Evidence map›Paper›PMID 26755361›Full record

ArticleParasitology research2016

DNA sequence analysis suggests that cytb-nd1 PCR-RFLP may not be applicable to sandfly species identification throughout the Mediterranean region.

Ivonne Pamela Llanes-Acevedo, Carolina Arcones, Rosa Gálvez, Oihane Martin, Rocío Checa, Ana Montoya, Carmen Chicharro, Susana Cruz, Guadalupe Miró, Israel Cruz

Open access · hybridAbstract read
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Article in Parasitology research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.8field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Ivonne Pamela Llanes-AcevedoServicio de Parasitología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, World Health Organization Collaborating Center for Leishmaniasis, Ctra. Majadahonda-Pozuelo Km2, Majadahonda, 28220, Madrid, Spain. pamellanes@isciii.es.
Carolina ArconesServicio de Parasitología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, World Health Organization Collaborating Center for Leishmaniasis, Ctra. Majadahonda-Pozuelo Km2, Majadahonda, 28220, Madrid, Spain. c.arcones@isciii.es.
Rosa GálvezDepartamento de Sanidad Animal, Facultad de Veterinaria, Universidad Complutense de Madrid, Avda. Puerta de Hierro s/n, 28040, Madrid, Spain. r.galvez@ucm.es.
Oihane MartinDepartamento de Sanidad Animal, Facultad de Veterinaria, Universidad Complutense de Madrid, Avda. Puerta de Hierro s/n, 28040, Madrid, Spain. oihane.martin.s@gmail.com.
Rocío ChecaDepartamento de Sanidad Animal, Facultad de Veterinaria, Universidad Complutense de Madrid, Avda. Puerta de Hierro s/n, 28040, Madrid, Spain. rocichec@ucm.es.
Ana MontoyaDepartamento de Sanidad Animal, Facultad de Veterinaria, Universidad Complutense de Madrid, Avda. Puerta de Hierro s/n, 28040, Madrid, Spain. amontoya@ucm.es.
Carmen ChicharroServicio de Parasitología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, World Health Organization Collaborating Center for Leishmaniasis, Ctra. Majadahonda-Pozuelo Km2, Majadahonda, 28220, Madrid, Spain. cchichar@isciii.es.
Susana CruzServicio de Parasitología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, World Health Organization Collaborating Center for Leishmaniasis, Ctra. Majadahonda-Pozuelo Km2, Majadahonda, 28220, Madrid, Spain. susi_11@hotmail.com.
Guadalupe MiróDepartamento de Sanidad Animal, Facultad de Veterinaria, Universidad Complutense de Madrid, Avda. Puerta de Hierro s/n, 28040, Madrid, Spain. gmiro@ucm.es.
Israel CruzNeglected Tropical Diseases Programme, Foundation for Innovative New Diagnostics-FIND, Chemin des Mines 9, Campus Biotech, 1202, Geneva, Switzerland. isra.cruz@finddx.org.
Universidad Complutense de Madrid · ESCentro Nacional de Microbiologia · ESInstituto de Salud Carlos III · ESFoundation for Innovative New Diagnostics · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular methods are increasingly used for both species identification of sandflies and assessment of their population structure. In general, they are based on DNA sequence analysis of targets previously amplified by PCR. However, this approach requires access to DNA sequence facilities, and in some circumstances, it is time-consuming. Though DNA sequencing provides the most reliable information, other downstream PCR applications are explored to assist in species identification. Thus, it has been recently proposed that the amplification of a DNA region encompassing partially both the cytochrome-B (cytb) and the NADH dehydrogenase 1 (nd1) genes followed by RFLP analysis with the restriction enzyme Ase I allows the rapid identification of the most prevalent species of phlebotomine sandflies in the Mediterranean region. In order to confirm the suitability of this method, we collected, processed, and molecularly analyzed a total of 155 sandflies belonging to four species including Phlebotomus ariasi, P. papatasi, P. perniciosus, and Sergentomyia minuta from different regions in Spain. This data set was completed with DNA sequences available at the GenBank for species prevalent in the Mediterranean basin and the Middle East. Additionally, DNA sequences from 13 different phlebotomine species (P. ariasi, P. balcanicus, P. caucasicus, P. chabaudi, P. chadlii, P. longicuspis, P. neglectus, P. papatasi, P. perfiliewi, P. perniciosus, P. riouxi, P. sergenti, and S. minuta), from 19 countries, were added to the data set. Overall, our molecular data revealed that this PCR-RFLP method does not provide a unique and specific profile for each phlebotomine species tested. Intraspecific variability and similar RFLP patterns were frequently observed among the species tested. Our data suggest that this method may not be applicable throughout the Mediterranean region as previously proposed. Other molecular approaches like DNA barcoding or phylogenetic analyses would allow a more precise molecular species identification.

Indexed as

AnimalsBase SequenceClimateCytochromes bDatabases, Nucleic AcidDNAElectron Transport Complex IFemaleMaleMediterranean RegionMiddle EastPhlebotomusPhylogenyPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthPsychodidaeCytochromes bDNAElectron Transport Complex IcytbMediterranean phlebotomine sandfliesMitochondrial DNAPCR-RFLP

Identifiers

PMID26755361
PMCPMC4759228
OpenAlexW2239706193

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.