Evidence map›Paper›PMID 32401754›Full record

ArticlePLoS neglected tropical diseases2020

Genetic diversity of Echinococcus multilocularis and Echinococcus granulosus sensu lato in Kyrgyzstan: The A2 haplotype of E. multilocularis is the predominant variant infecting humans.

Cristian A Alvarez Rojas, Philipp A Kronenberg, Sezdbek Aitbaev, Rakhatbek A Omorov, Kubanychbek K Abdykerimov, Giulia Paternoster, Beat Müllhaupt, Paul Torgerson, Peter Deplazes

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Article in PLoS neglected tropical diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Transboundary and emerging diseases · 2026
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  8. Genetic diversity and genotyping ofFrontiers in parasitology · 2025
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  13. Molecular phylogenetic analysis ofFood and waterborne parasitology · 2024
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  14. Case report:Frontiers in veterinary science · 2024
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  15. Journal of veterinary research · 2023
    Article
  16. Article
  17. Co-infection ofInternational journal for parasitology. Parasites and wildlife · 2023
    Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Cristian A Alvarez RojasInstitute of Parasitology, Vetsuisse and Medical Faculty, University of Zürich, Zürich, Switzerland.ORCID 0000-0002-8069-7607
Philipp A KronenbergInstitute of Parasitology, Vetsuisse and Medical Faculty, University of Zürich, Zürich, Switzerland.
Sezdbek AitbaevCity Clinical Hospital #1, Surgical Department, Faculty of Surgery of the Kyrgyz State Medical Academy, Bishkek, Kyrgyzstan.
Rakhatbek A OmorovCity Clinical Hospital #1, Surgical Department, Faculty of Surgery of the Kyrgyz State Medical Academy, Bishkek, Kyrgyzstan.
Kubanychbek K AbdykerimovSection of Epidemiology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.
Giulia PaternosterSection of Epidemiology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.
Beat MüllhauptClinics of Hepatology and Gastroenterology, University Hospital of Zürich, Zürich, Switzerland.
Paul TorgersonSection of Epidemiology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.
Peter DeplazesInstitute of Parasitology, Vetsuisse and Medical Faculty, University of Zürich, Zürich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alveolar and cystic echinococcosis (AE, CE) caused by E. multilocularis and E. granulosus s.l., respectively, are considered emerging zoonotic diseases in Kyrgyzstan with some of the world highest regional incidences. Little is known regarding the molecular variability of both species in Kyrgyzstan. In this study we provide molecular data from a total of 72 parasite isolates derived from humans (52 AE and 20 CE patients) and 43 samples from dogs (23 infected with E. multilocularis and 20 with E. granulosus s.l.).Genetic variability in E. multilocularis was studied using the concatenated complete sequences of the cob, nad2 and cox1 mitochondrial genes adding a total of 3,558bp per isolate. The cob/nad2/cox1 A2 haplotype was identified in 63.4% of the human and in 65.2% of the dog samples. This haplotype was originally described in samples from Kazakhstan and St. Lawrence Island (Alaska, USA). We also describe here 16 non-previously defined variants of E. multilocularis (called A11-A26). All haplotypes cluster together within the Asian group in the haplotype network. Based on Fst values, low level of genetic differentiation was found between the populations of E. multilocularis isolated from different regions within the country. However, high degree of differentiation was found when all the concatenated sequences from Kyrgyzstan are considered as a single population and compared with the population of the parasite from the neighbouring country China. In the case of E. granulosus s.l. the analysis was based in 1,609bp of the cox1 gene. One isolate from a dog was identified as E. equinus, while all the other sequences were identified belonging to E. granulosus s.s. In total, 24 cox1 haplotypes of E. granulosus s.s. were identified including the already described variants: Eg01 (in 6 samples), Eg33 (in 4 samples), EgCl04 (in 2 samples), Eg03 (in 1 sample) and Eg32 (in 1 sample). From the twenty-five other isolates of E. granulosus s.s. a total of 19 non-previously described cox1 haplotypes were identified and named as EgKyr1 to EgKyr19. The most common haplotype infecting human is the EgKyr1 which was found in 5 isolates.The cob/nad2/cox1 A2 haplotype of E. multilocularis is responsible for the majority of human infections in Kyrgyzstan and is also found in the majority of dogs included in this study. Further similar studies in different parts of Asia could elucidate if it is also the most common variant infecting humans in other countries. It remains unknown if this particular haplotype presents differences in virulence which could have contributed to the emergency of alveolar echinococcosis in Kyrgyzstan. In the case of E. granulosus s.s. it seems that there is no dominant haplotype infecting humans in Kyrgzstan. Further characterization of biological or antigenic features of dominant mitochondrial haplotypes could help to elucidate if they present differences which could be relevant in the diagnostic, pathogenicity or in the host/parasite interaction when infecting humans.

Indexed as

Genetic VariationAdultAnimalsCluster AnalysisCommunicable Diseases, EmergingDog DiseasesDogsEchinococcosisEchinococcus granulosusEchinococcus multilocularisElectron Transport Complex IVFemaleHaplotypesHelminth ProteinsHumansIncidenceElectron Transport Complex IVHelminth ProteinsNADH Dehydrogenase

Identifiers

PMID32401754
PMCPMC7219741

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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.