Epidemiological study of pap genes among diarrheagenic or septicemic Escherichia coli strains producing CS31A and F17 adhesins and characterization of Pap(31A) fimbriae

Citation
Y. Bertin et al., Epidemiological study of pap genes among diarrheagenic or septicemic Escherichia coli strains producing CS31A and F17 adhesins and characterization of Pap(31A) fimbriae, J CLIN MICR, 38(4), 2000, pp. 1502-1509
Citations number
43
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
38
Issue
4
Year of publication
2000
Pages
1502 - 1509
Database
ISI
SICI code
0095-1137(200004)38:4<1502:ESOPGA>2.0.ZU;2-Y
Abstract
The association of the pap operon with the CS31A and F17 adhesins was studi ed with 255 Escherichia coli strains isolated from calves, lambs, or humans with diarrhea, The three classes of PapG adhesin with different receptor b inding preferences were also screened. The pap operon was associated with 5 0 and 36% of human strains that produced CS31A and ovine strains that produ ced F17, respectively, Among the bovine isolates, the pap operon was detect ed in 61% of the CS31A-positive isolates and 72% of the strains that produc e both CS31A and F17, The class II adhesin gene was present in bovine (20%) and ovine (71%) isolates, Both class II and III adhesins were genetically associated with 36% of the human strains. The highest prevalence of the pap operon was observed among E. coli strains that produce additional adhesins involved in the binding of bacteria to intestinal cells. Among the bovine isolates, the reference strain for CS31A and F17c was found to be positive for the pap operon, Phenotypic and genotypic characterizations were underta ken. Pap(31A) appeared as fine and flexible fimbriae surrounding the bacter ia but did not mediate adhesion to calf intestinal villi. Pap(31A) producti on was optimal with bacteria cultured on minimal growth media and repressed by addition of exogenous leucine, The deduced amino acid sequence of the P apA(31A) structural subunit shelved 57 to 97% identity with the different P -related structural subunits produced by E. coli strains isolated from pigs with septicemia or humans with urinary trace infections. None of the three papG allelic variants was detected, but a homologous papG gene was present in the chromosome of strain 31A.