt, Ulrich ;
Gaertner, Julia ;
Gallitz, Inka ;
Hacker, Jorg ;
Karch, Helge ;
Mueller, Daniel ;
Schubert, Soren ;
Schmidt, M. Alexander ;
Sorsa, Liisa Johanna ;
Zdziarski, Jaroslaw .
INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2007, 297 (7-8) :625-639
[7]   Shiga toxin gene loss and transfer in vitro and in vivo during enterohemorrhagic Escherichia coli O26 infection in humans [J].
Bielaszewska, Martina ;
Prager, Rita ;
Koeck, Robin ;
Mellmann, Alexander ;
Zhang, Wenlan ;
Tschaepe, Helmut ;
Tarr, Phillip I. ;
Karch, Helge .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (10) :3144-3150
[8]   Enterohemorrhagic Escherichia coli O26: H11/H-: A New Virulent Clone Emerges in Europe [J].
Bielaszewska, Martina ;
Mellmann, Alexander ;
Bletz, Stefan ;
Zhang, Wenlan ;
Koeck, Robin ;
Kossow, Annelene ;
Prager, Rita ;
Fruth, Angelika ;
Orth-Hoeller, Dorothea ;
Marejkova, Monika ;
Morabito, Stefano ;
Caprioli, Alfredo ;
Pierard, Denis ;
Smith, Geraldine ;
Jenkins, Claire ;
Curova, Katarina ;
Karch, Helge .
CLINICAL INFECTIOUS DISEASES, 2013, 56 (10) :1373-1381
[9]   Typing of intimin (eae) enteropathogenic from children with genes from Escherichia coli (EPEC) isolated diarrhoea in Montevideo, Uruguay:: identification of two novel intimin variants (μB and ξR/β2B) [J].
Blanco, Miguel ;
Blanco, Jesus E. ;
Dahbi, Ghizlane ;
Mora, Azucena ;
Pilar Alonso, Maria ;
Varela, Gustavo ;
Pilar Gadea, Maria ;
Schelotto, Felipe ;
Gonzalez, Enrique A. ;
Blanco, Jorge .
JOURNAL OF MEDICAL MICROBIOLOGY, 2006, 55 (09) :1165-1174
[10]   Non-O157 shiga toxin-producing Escherichia coli infections in the United States, 1983-2002 [J].
Brooks, JT ;
Sowers, EG ;
Wells, JG ;
Greene, KD ;
Griffin, PM ;
Hoekstra, RM ;
Strockbine, NA .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (08) :1422-1429