scholarly journals Detecting differential growth of microbial populations with Gaussian process regression

2016 ◽  
Author(s):  
Peter D Tonner ◽  
Cynthia L Darnell ◽  
Barbara E Engelhardt ◽  
Amy K Schmid

AbstractMicrobial growth curves are used to study differential effects of media, genetics, and stress on microbial population growth. Consequently, many modeling frameworks exist to capture microbial population growth measurements. However, current models are designed to quantify growth under conditions that produce a specific functional form. Extensions to these models are required to quantify the effects of perturbations, which often exhibit non-standard growth curves. Rather than fix expected functional forms of different experimental perturbations, we developed a general and robust model of microbial population growth curves using Gaussian process (GP) regression. GP regression modeling of high resolution time-series growth data enables accurate quantification of population growth, and can be extended to identify differential growth phenotypes due to genetic background or stress. Additionally, confounding effects due to experimental variation can be controlled explicitly. Our framework substantially outperforms commonly used microbial population growth models, particularly when modeling growth data from environmentally stressed populations. We apply the GP growth model to a collection of growth measurements for seven transcription factor knockout strains of a model archaeal organism,Halobacterium salinarum. Using these models fitted to growth data, two statistical tests were developed to quantify the differential effects of genetic and environmental perturbations on microbial growth. These statistical tests accurately identify known regulators and implicate novel regulators of growth under standard and stress conditions. Furthermore, the fitted GP regression models are interpretable, recapitulating biological knowledge of growth response while providing new insights into the relevant parameters affecting microbial population growth.

2016 ◽  
Vol 1 (2) ◽  
pp. 63 ◽  
Author(s):  
Ji-Dong Gu

Bacterial growth is a very important piece of information in a wide range of investigation and, in most of the time the data are simply shown directly without any further processing. In a single factor investigation without comparative information to be extracted, this simple approach can be used together with other data to form a comprehensive set of results. When comparison is involved, such direct showing of bacterial growth curves without processing cannot warrant a meaningful comparison thoroughly and further processing of data is necessary. In addition, there is little, if any, quantitative data for the comparison from the display of growth curves and description of a number of curves is not a simple task, especially in a meaningful way for assimilation of the data to readers. With this in mind, I would like to remind of those who plan to show such data as growth curves for their potential publication to carry this further to generate comparative results for a much meaningful interpretation by modeling and calculation from the raw growth data over time of incubation. By calculating with existing equations, the lag phase, growth rate and the biomass can be derived from a series of growth curves for a more effective and meaningful analysis. This approach is not new, but remembrance of such available tool is more important so that research data are shown professionally and also scientifically for meaning presentation and effective assimilation.


2020 ◽  
Author(s):  
Firas S. Midani ◽  
James Collins ◽  
Robert A. Britton

ABSTRACTThe analysis of microbial growth is one of the central methods in the field of microbiology. Microbial growth dynamics can be characterized by growth parameters including carrying capacity, exponential growth rate, and growth lag. However, growth assays with clinical isolates, fastidious organisms, or microbes under stress often produce atypical growth shapes that do not follow the classical microbial growth pattern. Here, we introduce the Analysis of Microbial Growth Assays (AMiGA) software which streamlines the analysis of growth curves without any assumptions about their shapes. AMiGA can pool replicates of growth curves and infer summary statistics for biologically meaningful growth parameters. In addition, AMiGA can quantify death phases and characterize diauxic shifts. It can also statistically test for differential growth under distinct experimental conditions. Altogether, AMiGA streamlines the organization, analysis, and visualization of microbial growth assays.IMPORTANCEOur current understanding of microbial physiology relies on the simple method of measuring microbial populations’ size over time and under different conditions. Many advances have increased the throughput of those assays and enabled the study of non-lab adapted microbes under diverse conditions that widely affect their growth dynamics. Our software provides an all-in-one tool for estimating the growth parameters of microbial cultures and testing for differential growth in a high-throughput and user-friendly fashion without any underlying assumptions about how microbes respond to their growth conditions.


2020 ◽  
Vol 16 (10) ◽  
pp. e1008366
Author(s):  
Peter D. Tonner ◽  
Cynthia L. Darnell ◽  
Francesca M. L. Bushell ◽  
Peter A. Lund ◽  
Amy K. Schmid ◽  
...  

Substantive changes in gene expression, metabolism, and the proteome are manifested in overall changes in microbial population growth. Quantifying how microbes grow is therefore fundamental to areas such as genetics, bioengineering, and food safety. Traditional parametric growth curve models capture the population growth behavior through a set of summarizing parameters. However, estimation of these parameters from data is confounded by random effects such as experimental variability, batch effects or differences in experimental material. A systematic statistical method to identify and correct for such confounding effects in population growth data is not currently available. Further, our previous work has demonstrated that parametric models are insufficient to explain and predict microbial response under non-standard growth conditions. Here we develop a hierarchical Bayesian non-parametric model of population growth that identifies the latent growth behavior and response to perturbation, while simultaneously correcting for random effects in the data. This model enables more accurate estimates of the biological effect of interest, while better accounting for the uncertainty due to technical variation. Additionally, modeling hierarchical variation provides estimates of the relative impact of various confounding effects on measured population growth.


Genetics ◽  
1997 ◽  
Vol 147 (2) ◽  
pp. 915-925 ◽  
Author(s):  
Yun-Xin Fu

The main purpose of this article is to present several new statistical tests of neutrality of mutations against a class of alternative models, under which DNA polymorphisms tend to exhibit excesses of rare alleles or young mutations. Another purpose is to study the powers of existing and newly developed tests and to examine the detailed pattern of polymorphisms under population growth, genetic hitchhiking and background selection. It is found that the polymorphic patterns in a DNA sample under logistic population growth and genetic hitchhiking are very similar and that one of the newly developed tests, FS, is considerably more powerful than existing tests for rejecting the hypothesis of neutrality of mutations. Background selection gives rise to quite different polymorphic patterns than does logistic population growth or genetic hitchhiking, although all of them show excesses of rare alleles or young mutations. We show that Fu and Li's tests are among the most powerful tests against background selection. Implications of these results are discussed.


2007 ◽  
Vol 1064 ◽  
Author(s):  
Somesree GhoshMitra ◽  
Tong Cai ◽  
Santaneel Ghosh ◽  
Arup Neogi ◽  
Zhibing Hu ◽  
...  

ABSTRACTQuantum dots (QDs) are now used extensively for labeling in biomedical research due to their unique photoluminescence behavior, involving size-tunable emission color, a narrow and symmetric emission profile and a broad excitation range [1]. Uncoated QDs made of CdTe core are toxic to cells because of release of Cd2+ ions into the cellular environment. This problem can be partially solved by encapsulating QDs with polymers, like poly(N-isopropylacrylamide) (PNIPAM) or poly(ethylene glycol) (PEG). Based on biological compatibility, fast response as well as pH, temperature and magnetic field dependent swelling properties, hydrogel nanospheres has become carriers of drugs, fluorescence labels, magnetic particles for hyperthermia applications and particles that have strong optical absorption profiles for optical excitation. The toxicity of uncoated QDs are known; however, there have been a very limited number of studies specially designed to assess thoroughly the toxicity of nanosphere encapsulated QDs against QD density and dosing level.In this work, we present preliminary studies of biological effects of a novel QD based nanomaterial system on Escherichia coli (E. coli) bacteria. Cadmium chalcogenide QDs provide the most attractive fluorescence labels in comparison with routine dyes or metal complexes. Nanospheres on the other hand are the most commonly used carriers of fluorescence labels for fluorescence detection. The integration of fluorescent QDs in nanospheres therefore provides a new generation of fluorescence markers for biological assays. Hydrogels based on PNIPAM is a well known thermoresponsive polymer that undergoes a volume phase transition across the low critical solution (LCST) [2]. Therefore, the inherent temperature-sensitive swelling properties of PNIPAM offer the potentiality to control QD density within the nanospheres. In the present work, E. coli growth was monitored as E. coli served as a representation of how cells might respond in the presence of hydrogel encapsulated QDs in their growth environment. The present work describes the successful encapsulation of CdTe QDs in PNIPAM gel network. Microgel encapsulated QDs were synthesized by first preparing PNIPAM microspheres with cystaminebisacrylamide as a crosslinker and CdTe QDs capped with a stabilizer. The CdTe QDs were bonded into PNIPAM microgels through the replacement of CdTe's stabilizer inside PNIPAM microspheres. Growth curves were generated for E. coli growing in 20 mL of LB media containing hydrogel encapsulated QD nanospheres (400 nm diameter) at relatively higher (0.5mg/mL) and lower (0.01mg/mL) concentration of solution. From the growth curves, there was no evidence at lower concentration (0.01mg/mL) that the hydrogel encapsulated QDs prevent the microbial cells from growing but at higher concentration (0.5mg/mL), microbial growth was inhibited. Transmission Electron Microscopy (TEM) was used to characterize QD size and density inside the hydrogel nanospheres. Scanning Electron Microscopy (SEM) was used to observe size and morphology of the hydrogel particles. Further investigation is going on cell growth response at different QD density and to evaluate the limiting hydrogel concentration for different QD densities.


2008 ◽  
Vol 355 (1) ◽  
pp. 27-40 ◽  
Author(s):  
G.A.P. dos Santos ◽  
S. Derycke ◽  
V.G. Fonsêca-Genevois ◽  
L.C.B.B. Coelho ◽  
M.T.S. Correia ◽  
...  

1988 ◽  
Vol 2 (3) ◽  
pp. 304-309 ◽  
Author(s):  
Jerry L. Flint ◽  
Paul L. Cornelius ◽  
Michael Barrett

A model and a proposed method for testing herbicide interactions were modified from an analysis of variance (ANOVA) model for a 2 by 2 factorial experiment. Statistical tests for either synergism, antagonism, or additivity of herbicide combinations were developed through transforming growth data to logarithms followed by significance tests of 2 by 2 contrasts of the form μii- μi0- μ0i+ μ00with respect to the log-transformed data. Using actual experimental data, heterogeneity of variance was less severe on the log scale compared to the original measurement scale. An expedient SAS(R)program for obtaining the desired significance tests was developed.


2004 ◽  
Vol 21 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Paula Beatriz Araujo ◽  
Georgina Bond-Buckup

The terrestrial isopod Atlantoscia floridana (van Name, 1940) occurs from the U.S.A. (Florida) to Brazil and Argentina. In the southernmost Brazilian State, Rio Grande do Sul, the species is recorded in many localities, in urban and in non-urban areas. The growth curve of Atlantoscia floridana based on field data is presented. The specimens were sampled from April, 2000 to October, 2001 at the Reserva Biológica do Lami (RBL), Rio Grande do Sul. Captured individuals were sexed and had their cephalothorax width measured, with the data analyzed with von Bertalanffy's model. The growth curves for males and females are described, respectively, by the equations: Wt = 1.303 [1 - e-0.00941 (t + 50.37)] and Wt = 1.682 [1 - e-0.00575 (t + 59.13)]. The curves showed differential growth between sexes, where females reach a higher Wµ with a slower growth rate. Based on the growth curves it was also possible to estimate life expectancy for males and females.


2018 ◽  
Vol 80 (01) ◽  
pp. 072-078 ◽  
Author(s):  
Berdine Heesterman ◽  
John-Melle Bokhorst ◽  
Lisa de Pont ◽  
Berit Verbist ◽  
Jean-Pierre Bayley ◽  
...  

Background To improve our understanding of the natural course of head and neck paragangliomas (HNPGL) and ultimately differentiate between cases that benefit from early treatment and those that are best left untreated, we studied the growth dynamics of 77 HNPGL managed with primary observation. Methods Using digitally available magnetic resonance images, tumor volume was estimated at three time points. Subsequently, nonlinear least squares regression was used to fit seven mathematical models to the observed growth data. Goodness of fit was assessed with the coefficient of determination (R 2) and root-mean-squared error. The models were compared with Kruskal–Wallis one-way analysis of variance and subsequent post-hoc tests. In addition, the credibility of predictions (age at onset of neoplastic growth and estimated volume at age 90) was evaluated. Results Equations generating sigmoidal-shaped growth curves (Gompertz, logistic, Spratt and Bertalanffy) provided a good fit (median R 2: 0.996–1.00) and better described the observed data compared with the linear, exponential, and Mendelsohn equations (p < 0.001). Although there was no statistically significant difference between the sigmoidal-shaped growth curves regarding the goodness of fit, a realistic age at onset and estimated volume at age 90 were most often predicted by the Bertalanffy model. Conclusions Growth of HNPGL is best described by decelerating tumor growth laws, with a preference for the Bertalanffy model. To the best of our knowledge, this is the first time that this often-neglected model has been successfully fitted to clinically obtained growth data.


2021 ◽  
Author(s):  
Milanka Radulovic ◽  
◽  
Svetlana Mitrovski

Peat is a natural substrate for growth of microorganisms because it is rich in compounds that microorganisms can use as sources of carbon, nitrogen and growth factors. Peat originating from Vlasina lake in Eastern Serbia is especially rich in organic matter. The content of humic substances (humic acid, fulvic acid and humine) is almost twice that found in other peat-rich regions of similar origin and geochemical age. Humic and fluvic acids are known to promote microbial growth. In this work, humic and fulvic acids were first extracted from Vlasina lake peat and then added to minimal medium (synthetic, low ionic strength medium). The humic substances were added separately and combined in a 1:1 ratio by mass to study their individual and combined effect on microbial growth of Escherichia coli ATCC 25922 (Gr–), Staphyloccocus aureus (Gr+) i Aureobasidium pullulans, strain CH-1. The microbial growth was measured microspectrophotometrically over a 24-hour period and growth curves were obtained for a range of acid concentrations between 25 µg cm-3 and 100 µg cm-3. It was found that both humic and fulvic acids promote the growth of all three microorganisms by up to a maximum of 40%-80% the extent of which varied with the concentration of the acid and the identity of the microorganism. In general, humic acid was found to result in higher microbial growth (at highest concentrations, up to ~80% for all three microbial species).


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