A discrete time model for the analysis of medium-throughput C. elegans growth data
As part of a program to predict the toxicity of environmental agents on human health using alternative methods, several in vivo high- and medium-throughput assays are being developed that use C. elegans as a model organism. C. elegans-based toxicological assays utilize the COPAS Biosort flow sorting...
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Published in | PloS one Vol. 4; no. 9; p. e7018 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Public Library of Science
15.09.2009
Public Library of Science (PLoS) |
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Abstract | As part of a program to predict the toxicity of environmental agents on human health using alternative methods, several in vivo high- and medium-throughput assays are being developed that use C. elegans as a model organism. C. elegans-based toxicological assays utilize the COPAS Biosort flow sorting system that can rapidly measure size, extinction (EXT) and time-of-flight (TOF), of individual nematodes. The use of this technology requires the development of mathematical and statistical tools to properly analyze the large volumes of biological data.
Findings A Markov model was developed that predicts the growth of populations of C. elegans. The model was developed using observations from a 60 h growth study in which five cohorts of 300 nematodes each were aspirated and measured every 12 h. Frequency distributions of log(EXT) measurements that were made when loading C. elegans L1 larvae into 96 well plates (t = 0 h) were used by the model to predict the frequency distributions of the same set of nematodes when measured at 12 h intervals. The model prediction coincided well with the biological observations confirming the validity of the model. The model was also applied to log(TOF) measurements following an adaptation. The adaptation accounted for variability in TOF measurements associated with potential curling or shortening of the nematodes as they passed through the flow cell of the Biosort. By providing accurate estimates of frequencies of EXT or TOF measurements following varying growth periods, the model was able to estimate growth rates. Best model fits showed that C. elegans did not grow at a constant exponential rate. Growth was best described with three different rates. Microscopic observations indicated that the points where the growth rates changed corresponded to specific developmental events: the L1/L2 molt and the start of oogenesis in young adult C. elegans.
Quantitative analysis of COPAS Biosort measurements of C. elegans growth has been hampered by the lack of a mathematical model. In addition, extraneous matter and the inability to assign specific measurements to specific nematodes made it difficult to estimate growth rates. The present model addresses these problems through a population-based Markov model. |
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AbstractList | As part of a program to predict the toxicity of environmental agents on human health using alternative methods, several in vivo high- and medium-throughput assays are being developed that use C. elegans as a model organism. C. elegans-based toxicological assays utilize the COPAS Biosort flow sorting system that can rapidly measure size, extinction (EXT) and time-of-flight (TOF), of individual nematodes. The use of this technology requires the development of mathematical and statistical tools to properly analyze the large volumes of biological data.
Findings A Markov model was developed that predicts the growth of populations of C. elegans. The model was developed using observations from a 60 h growth study in which five cohorts of 300 nematodes each were aspirated and measured every 12 h. Frequency distributions of log(EXT) measurements that were made when loading C. elegans L1 larvae into 96 well plates (t = 0 h) were used by the model to predict the frequency distributions of the same set of nematodes when measured at 12 h intervals. The model prediction coincided well with the biological observations confirming the validity of the model. The model was also applied to log(TOF) measurements following an adaptation. The adaptation accounted for variability in TOF measurements associated with potential curling or shortening of the nematodes as they passed through the flow cell of the Biosort. By providing accurate estimates of frequencies of EXT or TOF measurements following varying growth periods, the model was able to estimate growth rates. Best model fits showed that C. elegans did not grow at a constant exponential rate. Growth was best described with three different rates. Microscopic observations indicated that the points where the growth rates changed corresponded to specific developmental events: the L1/L2 molt and the start of oogenesis in young adult C. elegans.
Quantitative analysis of COPAS Biosort measurements of C. elegans growth has been hampered by the lack of a mathematical model. In addition, extraneous matter and the inability to assign specific measurements to specific nematodes made it difficult to estimate growth rates. The present model addresses these problems through a population-based Markov model. As part of a program to predict the toxicity of environmental agents on human health using alternative methods, several in vivo high- and medium-throughput assays are being developed that use C. elegans as a model organism. C. elegans-based toxicological assays utilize the COPAS Biosort flow sorting system that can rapidly measure size, extinction (EXT) and time-of-flight (TOF), of individual nematodes. The use of this technology requires the development of mathematical and statistical tools to properly analyze the large volumes of biological data. Quantitative analysis of COPAS Biosort measurements of C. elegans growth has been hampered by the lack of a mathematical model. In addition, extraneous matter and the inability to assign specific measurements to specific nematodes made it difficult to estimate growth rates. The present model addresses these problems through a population-based Markov model. BackgroundAs part of a program to predict the toxicity of environmental agents on human health using alternative methods, several in vivo high- and medium-throughput assays are being developed that use C. elegans as a model organism. C. elegans-based toxicological assays utilize the COPAS Biosort flow sorting system that can rapidly measure size, extinction (EXT) and time-of-flight (TOF), of individual nematodes. The use of this technology requires the development of mathematical and statistical tools to properly analyze the large volumes of biological data.Methodology/principal findingsFindings A Markov model was developed that predicts the growth of populations of C. elegans. The model was developed using observations from a 60 h growth study in which five cohorts of 300 nematodes each were aspirated and measured every 12 h. Frequency distributions of log(EXT) measurements that were made when loading C. elegans L1 larvae into 96 well plates (t = 0 h) were used by the model to predict the frequency distributions of the same set of nematodes when measured at 12 h intervals. The model prediction coincided well with the biological observations confirming the validity of the model. The model was also applied to log(TOF) measurements following an adaptation. The adaptation accounted for variability in TOF measurements associated with potential curling or shortening of the nematodes as they passed through the flow cell of the Biosort. By providing accurate estimates of frequencies of EXT or TOF measurements following varying growth periods, the model was able to estimate growth rates. Best model fits showed that C. elegans did not grow at a constant exponential rate. Growth was best described with three different rates. Microscopic observations indicated that the points where the growth rates changed corresponded to specific developmental events: the L1/L2 molt and the start of oogenesis in young adult C. elegans.ConclusionsQuantitative analysis of COPAS Biosort measurements of C. elegans growth has been hampered by the lack of a mathematical model. In addition, extraneous matter and the inability to assign specific measurements to specific nematodes made it difficult to estimate growth rates. The present model addresses these problems through a population-based Markov model. Background As part of a program to predict the toxicity of environmental agents on human health using alternative methods, several in vivo high- and medium-throughput assays are being developed that use C. elegans as a model organism. C. elegans-based toxicological assays utilize the COPAS Biosort flow sorting system that can rapidly measure size, extinction (EXT) and time-of-flight (TOF), of individual nematodes. The use of this technology requires the development of mathematical and statistical tools to properly analyze the large volumes of biological data. Methodology/Principal Findings Findings A Markov model was developed that predicts the growth of populations of C. elegans. The model was developed using observations from a 60 h growth study in which five cohorts of 300 nematodes each were aspirated and measured every 12 h. Frequency distributions of log(EXT) measurements that were made when loading C. elegans L1 larvae into 96 well plates (t = 0 h) were used by the model to predict the frequency distributions of the same set of nematodes when measured at 12 h intervals. The model prediction coincided well with the biological observations confirming the validity of the model. The model was also applied to log(TOF) measurements following an adaptation. The adaptation accounted for variability in TOF measurements associated with potential curling or shortening of the nematodes as they passed through the flow cell of the Biosort. By providing accurate estimates of frequencies of EXT or TOF measurements following varying growth periods, the model was able to estimate growth rates. Best model fits showed that C. elegans did not grow at a constant exponential rate. Growth was best described with three different rates. Microscopic observations indicated that the points where the growth rates changed corresponded to specific developmental events: the L1/L2 molt and the start of oogenesis in young adult C. elegans. Conclusions Quantitative analysis of COPAS Biosort measurements of C. elegans growth has been hampered by the lack of a mathematical model. In addition, extraneous matter and the inability to assign specific measurements to specific nematodes made it difficult to estimate growth rates. The present model addresses these problems through a population-based Markov model. Background As part of a program to predict the toxicity of environmental agents on human health using alternative methods, several in vivo high- and medium-throughput assays are being developed that use C. elegans as a model organism. C. elegans-based toxicological assays utilize the COPAS Biosort flow sorting system that can rapidly measure size, extinction (EXT) and time-of-flight (TOF), of individual nematodes. The use of this technology requires the development of mathematical and statistical tools to properly analyze the large volumes of biological data. Methodology/Principal Findings Findings A Markov model was developed that predicts the growth of populations of C. elegans. The model was developed using observations from a 60 h growth study in which five cohorts of 300 nematodes each were aspirated and measured every 12 h. Frequency distributions of log(EXT) measurements that were made when loading C. elegans L1 larvae into 96 well plates (t = 0 h) were used by the model to predict the frequency distributions of the same set of nematodes when measured at 12 h intervals. The model prediction coincided well with the biological observations confirming the validity of the model. The model was also applied to log(TOF) measurements following an adaptation. The adaptation accounted for variability in TOF measurements associated with potential curling or shortening of the nematodes as they passed through the flow cell of the Biosort. By providing accurate estimates of frequencies of EXT or TOF measurements following varying growth periods, the model was able to estimate growth rates. Best model fits showed that C. elegans did not grow at a constant exponential rate. Growth was best described with three different rates. Microscopic observations indicated that the points where the growth rates changed corresponded to specific developmental events: the L1/L2 molt and the start of oogenesis in young adult C. elegans. Conclusions Quantitative analysis of COPAS Biosort measurements of C. elegans growth has been hampered by the lack of a mathematical model. In addition, extraneous matter and the inability to assign specific measurements to specific nematodes made it difficult to estimate growth rates. The present model addresses these problems through a population-based Markov model. |
Audience | Academic |
Author | Snyder, Daniel W Kissling, Grace E Smith, Marjolein V Portier, Christopher J Freedman, Jonathan H Rice, Julie R Boyd, Windy A |
AuthorAffiliation | Massachusetts General Hospital/Harvard Medical School, United States of America 4 Laboratory of Molecular Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health (NIH), Research Triangle Park, North Carolina, United States of America 2 Biomoleclular Screening Branch, National Toxicology Program, Research Triangle Park, North Carolina, United States of America 1 SRA International, Durham, North Carolina, United States of America 3 Biostatistics Branch, National Institute of Environmental Health Sciences, National Institutes of Health (NIH), Research Triangle Park, North Carolina, United States of America |
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Author_xml | – sequence: 1 givenname: Marjolein V surname: Smith fullname: Smith, Marjolein V organization: SRA International, Durham, North Carolina, USA – sequence: 2 givenname: Windy A surname: Boyd fullname: Boyd, Windy A – sequence: 3 givenname: Grace E surname: Kissling fullname: Kissling, Grace E – sequence: 4 givenname: Julie R surname: Rice fullname: Rice, Julie R – sequence: 5 givenname: Daniel W surname: Snyder fullname: Snyder, Daniel W – sequence: 6 givenname: Christopher J surname: Portier fullname: Portier, Christopher J – sequence: 7 givenname: Jonathan H surname: Freedman fullname: Freedman, Jonathan H |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/19753303$$D View this record in MEDLINE/PubMed |
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Notes | Conceived and designed the experiments: MVS WAB JHF. Performed the experiments: WAB JRR DWS. Analyzed the data: MVS GEK CJP. Wrote the paper: MVS WAB JHF. |
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References_xml | – volume: 319 start-page: 906 year: 2008 ident: ref1 article-title: Toxicology. Transforming environmental health protection. publication-title: Science doi: 10.1126/science.1154619 contributor: fullname: FS Collins – volume: 77 start-page: 71 year: 1974 ident: ref11 article-title: The genetics of Caenorhabditis elegans. publication-title: Genetics doi: 10.1093/genetics/77.1.71 contributor: fullname: S Brenner – start-page: 1 year: 1988 ident: ref5 article-title: Introduction to C. elegans Biology. In: Wood WB, editor. The Nematode Caenorhabditis elegans. contributor: fullname: WB Wood – volume: 4 start-page: 16 year: 2002 ident: ref7 article-title: A novel mode of ecdysozoan growth in Caenorhabditis elegans. publication-title: Evol Dev doi: 10.1046/j.1525-142x.2002.01058.x contributor: fullname: CG Knight – volume: 282 start-page: 2012 year: 1998 ident: ref3 article-title: Genome sequence of the nematode C. elegans: a platform for investigating biology. publication-title: Science doi: 10.1126/science.282.5396.2012 – volume: x year: 2008 ident: ref4 article-title: C. elegans atlas. contributor: fullname: DH Hall – year: 2009 ident: ref8 article-title: Medium- and high-throughput screening of neurotoxicants using C. elegans. publication-title: Neurotoxicol Teratol contributor: fullname: WA Boyd – volume: xvi year: 1984 ident: ref14 article-title: Elements of applied stochastic processes. contributor: fullname: UN Bhat – volume: 29 start-page: 546 year: 2008 ident: ref2 article-title: Use of non-mammalian alternative models for neurotoxicological study. publication-title: Neurotoxicology doi: 10.1016/j.neuro.2008.04.006 contributor: fullname: RT Peterson – volume: 32 start-page: 110 year: 1997 ident: ref12 article-title: Tolerance of the nematode Caenorhabditis elegans to pH, salinity, and hardness in aquatic media. publication-title: Arch Environ Contam Toxicol doi: 10.1007/s002449900162 contributor: fullname: N Khanna – volume: 51 start-page: 23 year: 1976 ident: ref6 article-title: The life cycle of the nematode Caenorhabditis elegans. I. Wild-type growth and reproduction. publication-title: Dev Biol doi: 10.1016/0012-1606(76)90119-6 contributor: fullname: L Byerly – volume: 4 start-page: 469 year: 1988 ident: ref10 article-title: Using the nematode Caenorhabditis elegans to predict mammalian acute lethality to metallic salts. publication-title: Toxicol Ind Health doi: 10.1177/074823378800400406 contributor: fullname: PL Williams – volume: 325 start-page: 167 year: 2009 ident: ref15 article-title: Cell growth and size homeostasis in proliferating animal cells. publication-title: Science doi: 10.1126/science.1174294 contributor: fullname: A Tzur – volume: 351 start-page: 275 year: 2006 ident: ref9 article-title: Techniques for analysis, sorting, and dispensing of C. elegans on the COPAS flow-sorting system. publication-title: Methods Mol Biol contributor: fullname: R Pulak – volume: 48 start-page: 3 year: 1995 ident: ref13 article-title: Basic culture methods. publication-title: Methods Cell Biol doi: 10.1016/S0091-679X(08)61381-3 contributor: fullname: JA Lewis |
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Title | A discrete time model for the analysis of medium-throughput C. elegans growth data |
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