TY - JOUR
T1 - Rapid degradation of longer DNA fragments enables the improved estimation of distribution and biomass using environmental DNA
AU - Jo, Toshiaki
AU - Murakami, Hiroaki
AU - Masuda, Reiji
AU - Sakata, Masayuki K.
AU - Yamamoto, Satoshi
AU - Minamoto, Toshifumi
N1 - Funding Information:
We thank Dr. Atushi Ushimaru and Dr. Yasuoki Takami (Kobe University) for helpful comments and suggestions to the experimental design and interpretation of results. This work was supported by JST CREST Grant Number JPMJCR13A2, Japan.
Publisher Copyright:
© 2017 John Wiley & Sons Ltd
PY - 2017/11
Y1 - 2017/11
N2 - The advent of environmental DNA (eDNA) analysis methods has enabled rapid and wide-range ecological monitoring in aquatic ecosystems, but there is a dearth of information on eDNA degradation. The results of previous studies suggest that the decay rate of eDNA varies depending on the length of DNA fragments. To examine this hypothesis, we compared temporal change in copy number of long eDNA fragments (719 bp) with that of short eDNA fragments (127 bp). First, we isolated rearing water from a target fish species, Japanese Jack Mackerel (Trachurus japonicus), and then quantified the copy number of the long and short eDNA fragments in 1 L water samples after isolating the water from the fish. Long DNA fragments showed a higher decay rate than short fragments. Next, we measured the eDNA copy numbers of long and short DNA fragments using field samples, and compared them with fish biomass as measured by echo intensity. Although a previous study suggested that short eDNA fragments could be overestimated because of nontarget eDNA from a nearby fish market and carcasses, the eDNA concentrations of long fragments were correlated with echo intensity. This suggests that the concentration of longer eDNA fragments reflects fish biomass more accurately than the previous study by removing the effects of the fish market and carcasses. The length-related differences in eDNA have a substantial potential to improve estimation of species biomass.
AB - The advent of environmental DNA (eDNA) analysis methods has enabled rapid and wide-range ecological monitoring in aquatic ecosystems, but there is a dearth of information on eDNA degradation. The results of previous studies suggest that the decay rate of eDNA varies depending on the length of DNA fragments. To examine this hypothesis, we compared temporal change in copy number of long eDNA fragments (719 bp) with that of short eDNA fragments (127 bp). First, we isolated rearing water from a target fish species, Japanese Jack Mackerel (Trachurus japonicus), and then quantified the copy number of the long and short eDNA fragments in 1 L water samples after isolating the water from the fish. Long DNA fragments showed a higher decay rate than short fragments. Next, we measured the eDNA copy numbers of long and short DNA fragments using field samples, and compared them with fish biomass as measured by echo intensity. Although a previous study suggested that short eDNA fragments could be overestimated because of nontarget eDNA from a nearby fish market and carcasses, the eDNA concentrations of long fragments were correlated with echo intensity. This suggests that the concentration of longer eDNA fragments reflects fish biomass more accurately than the previous study by removing the effects of the fish market and carcasses. The length-related differences in eDNA have a substantial potential to improve estimation of species biomass.
KW - DNA fragment length
KW - Japanese Jack Mackerel (Trachurus japonicus)
KW - decay rate
KW - echo intensity
KW - environmental DNA (eDNA)
KW - quantitative real-time PCR
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U2 - 10.1111/1755-0998.12685
DO - 10.1111/1755-0998.12685
M3 - Article
C2 - 28449215
AN - SCOPUS:85019695817
SN - 1755-098X
VL - 17
SP - e25-e33
JO - Molecular Ecology Resources
JF - Molecular Ecology Resources
IS - 6
ER -