The Barcode Blog

A mostly scientific blog about short DNA sequences for species identification and discovery. I encourage your commentary. -- Mark Stoeckle

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Tracking disease vectors with DNA

mosquitofedWhat hosts sustain arthropod disease vectors when they are not biting humans? In September 2009 PLoS ONE, researchers from DoƱana Research Station, Seville, Spain, report on a “universal DNA barcoding method to identify vertebrate hosts from arthropod bloodmeals.” The investigators collected “wildlife engorged mosquitoes, culicoids [biting midges] and sand flies (Phlebotomiae)…using CDC traps supplied with dry ice to attract ectoparasites through light and CO2.”

To design vertebrate-specific primers that would not amplify the more abundant arthropod DNA, Alcaide and colleagues “downloaded all vertebrate COI sequences (N = 18,2980 from the Classes Mammalia, Aves, Amphibia, and Reptilia that were available in the public domain managed by BOLD Systems database in January 2009” and compared these to “6,784 arthropod COI sequences from taxonomic groups that included blood-feeding species.” From this comparison they designed degenerate (multiple nucleotides at some positions) primers that were >99% matched to vertebrate target sequences and >99% mismatched to invertebrate targets. It would be helpful in this and other studies if the description of new primer(s) gave the position of the 3′ end of each primer as compared to mouse mitochondrial COI for instance. This would make it clear which portion of the COI barcode region is being amplified.

The first pass test with these primers gave PCR products in 43 of 100 mosquito bloodmeals, and reamplification with a slightly different primer set yielded sequenceable products in 97 of 100 cases; this re-amplification protocol was applied to the other vector species with “satisfactory” results. All except 5 matched at >99% level to vertebrate sequences from museum voucher specimens. For 3 of the uncertain identity sequences, they used the closest BOLD matches and knowledge of local fauna to “deduce that these species could be the Iberian hare Lepus granatensis, the red-legged partridge Alectoris rufa and the Egyptian mongoose Herpestes ichneumon.” The other two without close matches were from ticks collected while still feeding so the hosts were known. By my count they detected 18 mammalian and 26 avian host species in arthropod bloodmeals; to me this is remarkable variety given the relatively small number of bloodmeals tested. I look forward to learning more through DNA tracking of biting arthropods.

This entry was posted on Saturday, November 7th, 2009 at 9:10 pm and is filed under General. You can follow any responses to this entry through the RSS 2.0 feed. Both comments and pings are currently closed.

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Contact: mark.stoeckle@rockefeller.edu

About this site

This web site is an outgrowth of the Taxonomy, DNA, and Barcode of Life meeting held at Banbury Center, Cold Spring Harbor Laboratory, September 9-12, 2003. It is designed and managed by Mark Stoeckle, Perrin Meyer, and Jason Yung at the Program for the Human Environment (PHE) at The Rockefeller University.

About the Program for the Human Environment

The involvement of the Program for the Human Environment in DNA barcoding dates to Jesse Ausubel's attendance in February 2002 at a conference in Nova Scotia organized by the Canadian Center for Marine Biodiversity. At the conference, Paul Hebert presented for the first time his concept of large-scale DNA barcoding for species identification. Impressed by the potential for this technology to address difficult challenges in the Census of Marine Life, Jesse agreed with Paul on encouraging a conference to explore the contribution taxonomy and DNA could make to the Census as well as other large-scale terrestrial efforts. In his capacity as a Program Director of the Sloan Foundation, Jesse turned to the Banbury Conference Center of Cold Spring Harbor Laboratory, whose leader Jan Witkowski prepared a strong proposal to explore both the scientific reliability of barcoding and the processes that might bring it to broad application. Concurrently, PHE researcher Mark Stoeckle began to work with the Hebert lab on analytic studies of barcoding in birds. Our involvement in barcoding now takes 3 forms: assisting the organizational development of the Consortium for the Barcode of Life and the Barcode of Life Initiative; contributing to the scientific development of the field, especially by studies in birds, and contributing to public understanding of the science and technology of barcoding and its applications through improved visualization techniques and preparation of brochures and other broadly accessible means, including this website. While the Sloan Foundation continues to support CBOL through a grant to the Smithsonian Institution, it does not provide financial support for barcoding research itself or support to the PHE for its research in this field.