Cargando…
Genome Size, rDNA Copy, and qPCR Assays for Symbiodiniaceae
Symbiodiniaceae community structure in corals is crucial for understanding the plasticity of different holobionts under environmental stress. While this relies on molecular analyses, accuracy of molecular quantification, as influenced by DNA extraction efficiency and rDNA copy number variations in p...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264167/ https://www.ncbi.nlm.nih.gov/pubmed/32528423 http://dx.doi.org/10.3389/fmicb.2020.00847 |
_version_ | 1783540917646393344 |
---|---|
author | Saad, Osama S. Lin, Xin Ng, Tsz Yan Li, Ling Ang, Put Lin, Senjie |
author_facet | Saad, Osama S. Lin, Xin Ng, Tsz Yan Li, Ling Ang, Put Lin, Senjie |
author_sort | Saad, Osama S. |
collection | PubMed |
description | Symbiodiniaceae community structure in corals is crucial for understanding the plasticity of different holobionts under environmental stress. While this relies on molecular analyses, accuracy of molecular quantification, as influenced by DNA extraction efficiency and rDNA copy number variations in particular, has rarely been systematically investigated. Here, we report the development of a set of genus-specific qPCR assays. First, a protocol for efficient DNA isolation and accurate measurements of genome size and rDNA copy number was established. Second, seven newly designed genus-specific ITS2 primer sets were validated using computational and empirical analyses and qPCR assays were developed. We find that while the genome size ranges between 1.75 ± 0.21 and 4.5 ± 0.96 Gbp, rDNA copy number shows over 10-fold variation among Symbiodiniaceae species. Our protocol produced standard curves with high efficiencies (89.8–99.3%; R(2) ≥ 0.999) and tight Cq values over different PCR conditions, illustrating high specificity and sensitivity of the qPCR assays. Tested on mock communities of mixed culture species, our qPCR results agreed well with microscopic counts and facilitated calibration of metabarcoding data. To test the applicability of our protocol for field samples, we analyzed three different Hong Kong coral samples. Six Symbiodiniaceae genera were detected in Acropora valida, Oulastrea crispata, and Platygyra acuta, with Breviolum, Effrenium, Fugacium, and Gerakladium sp. being reported for the first time. Our results suggest that aggressively disrupting cells to ensure thorough cell lysis, estimating cell loss and DNA loss, and validating qPCR assays are critical for success. The number of species examined here is limited, but the primers are potentially applicable to most species in respective genera, and the protocol and the approach to develop it provide a base and template toward a standardized procedure for quantitatively characterizing Symbiodiniaceae communities in corals. |
format | Online Article Text |
id | pubmed-7264167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72641672020-06-10 Genome Size, rDNA Copy, and qPCR Assays for Symbiodiniaceae Saad, Osama S. Lin, Xin Ng, Tsz Yan Li, Ling Ang, Put Lin, Senjie Front Microbiol Microbiology Symbiodiniaceae community structure in corals is crucial for understanding the plasticity of different holobionts under environmental stress. While this relies on molecular analyses, accuracy of molecular quantification, as influenced by DNA extraction efficiency and rDNA copy number variations in particular, has rarely been systematically investigated. Here, we report the development of a set of genus-specific qPCR assays. First, a protocol for efficient DNA isolation and accurate measurements of genome size and rDNA copy number was established. Second, seven newly designed genus-specific ITS2 primer sets were validated using computational and empirical analyses and qPCR assays were developed. We find that while the genome size ranges between 1.75 ± 0.21 and 4.5 ± 0.96 Gbp, rDNA copy number shows over 10-fold variation among Symbiodiniaceae species. Our protocol produced standard curves with high efficiencies (89.8–99.3%; R(2) ≥ 0.999) and tight Cq values over different PCR conditions, illustrating high specificity and sensitivity of the qPCR assays. Tested on mock communities of mixed culture species, our qPCR results agreed well with microscopic counts and facilitated calibration of metabarcoding data. To test the applicability of our protocol for field samples, we analyzed three different Hong Kong coral samples. Six Symbiodiniaceae genera were detected in Acropora valida, Oulastrea crispata, and Platygyra acuta, with Breviolum, Effrenium, Fugacium, and Gerakladium sp. being reported for the first time. Our results suggest that aggressively disrupting cells to ensure thorough cell lysis, estimating cell loss and DNA loss, and validating qPCR assays are critical for success. The number of species examined here is limited, but the primers are potentially applicable to most species in respective genera, and the protocol and the approach to develop it provide a base and template toward a standardized procedure for quantitatively characterizing Symbiodiniaceae communities in corals. Frontiers Media S.A. 2020-05-26 /pmc/articles/PMC7264167/ /pubmed/32528423 http://dx.doi.org/10.3389/fmicb.2020.00847 Text en Copyright © 2020 Saad, Lin, Ng, Li, Ang and Lin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Saad, Osama S. Lin, Xin Ng, Tsz Yan Li, Ling Ang, Put Lin, Senjie Genome Size, rDNA Copy, and qPCR Assays for Symbiodiniaceae |
title | Genome Size, rDNA Copy, and qPCR Assays for Symbiodiniaceae |
title_full | Genome Size, rDNA Copy, and qPCR Assays for Symbiodiniaceae |
title_fullStr | Genome Size, rDNA Copy, and qPCR Assays for Symbiodiniaceae |
title_full_unstemmed | Genome Size, rDNA Copy, and qPCR Assays for Symbiodiniaceae |
title_short | Genome Size, rDNA Copy, and qPCR Assays for Symbiodiniaceae |
title_sort | genome size, rdna copy, and qpcr assays for symbiodiniaceae |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264167/ https://www.ncbi.nlm.nih.gov/pubmed/32528423 http://dx.doi.org/10.3389/fmicb.2020.00847 |
work_keys_str_mv | AT saadosamas genomesizerdnacopyandqpcrassaysforsymbiodiniaceae AT linxin genomesizerdnacopyandqpcrassaysforsymbiodiniaceae AT ngtszyan genomesizerdnacopyandqpcrassaysforsymbiodiniaceae AT liling genomesizerdnacopyandqpcrassaysforsymbiodiniaceae AT angput genomesizerdnacopyandqpcrassaysforsymbiodiniaceae AT linsenjie genomesizerdnacopyandqpcrassaysforsymbiodiniaceae |