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.
Journal Information
Vol. 15. Issue 2.
Pages 144-150 (March - April 2011)
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
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Monique Ribeiro Tiba1,
, Claúdia de Moura2, Marcelo Falsarella Carazzolle3, Domingos da Silva Leite4
Corresponding author
mrtiba@gmail.com
Correspondence to: Monique Ribeiro Tiba Rua Visconde de Taunay, 147/41, Vila Itapura, Campinas, SP, Brazil.
Correspondence to: Monique Ribeiro Tiba Rua Visconde de Taunay, 147/41, Vila Itapura, Campinas, SP, Brazil.
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Article information
Abstract
Keywords:
Escherichia coli
antigens
bacterial
polymerase chain reaction
polymorphism
restriction fragment length
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