TY - JOUR
T1 - An optimized metabarcoding method for mimiviridae
AU - Prodinger, Florian
AU - Endo, Hisashi
AU - Gotoh, Yasuhiro
AU - Li, Yanze
AU - Morimoto, Daichi
AU - Omae, Kimiho
AU - Tominaga, Kento
AU - Blanc-Mathieu, Romain
AU - Takano, Yoshihito
AU - Hayashi, Tetsuya
AU - Nagasaki, Keizo
AU - Yoshida, Takashi
AU - Ogata, Hiroyuki
N1 - Funding Information:
Funding: This research was funded by The Canon Foundation (No. 203143100025), JSPS/KAKENHI (Nos. 26430184, 17H03850, 18H02279, 16H06279 (PAGS)), Scientific Research on Innovative Areas from the Ministry of Education, Culture, Science, Sports and Technology (MEXT) of Japan (Nos. 16H06429, 16K21723, 16H06437), The Kyoto University Foundation, and the Collaborative Research Program of the Institute for Chemical Research, Kyoto University (Nos. 2019-33, 2018-31, 2017-25, 2016-28).
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/4
Y1 - 2020/4
N2 - Mimiviridae is a group of viruses with large genomes and virions. Ecological relevance of Mimiviridae in marine environments has been increasingly recognized through the discoveries of novel isolates and metagenomic studies. To facilitate ecological profiling of Mimiviridae, we previously proposed a meta-barcoding approach based on 82 degenerate primer pairs (i.e., MEGAPRIMER) targeting the DNA polymerase gene of Mimiviridae. The method detected a larger number of operational taxonomic units (OTUs) in environmental samples than previous methods. However, it required large quantities of DNA and was laborious due to the use of individual primer pairs. Here, we examined coastal seawater samples using varying PCR conditions and purification protocols to streamline the MEGAPRIMER method. Mixing primer pairs in “cocktails” reduced the required amount of environmental DNA by 90%, while reproducing the results obtained by the original protocol. We compared the results obtained by the meta-barcoding approach with quantifications using qPCR for selected OTUs. This revealed possible amplification biases among different OTUs, but the frequency profiles for individual OTUs across multiple samples were similar to those obtained by qPCR. We anticipate that the newly developed MEGAPRIMER protocols will be useful for ecological investigation of Mimiviridae in a larger set of environmental samples.
AB - Mimiviridae is a group of viruses with large genomes and virions. Ecological relevance of Mimiviridae in marine environments has been increasingly recognized through the discoveries of novel isolates and metagenomic studies. To facilitate ecological profiling of Mimiviridae, we previously proposed a meta-barcoding approach based on 82 degenerate primer pairs (i.e., MEGAPRIMER) targeting the DNA polymerase gene of Mimiviridae. The method detected a larger number of operational taxonomic units (OTUs) in environmental samples than previous methods. However, it required large quantities of DNA and was laborious due to the use of individual primer pairs. Here, we examined coastal seawater samples using varying PCR conditions and purification protocols to streamline the MEGAPRIMER method. Mixing primer pairs in “cocktails” reduced the required amount of environmental DNA by 90%, while reproducing the results obtained by the original protocol. We compared the results obtained by the meta-barcoding approach with quantifications using qPCR for selected OTUs. This revealed possible amplification biases among different OTUs, but the frequency profiles for individual OTUs across multiple samples were similar to those obtained by qPCR. We anticipate that the newly developed MEGAPRIMER protocols will be useful for ecological investigation of Mimiviridae in a larger set of environmental samples.
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U2 - 10.3390/microorganisms8040506
DO - 10.3390/microorganisms8040506
M3 - Article
AN - SCOPUS:85083211078
SN - 2076-2607
VL - 8
JO - Microorganisms
JF - Microorganisms
IS - 4
M1 - 506
ER -