Affiliation:
1. Medicine Service, Veterans Affairs Medical Center, and Department of Medicine, University of Minnesota, Minneapolis, Minnesota
Abstract
ABSTRACT
Data regarding the hemagglutination (HA) patterns of the three variants (classes I, II, and III) of the
Escherichia coli
adhesin PapG are conflicting. These HA patterns usually have been assessed for each
papG
allele separately with recombinant strains in slide HA assays. We rigorously evaluated an alternative microtiter tray HA assay and then used it to assess the HA of four erythrocyte types (human A
1
P
1
and OP
1
, rabbit, and sheep erythrocytes) by multiple wild-type
E. coli
strains representing the four naturally occurring combinations of the
papG
alleles, i.e., class I plus III, class III only, class II plus III, and class II only. The microtiter tray HA assay displayed significantly better reproducibility of intraobserver (83%) and interobserver (86%) results than did slide HA assays (39 and 73%, respectively). Novel findings from the study of 32 wild-type P-fimbriated strains included reproducible determinations of phenotypic diversity among different
papG
categories, among strains within each
papG
category, and from day to day for individual strains. There was also substantial overlap of phenotypes between
papG
categories I plus III and III only and between II plus III and II only. A class III
papG
recombinant strain’s HA pattern differed significantly from that of the wild-type class III strains. These data demonstrate that HA phenotypes of wild-type P-fimbriated
E. coli
strains can be reproducibly assessed by a microtiter HA assay and that they correspond broadly to
papG
genotype but in a more complex and varied fashion than previously recognized.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
Cited by
20 articles.
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