Table 1. Virulence-associated genes typical for E. coli isolated from diarrheic pigs (iVAGs) and isolated from extraintestinal disease (eVAGs) and phylogenetic origin of 104 porcine non-hemolytic E. coli isolates.
gene(s) or operon | description | prevalence in E. coli (n = 104) from healthy pigs of this study in% | prevalence in E. coli (n = 93) from wild boars of the study Römer et al. [17] and of our actual study (#) in% |
iVAGs 1 | |||
est-1a | Heat stabile enterotoxin 1 | 0 | 3.2 |
est-2 | Heat stabile enterotoxin 2 | 2.9 | 3.2 |
fedA | Subunit of F18 fimbriae | 0 | 1.1 |
stx2e | Shigatoxin 2e | 1.9 | 5.4 |
fanA | Subunit of F5 fimbriae | 0 | 0 |
fimF41a | Subunit of F41 fimbriae | 0 | 0 |
fasA | Subunit of F6 fimbriae | 1.0 | 0 |
eltB-Ip | Heat labile enterotoxin 1 | 0 | 0 |
faeG | Subunit of F4 fimbriae | 0 | 0 |
eVAGs 2 | |||
Adhesins | |||
aatA | APEC autotransporter | 16.3* | 1.1 #* |
afa/draB | Afimbrial/Dr antigen-specific adhesin | 1.0 | 0 |
csgA | Curli fibre-encoding gene | 78.8 | 87.1 |
fimC | Type 1 fimbriae (D-mannose specific adhesin) | 91.3* | 100* |
fimH | Type 1 fimbriae (D-mannose specific adhesin) | 96.1* | 83.9 #* |
hra | Heat-resistant agglutinin | 13.5* | 23.7* |
H7 | H7 flagellar antigen | 15.4 | 11.8 # |
iha | Iron-regulated-gene-homologue adhesin | 0* | 5.4* |
mat | Meningitis-associated and temperature-regulated fimbriae | 81.7* | 48.4* |
papAH | Pilus associated with pyelonephritis | 1.9 | 0 |
papC | Pilus associated with pyelonephritis | 9.6* | 0* |
papEF | Pilus associated with pyelonephritis | 4.8 | 0 |
papGII | Pilus associated with pyelonephritis | 5.8 | 0 |
papGIII | Pilus associated with pyelonephritis | 1.0 | 0 |
papGII/III | Pilus associated with pyelonephritis | 0 | 0 |
sfa/focCD | S fimbriae (sialic acid-specific) and F1C fimbriae | 4.8 | 5.4 |
tsh 1 | Temperature sensitive hemagglutinin | 16.3* | 4.3* |
yqi | APEC fimbrial adhesin | 27.9 | 30.1 # |
Iron acquisition | |||
chuA | Heme receptor gene (E. coli haem utilization) | 19.2* | 39.8* |
feoB | Major bacterial ferrous iron transporter, iron(II) transport system | 98.1* | 73.1 #* |
fyuA | Ferric Yersinia uptake (yersiniabactin receptor) | 26.9 | 30.0 |
ireA | Iron-responsive element (putative catecholate siderophore receptor) | 9.6 | 3.2 |
iroN 1 | Catecholate siderophore (salmochelin) receptor | 21.2* | 10.8* |
irp2 | Iron repressible protein (yersiniabactin synthesis) | 22.1 | 19.4 |
iucD 1 | Aerobactin synthesis | 26.0* | 1.1* |
sitD chr. | Salmonella iron transport system gene | 1.0* | 11.8* |
sitD ep.1 | Salmonella iron transport system gene | 14.4* | 5.4* |
iutA | Aerobactin receptor | 36.5* | 5.4 #* |
Protectins/Serum resistance | |||
cvi/cva 1 | Structural genes of colicin V operon (Microcin ColV) | 19.2* | 6.5* |
neuC | K1 capsular polysaccharide | 2.9 | 0 |
kpsMT II | Group II capsule antigens | 21.2 | 24.7 |
ompA | Outer membrane protein | 94.2* | 100* |
traT 1 | Transfer Protein | 51.9 | 45.2 |
Toxins | |||
astA | EAST1 (heat stable cytotoxin associated with enteroaggregative E. coli) | 43.3 | 39.2 # |
sat | Secreted autotransporter toxin | 1.0 | 3.2 |
hlyA | Haemolysin A | 3.8 | 0 |
cnf1/2 | Cytotoxic necrotising factor 1/2 | 6.7 | 10.8 |
Invasins | |||
gimB | Genetic island associated with neonatal meningitis | 0 | 0 |
ibeA | Invasion of brain endothelium | 3.8* | 16.1* |
tia | Toxigenic invasion locus in ETEC isolates | 3.8 | 5.4 |
Miscellaneous | |||
pic | Serine protease autotransporter | 4.8 | 6.5 |
malX | Pathogenicity-associated island marker CFT073 | 7.7 | 16.1 |
ECoR group | |||
A | 63.5* | 29.0* | |
B1 | 17.3* | 32.3* | |
B2 | 4.8* | 21.5* | |
D | 14.4 | 17.2 |
Comparison to E. coli from wild boars of an already published study.
differences between both groups statistically significant with p<0.05
n.t. = not tested
iVAGs were included since it was shown that an iVAG can affect colonization [58].
eVAGs were included since it was shown that eVAGs correlated with successful intestinal E. coli colonization in pigs [29].