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Construction of A New Dose–Response Model for Staphylococcus aureus Considering Growth and Decay Kinetics on Skin

In order to determine the relationship between an exposure dose of Staphylococcus aureus (S. aureus) on the skin and the risk of infection, an understanding of the bacterial growth and decay kinetics is very important. Models are essential tools for understanding and predicting bacterial kinetics an...

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Autores principales: Esfahanian, Elaheh, Adhikari, Umesh, Dolan, Kirk, Mitchell, Jade
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963640/
https://www.ncbi.nlm.nih.gov/pubmed/31766315
http://dx.doi.org/10.3390/pathogens8040253
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author Esfahanian, Elaheh
Adhikari, Umesh
Dolan, Kirk
Mitchell, Jade
author_facet Esfahanian, Elaheh
Adhikari, Umesh
Dolan, Kirk
Mitchell, Jade
author_sort Esfahanian, Elaheh
collection PubMed
description In order to determine the relationship between an exposure dose of Staphylococcus aureus (S. aureus) on the skin and the risk of infection, an understanding of the bacterial growth and decay kinetics is very important. Models are essential tools for understanding and predicting bacterial kinetics and are necessary to predict the dose of organisms post-exposure that results in a skin infection. One of the challenges in modeling bacterial kinetics is the estimation of model parameters, which can be addressed using an inverse problem approach. The objective of this study is to construct a microbial kinetic model of S. aureus on human skin and use the model to predict concentrations of S. aureus that result in human infection. In order to model the growth and decay of S. aureus on skin, a Gompertz inactivation model was coupled with a Gompertz growth model. A series of analyses, including ordinary least squares regression, scaled sensitivity coefficient analysis, residual analysis, and parameter correlation analysis were conducted to estimate the parameters and to describe the model uncertainty. Based on these analyses, the proposed model parameters were estimated with high accuracy. The model was then used to develop a new dose-response model for S. aureus using the exponential dose–response model. The new S. aureus model has an optimized k parameter equivalent to 8.05 × 10(−8) with 95(th) percentile confidence intervals between 6.46 × 10(−8) and 1.00 × 10(−7).
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spelling pubmed-69636402020-01-27 Construction of A New Dose–Response Model for Staphylococcus aureus Considering Growth and Decay Kinetics on Skin Esfahanian, Elaheh Adhikari, Umesh Dolan, Kirk Mitchell, Jade Pathogens Article In order to determine the relationship between an exposure dose of Staphylococcus aureus (S. aureus) on the skin and the risk of infection, an understanding of the bacterial growth and decay kinetics is very important. Models are essential tools for understanding and predicting bacterial kinetics and are necessary to predict the dose of organisms post-exposure that results in a skin infection. One of the challenges in modeling bacterial kinetics is the estimation of model parameters, which can be addressed using an inverse problem approach. The objective of this study is to construct a microbial kinetic model of S. aureus on human skin and use the model to predict concentrations of S. aureus that result in human infection. In order to model the growth and decay of S. aureus on skin, a Gompertz inactivation model was coupled with a Gompertz growth model. A series of analyses, including ordinary least squares regression, scaled sensitivity coefficient analysis, residual analysis, and parameter correlation analysis were conducted to estimate the parameters and to describe the model uncertainty. Based on these analyses, the proposed model parameters were estimated with high accuracy. The model was then used to develop a new dose-response model for S. aureus using the exponential dose–response model. The new S. aureus model has an optimized k parameter equivalent to 8.05 × 10(−8) with 95(th) percentile confidence intervals between 6.46 × 10(−8) and 1.00 × 10(−7). MDPI 2019-11-21 /pmc/articles/PMC6963640/ /pubmed/31766315 http://dx.doi.org/10.3390/pathogens8040253 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Esfahanian, Elaheh
Adhikari, Umesh
Dolan, Kirk
Mitchell, Jade
Construction of A New Dose–Response Model for Staphylococcus aureus Considering Growth and Decay Kinetics on Skin
title Construction of A New Dose–Response Model for Staphylococcus aureus Considering Growth and Decay Kinetics on Skin
title_full Construction of A New Dose–Response Model for Staphylococcus aureus Considering Growth and Decay Kinetics on Skin
title_fullStr Construction of A New Dose–Response Model for Staphylococcus aureus Considering Growth and Decay Kinetics on Skin
title_full_unstemmed Construction of A New Dose–Response Model for Staphylococcus aureus Considering Growth and Decay Kinetics on Skin
title_short Construction of A New Dose–Response Model for Staphylococcus aureus Considering Growth and Decay Kinetics on Skin
title_sort construction of a new dose–response model for staphylococcus aureus considering growth and decay kinetics on skin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963640/
https://www.ncbi.nlm.nih.gov/pubmed/31766315
http://dx.doi.org/10.3390/pathogens8040253
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