Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Mar 3;18(3):e0279268.
doi: 10.1371/journal.pone.0279268. eCollection 2023.

Elucidating the life cycle of opossum parasites: DNA sequences reveal the involvement of planorbid snails as intermediate hosts of Rhopalias spp. (Trematoda: Echinostomatidae) in Brazil

Affiliations

Elucidating the life cycle of opossum parasites: DNA sequences reveal the involvement of planorbid snails as intermediate hosts of Rhopalias spp. (Trematoda: Echinostomatidae) in Brazil

Danimar López-Hernández et al. PLoS One. .

Abstract

Echinostomatid digeneans belonging to the genus Rhopalias are intestinal trematodes found mainly in opossums in the New World. The genus comprises seven species, but their life cycles and intermediate hosts have been unknown until now. During our long-term study carried out in freshwater habitats within the state of Minas Gerais, Southeast Brazil, echinostomatid cercariae lacking collar spines were found in planorbid snails Biomphalaria glabrata, Biomphalaria straminea, Drepanotrema lucidum and Gundlachia ticaga in six different batches of snail samples collected between 2010 and 2019. Morphologically, the larvae reported herein are morphologically consistent with each other and characterized by the presence of 2-3 large ovoid or spherical corpuscles in each main duct of the excretory system, resembling to Cercaria macrogranulosa previously described from the same region of Brazil. Partial sequences of the ITS (ITS1-5.8S-ITS2) region and 28S gene of the nuclear ribosomal RNA operon, and partial sequences of mitochondrial nad1 and cox1 genes were obtained and compared with the data available for members of the family Echinostomatidae. Nuclear markers indicate that all samples of cercariae evaluated in the present study can be assigned to Rhopalias, but distinct from North American isolates of Rhopalias macracanthus, Rhopalias coronatus and Rhopalias oochi (divergence 0.2-1.2% in 28S and 0.8-4.7% in ITS). The lack of differences verified in both 28S and ITS in 5 out 6 studied samples suggested that they belong to the same species. However, nad1 sequences revealed that our cercariae correspond to three distinct species of Rhopalias (interspecific divergence: 7.7-9.9%), named here as Rhopalias sp. 1, found in B. straminea and G. ticaga, Rhopalias sp. 2 found in B. glabrata and D. lucidum, and Rhopalias sp. 3 also found in D. lucidum. They also differ by 10.8-17.2% from a North American isolate of R. macracanthus sequenced in this study. The cox1 sequences obtained for Rhopalias sp. 1 and Rhopalias sp. 2 (but not Rhopalias sp. 3) reveal that they are distinct from North American isolates of R. macracanthus (genetic divergence 16.3-16.5% and 15.6-15.7%, respectively), R. coronatus (9.2-9.3% and 9.3-9.5%) and Rhopalias oochi (9.0% and 9.5-10.1%). Encysted metacercariae with general morphology similar to that of the body of cercariae were found in tadpoles of Rhinella sp. from the same stream where snails harbored Rhopalias sp. 2, suggesting that the amphibians could act as second intermediate hosts of species of Rhopalias. Data obtained provide the first insights into the life cycle of this unusual echinostomatid genus.

PubMed Disclaimer

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Phylogenetic relationships between Rhopalias spp. found in planorbids from Brazil and members of the family Echinostomatidae inferred from partial 28S sequence data (1077 bp).
The trees were generated by Bayesian Inference (BI) and Maximum Likelihood (ML) methods. New sequences from the present study are in bold. Scale bar represents the number of nucleotide substitutions per site.
Fig 2
Fig 2
Phylogenetic relationships between Rhopalias spp. found in planorbids from Brazil and members of the family Echinostomatidae inferred from (A) ITS1-5.8S-ITS-2 (954 bp) and (B) ITS2 (378 bp) sequence data. The trees were generated by Bayesian Inference (BI) and Maximum Likelihood (ML) methods. New sequences from the present study are in bold. Scale bar represents the number of nucleotide substitutions per site.
Fig 3
Fig 3
Phylogenetic relationships between Rhopalias spp. found in planorbids from Brazil and members of the family Echinostomatidae inferred from (A) nad1 (397 bp) and (B) cox1 (612 bp) sequence data. The trees were generated by Bayesian Inference (BI) and Maximum Likelihood (ML) methods. New sequences from the present study are in bold. Scale bar represents the number of nucleotide substitutions per site.
Fig 4
Fig 4. Cercaria of Rhopalias from Biomphalaria straminea from Brazil.
(A) Whole view. (B) Detail of body. Cercariae from the same infected snail were genetically identified as Rhopalias sp. 1. Scale bars: 50 μm.
Fig 5
Fig 5. Larval stages of Rhopalias found in Biomphalaria straminea from Brazil.
(A) Whole view of the cercaria stained with Nile blue sulphate. (B) Detail of the cercarial body stained with Nile blue sulphate. (C) Whole view of a redia. (D) Detail of the anterior region of a redia. (E) Metacercaria obtained experimentally in Poecilia reticulata. Cercariae from the same infected snail were molecularly identified as Rhopalias sp. 1. Scale bars: (A, B, D, E) 50 μm, (C) 100 μm.
Fig 6
Fig 6. Larval stages of Rhopalias found in Biomphalaria glabrata and Rhinella sp. from Brazil.
(A) Whole view of a cercaria stained with Nile blue sulphate. (B) Detail of the body of a cercaria stained with neutral red. (C) Metacercariae found in a naturally infected tadpole. (D) Detail of a metacercaria. Cercariae from the same infected snail were genetically identified as Rhopalias sp. 2. Scale bars: (A, B, D) 50 μm, (C) 200 μm.

Similar articles

Cited by

References

    1. Yamaguti S. Synopsis of Digenetic Trematodes of Vertebrates. vol. 1. Keigaku Publishing Company: Tokyo; 1971.
    1. Marshall ME, Miller GC. Some digenetic trematodes from Ecuadorian bats including five new species and one new genus. J. Parasitol. 1979;65: 909–917.
    1. Radev V, Gardner SL, Kanev I. Family Rhopaliidae Looss, 1899. In: Keys to the Trematoda, Jones A, Bray RA, and Gibson DI (eds). London, U.K.: CAB International and The Natural History Museum; 2005. p. 119–120.
    1. Haverkost TR, Gardner SL. A review of species in the genus Rhopalias (Rudolphi, 1819). J. Parasitol. 2008;94: 716–726. - PubMed
    1. López-Caballero J, Mata-López R, Pérez Ponce de León G. Molecular data reveal a new species of Rhopalias Stiles & Hassall, 1898 (Digenea, Echinostomatidae) in the Common opossum, Didelphis marsupialis L. (Mammalia, Didelphidae) in the Yucatán Peninsula, Mexico. ZooKeys 2019;854: 145. - PMC - PubMed