Evidence map›Paper›PMID 39300564›Full record

ArticleParasites & vectors2024

Seasonal dynamics, Leishmania diversity, and nanopore-based metabarcoding of blood meal origins in Culicoides spp. in the newly emerging focus of leishmaniasis in Northern Thailand.

Chulaluk Promrangsee, Sira Sriswasdi, Sakone Sunantaraporn, Chatuthanai Savigamin, Thanapat Pataradool, Chatchapon Sricharoensuk, Rungfar Boonserm, Rinnara Ampol, Pitchayaporn Pruenglampoo, Mathirut Mungthin and 3 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

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  6. Molecular identification and characterization ofCurrent research in parasitology & vector-borne diseases · 2026
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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

13 authors.

Chulaluk PromrangseeInterdisciplinary Program of Biomedical Sciences, Graduate School, Chulalongkorn University, Bangkok, Thailand.
Sira SriswasdiCenter of Excellence in Computational Molecular Biology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Sakone SunantarapornCenter of Excellence in Vector Biology and Vector-Borne Disease, Chulalongkorn University, Bangkok, Thailand.
Chatuthanai SavigaminDepartment of Parasitology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Thanapat PataradoolDepartment of Parasitology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Chatchapon SricharoensukDepartment of Parasitology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Rungfar BoonsermCenter of Excellence in Vector Biology and Vector-Borne Disease, Chulalongkorn University, Bangkok, Thailand.
Rinnara AmpolCenter of Excellence in Vector Biology and Vector-Borne Disease, Chulalongkorn University, Bangkok, Thailand.
Pitchayaporn PruenglampooDivision of Medical Technical and Academic Affairs, Department of Medical Services, Ministry of Public Health, Nonthaburi, Thailand.
Mathirut MungthinDepartment of Parasitology, Phramongkutklao College of Medicine, Bangkok, Thailand.
Jonas Schmidt-ChanasitBernhard-Nocht-Institute for Tropical Medicine, Bernhard-Nocht-Str. 74, Hamburg, Germany.
Padet SiriyasatienCenter of Excellence in Vector Biology and Vector-Borne Disease, Chulalongkorn University, Bangkok, Thailand.
Kanok PreativatanyouCenter of Excellence in Vector Biology and Vector-Borne Disease, Chulalongkorn University, Bangkok, Thailand. kanok.pr@chula.ac.th.

Funding

the Ratchadapiseksompote Fund, Graduate Affairs, Faculty of Medicine, Chulalongkorn University GA68/001
6 · The paper itself

Abstract

backgroundClinical cases of leishmaniasis caused by Leishmania (Mundinia) parasites have been increasingly reported in Southeast Asia, particularly Thailand. Recent evidence has shown that Leishmania (Mundinia) parasites successfully developed into infective metacyclic promastigotes in Culicoides biting midges, strongly supporting their putative role in disease transmission. However, Culicoides diversity, host preference, and Leishmania prevalence in endemic areas remain largely unknown.

methodsWe investigated the seasonal dynamics, infection prevalence, and blood meal identification of Culicoides collected from the emerging focus of visceral leishmaniasis in Lampang Province, Northern Thailand, during 2021-2023. Midge samples were molecularly screened for Leishmania using SSU rRNA-qPCR and ITS1-PCR, followed by Sanger plasmid sequencing, and parasite haplotype diversity was analyzed. Host blood meal origins were comparatively identified using host-specific Cytb-PCRs and a nanopore-based metabarcoding approach.

resultsA total of 501 parous and gravid females and 46 blood-engorged ones belonging to at least 17 species of five subgenera (Remmia, Trithecoides, Avaritia, Hoffmania, and Meijerehelea) and two species groups (Shortti and Calvipalpis) were collected with temporal differences in abundance. Leishmania was detected by SSU rRNA-qPCR in 31 samples of at least 11 midge species, consisting of Culicoides oxystoma, C. guttifer, C. orientalis, C. mahasarakhamense, C (Trithecoides) spp., C. innoxius, C. shortti, C. arakawae, C. sumatrae, C. actoni, and C. fulvus, with the overall infection prevalence of 5.7%. The latter six species represent the new records as putative leishmaniasis vectors in Northern Thailand. The ITS1-PCR and plasmid sequencing revealed that Leishmania martiniquensis was predominantly identified in all qPCR-positive species, whereas L. orientalis was identified only in three C. oxystoma samples. The most dominant haplotype of L. martiniquensis in Thailand was genetically intermixed with those from other geographical regions, confirming its globalization. Neutrality test statistics were also significantly negative on regional and country-wide scales, suggesting rapid population expansion or selective sweeps. Nanopore-based blood meal analysis revealed that most Culicoides species are mammalophilic, with peridomestic and wild mammals (cow, pig, deer, and goat-like species) and humans as hosts, while C. guttifer and C. mahasarakhamense fed preferentially on chickens.

conclusionsThis study revealed seasonal dynamics and sympatric circulation of L. martiniquensis and L. orientalis in different species of Culicoides. Evidence of human blood feeding was also demonstrated, implicating Culicoides as putative vectors of human leishmaniasis in endemic areas. Further research is therefore urgently needed to develop vector control strategies and assess the infection status of their reservoir hosts to effectively minimize disease transmission.

Indexed as

CeratopogonidaeInsect VectorsLeishmaniaSeasonsAnimalsDNA Barcoding, TaxonomicFemaleGenetic VariationHumansLeishmaniasisLeishmaniasis, VisceralNanoporesThailandCulicoides biting midgesHost preferenceKillick-Kendrick’s criteriaLeishmaniaMundiniaNanopore metabarcodingNorthern Thailand

Identifiers

PMID39300564
PMCPMC11414243

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.