scholarly journals Imprecise excision of insertion element IS5 from the fliC gene contributes to flagellar diversity in Escherichia coli

2006 ◽  
Vol 256 (2) ◽  
pp. 195-202 ◽  
Author(s):  
Eckhard Strauch ◽  
Lothar Beutin
1984 ◽  
Vol 81 (14) ◽  
pp. 4500-4504 ◽  
Author(s):  
L. Green ◽  
R. D. Miller ◽  
D. E. Dykhuizen ◽  
D. L. Hartl

2020 ◽  
Vol 10 (1) ◽  
pp. 14-23
Author(s):  
William R Schwan ◽  
Nicole L Flohr ◽  
Abigail R Multerer ◽  
Jordan C Starkey

2008 ◽  
Vol 28 (10) ◽  
pp. 508-514 ◽  
Author(s):  
Tatiana Amabile de Campos ◽  
Gerson Nakazato ◽  
Eliana Guedes Stehling ◽  
Marcelo Brocchi ◽  
Wanderley Dias da Silveira

The clonal relationship among avian Escherichia coli strains and their genetic proximity with human pathogenic E. coli, Salmonela enterica, Yersinia enterocolitica and Proteus mirabilis, was determined by the DNA sequencing of the conserved 5' and 3'regions fliC gene (flagellin encoded gene). Among 30 commensal avian E. coli strains and 49 pathogenic avian E. coli strains (APEC), 24 commensal and 39 APEC strains harbored fliC gene with fragments size varying from 670bp to 1,900bp. The comparative analysis of these regions allowed the construction of a dendrogram of similarity possessing two main clusters: one compounded mainly by APEC strains and by H-antigens from human E. coli, and another one compounded by commensal avian E. coli strains, S. enterica, and by other H-antigens from human E. coli. Overall, this work demonstrated that fliC conserved regions may be associated with pathogenic clones of APEC strains, and also shows a great similarity among APEC and H-antigens of E. coli strains isolated from humans. These data, can add evidence that APEC strains can exhibit a zoonotic risk.


2013 ◽  
Vol 33 (4) ◽  
pp. 417-422 ◽  
Author(s):  
Cláudia de Moura ◽  
Monique Ribeiro Tiba ◽  
Marcio José da Silva ◽  
Domingos da Silva Leite

Identification of Escherichia coli requires knowledge regarding the prevalent serotypes and virulence factors profiles allows the classification in pathogenic/non-pathogenic. However, some of these bacteria do not express flagellar antigen invitro. In this case the PCR-restriction fragment length polymorphism (RFLP-PCR) and sequencing of the fliC may be suitable for the identification of antigens by replacing the traditional serology. We studied 17 samples of E. coli isolated from animals and presenting antigen H nontypeable (HNT). The H antigens were characterized by PCR-RFLP and sequencing of fliC gene. Three new flagellin genes were identified, for which specific antisera were obtained. The PCR-RFLP was shown to be faster than the serotyping H antigen in E. coli, provided information on some characteristics of these antigens and indicated the presence of new genes fliC.


2000 ◽  
Vol 151 (7) ◽  
pp. 535-546 ◽  
Author(s):  
Jorge Machado ◽  
Francine Grimont ◽  
Patrick A.D. Grimont
Keyword(s):  

2008 ◽  
Vol 52 (8) ◽  
pp. 2929-2932 ◽  
Author(s):  
Vincent Cattoir ◽  
Patrice Nordmann ◽  
Jesus Silva-Sanchez ◽  
Paula Espinal ◽  
Laurent Poirel

ABSTRACT A novel QnrB-like plasmid-mediated resistance determinant, QnrB19, was identified from an Escherichia coli clinical isolate from Colombia. Its gene was associated with an ISEcp1-like insertion element that did not act as a promoter for its expression. Using an in vitro model of transposition, we showed that the ISEcp1-like element was able to mobilize the qnrB19 gene.


Pathogens ◽  
2020 ◽  
Vol 9 (2) ◽  
pp. 73
Author(s):  
Roman Kotłowski ◽  
Katarzyna Grecka ◽  
Barbara Kot ◽  
Piotr Szweda

Easy-to-perform, fast, and inexpensive methods of differentiation of Escherichia coli strains beyond the species level are highly required. Herein two new, original tools for genotyping of E. coli isolates are proposed. The first of the developed method, a PCR-RFLP (polymerase chain reaction-restriction fragment length polymorphism) test uses a highly variable fliC gene, encoding the H antigen as a molecular target. The designing of universal pair of primers and selection of the optimal restriction enzyme RsaI was preceded by in silico comparative analysis of the sequences of the genes coding for 53 different serotypes of H-antigen (E. coli flagellin). The target fragments of E. coli genomes for MLST method were selected on the basis of bioinformatics analysis of complete sequences of 16 genomes of E. coli. Initially, seven molecular targets were proposed (seven pairs of primers) and five of them were found useful for effective genotyping of E. coli strains. Both developed methods revealed high differentiation power, and a high genetic diversity of the strains tested was observed. Within the group of 71 strains tested, 29 and 47 clusters were revealed with fliC RFLP-PCR and MLST methods, respectively. Differentiation of the strains with the reference BOX-PCR method revealed 31 different genotypes. The in silico analysis revealed that the discriminatory power of the new MLST method is comparable to the Pasteur and Achtman schemes and is higher than the discriminatory power of the method developed by Clermont. From the epidemiology point of view, the outcomes of our investigation revealed that in most cases, the patients were infected with unique strains, probably from environmental sources. However, some strains isolated from different patients of the wards of pediatrics, internal medicine, and neurology were classified to the same genotype when the results of all three methods were taken into account. It could suggest that they were transferred between the patients.


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