Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 148 (2002), 1513-1522
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Gordon, D. M.
Right arrow Articles by Johnson, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gordon, D. M.
Right arrow Articles by Johnson, J. R.
Agricola
Right arrow Articles by Gordon, D. M.
Right arrow Articles by Johnson, J. R.
Microbiology (2002), 148, 1513-1522.
© 2002 Society for General Microbiology


Research Paper

The genetic structure of Escherichia coli populations in primary and secondary habitats

David M. Gordon1, Sonja Bauer1 and James R. Johnson2

School of Botany and Zoology, Australian National University, Canberra, ACT, Australia1
Medical Service, VA Medical Center and Department of Medicine, University of Minnesota, Minneapolis, MN, USA2

Author for correspondence: David M. Gordon. Tel: +61 02 6125 3552. Fax: +61 02 6125 5573. e-mail: David.Gordon{at}anu.edu.au

Escherichia coli were recovered from the members of two two-person households and their associated septic tanks. The E. coli were isolated using selective and non-selective isolation techniques, characterized using the method of multi-locus enzyme electrophoresis and screened for the presence of virulence factors associated with extra-intestinal disease by using PCR. The growth rate–temperature relationships of strains from the two habitats were also determined. Temporal variation explained 25% of the observed electrophoretic type (ET) diversity in the humans. Among-host variation accounted for 29% of the observed allelic diversity. In one household, ET diversity of the E. coli population in the septic tank was significantly lower than ET diversity in the humans providing the inputs to the septic tank. Molecular analysis of variance revealed that, on average, strains recovered from the septic tank of this household were genetically distinct from strains recovered from the humans providing the faecal inputs to the septic tank. Further, the growth rate–temperature response of strains differed between strains isolated from the septic tank and strains isolated from the humans. Septic tank isolates grew better at low temperatures than strains isolated from humans, but more slowly at high temperatures compared to the human isolates. By contrast, no real differences in ET diversity, allelic diversity, or the growth charcteristics of strains could be detected between strains from the humans and strains from the septic tank of the other household. The results of this study suggest there are strains of E. coli that are better ‘adapted’ to conditions found in the external environment compared to strains isolated from the gastrointestinal habitat. Further, the finding that the numerically dominant clones and clonal diversity in secondary habitats can differ substantially from those found in the source populations will confound efforts to identify the sources of faecal pollution in the environment.

Keywords: population structure, coliforms, human, septic tank

Abbreviations: AMOVA, molecular analysis of variance; ET, electrophoretic type; MLEE, multi-locus enzyme electrophoresis




This article has been cited by other articles:


Home page
Appl. Environ. Microbiol.Home page
T. W. Alexander, T. Reuter, R. Sharma, L. J. Yanke, E. Topp, and T. A. McAllister
Longitudinal Characterization of Resistant Escherichia coli in Fecal Deposits from Cattle Fed Subtherapeutic Levels of Antimicrobials
Appl. Envir. Microbiol., November 15, 2009; 75(22): 7125 - 7134.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
S. T. Walk, E. W. Alm, D. M. Gordon, J. L. Ram, G. A. Toranzos, J. M. Tiedje, and T. S. Whittam
Cryptic Lineages of the Genus Escherichia
Appl. Envir. Microbiol., October 15, 2009; 75(20): 6534 - 6544.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
T. M. Bergholz, C. L. Tarr, L. M. Christensen, D. J. Betting, and T. S. Whittam
Recent Gene Conversions between Duplicated Glutamate Decarboxylase Genes (gadA and gadB) in Pathogenic Escherichia coli
Mol. Biol. Evol., October 1, 2007; 24(10): 2323 - 2333.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
P. Duriez and E. Topp
Temporal Dynamics and Impact of Manure Storage on Antibiotic Resistance Patterns and Population Structure of Escherichia coli Isolates from a Commercial Swine Farm
Appl. Envir. Microbiol., September 1, 2007; 73(17): 5486 - 5493.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
W. B. Ksoll, S. Ishii, M. J. Sadowsky, and R. E. Hicks
Presence and Sources of Fecal Coliform Bacteria in Epilithic Periphyton Communities of Lake Superior
Appl. Envir. Microbiol., June 15, 2007; 73(12): 3771 - 3778.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
H. Wildschutte and J. G. Lawrence
Differential Salmonella survival against communities of intestinal amoebae
Microbiology, June 1, 2007; 153(6): 1781 - 1789.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
D. M. Stoeckel and V. J. Harwood
Performance, Design, and Analysis in Microbial Source Tracking Studies
Appl. Envir. Microbiol., April 15, 2007; 73(8): 2405 - 2415.
[Full Text] [PDF]


Home page
J. Environ. Qual.Home page
J. R. Vogel, D. M. Stoeckel, R. Lamendella, R. B. Zelt, J. W. Santo Domingo, S. R. Walker, and D. B. Oerther
Identifying Fecal Sources in a Selected Catchment Reach Using Multiple Source-Tracking Tools
J. Environ. Qual., April 5, 2007; 36(3): 718 - 729.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
S. Ishii, W. B. Ksoll, R. E. Hicks, and M. J. Sadowsky
Presence and Growth of Naturalized Escherichia coli in Temperate Soils from Lake Superior Watersheds
Appl. Envir. Microbiol., January 1, 2006; 72(1): 612 - 621.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
Z. Lu, D. Lapen, A. Scott, A. Dang, and E. Topp
Identifying Host Sources of Fecal Pollution: Diversity of Escherichia coli in Confined Dairy and Swine Production Systems
Appl. Envir. Microbiol., October 1, 2005; 71(10): 5992 - 5998.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
K. L. Anderson, J. E. Whitlock, and V. J. Harwood
Persistence and Differential Survival of Fecal Indicator Bacteria in Subtropical Waters and Sediments
Appl. Envir. Microbiol., June 1, 2005; 71(6): 3041 - 3048.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
D. M. Gordon, S. E. Stern, and P. J. Collignon
Influence of the age and sex of human hosts on the distribution of Escherichia coli ECOR groups and virulence traits
Microbiology, January 1, 2005; 151(1): 15 - 23.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
S. L. McLellan
Genetic Diversity of Escherichia coli Isolated from Urban Rivers and Beach Water
Appl. Envir. Microbiol., August 1, 2004; 70(8): 4658 - 4665.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
H. Wildschutte, D. M. Wolfe, A. Tamewitz, and J. G. Lawrence
Protozoan predation, diversifying selection, and the evolution of antigenic diversity in Salmonella
PNAS, July 20, 2004; 101(29): 10644 - 10649.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
S. M. Dixit, D. M. Gordon, X.-Y. Wu, T. Chapman, K. Kailasapathy, and J. J.-C. Chin
Diversity analysis of commensal porcine Escherichia coli - associations between genotypes and habitat in the porcine gastrointestinal tract
Microbiology, June 1, 2004; 150(6): 1735 - 1740.
[Abstract] [Full Text] [PDF]


Home page
J. Environ. Qual.Home page
J. L. Ram, R. P. Ritchie, J. Fang, F. S. Gonzales, and J. P. Selegean
Sequence-Based Source Tracking of Escherichia coli Based on Genetic Diversity of {beta}-Glucuronidase
J. Environ. Qual., May 1, 2004; 33(3): 1024 - 1032.
[Abstract] [Full Text] [PDF]


Home page
J. Environ. Qual.Home page
R. L. Kuntz, P. G. Hartel, D. G. Godfrey, J. L. McDonald, K. W. Gates, and W. I. Segars
Targeted Sampling Protocol as Prelude to Bacterial Source Tracking with Enterococcus faecalis
J. Environ. Qual., November 1, 2003; 32(6): 2311 - 2318.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
S. Seurinck, W. Verstraete, and S. D. Siciliano
Use of 16S-23S rRNA Intergenic Spacer Region PCR and Repetitive Extragenic Palindromic PCR Analyses of Escherichia coli Isolates To Identify Nonpoint Fecal Sources
Appl. Envir. Microbiol., August 1, 2003; 69(8): 4942 - 4950.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
M. D. Winfield and E. A. Groisman
Role of Nonhost Environments in the Lifestyles of Salmonella and Escherichia coli
Appl. Envir. Microbiol., July 1, 2003; 69(7): 3687 - 3694.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2002 Society for General Microbiology.