Journal Information
Vol. 15. Issue 2.
Pages 144-150 (March - April 2011)
Share
Share
Download PDF
More article options
Vol. 15. Issue 2.
Pages 144-150 (March - April 2011)
Original article
Open Access
Identification of putative new Escherichia coli flagellar antigens from human origin using serology, PCR-RFLP and DNA sequencing methods
Visits
2531
Monique Ribeiro Tiba1,
Corresponding author
mrtiba@gmail.com

Correspondence to: Monique Ribeiro Tiba Rua Visconde de Taunay, 147/41, Vila Itapura, Campinas, SP, Brazil.
, Claúdia de Moura2, Marcelo Falsarella Carazzolle3, Domingos da Silva Leite4
1 MSc; Dr.; Post-doctorate, Universidade Estadual de Campinas - UNICAMP, São Paulo, Brazil
2 MSc; PhD Candidate, UNICAMP, São Paulo, Brazil
3 MSc, Dr.; Physicist, UNICAMP, São Paulo, Brazil
4 MSc, Dr.; Professor, UNICAMP, São Paulo, Brazil
This item has received

Under a Creative Commons license
Article information
Abstract

Escherichia coli has been isolated frequently, showing flagellar antigens that are not recognized by any of the 53 antisera, provided by the most important reference center of E. coli, The International Escherichia and Klebsiella Center (WHO) of the Statens Serum Institute, Copenhagen, Denmark. The objective of this study was to characterize flagellar antigens of E. coli that express non-typeable H antigens. The methods used were serology, PCR-RFLP and DNA sequencing. This characterization was performed by gene amplification of the fliC (flagellin protein) by polymerase chain reaction in all 53 standards E.coli strains for the H antigens and 20 E. coli strains for which the H antigen was untypeable. The amplicons were digested by restriction enzymes, and different restriction enzyme profiles were observed. Anti-sera were produced in rabbits, for the non-typeable strains, and agglutination tests were carried out. In conclusion,the results showed that although non-typeable and typable H antigens strains had similar flagellar antigens, the two types of strains were distinct in terms of nucleotide sequence, and did not phenotypically react with the standard antiserum, as expected. Thirteen strains had been characterized as likely putative new H antigen using PCR-RFLP techniques, DNA sequencing and/or serology.

Keywords:
Escherichia coli
antigens
bacterial
polymerase chain reaction
polymorphism
restriction fragment length
Full text is only aviable in PDF
References
[1.]
J. Machado, F. Grimont, P.A.D. Grimont.
Identification of Escherichia coli flagellar types by restriction of the amplified fliC gene.
Res Microbiol, 151 (2000), pp. 535-546
[2.]
R. Prager, U. Strutz, A. Fruth, H. Tschäpe.
Subtyping of pathogenic Escherichia coli strains using flagellar (H) – antigens: serotyping versus fliC polymorphisms.
Int J Med Microbiol, 292 (2003), pp. 477-486
[3.]
L. Wang, D. Rothemund, H. Curd, P.R. Reeves.
Species-wide variation in the Escherichia coli flagellin (H-antigen) gene.
J Bacteriol, 185 (2003), pp. 2936-2943
[4.]
I. Ørskov, F. Ørskov.
Escherichia coli serotyping and in man and animals.
Can J Microbiol, 38 (1992), pp. 699-704
[5.]
Y.A. Ratiner.
Temperature-dependent flagellar antigen phase variation in Escherichia coli.
Res Microbiol, 150 (1999), pp. 457-463
[6.]
G. Schoenhals, C. Whitfield.
Comparative analysis of flagellin sequences from Escherichia coli strains possessing serologically distinct flagellar filaments with a shared complex surface pattern.
J Bacteriol, 175 (1993), pp. 5395-5402
[7.]
P.I. Fields, K. Blom, H.J. Hughes, L.O. Helsel, P. Feng, B. Swaminathan.
Molecular characterization of the gene encoding H antigen in Escherichia coli and development of a PCR-Restriction fragment length polymorphism test for identification of E. coli O157:H7 and O157:NM.
J Clin Microbiol, 35 (1997), pp. 1066-1070
[8.]
J.MK. Amhaz, A. Andrade, S.Y. Bando, T.L. Tanaka, C.A. Moreira-Filha, M.B. Martinez.
Molecular typing and phylogenetic analysis of enteroinvasive Escherichia coli using the fliC gene sequence.
FEMS Microbiol Lett, 235 (2004), pp. 259-264
[9.]
F. Scheutz, T. Cheasty, D. Woodward, H.R. Smith.
Designation of O174 and O175 to temporary O groups OX3 and OX7, and six new E. coli O groups that include Verocytotoxin-producing E. coli (VTEC): O176, O177, O178, O179, O180 and O181.
[10.]
F. Ørskov, I. Ørskov, B. Jann, K. Jann.
Serology, chemistry, and genetics of O and K antigens of Escherichia coli.
Bacteriol Rev, 41 (1977), pp. 667-710
[11.]
W.H. Ewing, P.R. Edwards.
The genus Escherichia. Identification of Enterobacteriaceae.
Burgess, (1983),
[12.]
J. Sambrook, E.F. Fritsch, T. Maniatis.
Molecular cloning: A laboratory manual.
CSHL, (1989),
Copyright © 2011. Elsevier Editora Ltda.. All rights reserved
The Brazilian Journal of Infectious Diseases
Article options
Tools