The first mitogenome of Petrovinema skrjabini from Equus ferus przewalskii: a phylogenetic analysis within the Strongylidae family.
Abstract: Petrovinema skrjabini (Nematoda: Strongylidae, Cyathostominae) is a parasitic nematode colonizing the cecum and colon of equids. Like other cyathostomins, its larvae (L3) invade the intestinal mucosa, forming encysted nodules that may remain dormant for years. Mass larval emergence triggers larval cyathostominosis-a severe syndrome characterized by hemorrhagic typhlocolitis and diarrhea, with mortality rates exceeding 50%. However, owing to the morphological indistinguishability of cyathostomin and frequent mixed infections in natural settings, species-specific contributions to pathogenesis remain unresolved. Previous studies on P. skrjabini have predominantly focused on its morphology, with limited molecular information available. Methods: The complete mitogenome of Petrovinema skrjabini was sequenced using the Illumina NovaSeq 6000 platform, followed by assembly and annotation. We performed a phylogenetic analysis using Bayesian inference (BI) and maximum likelihood (ML) methods, based on 12 protein-coding genes from mitogenomes, to assess the evolutionary relationships of 34 Strongylidae species. Results: The complete mitogenome of P. skrjabini comprises 13,885 base pairs with 12 protein-coding genes, two ribosomal-RNA genes, 22 transfer-RNA genes, and two non-coding regions. The gene arrangement of the P. skrjabini mitogenome was consistent with the GA3 arrangement found in other Strongylidae species. The mitogenome exhibited a high AT bias (75.4%), which is consistent with other species in other Strongylidae species. Phylogenetic analysis showed that two Strongylus species (belonging to subfamily Strongylinae) formed a clade and located in the base of Strongylidae, while three Triodontophorus (belonging to subfamily Strongylinae) species and P. skrjabini formed another clade within in subfamily Cyathostominae within Strongylidae, based on 12 protein-coding genes from mitogenomes, suggesting that the genus Triodontophorus should transfer to the subfamily Cyathostominae. Conclusions: The characterization of the complete mitochondrial genomes of P. skrjabini is reported for the first time. This study provided helpful genetic markers for P. skrjabini identification and taxonomy, facilitating early nematode diagnosis and treatment to decrease equine parasitic nematode burdens. Our mitochondrial phylogeny analyses further corroborate the hypothesis that the genus Triodontophorus belongs to Cyathostominae. The present study enriches the database of strongylids mitogenomes and provides a new insight into the systematics of the family Strongylidae.
© 2025. The Author(s).
Publication Date: 2025-07-11 PubMed ID: 40646541PubMed Central: PMC12247273DOI: 10.1186/s13071-025-06851-7Google Scholar: Lookup
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Summary
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The research work focuses on the genetic analysis of Petrovinema skrjabini, a parasitic worm species found in horses, with the aim of providing genetic markers for better diagnosis of nematode infections and to refine the taxonomy of the family Strongylidae.
Objective and Importance of the Research
- The key goal of the research is to analyze the mitochondrial genome, or mitogenome, of Petrovinema skrjabini – a parasitic nematode found in some horse species.
- Understanding the complete genetic makeup of this worm species is crucial due to its potential fatal impact; mass hatching of its larvae could cause a severe syndrome in the horses with a mortality rate exceeding 50%.
- Additionally, past studies on this species have been primarily morphological, while molecular information remains limited. Hence, this study might help fill in the gaps in molecular research on this nematode.
Methodology and Results
- The mitogenome of P. skrjabini was sequenced using the Illumina NovaSeq 6000 platform, and assembled and annotated thereafter.
- After the sequencing, a phylogenetic analysis was performed using Bayesian Inference and Maximum Likelihood methods. They assessed the evolutionary relationships of 34 species within the Strongylidae family based on 12 protein-coding genes.
- The sequencing revealed that the complete mitogenome of P. skrjabini has 13,885 base pairs including 12 protein-coding genes, two ribosomal-RNA genes, 22 transfer-RNA genes, and two non-coding regions.
- A high AT bias (75.4%) was also observed in the mitogenome of P. skrjabini, which is an expected trait in Strongylidae species.
Key Findings and Conclusion
- The phylogenetic analysis gathered from the study revealed that two Strongylus species and three Triodontophorus species, together with P. skrjabini, formed distinct clusters within the Cyathostominae subfamily of the Strongylidae family.
- This could suggest that the genus Triodontophorus should be transferred to the Cyathostominae subfamily, which offers a new perspective on the taxonomy of Strongylidae.
- The first-ever reported characterization of the complete mitochondrial genomes of P. skrjabini provides useful genetic markers for this species’ identification and taxonomy.
- This study facilitates early diagnosis and treatment of nematode infections, potentially reducing the burdens of equine parasitic nematodes.
- The study enriches the genetic database of strongylids and offers a fresh insight into the taxonomy of the Strongylidae family.
Cite This Article
APA
Jia H, Tang L, Fu Y, Xiong Y, Yan L, Shao C, Li K, Zhang D, Hu D.
(2025).
The first mitogenome of Petrovinema skrjabini from Equus ferus przewalskii: a phylogenetic analysis within the Strongylidae family.
Parasit Vectors, 18(1), 278.
https://doi.org/10.1186/s13071-025-06851-7 Publication
Researcher Affiliations
- School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, 100083, China.
- School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, 100083, China.
- School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, 100083, China.
- School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, 100083, China.
- School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, 100083, China.
- Xinjiang Kalamaili Mountain Ungulate Nature Reserve Management Center, Xinjiang, China.
- School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, 100083, China.
- School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, 100083, China. ernest8445@163.com.
- School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, 100083, China. hudf@bjfu.edu.cn.
MeSH Terms
- Animals
- Phylogeny
- Genome, Mitochondrial
- Equidae / parasitology
- Strongyloidea / genetics
- Strongyloidea / classification
- Horses / parasitology
- Horse Diseases / parasitology
Grant Funding
- 2022YFC2601601 / The National Key R&D Program of China
- 2019JQ0318 / The Beijing Forestry University Outstanding Young Talent Cultivation Project
Conflict of Interest Statement
Declarations. Ethics approval and consent to participate: Not applicable. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.
References
This article includes 60 references
- Clark A, Sallé G, Ballan V, Reigner F, Meynadier A, Cortet J. Strongyle infection and gut microbiota: profiling of resistant and susceptible horses over a grazing season. Front Physiol 2018;9:272.
- Kuzmina TA, Tolliver SC, Lyons ET. Three recently recognized species of cyathostomes (Nematoda: Strongylidae) in equids in Kentucky. Parasitol Res 2011;108:1179–84.
- SSaeed MA, Beveridge I, Abbas G, Beasley A, Bauquier J, Wilkes E. Systematic review of gastrointestinal nematodes of horses from Australia. Parasit Vectors 2019;12:188.
- Corning S. Equine cyathostomins: a review of biology, clinical significance and therapy. Parasit Vectors 2009;2:S1.
- Krecek RC, Guthrie AJ. Alternative approaches to control of cyathostomes: an African perspective. Vet Parasitol 1999;85:151–62.
- Morariu S, Mederle N, Badea C, Dărăbuş G, Ferrari N, Genchi C. The prevalence, abundance and distribution of cyathostomins (small stongyles) in horses from Western Romania. Vet Parasitol 2016;223:205–9.
- Painer J, Kaczensky P, Ganbaatar O, Huber K, Walzer C. Comparative parasitological examination on sympatric equids in the great gobi “B” strictly protected area, Mongolia. Eur J Wildl Res 2011;57:225–32.
- Baptista CJ, Sós E, Madeira de Carvalho L. Gastrointestinal parasitism in Przewalski horses (). Acta Parasitol 2021;66:1095–101.
- Kuzmina T, Zvegintsova N, Zharkikh T. Strongylid community structure of the przewalski’s horses () from the biosphere reserve “askania-Nova”, Ukraine. Vestn Zool 2009;43:e5.
- Slivinska K, Klich D, Yasynetska N, Zygowska M. The effects of seasonality and group size on fecal egg counts in wild Przewalski’s horses (, Poljakov, 1881) in the Chernobyl exclusion zone, Ukraine during 2014–2018. Helminthologia (Poland) 2020;57:314–21.
- Ferrari N, Cattadori IM, Rizzoli A, Hudson PJ. reduces infestation of in free-living yellow-necked mice, .. Parasitology 2009;136:305–16.
- Lass S, Hudson PJ, Thakar J, Saric J, Harvill E, Albert R. Generating super-shedders: co-infection increases bacterial load and egg production of a gastrointestinal helminth. J R Soc Interf 2013;10:20120588.
- Lello J, Boag B, Fenton A, Stevensonlan R, Hudson PJ. Competition and mutualism among the gut helminths of a mammalian host. Nature 2004;428:837–40.
- Randall J, Cable J, Guschina IA, Harwood JL, Lello J. Endemic infection reduces transmission potential of an epidemic parasite during co-infection. Proc Roy Soc B Biol Sci 2013;280:20131500.
- Tombak KJ, Hansen CB, Kinsella JM, Pansu J, Pringle RM, Rubenstein DI. The gastrointestinal nematodes of plains and Grevy’s zebras: phylogenetic relationships and host specificity. Int J Parasitol Parasites Wildl 2021;16:228–35.
- Bredtmann CM, Krücken J, Murugaiyan J, Kuzmina T, von Samson-Himmelstjerna G. Nematode species identification—current status, challenges and future perspectives for cyathostomins. Front Cell Infect Microbiol 2017;7:283.
- Blouin MS. Molecular prospecting for cryptic species of nematodes: mitochondrial DNA versus internal transcribed spacer. Int J Parasitol 2002;32:527–31.
- Gasser RB, Newton SE. Genomic and genetic research on bursate nematodes: significance, implications and prospects. Int J Parasitol 2000;30:509–34.
- Hung GC, Chilton NB, Beveridge I, Gasser RB. Secondary structure model for the ITS-2 precursor rRNA of strongyloid nematodes of equids: implications for phylogenetic inference. Int J Parasitol 1999;29:1949–64.
- Nisa RU, Tantray AY, Shah AA. Shift from morphological to recent advanced molecular proaches for the identification of nematodes. Genomics 2022;2:114.
- Blaxter ML, De Ley P, Garey JR, Llu LX, Scheldeman P, Vierstraete A. A molecular evolutionary framework for the phylum Nematoda. Nature 1998;392:71–5.
- Lichtenfels JR, Kharchenko VA, Dvojnos GM. Illustrated identification keys to strongylid parasites (Strongylidae: Nematoda) of horses, zebras and asses (Equidae). Vet Parasitol 2008;156:4–161.
- Gao Y, Wang XX, Ma XX, Zhang ZH, Lan Z, Qiu YY. Characterization of the complete mitochondrial genomes of and : comparison with Strongylidae species and phylogenetic implication. Vet Parasitol 2021;290:109359.
- Hu L, Zhang M, Sun Y, Bu Y. Characterization and phylogenetic analysis of the first complete mitochondrial genome of .. Vet Parasitol 2020;281:109097.
- McDonnell A, Love S, Tait A, Lichtenfels JR, Matthews JB. Phylogenetic analysis of partial mitochondrial cytochrome oxidase c subunit I and large ribosomal RNA sequences and nuclear internal transcribed spacer I sequences from species of Cyathostominae and Strongylinae (Nematoda, Order Strongylida), parasites of.. Parasitology 2000;121:649–59.
- Zhang L, Hu M, Chilton NB, Huby-Chilton F, Beveridge I, Gasser RB. Nucleotide alterations in the D3 domain of the large subunit of ribosomal DNA among 21 species of equine strongyle. Mol Cell Probes 2007;21:111–5.
- Gao Y, Zhang Y, Yang X, Qiu JH, Duan H, Xu WW. Mitochondrial DNA evidence supports the hypothesis that species belong to cyathostominae. Front Microbiol 2017;8:1–10.
- Peregrine AS, Mcewen B, Bienzle D, Koch TG, Weese JS. Larval cyathostominosis in horses in Ontario: an emerging disease?. Can Vet J 2006;47:80.
- Zhang LP, Kong FY. Parasitic nematodes from spp.Beijing: China Agriculture Press; 2002. .
- Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 2014;30:2114–20.
- Bernt M, Donath A, Jühling F, Externbrink F, Florentz C, Fritzsch G. MITOS: improved de novo metazoan mitochondrial genome annotation. Mol Phylogenet Evol 2013;69:313–9.
- Tamura K, Stecher G, Peterson D, Filipski A, Kumar S. MEGA6: molecular evolutionary genetics analysis version 6. Mol Biol Evol 2013;30:2725–9.
- Perna NT, Kocher TD. Patterns of nucleotide composition at fourfold degenerate sites of animal mitochondrial genomes. J Mol Evol 1995;41:353–8.
- Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. MEGA5: Molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 2011;28:2731–9.
- Rozas J, Ferrer-Mata A, Sánchez-DelBarrio JC, Guirao-Rico S, Librado P, Ramos-Onsins SE. DnaSP 6: DNA sequence polymorphism analysis of large data sets. Mol Biol Evol 2017;34:3299–302.
- Gómez-Rubio V. ggplot2 - elegant graphics for data analysis. J Stat Softw 2017;77:1–3.
- Librado P, Rozas J. DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics 2009;25:1451–2.
- Liu GH, Zhao L, Song HQ, Zhao GH, Cai JZ, Zhao Q. (Nematoda) is a distinct species based on nuclear ribosomal DNA sequences and mitochondrial DNA sequences. Parasit Vectors 2014;7:1–8.
- Xia X, Xie Z, Salemi M, Chen L, Wang Y. An index of substitution saturation and its application. Mol Phylogenet Evol 2003;26:1–7.
- Gao JF, Zhao Q, Liu GH, Zhang Y, Zhang Y, Wang WT. Comparative analyses of the complete mitochondrial genomes of the two ruminant hookworms and. Gene 2014;541:92–100.
- Stamatakis A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 2014;30:1312–3.
- Ronquist F, Teslenko M, Van Der Mark P, Ayres DL, Darling A, Höhna S. Mrbayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol 2012;61:539–42.
- Zhao H, Zhu J, Zong TK, Liu XL, Ren LY, Lin Q. Two new species in the family Cunninghamellaceae from China. Mycobiology 2021;49:142–50.
- Zhao H, Nie Y, Zong TK, Wang YJ, Wang M, Dai YC. Species diversity and ecological habitat of (Cunninghamellaceae, Mucorales) with emphasis on five new species from forest and grassland soil in China. Journal of Fungi 2022;8:471.
- Darriba D, Posada D, Kozlov AM, Stamatakis A, Morel B, Flouri T. ModelTest-NG: a new and scalable tool for the selection of DNA and protein evolutionary models. Mol Biol Evol 2020;37:291–4.
- Letunic I, Bork P. Interactive Tree of Life (iTOL) v4: recent updates and new developments. Nucleic Acids Res 2019;47:W256.
- Liu GH, Shao R, Li JY, Zhou DH, Li H, Zhu XQ. The complete mitochondrial genomes of three parasitic nematodes of birds: a unique gene order and insights into nematode phylogeny. BMC Genomics 2013;14:1.
- Duan H, Gao JF, Hou MR, Zhang Y, Liu ZX, Gao DZ. Complete mitochondrial genome of an equine intestinal parasite, (Chromadorea: Strongylidae): the first characterization within the genus. Parasitol Int 2015;64:429–34.
- Xu WW, Qiu JH, Liu GH, Zhang Y, Liu ZX, Duan H. The complete mitochondrial genome of (Chromadorea: Strongylidae): comparison with other closely related species and phylogenetic analyses. Exp Parasitol 2015;159:94–9.
- Gao JF, Liu GH, Duan H, Gao Y, Zhang Y, Chang QC. Complete mitochondrial genomes of and , and their comparison with. Exp Parasitol 2017;181:88–93.
- Qiu YY, Zeng MH, Diao PW, Wang XX, Li Q, Li Y. Comparative analyses of the complete mitochondrial genomes of and provide new molecular data for the evolution of Cyathostominae nematodes. J Helminthol 2019;93:643–7.
- Gao Y, Qiu JH, Zhang BB, Su X, Fu X, Yue DM. Complete mitochondrial genome of parasitic nematode and comparative analyses with. Exp Parasitol 2017;172:18–22.
- Kim T, Kim J, Cho S, Min GS, Park C, Carreno RA. Phylogeny of Rhigonematomorpha based on the complete mitochondrial genome of (Nematoda: Chromadorea). Zool Scr 2014;43:289–303.
- Palomares-Rius JE, Cantalapiedra-Navarrete C, Archidona-Yuste A, Blok VC, Castillo P. Mitochondrial genome diversity in dagger and needle nematodes (Nematoda: Longidoridae). Sci Rep 2017;7:41813.
- Li Q, Gao Y, Wang XX, Li Y, Gao JF, Wang CR. The complete mitochondrial genome of (Rhabditida: Cyathostominae). Mitochondrial DNA B Resour 2019;4:1225–6.
- Fu YT, Jin YC, Liu GH. The complete mitochondrial genome of the Caecal fluke of poultry, , as the first representative from the superfamily Brachylaimoidea. Front Genet 2019;10:1–13.
- Deng YP, Zhang XL, Li LY, Yang T, Liu GH, Fu YT. Characterization of the complete mitochondrial genome of the swine kidney worm (Nematoda: Syngamidae) and phylogenetic implications. Vet Parasitol 2021;295:109475.
- Zhao L, Liu GH, Zhao GH, Cai JZ, Zhu XQ, Qian AD. Genetic differences between and revealed by sequence analysis of four mitochondrial genes. Mitochondrial DNA 2015;26:167–70.
- Bu YZ. Studies on Strongylid Nematodes in Henan Province. .
- Hung GC, Chilton NB, Beveridge I, Gasser RB. A molecular systematic framework for equine strongyles based on ribosomal DNA sequence data. Int J Parasitol 2000;30:95–103.
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