Skip to main content Skip to main navigation menu Skip to site footer
Type: Article
Published: 2026-01-21
Page range: 429-437
Abstract views: 18
PDF downloaded: 0

Kudoa stigmatias sp. nov. (Cnidaria: Multivalvulida) infecting the brain of the marine fish Chaeturichthys stigmatias (Gobiiformes: Gobiidae) in the Yellow Sea, China

The Laboratory of Aquatic Parasitology and Microbial Resources; School of Marine Science and Engineering; Qingdao Agricultural University; Qingdao City; Shandong Province; China
Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Aquality; Ministry of Agriculture and Rural Affairs; Yellow Sea Fisheries Research Institute; Chinese Acaademy of Fishery Sciences; China
Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Aquality; Ministry of Agriculture and Rural Affairs; Yellow Sea Fisheries Research Institute; Chinese Acaademy of Fishery Sciences; China
Key Laboratory of Testing and Evaluation for Aquatic Product Safety and Aquality; Ministry of Agriculture and Rural Affairs; Yellow Sea Fisheries Research Institute; Chinese Acaademy of Fishery Sciences; China
School of Animal Science and Technology; Foshan University; Nanhai District; Foshan City; Guangdong Province; China
The Laboratory of Aquatic Parasitology and Microbial Resources; School of Marine Science and Engineering; Qingdao Agricultural University; Qingdao City; Shandong Province; China
The Laboratory of Aquatic Parasitology and Microbial Resources; School of Marine Science and Engineering; Qingdao Agricultural University; Qingdao City; Shandong Province; China
Protist Molecular Biology Brain Myxozoa Chaeturichthys stigmatias Kudoa stigmatias sp. nov.

Abstract

In this study, 20 specimens of Chaeturichthys stigmatias were collected from a fishing dock in Qingdao city, Shandong Province, China, and examined for parasitic infections. Kudoa spores were detected in the brains of 35% of the specimens. The mature spores were quadrate and hemispherical in lateral view, measuring 8.1±0.4 (7.1–8.8) μm in length, 13.5±0.4 (12.1–13.8) μm in width, and 11.8±0.4 (10.6–12.5) μm in thickness (n = 50). Each spore possessed four shell valves and four pyriform polar capsules measuring 4.0±0.2 (3.5–4.2) × 3.1±0.2 (2.7–3.5) μm. Morphological comparisons revealed distinct differences from previously described Kudoa species. Sequence analysis of the partial LSU rDNA further confirmed that this species did not match any known Kudoa species. Furthermore, the phylogenetic tree showed that it clusters with muscle-infecting Kudoa species but is distantly related to brain-infecting taxa. Based on morphological and molecular evidence, we describe Kudoa stigmatias sp. nov. as a novel species, representing the first documented case of myxosporean infection in Chaeturichthys species.

 

References

  1. Abdel-Baki, A.-A.S., Abdel-Haleem, H.M., Al-Quraishy, S., Azevedo, C. & Mansour, L. (2018) Ultrastructural and molecular characteristics of Kudoa crenimugilis n. sp. infecting intestinal smooth muscle of fringelip mullet Crenimugil crenilabis in the Red Sea. Diseases of aquatic organisms, 129, 53–62. https://doi.org/10.3354/dao03225
  2. Bartošová, P., Fiala, I. & Hypša, V. (2009) Concatenated SSU and LSU rDNA data confirm the main evolutionary trends within myxosporeans (Myxozoa: Myxosporea) and provide an effective tool for their molecular phylogenetics. Molecular phylogenetics and evolution, 53, 81–93. https://doi.org/10.1016/j.ympev.2009.05.018
  3. Cardim, J., Araújo-Neto, J., da Silva, D.T., Hamoy, I., Matos, E. & Abrunhosa, F. (2020) Kudoa yasai n. sp. (Multivalvulida: Kudoidae) from the skeletal muscle of Macrodon ancylodon (Sciaenidae) on the northern Atlantic coast, Brazil. Parasitology Research, 119, 1743–1752. https://doi.org/10.1007/s00436-020-06679-3
  4. Colunga-Ramírez, G., Aguirre-Macedo, M.L., Molnár, K., Székely, C., Sellyei, B. & Cech, G. (2025) Two new myxozoan parasites, Myxobolus mayarum n. sp. and Kudoa mayarum n. sp., infecting the Neotropical fish Mayan cichlid, Mayaheros urophthalmus (Günther, 1862) in the Yucatán Peninsula, Mexico. Acta Tropica, 262, 107527. https://doi.org/10.1016/j.actatropica.2025.107527
  5. Dyková, I., Buron, I.D., Fiala, I. & Roumillat, W.A. (2009) Kudoa inornata sp. n. (Myxosporea: Multivalvulida) from the skeletal muscles of Cynoscion nebulosus (Teleostei: Sciaenidae). Folia Parasitologica, 56, 91–8. https://doi.org/10.14411/fp.2009.014
  6. Eiras, J.C., Saraiva, A. & Cruz, C. (2014) Synopsis of the species of Kudoa Meglitsch, 1947 (Myxozoa: Myxosporea: Multivalvulida). Systematic Parasitology, 87, 153–180. https://doi.org/10.1007/s11230-013-9461-4
  7. Fiala, I. (2006) The phylogeny of Myxosporea (Myxozoa) based on small subunit ribosomal RNA gene analysis. International Journal for Parasitology, 36, 1521–1534. https://doi.org/10.1016/j.ijpara.2006.06.016
  8. Fiala, I., Bartošová-Sojková, P. & Whipps, C.M. (2015) Classification and phylogenetics of Myxozoa. In: Okamura, B., Gruhl, A. & Bartholomew, J. (Eds.), Myxozoan evolution, ecology and development. Springer, Cham, pp. 85–110. https://doi.org/10.1007/978-3-319-14753-6_5
  9. Kasai, A., Li, Y.C., Mafie, E. & Sato, H. (2016) New host records of monacanthid fish for three Kudoa spp. (K. septempunctata, K. thyrsites and K. shiomitsui) prevalent in the olive flounder (Paralichthys olivaceus), with the description of K. parathyrsites n. sp. from a black scraper (Thamnaconus modestus). Parasitology Research, 115, 2741–2755. https://doi.org/10.1007/s00436-016-5023-4
  10. Kasai, A., Tsuduki, H., Jimenez, L.A., Li, Y.C., Tanaka, S. & Sato, H. (2017) Incidence of three Kudoa spp., K. neothunni, K. hexapunctata and K. thunni (Myxosporea: Multivalvulida), in Thunnus tunas distributed in the western Pacific Ocean. Parasitology Research, 116, 1137–1150. https://doi.org/10.1007/s00436-016-5369-7
  11. Li, X.B., He, J., Ma, R.R., Sun, F.Y., Wu, W.X., Luo, H.M., Bai, L.H. & Qian, D. (2022) Morphological characterization and molecular phylogenetic analysis of Kudoa iwatai from large yellow croaker (Larimichthys crocea) as a new host in China. Animals, 12, 1145. https://doi.org/10.3390/ani12091145
  12. Li, Y.C., Inoue, K., Zhang, J.Y. & Sato, H. (2020a) Phylogenetic relationships of three Kudoa spp. with morphologically similar myxospores (K. iwatai, K. lutjanus and K. bora), with the redescription of K. uncinata and K. petala and description of a new species (K. fujitai n. sp.) in fishes in the South China Sea. Parasitology Research, 119, 1221–1236. https://doi.org/10.1007/s00436-020-06636-0
  13. Li, Y.C., Inoue, K., Tanaka, S., Zhang, J.Y. & Sato, H. (2020b) Identification of four new Kudoa spp. (Myxozoa: Myxosporea: Multivalvulida) in commercial fishes collected from South China Sea, Atlantic Ocean and Bering Sea by integrated taxonomic approach. Parasitology Research, 119, 2113–2128. https://doi.org/10.1007/s00436-020-06707-2
  14. Li, Y.C., Inoue, K., Zhang, J.Y. & Sato, H. (2024) Description of three new species of Kudoa Meglitsch, 1947 (Myxozoa: Multivalvulida) in commercial marine fishes from southern China, and new host records. Folia Parasitologica, 71, 1–19. https://doi.org/10.14411/fp.2024.018
  15. Liu, X., Zhang, C., Ren, Y. & Xu, B. (2015) Spatiotemporal variation in the distribution and abundance of Chaeturichthys stigmatias in the Yellow River estuary and adjacent waters. Journal of Fishery Sciences of China, 22, 791–798. https://doi.org/10.3724/SP.J.1118.2015.140426
  16. Lom, J. & Arthur, J. (1989) A guideline for the preparation of species descriptions in Myxosporea. Journal of Fish Diseases, 12, 151–156. https://doi.org/10.1111/j.1365-2761.1989.tb00287.x
  17. Lom, J. & Dyková, I. (2006) Myxozoan genera: definition and notes on taxonomy, life-cycle terminology and pathogenic species. Folia Parasitologica, 53, 1–36. https://doi.org/10.14411/fp.2006.001
  18. Mansour, L., Harrath, A.H., Abdel-Baki, A.A.S., Alwasel, S., Al-Quraishy, S. & Al Omar, S.Y. (2015) Kudoa saudiensis sp. n. (Myxosporea: Multivalvulida) infecting oocytes of the Indian mackerel Rastrelliger kanagurta (Perciformes: Scombridae). Folia Parasitologica, 62 (1), 10. https://doi.org/10.14411/fp.2015.010
  19. Meng, K., Wang, J., Zhang, C., Ren, Y. & Xu, B. (2017) The fishery biological characteristics of Chaeturichthys stigmatias in the Yellow River estuary and its adjacent waters. Journal of Fishery Sciences of China, 24, 939–945. https://doi.org/10.3724/SP.J.1118.2017.17083
  20. Moran, J.D.W., Whitaker, D.J. & Kent, M.L. (1999) A review of the myxosporean genus Kudoa Meglitsch, 1947, and its impact on the international aquaculture industry and commercial fisheries. Aquaculture, 172, 163–196. https://doi.org/10.1016/S0044-8486(98)00437-2
  21. Ohnishi, T., Obara, T., Arai, S., Yoshinari, T. & Sugita-Konishi, Y. (2018) Quantitative analysis of Unicapsula seriolae in greater amberjack associated with unidentified food-borne disease. Journal of the Food Hygienic Society of Japan, 59, 24–29. https://doi.org/10.3358/shokueishi.59.24
  22. Posada, D. (2008) jModelTest: phylogenetic model averaging. Molecular Biology and Evolution, 25, 1253–1256. https://doi.org/10.1093/molbev/msn083
  23. Ren, Y. (2022) Fishery Resources and Habitat Environment in Haizhou Bay. China Agriculture Press, Beijing, 187 pp.
  24. Sakai, H., Kawai, T., Zhang, J. & Sato, H. (2019) New host records of three Kudoa spp. (K. yasunagai, K. thalassomi and K. igami) with notable variation in the number of shell valves and polar capsules in spores. Parasitology Research, 118, 143–157. https://doi.org/10.1007/s00436-018-6144-8
  25. Shirakashi, S., Morita, A., Ishimaru, K. & Miyashita, S. (2012) Infection dynamics of Kudoa yasunagai (Myxozoa: Multivalvulida) infecting brain of cultured yellowtail Seriola quinqueradiata in Japan. Diseases of aquatic organisms, 101, 123–130. https://doi.org/10.3354/dao02513
  26. Sun, Y., Wei, T. & Jin, X. (2015) Unusual features of control region and a novel NADH 6 genes in mitochondrial genome of the finespot goby, Chaeturichthys stigmatias (Perciformes, Gobiidae). Mitochondrial DNA, 26, 665–667. https://doi.org/10.3109/19401736.2013.840598
  27. Suzuki, J., Murata, R., Yokoyama, H., Sadamasu, K. & Kai, A. (2015) Detection rate of diarrhoea-causing Kudoa hexapunctata in Pacific bluefin tuna Thunnus orientalis from Japanese waters. International Journal of Food Microbiology, 194, 1–6. https://doi.org/10.1016/j.ijfoodmicro.2014.11.001
  28. Tamura, K., Stecher, G., Peterson, D., Filipski, A. & Kumar, S. (2013) MEGA6: molecular evolutionary genetics analysis version 6.0. Molecular Biology and Evolution, 30, 2725–2729. https://doi.org/10.1093/molbev/mst197
  29. Thompson, J.D., Gibson, T.J., Plewniak, F., Jeanmougin, F. & Higgins, D.G. (1997) The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic acids research, 25, 4876–4882. https://doi.org/10.1093/nar/25.24.4876
  30. Velasco, M., Eduard, J., Neto, J.L.S., Dias, L.d.N.S., Matos, E. & Gonçalves, E.C. (2022) Kudoa rousseauxii n. sp.(Cnidaria: Multivalvulida) infects the skeletal muscles of the freshwater fish Brachyplatystoma rousseauxii in the Amazon River. Acta Parasitologica, 67, 962–969. https://doi.org/10.1007/s11686-022-00539-z
  31. Wang, H.W., Zhu, N., Cai, D.B., Wang, Y.F., Liu, Y.W., Tian, S.Q., Wang, Y. & Huo, R. (2014) Evaluation and content of various heavy metals found in the fish (Chaeturichthys stigmatias Richardson) collected from the oil spill area of Bohai Bay (China) during the Summer. Advanced Materials Research, 955, 1448–1451. https://doi.org/10.4028/www.scientific.net/AMR.955-959.1448
  32. Whipps, C., Grossel, G., Adlard, R., Yokoyama, H., Bryant, M., Munday, B. & Kent, M. (2004) Phylogeny of the Multivalvulidae (Myxozoa: Myxosporea) based on comparative ribosomal DNA sequence analysis. Journal of Parasitology, 90, 618–622. https://doi.org/10.1645/GE-153R
  33. Whipps, C.M. & Kent, M.L. (2006) Phylogeography of the cosmopolitan marine parasite Kudoa thyrsites (Myxozoa: Myxosporea). Journal of Eukaryotic Microbiology, 53, 364–373. https://doi.org/10.1111/j.1550-7408.2006.00114.x
  34. Wu, H.L. & Zhong, J.S. (2008) n.k. In: Fauna Sinica, Osteichthyes, Perciformes. Science Press, Beijing, pp. 311–312.
  35. Xu, L., Zhao, X., Huang, Y., Xin, Z. & Zhang, J. (2025) Morphological and molecular characterization of Myxobolus aculeatus n. sp. (Myxozoa: Myxosporea) from the ovary of Macrognathus aculeatus, Bloch, 1786 (Synbranchiformes: Mastacembelidae) in China. Parasitology International, 106, 103039. https://doi.org/10.1016/j.parint.2025.103039
  36. Yu, X., Cao, L., Liu, J., Zhao, B., Shan, X. & Dou, S. (2014) Application of otolith shape analysis for stock discrimination and species identification of five goby species (Perciformes: Gobiidae) in the northern Chinese coastal waters. Journal of Oceanology and Limnology, 32, 1060–1073. https://doi.org/10.1007/s00343-015-4022-0
  37. Zhang, D., Gao, F., Jakovlić, I., Zou, H., Zhang, J., Li, W.X. & Wang, G.T. (2020) PhyloSuite: An integrated and scalable desktop platform for streamlined molecular sequence data management and evolutionary phylogenetics studies. Molecular Ecology Resources, 20, 348–355. https://doi.org/10.1111/1755-0998.13096

How to Cite

Dong, J., Jiang, Y., Tan, Z., Yao, L., Liu, P., Zhao, X. & Zhang, J. (2026) Kudoa stigmatias sp. nov. (Cnidaria: Multivalvulida) infecting the brain of the marine fish Chaeturichthys stigmatias (Gobiiformes: Gobiidae) in the Yellow Sea, China. Zootaxa, 5750 (3), 429–437. https://doi.org/10.11646/zootaxa.5750.3.8