Evidence map›Paper›PMID 25274259›Full record

ArticleParasites & vectors2014

Comparison of PCR methods for detection of Leishmania siamensis infection.

Atitaya Hitakarun, Peerapan Tan-ariya, Suradej Siripattanapipong, Mathirut Mungthin, Phunlerd Piyaraj, Tawee Naaglor, Padet Siriyasatien, Saruda Tiwananthagorn, Saovanee Leelayoova

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 43 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Atitaya HitakarunDepartment of Microbiology, Faculty of Science, Mahidol University, Ratchawithi Rd., Ratchathewi, Bangkok, 10400, Thailand. aor_meddream@hotmail.com.
Peerapan Tan-ariyaDepartment of Microbiology, Faculty of Science, Mahidol University, Ratchawithi Rd., Ratchathewi, Bangkok, 10400, Thailand. scptn@mahidol.ac.th.
Suradej SiripattanapipongDepartment of Parasitology, Phramongkutklao College of Medicine, Bangkok, 10400, Thailand. suradejs@rocketmail.com.
Mathirut MungthinDepartment of Parasitology, Phramongkutklao College of Medicine, Bangkok, 10400, Thailand. mathirut@pmk.ac.th.
Phunlerd PiyarajDepartment of Parasitology, Phramongkutklao College of Medicine, Bangkok, 10400, Thailand. p_phunlerd@yahoo.com.
Tawee NaaglorDepartment of Parasitology, Phramongkutklao College of Medicine, Bangkok, 10400, Thailand. tawee_narkloar@hotmail.com.
Padet SiriyasatienDepartment of Parasitology, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand. padet.s@chula.ac.th.
Saruda TiwananthagornDepartment of Veterinary Biosciences and Veterinary Public Health, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai, 50100, Thailand. saruda.t@cmu.ac.th.
Saovanee LeelayoovaDepartment of Parasitology, Phramongkutklao College of Medicine, Bangkok, 10400, Thailand. s_leelayoova@scientist.com.
Phramongkutklao Hospital · THMahidol University · THChiang Mai University · THChulalongkorn University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeishmania siamensis, a newly identified species, has been reported as a causative agent of leishmaniasis in Thailand. This organism has been identified and genetically characterized using PCR techniques based on several target genes. However, the sensitivities and specificities of these methods for the diagnosis of L. siamensis infection have never been evaluated.

methodsTo evaluate the sensitivities and specificities of PCR methods to detect L. siamensis infection, PCR for different genetic markers, i.e., the small subunit ribosomal RNA region (SSU-rRNA), the internal transcribed spacer 1 region (ITS1), cysteine protease B (cpb), cytochrome b (cyt b), heat shock protein 70 (hsp70), the spliced leader mini-exon, and the triose-phosphate isomerase (tim) genes were compared.

resultsBoth the ITS1-PCR and the SSU rRNA-PCR could detect promastigote of L. siamensis at concentrations as low as 0.05 parasites/μl or the DNA concentration at 2.3 pg/μl. Though the ITS1-PCR method only recognized 8 samples as positive, all of these could be assessed as true positive according to microscopic diagnosis and/or amplifying the results of the PCR and their sequencing, while other methods also produced false positive results. Compared with the ITS1-PCR method, the PCR amplified SSU-rRNA and cpb gene showed 100% sensitivity for the detection of L. siamensis in clinical specimens. The PCR amplified mini-exon and hsp70 gene also gave a high sensitivity of 87.5%. In contrast, the PCR methods for cyt b and tim gene showed low sensitivity. The PCR methods for cyt b, mini-exon and tim gene showed 100% specificity compared with the ITS1-PCR.

conclusionAs a result, the ITS1-PCR method is a suitable target for PCR-based detection of L. siamensis infection in clinical specimens due to its high sensitivity and specificity. The results of this study can be used for molecular diagnosis as well as in epidemiological studies of L. siamensis in affected areas.

Indexed as

DNA, IntergenicDNA, ProtozoanGene Expression RegulationGenetic MarkersHSP70 Heat-Shock ProteinsHumansLeishmaniaLeishmaniasisPolymerase Chain ReactionRNA, ProtozoanRNA, RibosomalSensitivity and SpecificityDNA, IntergenicDNA, ProtozoanGenetic MarkersHSP70 Heat-Shock ProteinsRNA, ProtozoanRNA, Ribosomal

Identifiers

PMID25274259
PMCPMC4188918
OpenAlexW2104145751

What OpenQuestion holds

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LicenceCC BY
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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.