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.
Analysis of the genetic variability in Echinococcus species from different endemic countries have contributed to the knowledge in the taxonomy and phylogeography of these parasites. The most important species of this genus, Echinococcus granulosus sensu lato and Echinococcus multilocularis, co-exist in Kyrgyzstan causing serious public health issues. E. granulosus s.l. causes cystic echinococcosis and E. multilocularis is the causative agent of alveolar echinococcosis. The most relevant finding of our study is the identification of the cob/nad2/cox1 A2 haplotype of E. multilocularis as the most commonly found in humans and dogs. However, it remains unknown if this variant of E. multilocularis, based on genetic differences in mitochondrial genes, presents differences in virulence which could have contributed to the emergence of alveolar echinococcosis in Kyrgyzstan. The results also show a number of non-previously described genetic variants of E. multilocularis and E. granulosus s.s.
Citation: Alvarez Rojas CA, Kronenberg PA, Aitbaev S, Omorov RA, Abdykerimov KK, Paternoster G, et al. (2020) Genetic diversity of Echinococcus multilocularis and Echinococcus granulosus sensu lato in Kyrgyzstan: The A2 haplotype of E. multilocularis is the predominant variant infecting humans. PLoS Negl Trop Dis 14(5): e0008242. https://doi.org/10.1371/journal.pntd.0008242
Editor: Adriano Casulli, Istituto Superiore Di Sanita, ITALY
Received: January 17, 2020; Accepted: March 23, 2020; Published: May 13, 2020
Copyright: © 2020 Alvarez Rojas et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All sequence data are available at GenBank (accession numbers: MN829497-MN829544 and MN787537-MN787561).
Funding: PD, PT, BM received the grant number: SNF Project: No. 173131 – “Transmission modelling of emergent echinococcosis in Kyrgyzstan” from the Swiss National Foundation (http://www.snf.ch). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Alveolar (AE) and cystic echinococcosis (CE), caused by Echinococcus multilocularis and Echinococcus granulosus sensu lato respectively, are serious zoonotic parasitic diseases with a considerable socioeconomic impact . While CE has a worldwide distribution, AE is confined to the northern hemisphere; thus, in some countries, both parasites co-exist as is the case of Kyrgyzstan . AE has become an increasing public health problem in Kyrgyzstan, as in other Asian countries [1,3,4,5], with a rise in the hospital incidence from 0–2 cases/year in the early 1990s to 148 cases reported in 2013 (2.6 cases per 105 inhabitants/year) with some districts in Kyrgyzstan reporting up to 58 cases per 105 inhabitants/year [6,7]. A recent detailed account of surgical incidence for AE shows values as high as 11.77/105 in Naryn and 7.94/105 in Osh . CE is also highly endemic in Kyrgyzstan with a hospital incidence which has increased almost three times between 1991 and 2013 (from 5.4 to 15.8 cases/105 inhabitants/year) [6,9]. However, the true incidence of both diseases is likely to have been underestimated as in other places in the world mostly due to underreporting of the diseases [6,10]. The increase of incidence of CE cases has been linked to changes in farming practices and the closing of meat-processing plants after the dissolution of the Soviet Union . In some areas, such as the Naryn region in central Kyrgyzstan, CE prevalence in sheep reaches 64% . The increase in dog population (especially stray dogs)  has influenced the rise in the incidence of both diseases. Particularly, in the case of AE high levels of infection in dogs have been reported, for example up to 18% in the Naryn district . On the other hand, the prevalence in red foxes (natural definitive host for E. multilocularis) can be as high as 64% in the same district . A common factor for the recent increase of the incidences of both diseases is the intensification in poverty after the economic changes since 1991 . There is a sparsity of information on the molecular variability of E. multilocularis in Kyrgyzstan, with a single study analyzing the EmsB microsatellite in two isolates from a vole and a dog from the Alay valley (Osh region) . In the case of E. granulosus s.l., the only genetic characterization of the parasite in Kyrgyzstan described the presence of E. granulosus s.s., Echinococcus equinus and Echinococcus intermedius G6/7 in dogs . No data from humans has been reported for Echinococcus species. In this study, we aim to investigate the genetic variability of E. multilocularis and E. granulosus s.l. in Kyrgyzstan. For this purpose, we have an unprecedentedly large number of human samples for both diseases and also dog faeces positives for either E. multilocularis or E. granulosus s.l.
Ethics approval for use of human samples
The Ministry of Health of the Kyrgyz Republic provided ethical approval for this study and patients signed a consent form to participate in the study.
Sixty-one samples consisting of parasite tissue derived from human patients diagnosed with AE (collected between Sept 2017 and Feb 2019) and twenty-three similar samples isolated from CE patients (collected in January and February 2019) were collected after surgery at the City Clinical Hospital in Bishkek, Kyrgyzstan. The discrimination between AE and CE was made by the surgeons in Kyrgyzstan supported by clinical data together with ultrasound and CT scan, Casoni skin test and histology of the resected liver lesions. For AE patients, the mean age of 26 men patients was 34 years, while the mean age of 35 female patients was 39 years. All patients had primary lesions in the liver, with 62% being located in the right liver lobe, 33% in the left liver lobe and 5% in both lobes. Of all 23 CE patients, 11 were male and 12 female (mean age: 33 and 29 years respectively). The diagnosis was mainly based on abdominal ultrasound scans, therefore there is only one case with an infected lung. All the rest of CE patients had lesions in the liver, with cyst localisation of 70% in the right, and 30% in the left liver lobe. Surgical specimens were stored in ethanol 70% and shipped to the Institute of Parasitology in Zürich, Switzerland for molecular analysis. Genomic DNA was isolated, after washing the samples three times with PBS1X, using the tissue protocol for the DNeasy Blood & Tissue Kit (Qiagen). DNA was used for routine PCR which can differentiate E. multilocularis from E. granulosus s.l. .
Dog faecal samples
Dog faecal samples from a parallel project studying the prevalence of Echinococcus species in Kyrgyzstan were selected for this study. These samples were collected from the ground in 10 villages located in the Alay and Kochkor districts of Kyrgyzstan (Osh and Naryn regions, respectively), during three expeditions carried out in September 2017, February and June 2018. Dog faeces were identified based on morphological criteria and color. In summary, the detection of taeniid eggs in faecal samples was accomplished through a combination of flotation with zinc chloride (density 1.45) and sieving through nylon meshes of 40 and 21 μm size as described before . The sediment retained in the 21 μm mesh was deposited in a flat-sided tube and examined for the presence of taeniid eggs using an inverted microscope. Positive samples to taeniid eggs were selected and centrifuged at 1,000g for 10 min. DNA was isolated from the sediment as previously described  and used as a template in a multiplex PCR to discriminate between E. granulosus s.l., E. multilocularis and other cestodes . In total, 28 samples positive to E. multilocularis and 24 positives to E. granulosus s.l. were identified and selected for further molecular analysis.
DNA identified as E. multilocularis from parasite tissue derived from human samples and from dog faeces was used as a template for the amplification of the full length of three mitochondrial genes. These genes were cytochrome b (cob), cytochrome c oxidase subunit 1 (cox1) and NADH dehydrogenase subunit 2 (nad2) using primers previously described . PCR products were visualized in a 2% agarose gel and purified using the MinElute PCR purification kit (Qiagen) for subsequent Sanger sequencing with the same primers used for amplification. In the case of the cox1 gene, an extra internal reverse sequencing primer was designed (5’-AGCCACCACAAATCAAGTATCG-3’) (Microsynth, Switzerland). Only electropherograms with clear single peaks were accepted, particular attention was given to samples from dogs taking into consideration that mixed haplotype infections can occur . Electropherograms with double peaks in any of the genes analysed from dog samples were considered to represent infections with two or more haplotypes, and therefore, were not considered in the study. Sequencing analysis was performed with Geneious v11.1.5 and the sequence of each gene was assembled following the reference mitochondrial genome for E. multilocularis (Accession number AB018440). Concatenated sequences of the cob (1,068bp), nad2 (882bp) and cox1 (1,608bp) genes for each DNA sample (adding 3,558bp) were aligned together with other similar available sequences from representative and distinct haplotypes from Asia (A1-A10), Europe (haplotypes E1-E5) and North America (N1-N2) from investigations by Nakao et al. . Alignments were exported as a PHYLIP and NEXUS extensions and used as input for TCS v1.21  and PopArt  for the identification of haplotypes, network construction and estimation of diversity indexes. Genetic distance between two subpopulations was analyzed by pairwise fixation index (Fst) calculated and statistically compared using Arlequin 3.5 .
E. granulosus s.l.
DNA identified as E. granulosus s.l., from parasitic tissue derived from humans cysts and dog faeces, was used for amplification of the cox1 gene using primers previously described . Sequences were assembled using the cox1 haplotype Eg01 as reference (JQ250806), with the same tools as explained above for E. multilocularis. As in the case of E. multilocularis, only electropherograms with single peaks were included in this study. Firstly, the genotypes of E. granulosus (G-system) present in the isolates characterized in this study were identified based on 366bp of the cox1 gene. The original reference sequences for the G1, G3 and other genotypes of E. granulosus s.l. described by Bowles et al  were used as reference in alignments for comparison with the sequences acquired in the present study. Subsequently, for the identification of the cox1 haplotypes of E. granulosus s.s. we included all sequences of the same length (1,609bp) deposited in GenBank. Network construction, estimation of diversity indexes and pairwise fixation index (Fst) were acquired as explained above for E. multilocularis.
PCR confirmed the presence of E. multilocularis in 60 out of 61 AE human patients diagnosed in Kyrgyzstan. The remnant sample was additionally confirmed as AE using immunohistochemichal-stainings with monoclonal antibodies . From the 60 samples mentioned above, it was possible to amplify and acquire good quality sequences from all the three genes of interest (cob, nad2 and cox1) in 52 isolates. From the 28 canine faecal samples identified positive for E. multilocularis, it was possible to amplify and sequence the same three genes in 23 samples. Therefore, the concatenated sequences of the cob, nad2 and cox1 genes from 75 DNA isolates of E. multilocularis (52 human and 23 dogs) were used for further haplotype analysis. In total, 17 different cob/nad2/cox1 haplotypes of E. multilocularis were identified in these 75 samples. When compared with the number of haplotypes using individual genes, the numbers of haplotypes decreased to 7 using only cob, 6 with nad2 and 9 with cox1. Forty-eight isolates representing 64% of the total number of samples, were identified as the haplotype A2, originally described by Nakao et al  from four samples from Kazakhstan and one from St. Lawrence Island (Alaska, USA). Within the human samples, the haplotype A2 was identified in 63.4% (33 out of 52 isolates). This haplotype was identified in 65.2% (15 out of 23 isolates) from dogs. The other twenty-seven concatenated cob/nad2/cox1 sequences were assigned to 16 not previously described haplotypes which were arbitrarily named A11-A26 (accession Numbers: MN829497-MN829544) following the nomenclature given by Nakao et al.  for isolates from Asia. The distribution of the 17 cob/nad2/cox1 haplotypes of E. multilocularis found in this study in Kyrgyzstan and the number of samples (from humans and dogs) identified with each haplotype is shown in Fig 1. The haplotype A2 is present in four out of five regions from where human E. multilocularis samples were available (Chuy, Issyk-Kul, Naryn and Osh) and is the most common haplotype infecting humans in each of these regions. From the Jalal-Abad region the single sample available was identified as the haplotype A23. Also, the haplotype A2 was found in 6 out of 7 dog samples from Osh and in 9 out of 16 dog samples from Naryn. The network of the haplotypes identified in this study is shown in Fig 2, including sequences previously described by Nakao et al.  from Europe, Asia and North America. It has the typical star-like shape with all haplotypes from Kyrgyzstan clustering with the Asian group but assembling a different subgroup compared with the haplotypes previously described from Sichuan in China. The cob/nad2/cox1 A2 haplotype is located in the central position for the Kyrgyzstan subgroup, while the haplotype cob/nad2/cox1 A5 seems to be the central haplotype in Sichuan. Nucleotide substitutions of the mitochondrial cob, nad2 and cox1 genes in the 17 haplotypes of E. multilocularis are shown in S1 Table, S2 Table and S3 Table, respectively. The haplotype A26 has 2 deletions in the sequence of the cox1 gene (positions 209 and 1,402) which produce internal stop codons, suggesting this is a pseudogene, and is not included in Fig 2. Table 1 shows values for genetic distance between subpopulations of E. multilocularis haplotypes identified in 3 regions of Kyrgyzstan where samples were available (Jalal-Abad and Chuy were excluded due to the low number of samples). Based on the values of pairwise fixation index (Fst), it is possible to say that there is no genetic differentiation between the regional parasite subpopulations found in Kyrgyzstan. Also, a low Fst value (-0.0494) was found when comparing the parasite populations of Kyrgyzstan and from the neighbouring country Kazakhstan (Table 2). However, Fst values near 1 were found when the total population of cob/nad2/cox1 haplotypes of E. multilocularis described in Kyrgyzstan were compared with haplotypes of the parasite described in Europe, Asia (Japan and Sichuan, China), and North America (including St. Lawrence Island, Alaska).
Haplotypes A1-A10 were previously identified by Nakao et al. 2009  when the haplotypes A11 to A27 are from this study. The number of samples belonging to each haplotype is shown between brackets. Map source: http://www.diva-gis.org/gdata.
Concatenated sequences from European haplotypes E1-E5, Asian haplotypes A1-A10 and North American haplotypes N1-N2 are also included; these sequences were downloaded from NCBI and were originally published by Nakao et al., . Haplotypes described in this study are named A11-A26 (Accession Numbers: MN829497-MN829544); haplotype A26 is not included in the figure due to a nucleotide deletion in the cox1 gene as explained in the results section. Nucleotide diversity n = 0.00333811, number of segregating sites = 83, number of parsimony-informative sites = 33, Tajima’s D: -0.611996 p (D<-0.611996) = 0.579195.
E. granulosus s.l.
It was possible to amplify the cox1 gene in 20 out of the 23 human CE samples and in 20 out of 24 canine faecal samples positive for E. granulosus s.l. In total, 24 samples have a sequence 100% homologous with the original description of G1 (366bp of the cox1) by Bowles et al, 1992 . While fifteen other samples have a sequence representing nine different genotypes which differ between one and three nucleotides with the G1 and G3 sequences therefore were identified as E. granulosus s.s. Finally, one isolate was identified as E. equinus (G4). A total of 24 different cox1 haplotypes of E. granulosus s.s. were identified from 39 cox1 sequences while a single sequence from a dog was identified as E. equinus. The sequence identified as E. equinus sequence (MN787562) shows 100% homology with isoales from Turkey (KY766905) and the United Kingdom (AB786665). Six samples (two from human and four from dogs), equivalent to 15.4% of the samples, were identified as Eg01 (JQ250806) which is the most commonly distributed cox1 haplotype of E. granulosus s.s. worldwide. Four samples (one human and three from dogs) were identified as Eg33 (AB688610), and one human sample was identified as the haplotype Eg32 (AB688609), both haplotypes previously described in China. Two samples from dogs were identified as EgCl04 (KX227119) initially described in Chile and another sample from a dog was identified as Eg03 (JQ250808) initially described in Iran and Jordan. The twenty-five remnant sequences were identified as 19 not previously described cox1 haplotypes of E. granulosus s.s. (named EgKyr1 to EgKyr19, accession numbers MN787537-MN787561). From these “new” haplotypes the most frequent was EgKyr1 present in 5 human samples. The distribution of the 24 cox1 haplotypes of E. granulosus s.s. and the single E. equinus sample found in this study in Kyrgyzstan and the number of samples (from humans and dogs) identified with particular haplotypes is shown in Fig 3. The most common and cosmopolitan cox1 haplotype, Eg01, was found in the provinces of Chuy and Naryn regions, but it was only in Naryn that this haplotype was found in both humans and dogs. The cox1 haplotype EgKyr1 is present in four out of six districts from where human samples were available (1 from Osh, Batken and Jalal-Abad and 2 from Chuy) (Fig 3). The haplotypes EgCl04 and Eg03 were found only in Naryn. The haplotype network built with the sequences of isolates from this study is shown in Fig 4. A typical star-like shape is observed with the Eg01 haplotype in the centre of the network and the other haplotypes from Kyrgyzstan differing between 1 and 8 nucleotides with the Eg01 sequence. Nucleotide substitutions of mitochondrial cox1 gene in the 24 haplotypes of E. granulosus s.s. identified in this study are shown in S4 Table. Similarly to E. multilocularis, based on Fst values it is possible to say that there is no genetic differentiation between the parasite subpopulations found within Kyrgyzstan for E. granulosus s.s. (Batken region was excluded due to the low number of samples) (Table 3).
The number of samples belonging to each haplotype is shown in brackets. Map source: http://www.diva-gis.org/gdata.
Haplotypes described in this study include EgKyr1-EgKyr19 (Accession numbers MN787537-MN787561). Sequences from haplotypes previously described were also included: Eg01 (JQ250806), Eg03 (JQ250808), Eg32 (AB688609), Eg33 (AB688610) and EgCl04 (KX227119). Nucleotide diversity n = 0.00197019, number of segregating sites = 40, number of parsimony-informative sites = 7, Tajima’s D: -2.34668 p (D<-2.34668) = 0.00351151.
The study of genetic variability in Echinococcus species has made a significant contribution to the knowledge of epidemiology, geographic distribution and phylogeny of these parasites. Since early studies in the 90’s it was clear that a higher degree of variability within E. granulosus s.l. was present compared with E. multilocularis [25,27]. Subsequent studies on the genetic variability of isolates causing CE have contributed clarifying the taxonomy of the parasite, grouping a number of species under the complex E. granulosus s.l. In the case of E. multilocularis the sequencing of the full length of three mitochondrial genes (cob, cox1 and nad2) clearly identified different haplotypes of the parasite clustering in European, Asian and North American clades . Genetic variability within E. multilocularis has also been extensively studied using microsatellite markers [28,29,30]. Although it is also possible to distinguish between Asian, European and North American clades, to date, there is no study discerning a possible connection between mitochondrial and microsatellite markers except for a conference paper in which no obvious correlation was found between individual EmsB profiles and certain mitochondrial haplotypes (cox1, nd1 and atp6 genes) . Using the methodology described by Nakao et al.  and Yanagida et al.  for the analysis of genetic variability within E. multilocularis and E. granulosus s.s., respectively, allowed us to produce datasets which are comparable with other sequences from different geographic regions. In total, 52 isolates from AE patients and 20 from CE patients were included in the study. In the case of E. multilocularis, Nakao et al  included only 5 human samples (from Sichuan, China) together with 24 samples from rodents, 6 from red foxes and 2 from dogs. The small number of samples from humans might reflect the difficulty in acquiring such parasite material. Other investigations which have included human samples have sequenced shorter sections of the mitochondrial genes  or the full length of different mitochondrial genes . Therefore, we cannot compare our dataset with such sequences. For E. granulosus, the analysis of genetic diversity using metacestode material derived from humans has been more extensively used  but mostly using short sequences of mitochondrial genes.
The cob/nad2/cox1 haplotype A2 of E. multilocularis, originally described in 4 isolates from Kazakhstan and in one isolate from St Lawrence island (Alaska, USA) , was the predominant E. multilocularis haplotype found in the human and dog samples in this study. Based on the finding of A2 and the haplotype A4 (in Japan and St. Lawrence Island), it was hypothesized that the long-distance dispersal of E. multilocularis in the Asian continent occurred during the Holocene to the present. Interestingly, the central location of the A2 haplotype in the network described in this study (Fig 2) suggests that this is an ancient haplotype from which other variants of the parasite have mutated. However, it is important to clarify that what is considered to be a cob/nad2/cox A2 haplotype could differ in the sequence in other mitochondrial genes. To confirm if all the sequences called A2 (by Nakao et al.  and in this study) are actually the same variant of the parasite it is necessary to sequence the whole mitochondrial genome of such isolates, however, this is not the objective of the present study. In fact, recent publications of nearly complete mitochondrial genome of different isolates of E. granulosus s.s. have shown that, in some cases, what was supposed to be the same haplotype (for example based on the sequence of the cox1 gene only) in reality corresponded to different variants of the parasite when the whole mitogenome is sequenced . Nevertheless, the identification of a single cob/nad2/cox1 haplotype of E. multilocularis in this study, as the most common variant of the parasite in humans (63.4%) and dogs (65.2%) from Kyrgyzstan is relevant to understand the transmission of the parasite to humans. This haplotype was not found in the Jalal-Abad region, however we had only one isolate from this region. Jalal-Abad is the region with the lowest incidence of AE in Kyrgyzstan and this explains the low number of samples from this area  and this explains the low number of samples from this area. It would be interesting to perform similar studies in E. multilocularis isolated from foxes in the same country to know if this is also the most common variant of the parasite in the wild animal cycle. Also, it would be interesting to study more human samples in Asia to see if the A2 haplotype is responsible for most human infections in the continent. It is possible to speculate that the emergence of echinococcosis in Kyrgyzstan could be partially attributed to a specific variant(s) of the parasite circulating in the country. However, there is no evidence which attributes differences in virulence or host/parasite interaction to specific mitochondrial haplotypes of E. multilocularis. A similar situation occurs describing the genetic variability within E. granulosus s.s. The sequencing of the full nuclear genome from isolates identified as different mitochondrial haplotypes of Echinococcus species could be useful information to better understand if different haplotypes vary in the sequence of important genes which allow the establishment and survival of the parasites at their different stages. Interestingly, the haplotypes of E. multilocularis found in this study differ from the ones described in neighbouring China, specifically from Sichuan and Inner Mongolia, clearly reflecting differences in the parasite population (Table 2). Such differences may have been facilitated by the physical barrier which separates China and Kyrgyzstan. This border is 1,063km in length with various mountain ridges and peaks of the Tian Shan mountain system, some of them reaching over 7,000 m and also includes the Turpan Depression 154 m below sea level which is also one of the hottest and driest areas in China during the summer. The endemic areas of Sichuan and Inner Mongolia are over 1,000 km east of these geographical barriers. However, there is no support for the differentiation of the parasite population found within the country in the studied regions (Table 1).
Regarding the analysis of E. granulosus s.s. samples, we found a high variability identifying 19 not previously described cox1 haplotypes. Interestingly, the most common and cosmopolitan cox1 haplotype of E. granulosus s.s. (Eg01) was described only in six samples from Chuy (one human sample) and Naryn (one human and four dog samples) regions. The most common cox1 haplotype infecting humans in Kyrgyzstan is EgKyr1 in 5 isolates from Osh, Batken, Jalal-Abad and Chuy. Unlike the case of E. multilocularis, there is no dominant haplotype of E. granulosus in the samples analysed (Fig 4). This could be the consequence of a low number of samples analysed or the higher variability of the sequences investigated. It is likely that the geographic isolation of Kyrgyzstan has allowed the parasite to mutate differently (at least in the cox1 gene), compared with other parts of the world. Fst values do not support the differentiation of the population of E. granulosus s.s. within the country (Table 3). After multiple investigations of genetic variability within E. granulosus s.s. (see [34,36]) it remains unknown if the variants of this parasite described (based on the sequence of the cox1 gene) are actually different in terms of pathogenicity, biological features and host response. In this study, we did not find any correlation between a specific haplotype and classification or size of the lesion. In the meantime, data from this study provides valuable information regarding the phylogeography and distribution of the parasite. Interestingly, we did not find other species than E. granulosus s.s. and E. equinus, although previous research has also identified E. intermedius G6/7 in dogs from Kyrgyzstan  and South-East Kazakhstan, close to the border with Kyrgyzstan .
In summary, we described that the cob/nad2/cox1 A2 haplotype of E. multilocularis is the most commonly found variant of the parasite in humans and dogs in Kyrgyzstan. Its central location in the haplotype network built here suggests that it is an ancient variant of the parasite. In the case of E. granulosus s.s. there is no dominant cox1 haplotype in the samples analysed, however a number of non previously described haplotypes have been characterized. Further investigations should clarify if the A2 haplotype is also the most relevant variant infecting humans in other countries in Asia.
S1 Table. Segregating sites between the concatenated sequences of the cob gene of the haplotypes of E. multilocularis identified in this study (haplotypes A11 to A26) compared with the sequence of the already described haplotypes of E. multilocularis by Nakao et al., 2009  (haplotypes A1-A10 excluding O1).
S2 Table. Segregating sites between the concatenated sequences of the nad2 gene of the haplotypes of E. multilocularis identified in this study (haplotypes A11 to A26) compared with the sequence of the already described haplotypes of E. multilocularis by Nakao et al., 2009  (haplotypes A1-A10 excluding O1).
S3 Table. Segregating sites between the concatenated sequences of the cox1 gene of the haplotypes of E. multilocularis identified in this study (haplotypes A11 to A26) compared with the sequence of the already described haplotypes of E. multilocularis by Nakao et al, 2009 (haplotypes A1-A10 excluding O1).
S4 Table. Segregating sites between the sequences of the cox1 gene of the haplotypes of E. granulosus sensu stricto identified in this study (haplotypes EgKyr1-EgKyr19) compared with the sequence of the already described haplotypes of E. granulosus s.s. Eg01 (JQ250806), Eg03 (JQ250808), Eg32 (AB688609), Eg33 (AB688610) and EgCl04 (KX227119) also present in Kyrgyzstan.
This research paper represents the veterinary doctoral thesis of Philipp Andreas Kronenberg (PAK).
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