A Mathematical Model for Escherichia coli Chemotaxis to Competing Stimuli

Author(s):  
Scott A. Middlebrooks ◽  
Xueying Zhao ◽  
Roseanne M. Ford ◽  
Peter T. Cummings

2014 ◽  
Vol 240 ◽  
pp. 1-9 ◽  
Author(s):  
R. Melgarejo-Torres ◽  
O. Castillo-Araiza ◽  
P. López-Ordaz ◽  
D. Torres-Martínez ◽  
M. Gutiérrez-Rojas ◽  
...  


2008 ◽  
Vol 6 (34) ◽  
pp. 463-469 ◽  
Author(s):  
Chrisantha T Fernando ◽  
Anthony M.L Liekens ◽  
Lewis E.H Bingle ◽  
Christian Beck ◽  
Thorsten Lenser ◽  
...  

We demonstrate how a single-celled organism could undertake associative learning. Although to date only one previous study has found experimental evidence for such learning, there is no reason in principle why it should not occur. We propose a gene regulatory network that is capable of associative learning between any pre-specified set of chemical signals, in a Hebbian manner, within a single cell. A mathematical model is developed, and simulations show a clear learned response. A preliminary design for implementing this model using plasmids within Escherichia coli is presented, along with an alternative approach, based on double-phosphorylated protein kinases.



2011 ◽  
Vol 9 (68) ◽  
pp. 518-527 ◽  
Author(s):  
Michael J. Tildesley ◽  
David L. Gally ◽  
Tom N. McNeilly ◽  
J. Chris Low ◽  
Arvind Mahajan ◽  
...  

Mathematical model-based statistical inference applied to within-host dynamics of infectious diseases can help dissect complex interactions between hosts and microbes. This work has applied advances in model-based inference to understand colonization of cattle by enterohaemorrhagic Escherichia coli O157 : H7 at the terminal rectum. A mathematical model was developed based on niche replication and transition rates at this site. A nested-model comparison, applied to excretion curves from 25 calves, was used to reduce complexity while maintaining integrity. We conclude that, 5–9 days post inoculation, the innate immune response negates bacterial replication on the epithelium and either reduces attachment to or increases detachment from the epithelium of the terminal rectum. Thus, we provide a broadly applicable model that gives novel insights into bacterial replication rates in vivo and the timing and impact of host responses.



2005 ◽  
Vol 49 (4) ◽  
pp. 1483-1494 ◽  
Author(s):  
C. Wiuff ◽  
R. M. Zappala ◽  
R. R. Regoes ◽  
K. N. Garner ◽  
F. Baquero ◽  
...  

ABSTRACT When growing bacteria are exposed to bactericidal concentrations of antibiotics, the sensitivity of the bacteria to the antibiotic commonly decreases with time, and substantial fractions of the bacteria survive. Using Escherichia coli CAB1 and antibiotics of five different classes (ampicillin, ciprofloxacin, rifampin, streptomycin, and tetracycline), we examine the details of this phenomenon and, with the aid of mathematical models, develop and explore the properties and predictions of three hypotheses that can account for this phenomenon: (i) antibiotic decay, (ii) inherited resistance, and (iii) phenotypic tolerance. Our experiments cause us to reject the first two hypotheses and provide evidence that this phenomenon can be accounted for by the antibiotic-mediated enrichment of subpopulations physiologically tolerant to but genetically susceptible to these antibiotics, phenotypic tolerance. We demonstrate that tolerant subpopulations generated by exposure to one concentration of an antibiotic are also tolerant to higher concentrations of the same antibiotic and can be tolerant to antibiotics of the other four types. Using a mathematical model, we explore the effects of phenotypic tolerance to the microbiological outcome of antibiotic treatment and demonstrate, a priori, that it can have a profound effect on the rate of clearance of the bacteria and under some conditions can prevent clearance that would be achieved in the absence of tolerance.



2018 ◽  
Author(s):  
Mehdi Snoussi ◽  
John Paul Talledo ◽  
Nathan-Alexander Del Rosario ◽  
Bae-Yeun Ha ◽  
Andrej Košmrlj ◽  
...  

AbstractAntimicrobial peptides (AMPs) are broad spectrum antibiotics that selectively target bacteria. Here we investigate the activity of human AMP LL37 againstEscherichia coliby integrating quantitative, population and single-cell level experiments with theoretical modeling. Our data indicate an unexpected, rapid absorption and retention of a large number of LL37 byE. colicells upon the inhibition of their growth, which increases the chance of survival for the rest of population. Cultures with high-enough cell density exhibit two distinct subpopulations: a non-growing population that absorb peptides and a growing population that survive owing to the sequestration of the AMPs by others. A mathematical model based on this binary picture reproduces the rather surprising behaviors ofE. colicultures in the presence of LL37, including the increase of the minimum inhibitory concentration with cell density (even in dilute cultures) and the extensive lag in growth introduced by sub-lethal dosages of LL37.



2020 ◽  
Vol 6 (10) ◽  
pp. eaaz5108 ◽  
Author(s):  
L. Galera-Laporta ◽  
J. Garcia-Ojalvo

Much is known about the effects of antibiotics on isolated bacterial species, but their influence on polybacterial communities is less understood. Here, we study the joint response of a mixed community of nonresistant Bacillus subtilis and Escherichia coli bacteria to moderate concentrations of the β-lactam antibiotic ampicillin. We show that when the two organisms coexist, their population response to the antibiotic is opposite to that in isolation: Whereas in monoculture B. subtilis is tolerant and E. coli is sensitive to ampicillin, in coculture it is E. coli who can proliferate in the presence of the antibiotic, while B. subtilis cannot. This antithetic behavior is predicted by a mathematical model constrained only by the responses of the two species in isolation. Our results thus show that the collective response of mixed bacterial ecosystems to antibiotics can run counter to what single-species potency studies tell us about their efficacy.



2013 ◽  
Vol 68 (4) ◽  
pp. 911-930 ◽  
Author(s):  
Zhigang Zhang ◽  
Jeffrey J. Morgan ◽  
Paul A. Lindahl


2005 ◽  
Vol 346 (2) ◽  
pp. 399-409 ◽  
Author(s):  
Kim Sneppen ◽  
Ian B. Dodd ◽  
Keith E. Shearwin ◽  
Adam C. Palmer ◽  
Rachel A. Schubert ◽  
...  




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