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Compared with conventional PCR assay, qPCR assay greatly improves the detection efficiency of predation

Studies of predation can contribute greatly to understanding predator–prey relationships and can also provide integral knowledge concerning food webs and multi‐trophic level interactions. Both conventional polymerase chain reaction (cPCR) and quantitative PCR (qPCR) have been employed to detect pred...

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Autores principales: Yang, Ting‐bang, Liu, Jie, Chen, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391540/
https://www.ncbi.nlm.nih.gov/pubmed/32760558
http://dx.doi.org/10.1002/ece3.6494
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author Yang, Ting‐bang
Liu, Jie
Chen, Jian
author_facet Yang, Ting‐bang
Liu, Jie
Chen, Jian
author_sort Yang, Ting‐bang
collection PubMed
description Studies of predation can contribute greatly to understanding predator–prey relationships and can also provide integral knowledge concerning food webs and multi‐trophic level interactions. Both conventional polymerase chain reaction (cPCR) and quantitative PCR (qPCR) have been employed to detect predation in the field because of their sensitivity and reproducibility. However, to date, few studies have been used to comprehensively demonstrate which method is more sensitive and reproducible in studies of predation. We used a Drosophila melanogaster‐specific DNA fragment (99 bp) to construct a tenfold gradient dilution of standards. Additionally, we obtained DNA samples from Pardosa pseudoannulata individuals that fed on D. melanogaster at various time since feeding. Finally, we compared the sensitivity and reproducibility between cPCR and qPCR assays for detecting DNA samples from feeding trials and standards. The results showed that the cPCR and qPCR assays could detect as few as 1.62 × 10(3) and 1.62 × 10(1) copies of the target DNA fragment, respectively. The cPCR assay could detect as few as 48 hr post‐feeding of the target DNA fragment. But the qPCR assay showed that all spiders were positive after consuming prey at various time intervals (0, 24, 48, 72, and 96 hr). A smaller proportion of the technical replicates were positive using cPCR, and some bands on the agarose gel were absent or gray, while some were white and bright for the same DNA samples after amplification by cPCR. By contrast, a larger proportion of the technical replicates were positive using qPCR and the coefficients of variation of the Ct value for the three technical replicates of each DNA sample were less than 5%. These data showed that qPCR was more sensitive and highly reproducible in detecting such degraded DNA from predator's gut. The present study provides an example of the use of cPCR and qPCR to detect the target DNA fragment of prey remains in predator's gut.
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spelling pubmed-73915402020-08-04 Compared with conventional PCR assay, qPCR assay greatly improves the detection efficiency of predation Yang, Ting‐bang Liu, Jie Chen, Jian Ecol Evol Original Research Studies of predation can contribute greatly to understanding predator–prey relationships and can also provide integral knowledge concerning food webs and multi‐trophic level interactions. Both conventional polymerase chain reaction (cPCR) and quantitative PCR (qPCR) have been employed to detect predation in the field because of their sensitivity and reproducibility. However, to date, few studies have been used to comprehensively demonstrate which method is more sensitive and reproducible in studies of predation. We used a Drosophila melanogaster‐specific DNA fragment (99 bp) to construct a tenfold gradient dilution of standards. Additionally, we obtained DNA samples from Pardosa pseudoannulata individuals that fed on D. melanogaster at various time since feeding. Finally, we compared the sensitivity and reproducibility between cPCR and qPCR assays for detecting DNA samples from feeding trials and standards. The results showed that the cPCR and qPCR assays could detect as few as 1.62 × 10(3) and 1.62 × 10(1) copies of the target DNA fragment, respectively. The cPCR assay could detect as few as 48 hr post‐feeding of the target DNA fragment. But the qPCR assay showed that all spiders were positive after consuming prey at various time intervals (0, 24, 48, 72, and 96 hr). A smaller proportion of the technical replicates were positive using cPCR, and some bands on the agarose gel were absent or gray, while some were white and bright for the same DNA samples after amplification by cPCR. By contrast, a larger proportion of the technical replicates were positive using qPCR and the coefficients of variation of the Ct value for the three technical replicates of each DNA sample were less than 5%. These data showed that qPCR was more sensitive and highly reproducible in detecting such degraded DNA from predator's gut. The present study provides an example of the use of cPCR and qPCR to detect the target DNA fragment of prey remains in predator's gut. John Wiley and Sons Inc. 2020-06-27 /pmc/articles/PMC7391540/ /pubmed/32760558 http://dx.doi.org/10.1002/ece3.6494 Text en © 2020 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Yang, Ting‐bang
Liu, Jie
Chen, Jian
Compared with conventional PCR assay, qPCR assay greatly improves the detection efficiency of predation
title Compared with conventional PCR assay, qPCR assay greatly improves the detection efficiency of predation
title_full Compared with conventional PCR assay, qPCR assay greatly improves the detection efficiency of predation
title_fullStr Compared with conventional PCR assay, qPCR assay greatly improves the detection efficiency of predation
title_full_unstemmed Compared with conventional PCR assay, qPCR assay greatly improves the detection efficiency of predation
title_short Compared with conventional PCR assay, qPCR assay greatly improves the detection efficiency of predation
title_sort compared with conventional pcr assay, qpcr assay greatly improves the detection efficiency of predation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391540/
https://www.ncbi.nlm.nih.gov/pubmed/32760558
http://dx.doi.org/10.1002/ece3.6494
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