» Articles » PMID: 32588173

Molecular Survey for Cyst-forming Coccidia (Toxoplasma Gondii, Neospora Caninum, Sarcocystis Spp.) in Mediterranean Periurban Micromammals

Overview
Journal Parasitol Res
Specialty Parasitology
Date 2020 Jun 27
PMID 32588173
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Rodents and other micromammals constitute important reservoirs of infectious diseases; their role in the life cycle of apicomplexan parasites such as Toxoplasma gondii, Neospora caninum, and Sarcocystis spp. still needs clarification. In the present study, we analyzed by PCR and Sanger sequencing methods the presence of specific parasite DNA within brain and heart tissues of 313 individuals of five synanthropic small mammal species (Apodemus sylvaticus, Mus spretus, M. musculus, Rattus rattus, and Crocidura russula) collected in Barcelona metropolitan area (NE Spain). In addition, PCR-RFLP and microsatellites were also used as tools for genotypic characterization of T. gondii and N. caninum, respectively. Specific DNA of T. gondii, N. caninum, and Sarcocystis spp. was detected in 0.3% (n = 1), 1.3% (n = 4), and 3.8% (n = 12) of the animals, respectively. No mixed infections were observed. Crocidura russula stood out as the main host for Sarcocystis spp. Toxoplasma gondii-specific DNA detected in a house rat was genetically characterized by PCR-RFLP, presenting type II and III alleles (SAG1 [II], SAG3 [II], GRA6 [II], c22-8 [III], Apico [III]). Also, unsuccessful DNA sequencing and microsatellite typing were attempted in N. caninum-positive samples, which suggested a lack of PCR specificity and open avenues to speculate the host competence of rodents for N. caninum. Likewise, Sarcocystis spp. identity was studied by alignment and phylogenetic analyses of cox1 and 28S rRNA sequences from the 14 positive samples. It resulted in at least three unknown organisms closely similar (95.7-100% cox1-sequence homology) to Sarcocystis pantherophisi from the Eastern rat snake (Pantherophis alleghaniensis) (KU891603), suggesting together with 28S rRNA sequences analyses, three Sarcocystis sp. with a life cycle conformed by rodents as intermediate host (IH) and snakes as definitive hosts (DH) infecting the periurban micromammals surveyed. Prevalence figures found in this first survey carried out in Spain agree with other international studies focused on periurban areas. Further surveys should be conducted in farms and their surroundings in order to unravel the role of wild micromammals in the epidemiology of such protozoan parasites affecting our livestock, and therefore human population.

Citing Articles

Molecular Confirmation of Raptors from Spain as Definitive Hosts of Numerous Species.

Juozaityte-Ngugu E, Svazas S, Bea A, Sneideris D, Villanua D, Butkauskas D Animals (Basel). 2025; 15(5).

PMID: 40075929 PMC: 11898200. DOI: 10.3390/ani15050646.


Detection of Three Species (Apicomplexa) in Blood Samples of the Bank Vole and Yellow-Necked Mouse from Lithuania.

Prakas P, Gudiskis N, Kitryte N, Bagdonaite D, Baltrunaite L Life (Basel). 2024; 14(3).

PMID: 38541690 PMC: 10971911. DOI: 10.3390/life14030365.


Serological and molecular detection of Toxoplasma gondii and Neospora caninum in free-ranging rats from Nagpur, India.

Mishra V, Mitra P, Barbuddhe S, Thorat Y, Chavan K, Shinde S Parasitol Res. 2023; 123(1):63.

PMID: 38114841 DOI: 10.1007/s00436-023-08095-9.


Protozoan Parasites of spp. in Rodents from Commercial Orchards.

Prakas P, Stirke V, Sneideris D, Rakauskaite P, Butkauskas D, Balciauskas L Animals (Basel). 2023; 13(13).

PMID: 37443884 PMC: 10339949. DOI: 10.3390/ani13132087.


Global prevalence of Neospora caninum in rodents: A systematic review and meta-analysis.

Hamzavi Y, Salimi Y, Ahmadi M, Adimi P, Falahi S, Bozorgomid A Vet Med Sci. 2023; 9(5):2192-2200.

PMID: 37417729 PMC: 10508548. DOI: 10.1002/vms3.1196.


References
1.
Barratt J, Al Qassab S, Reichel M, Ellis J . The development and evaluation of a nested PCR assay for detection of Neospora caninum and Hammondia heydorni in feral mouse tissues. Mol Cell Probes. 2008; 22(4):228-33. DOI: 10.1016/j.mcp.2008.03.001. View

2.
Calero-Bernal R, Perez-Martin J, Reina D, Serrano F, Frontera E, Fuentes I . Detection of Zoonotic Protozoa Toxoplasma gondii and Sarcocystis suihominis in Wild Boars from Spain. Zoonoses Public Health. 2015; 63(5):346-50. DOI: 10.1111/zph.12243. View

3.
Castano P, Fuertes M, Ferre I, Fernandez M, Ferreras M, Moreno-Gonzalo J . Placental thrombosis in acute phase abortions during experimental Toxoplasma gondii infection in sheep. Vet Res. 2014; 45:9. PMC: 3931317. DOI: 10.1186/1297-9716-45-9. View

4.
Dellarupe A, Fitte B, Pardini L, Campero L, Bernstein M, Robles M . Toxoplasma gondii and Neospora caninum infections in synanthropic rodents from Argentina. Rev Bras Parasitol Vet. 2019; 28(1):113-118. DOI: 10.1590/S1984-29612019009. View

5.
Donahoe S, Lindsay S, Krockenberger M, Phalen D, Slapeta J . A review of neosporosis and pathologic findings of Neospora caninum infection in wildlife. Int J Parasitol Parasites Wildl. 2015; 4(2):216-38. PMC: 4427759. DOI: 10.1016/j.ijppaw.2015.04.002. View