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Auteurs principaux: Bagdonaitė, Laima, Leder, Erica H, Lifjeld, Jan T, Johnsen, Arild, Mauvisseau, Quentin
Format: Artículo científico
Langue:en
Publié: PeerJ 2025
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Accès en ligne:https://pubmed.ncbi.nlm.nih.gov/40231068/
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author Bagdonaitė, Laima
Leder, Erica H
Lifjeld, Jan T
Johnsen, Arild
Mauvisseau, Quentin
author_facet Bagdonaitė, Laima
Leder, Erica H
Lifjeld, Jan T
Johnsen, Arild
Mauvisseau, Quentin
Bagdonaitė, Laima
Leder, Erica H
Lifjeld, Jan T
Johnsen, Arild
Mauvisseau, Quentin
collection PubMed - marine biology
contents Assessing reliability and accuracy of qPCR, dPCR and ddPCR for estimating mitochondrial DNA copy number in songbird blood and sperm cells. Bagdonaitė, Laima Leder, Erica H Lifjeld, Jan T Johnsen, Arild Mauvisseau, Quentin Animals Male DNA, Mitochondrial Spermatozoa Reproducibility of Results DNA Copy Number Variations Songbirds Polymerase Chain Reaction Real-Time Polymerase Chain Reaction Mitochondrial DNA (mtDNA) copy number varies across species, individuals, and cell types. In birds, there are two types of cells with a relatively low number of mitochondria: red blood cells and spermatozoa. Previous studies investigating variation of mitochondrial abundance in animal sperm have generally used quantitative PCR (qPCR), but this method shows potential limitations when quantifying targets at low abundance. To mitigate such issues, we investigated and compared the reliability and accuracy of qPCR, digital PCR (dPCR) and droplet digital PCR (ddPCR) to quantify high and low concentration DNA. We used synthetic DNA targets, to calculate the limit of detection and the limit of quantification and found that with both dPCR and ddPCR, these limits were lower than with qPCR. Then, to compare quantification accuracy and repeatability, we used DNA extracted from blood and sperm cells of Eurasian siskin. We found that qPCR, dPCR and ddPCR all reliably quantified mitochondrial DNA in sperm samples but showed significant differences when analyzing the typically lower levels of mtDNA in blood, with ddPCR consistently showing lower variation among replicates. Our study provides critical insights and recommendations for future studies aiming to quantify target mtDNA and indicates that dPCR and ddPCR are the preferred methods when working with samples with low abundance of mtDNA.
format Artículo científico
id pubmed_40231068
institution PubMed
language en
publishDate 2025
publisher PeerJ
record_format pubmed
spellingShingle Assessing reliability and accuracy of qPCR, dPCR and ddPCR for estimating mitochondrial DNA copy number in songbird blood and sperm cells.
Bagdonaitė, Laima
Leder, Erica H
Lifjeld, Jan T
Johnsen, Arild
Mauvisseau, Quentin
Animals
Male
DNA, Mitochondrial
Spermatozoa
Reproducibility of Results
DNA Copy Number Variations
Songbirds
Polymerase Chain Reaction
Real-Time Polymerase Chain Reaction
Assessing reliability and accuracy of qPCR, dPCR and ddPCR for estimating mitochondrial DNA copy number in songbird blood and sperm cells. Bagdonaitė, Laima Leder, Erica H Lifjeld, Jan T Johnsen, Arild Mauvisseau, Quentin Animals Male DNA, Mitochondrial Spermatozoa Reproducibility of Results DNA Copy Number Variations Songbirds Polymerase Chain Reaction Real-Time Polymerase Chain Reaction Mitochondrial DNA (mtDNA) copy number varies across species, individuals, and cell types. In birds, there are two types of cells with a relatively low number of mitochondria: red blood cells and spermatozoa. Previous studies investigating variation of mitochondrial abundance in animal sperm have generally used quantitative PCR (qPCR), but this method shows potential limitations when quantifying targets at low abundance. To mitigate such issues, we investigated and compared the reliability and accuracy of qPCR, digital PCR (dPCR) and droplet digital PCR (ddPCR) to quantify high and low concentration DNA. We used synthetic DNA targets, to calculate the limit of detection and the limit of quantification and found that with both dPCR and ddPCR, these limits were lower than with qPCR. Then, to compare quantification accuracy and repeatability, we used DNA extracted from blood and sperm cells of Eurasian siskin. We found that qPCR, dPCR and ddPCR all reliably quantified mitochondrial DNA in sperm samples but showed significant differences when analyzing the typically lower levels of mtDNA in blood, with ddPCR consistently showing lower variation among replicates. Our study provides critical insights and recommendations for future studies aiming to quantify target mtDNA and indicates that dPCR and ddPCR are the preferred methods when working with samples with low abundance of mtDNA.
title Assessing reliability and accuracy of qPCR, dPCR and ddPCR for estimating mitochondrial DNA copy number in songbird blood and sperm cells.
topic Animals
Male
DNA, Mitochondrial
Spermatozoa
Reproducibility of Results
DNA Copy Number Variations
Songbirds
Polymerase Chain Reaction
Real-Time Polymerase Chain Reaction
url https://pubmed.ncbi.nlm.nih.gov/40231068/