Evidence map›Paper›PMID 40774245›Full record

ArticleThe American journal of tropical medicine and hygiene2025

Polymerase Chain Reaction-Based Diagnosis of Leishmaniasis Targeting Kinetoplast Minicircle DNA in Infants with Hemophagocytic Lymphohistiocytosis.

Heng Zhao, Shulan Shi, Ying Zhang, Haijing Shi, Guorun Jiang, Lilian Yang, Heng Li, Huiwen Zheng, Li Yu, Yun Liao and 5 more

Abstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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

15 authors.

Heng ZhaoKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Shulan ShiClinical Laboratory, Kunming Children's Hospital, Kunming City, China.
Ying ZhangKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Haijing ShiKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Guorun JiangKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Lilian YangKunming Third People's Hospital, Kunming City, China.
Heng LiKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Huiwen ZhengKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Li YuKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Yun LiaoKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Xin ZhaoKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Mei YuanKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Na LiKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Longding LiuKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.
Dandan LiKey Laboratory of Systemic Innovative Research on Virus Vaccine, Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming City, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we aimed to assess the efficacy of polymerase chain reaction (PCR) targeting Leishmania kinetoplast minicircle DNA (kDNA) for diagnosing visceral leishmaniasis-associated hemophagocytic lymphohistiocytosis (VL-HLH). Three pediatric patients diagnosed with VL-HLH via the microscopic examination of bone marrow smears were selected to explore the diagnostic value of kDNA PCR in Leishmania species identification and parasite load quantification in three cases of visceral leishmaniasis. Total DNA was extracted from the bone marrow samples, and PCR testing targeting the Leishmania kDNA was conducted. The amplified PCR products were sequenced and analyzed by using National Center for Biotechnology Information Basic Local Alignment Search Tool for Leishmania species identification and homology cluster analysis. Furthermore, universal primers and probes were designed to quantify the kDNA load in patient samples through real-time quantitative PCR (qPCR) testing. Polymerase chain reaction testing targeting the kDNA gene yielded a specific 139 base pairs band in all samples. Real-time qPCR testing targeting the kDNA gene revealed significant amplification in all patients. The kDNA copy numbers for the three patients were 3,830/µL, 150/µL, and 77,168/µL, respectively. Homology analysis revealed 97.8% similarity between Patients 1 and 2, as well as 87.1% and 87.8% similarity between Patients 1 and 3 and Patients 2 and 3, respectively. All sequences were identified as belonging to the genus Leishmania, with Patients 1 and 2 clustering with Leishmania donovani sequences and Patient 3 clustering with Leishmania infantum. Polymerase chain reaction testing targeting the kDNA gene is a rapid, accurate, and sensitive method for detecting and quantifying Leishmania in VL-HLH patients. It also facilitates species identification through sequencing, demonstrating its potential as a valuable tool in clinical diagnostics.

Indexed as

DNA, KinetoplastLeishmaniasis, VisceralLymphohistiocytosis, HemophagocyticPolymerase Chain ReactionDNA, ProtozoanFemaleHumansInfantLeishmaniaMaleReal-Time Polymerase Chain ReactionDNA, KinetoplastDNA, Protozoan

Identifiers

PMID40774245
PMCPMC12493245

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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.