TY - JOUR
T1 - Phenotypic characteristics contributing to the enhanced growth of Escherichia coli bloom strains
AU - Nanayakkara, Buddhie S.
AU - O'Brien, Claire L.
AU - Gordon, David M.
N1 - Funding Information:
This study was funded in part by an Australian Research Council Linkage Grant (Grant No. LP120100327). Additional support was provided by Melbourne Water, Water Corporation of Western Australia, Queensland Bulk Water Authority, Hunter Water Corporation, South East Water, Yarra Valley Water, City West Water, Sydney Water Corporation, South Australian Water Corporation, Sydney Catchment Authority, Fitzroy River Water and Victorian Department of Health. Portions of the research were also funded by Water Research Australia (2018) Management of Environmental E. coli , Project 1101.
Funding Information:
This study was funded in part by an Australian Research Council Linkage Grant (Grant No. LP120100327). Additional support was provided by Melbourne Water, Water Corporation of Western Australia, Queensland Bulk Water Authority, Hunter Water Corporation, South East Water, Yarra Valley Water, City West Water, Sydney Water Corporation, South Australian Water Corporation, Sydney Catchment Authority, Fitzroy River Water and Victorian Department of Health. Portions of the research were also funded by Water Research Australia (2018) Management of Environmental E. coli, Project 1101.
Publisher Copyright:
© 2019 Society for Applied Microbiology and John Wiley & Sons Ltd
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019/12/1
Y1 - 2019/12/1
N2 - During bloom events, Escherichia coli cell counts increase to between 10,000 and 100,000 cfu/100 ml of water. The strains responsible for bloom events belong to E. coli phylogenetic groups A and B1, and all have acquired a capsule from Klebsiella. A pan-genome comparison of phylogroup A E. coli revealed that the ferric citrate uptake system (fecIRABCDE) was overrepresented in phylogroup A bloom strains compared with non-bloom E. coli. A series of experiments were carried out to investigate if the capsule together with ferric citrate uptake system could confer a growth rate advantage on E. coli. Capsulated strains had a growth rate advantage regardless of the media composition and the presence/absence of the fec operon, and they had a shorter lag phase compared with capsule-negative strains. The results suggest that the Klebsiella capsule may facilitate nutrient uptake or utilization by a strain. This, together with the protective roles played by the capsule and the shorter lag phase of capsule-positive strains, may explain why it is only capsule-positive strains that produce elevated counts in response to nutrient influx.
AB - During bloom events, Escherichia coli cell counts increase to between 10,000 and 100,000 cfu/100 ml of water. The strains responsible for bloom events belong to E. coli phylogenetic groups A and B1, and all have acquired a capsule from Klebsiella. A pan-genome comparison of phylogroup A E. coli revealed that the ferric citrate uptake system (fecIRABCDE) was overrepresented in phylogroup A bloom strains compared with non-bloom E. coli. A series of experiments were carried out to investigate if the capsule together with ferric citrate uptake system could confer a growth rate advantage on E. coli. Capsulated strains had a growth rate advantage regardless of the media composition and the presence/absence of the fec operon, and they had a shorter lag phase compared with capsule-negative strains. The results suggest that the Klebsiella capsule may facilitate nutrient uptake or utilization by a strain. This, together with the protective roles played by the capsule and the shorter lag phase of capsule-positive strains, may explain why it is only capsule-positive strains that produce elevated counts in response to nutrient influx.
UR - http://www.scopus.com/inward/record.url?scp=85074841801&partnerID=8YFLogxK
U2 - 10.1111/1758-2229.12801
DO - 10.1111/1758-2229.12801
M3 - Article
C2 - 31642169
AN - SCOPUS:85074841801
SN - 1758-2229
VL - 11
SP - 817
EP - 824
JO - Environmental Microbiology Reports
JF - Environmental Microbiology Reports
IS - 6
M1 - 31642169
ER -