Background: The past several years have seen a flurry of papers seeking to clarify the utility and limits of DNA barcoding, particularly in areas such as species discovery and paralogy due to nuclear pseudogenes. Heteroplasmy, the coexistence of multiple mitochondrial haplotypes in a single organism, has been cited as a potentially serious problem for DNA barcoding but its effect on identification accuracy has not been tested. In addition, few studies of barcoding have tested a large group of closely-related species with a well-established morphological taxonomy. In this study we examine both of these issues, by densely sampling the Hawaiian Hylaeus bee radiation. Results: Individuals from 21 of the 49 a priori morphologically-defined species exhibited coding sequence heteroplasmy at levels of 1-6% or more. All homoplasmic species were successfully identified by COI using standard methods of analysis, but only 71% of heteroplasmic species. The success rate in identifying heteroplasmic species was increased to 86% by treating polymorphisms as character states rather than ambiguities. Nuclear pseudogenes (numts) were also present in four species, and were distinguishable from heteroplasmic sequences by patterns of nucleotide and amino acid change. Conclusions: Heteroplasmy significantly decreased the reliability of species identification. In addition, the practical issue of dealing with large numbers of polymorphisms- and resulting increased time and labor required - makes the development of DNA barcode databases considerably more complex than has previously been suggested. The impact of heteroplasmy on the utility of DNA barcoding as a bulk specimen identification tool will depend upon its frequency across populations, which remains unknown. However, DNA barcoding is still likely to remain an important identification tool for those species that are difficult or impossible to identify through morphology, as is the case for the ecologically important solitary bee fauna.
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Univ Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
China Natl GeneBank Shenzhen, BGI Shenzhen, Beishan Rd,Beishan Ind Zone, Shenzhen 518083, Guangdong, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Tan, Meihua
Zhang, Rui
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China Natl GeneBank Shenzhen, BGI Shenzhen, Beishan Rd,Beishan Ind Zone, Shenzhen 518083, Guangdong, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Zhang, Rui
Hardman, Chloe
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Univ Reading, Sch Agr Policy & Dev, Reading, Berks, EnglandUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
Hardman, Chloe
Zhou, Xin
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China Natl GeneBank Shenzhen, BGI Shenzhen, Beishan Rd,Beishan Ind Zone, Shenzhen 518083, Guangdong, Peoples R ChinaUniv Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
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Univ Adelaide, Sch Agr Food & Wine, Adelaide, SA 5005, AustraliaUniv Adelaide, Sch Agr Food & Wine, Adelaide, SA 5005, Australia
Hogendoorn, Katja
Stevens, Mark
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S Australian Museum, Adelaide, SA 5000, Australia
Univ S Australia, Sch Pharm & Med Sci, Adelaide, SA 5000, AustraliaUniv Adelaide, Sch Agr Food & Wine, Adelaide, SA 5005, Australia
Stevens, Mark
Leijs, Remko
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S Australian Museum, Adelaide, SA 5000, AustraliaUniv Adelaide, Sch Agr Food & Wine, Adelaide, SA 5005, Australia