Affiliations 

  • 1 School of Ecology and Environmental Sciences and Yunnan International Joint Laboratory of Virology & Immunity, Yunnan University, Kunming, China
  • 2 Department of Pathology, AnaPath Services GmbH, Liestal, Switzerland
  • 3 Department Wildlife Diseases, Leibniz Institute for Zoo and Wildlife Research, Berlin, Germany
  • 4 Sabah Parks, Kota Kinabalu, Sabah, Malaysia
  • 5 Islamic University of North Sumatra, Medan, Indonesia
  • 6 Department of Agriculture, Plant Protection Research and Development Office, Bangkok, Thailand
  • 7 Department of Biosciences, Swansea University, Swansea, UK
  • 8 School of Ecology and Environmental Sciences and Yunnan International Joint Laboratory of Virology & Immunity, Yunnan University, Kunming, China. jjhu@ynu.edu.cn
  • 9 Department of Agriculture, Plant Protection Research and Development Office, Bangkok, Thailand. thom.jaekel@t-online.de
Parasit Vectors, 2024 Mar 15;17(1):135.
PMID: 38491403 DOI: 10.1186/s13071-024-06230-8

Abstract

BACKGROUND: The geographic distribution and host-parasite interaction networks of Sarcocystis spp. in small mammals in eastern Asia remain incompletely known.

METHODS: Experimental infections, morphological and molecular characterizations were used for discrimination of a new Sarcocystis species isolated from colubrid snakes and small mammals collected in Thailand, Borneo and China.

RESULTS: We identified a new species, Sarcocystis muricoelognathis sp. nov., that features a relatively wide geographic distribution and infects both commensal and forest-inhabiting intermediate hosts. Sarcocystis sporocysts collected from rat snakes (Coelognathus radiatus, C. flavolineatus) in Thailand induced development of sarcocysts in experimental SD rats showing a type 10a cyst wall ultrastructure that was identical with those found in Rattus norvegicus from China and the forest rat Maxomys whiteheadi in Borneo. Its cystozoites had equal sizes in all intermediate hosts and locations, while sporocysts and cystozoites were distinct from other Sarcocystis species. Partial 28S rRNA sequences of S. muricoelognathis from M. whiteheadi were largely identical to those from R. norvegicus in China but distinct from newly sequenced Sarcocystis zuoi. The phylogeny of the nuclear 18S rRNA gene placed S. muricoelognathis within the so-called S. zuoi complex, including Sarcocystis attenuati, S. kani, S. scandentiborneensis and S. zuoi, while the latter clustered with the new species. However, the phylogeny of the ITS1-region confirmed the distinction between S. muricoelognathis and S. zuoi. Moreover, all three gene trees suggested that an isolate previously addressed as S. zuoi from Thailand (KU341120) is conspecific with S. muricoelognathis. Partial mitochondrial cox1 sequences of S. muricoelognathis were almost identical with those from other members of the group suggesting a shared, recent ancestry. Additionally, we isolated two partial 28S rRNA Sarcocystis sequences from Low's squirrel Sundasciurus lowii that clustered with those of S. scandentiborneensis from treeshews.

CONCLUSIONS: Our results provide strong evidence of broad geographic distributions of rodent-associated Sarcocystis and host shifts between commensal and forest small mammal species, even if the known host associations remain likely only snapshots of the true associations.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.