The Tengmalm's owl Aegolius funereus (Aves, Strigidae) as the definitive host of Sarcocystis funereus sp. nov. (Apicomplexa)

. 2024 ; 11 () : 1356549. [epub] 20240207

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38384962

BACKGROUND: Owls have been reported as definitive hosts, whereas wild small mammals (naturally and experimentally) as intermediate hosts of several species of Sarcocystis. Recently, dead fledglings were found infected by an unnamed species of Sarcocystis since its intermediate host was unknown. After collecting additional samples of owls and wild small mammals, the present study focused on elucidating the identity, potential intermediate host, and complete life cycle of the found Sarcocystis through experimentally infected rodents. The developmental stages' morphological and molecular characterizations (28S rRNA gene, ITS1 region) are presented herein. METHODS: In total, 21 Tengmalm's owl carcasses (15 nestlings, 5 fledglings, and 1 adult male) were collected in Kauhava (west-central Finland) and parasitologically examined by wet mounts. Intestinal mucosa scrapings were used to isolate oocysts/sporocysts and employed for experimental infections in dexamethasone-immunosuppressed BALB/cOlaHsd mice. Additionally, sarcocysts were searched in the skeletal muscle of 95 samples from seven wild small mammal species. All these developmental stages were molecularly characterized by the 28S rRNA gene and ITS1 region. Experimental infections were carried out by using immunosuppressed female 8-week-old BALB/cOlaHsd mice, divided into three groups: (1) water with 15 μg/mL of dexamethasone, (2) water with 30 μg/mL of dexamethasone, (3) no dexamethasone treatment. Each group consisted of four individuals. In each group, two mice were infected with 1,000 sporocysts each, and the remaining two with 10,000 sporocysts each. All mice were euthanized on specific days post-infection. RESULTS: The intestinal mucosa of 11 nestlings and 5 fledglings of the Tengmalm's owl were positive for Sarcocystis funereus sp. nov. The adult male owl and all owls' breast and heart muscles were negative for Sarcocystis. Two dexamethasone-immunosuppressed BALB/cOlaHsd mice (group 2) were positive to S. funereus sp. nov. in diaphragm and leg muscles after 22- and 24-day post-infection. Some sarcocysts were found in the wild small mammals. Molecular identification at 28S rRNA revealed sequences from naturally infected Tengmalm's owls, as well as sarcocysts of dexamethasone-immunosuppressed BALB/cOlaHsd mice were 99.87-100% similar to Sarcocystis sp. isolate Af1 previously found in the Tengmalm's owl. At the ITS1 region, the S. funereus sp. nov. isolates Af2 haplotype B and Af3 haplotype A were 98.77-100% identical to Sarcocystis sp. isolate Af1. The sequences from sarcocysts of naturally infected wild small mammals were 75.23-90.30% similar at ITS1 region to those of S. funereus sp. nov. CONCLUSION: The morphological and molecular characterizations and phylogenetic placement of S. funereus sp. nov. are presented here for the first time and support the erection of the new species.

Zobrazit více v PubMed

Černá Z. Multiplication of merozoites of Sarcocystis dispersa Černa, Kolařova et Šulc, 1978 and Sarcocystis cernae Levine, 1977 in the blood stream of the intermediate host. Folia Parasit. (1983) 30:5–8.

Černá Ž, Kolařova I, Šulc P. Contribution to the problem of cyst-producing coccidians. Folia Parasit. (1978) 25:9–16. PubMed

Munday BL. A species of Sarcocystis using owls as definitive hosts. J Wildlife Dis. (1977) 13:205–7. doi: 10.7589/0090-3558-13.2.205, PMID: PubMed DOI

Espinosa R, Sterner M, Blixt J, Cawthorn R. Description of a species of Sarcocystis (Apicomplexa: Sarcocystidae), a parasite of the northern saw-whet owl, Aegolius acadicus, and experimental transmission to deer mice Peromyscus maniculatus. Can J Zool. (1988) 66:2118–21. doi: 10.1139/z88-31 DOI

Dubey JP, Calero-Bernal R, Rosenthal BM, Speer CA, Fayer R. Sarcocystosis of animals and humans. Boca Raton: CRC Press; (2016).

Levine ND, Tadros W. Named species and hosts of Sarcocystis (Protozoa: Apicomplexa: Sarcocystidae). Syst Parasit. (1980) 2:41–59. doi: 10.1007/BF00015094 DOI

Tadros W, Laarman JJ. The tawny owl, Strix aluco as final host of a new species of Sarcocystis with Mus musculus as intermediate host. Trop Geogr Med. (1980) 32:364.

Tadros W, Laarman JJ. Sarcocystis and related coccidian parasites: a brief general review, together with a discussion on some biological aspects of their life cycles and a new proposal for their classification. Act Leidens. (1976) 44:1107. PubMed

Tadros W, Laarman JJ. Current concepts on the biology, evolution and taxonomy of tissue cyst-forming eimeriid coccidia. Adv Parasit. (1982) 20:293–468. doi: 10.1016/S0065-308X(08)60540-0 PubMed DOI

Cawthorn RJ, Gajadhar AA, Brooks RJ. Description of Sarcocystis rauschorum sp. n. (Protozoa: Sarcocystidae) with experimental cyclic transmission between varying lemmings (Dicrostonyx richardsoni) and snowy owls (Nyctea scandiaca). Can J Zool. (1984) 62:217–25. doi: 10.1139/z84-036 DOI

Cawthorn RJ, Brooks RJ. Histological observations on precystic merogony and metrocyte formation of Sarcocystis rauschorum (Apicomplexa: Sarcocystidae) in varying lemmings, Dicrostonyx richardsoni. Can J Zool. (1985) 63:2907–12. doi: 10.1139/z85-435 DOI

Wiesner J. A new sarcosporidian species of Clethrionomys glareolus inhabiting the owl Aegolius funereus as definitive host. J Protozool. (1980) 27:72A.

Kouba M, Bartoš L, Bartošová J, Hongisto K, Korpimäki E. Interactive influences of fluctuations of main food resources and climate change on long-term population decline of Tengmalm’s owls in the boreal forest. Sci Rep. (2020) 10:20429. doi: 10.1038/s41598-020-77531-y, PMID: PubMed DOI PMC

Kouba M, Bartoš L, Bartošová J, Hongisto K, Korpimäki E. Long-term trends in the body condition of parents and offspring of Tengmalm’s owls under fluctuating food conditions and climate change. Sci Rep. (2021) 11:18893. doi: 10.1038/s41598-021-98447-1, PMID: PubMed DOI PMC

Máca O, Kouba M, Korpimäki E, González-Solís D. Molecular identification of Sarcocystis sp. (Apicomplexa, Sarcocystidae) in offspring of Tengmalmʼs owls, Aegolius funereus (Aves, Strigidae). Front Vet Sc. (2021) 8:804096. doi: 10.3389/fvets.2021.804096, PMID: PubMed DOI PMC

Kouba M, Bartoš L, Tulis F, Ševčík M, Sovadinová S, Bušina T, et al. . Post-fledging survival of Tengmalm’s owl offspring in boreal forests: interactive effects of varying dynamics of main prey and habitat composition. Front Ecol Evol. (2023) 11:1151622. doi: 10.3389/fevo.2023.1151622 DOI

Kutkienė L, Prakas P, Sruoga A, Butkauskas D. The mallard duck (Anas platyrhynchos) as intermediate host for Sarcocystis wobeseri sp. nov. from the barnacle goose (Branta leucopsis). Parasit Res. (2010) 107:879–88. doi: 10.1007/s00436-010-1945-4, PMID: PubMed DOI

Katoh K, Rozewicki J, Yamada KD. MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization. Brief Bioinform. (2019) 20:1160–6. doi: 10.1093/bib/bbx108, PMID: PubMed DOI PMC

Tamura K, Stecher G, Kumar S. MEGA11: molecular evolutionary genetics analysis version 11. Mol Biol Evol. (2021) 38:3022–7. doi: 10.1093/molbev/msab120, PMID: PubMed DOI PMC

Hasegawa M, Kishino H, Yano T. Dating the human-ape split by a molecular clock of mitochondrial DNA. J Mol Evol. (1985) 22:160–74. doi: 10.1007/BF02101694, PMID: PubMed DOI

ICZN (International Commission on Zoological Nomenclature) . Amendment of articles 8, 9, 10, 21 and 78 of the international code of zoological nomenclature to expand and refine methods of publication. Bull Zool Nom. (2012) 69:1–10. doi: 10.3897/zookeys.219.3994, PMID: PubMed DOI PMC

Gjerde B, Vikøren T, Hamnes IS. Molecular identification of Sarcocystis halieti n. sp., Sarcocystis lari and Sarcocystis truncata in the intestine of a white-tailed sea eagle (Haliaeetus albicilla) in Norway. Int J Parasitol. (2018) 7:1–11. doi: 10.1016/j.ijppaw.2017.12.001, PMID: PubMed DOI PMC

Levine ND, Ivens V. The coccidian parasites (Protozoa, Sporozoa) of rodents. Ill Biol Mongr. (1965) 33:1–365. doi: 10.5962/bhl.title.50242 DOI

Cutler TJ, MacKay RJ, Ginn PE, Gillis K, Tanhauser SM, LeRay EV, et al. . Immunoconversion against Sarcocystis neurona in normal and dexamethasone-treated horses challenged with S. Neurona sporocysts. Vet Parasitol. (2001) 95:197–210. doi: 10.1016/s0304-4017(00)00420-9, PMID: PubMed DOI

Giles AJ, Hutchinson MKND, Sonnemann HM, Jung J, Fecci PE, Ratnam NM, et al. . Dexamethasone-induced immunosuppression: mechanisms and implications for immunotherapy. J Immunother Cancer. (2018) 6:51. doi: 10.1186/s40425-018-0371-5, PMID: PubMed DOI PMC

Chen L, Jondal M, Yakimchuk K. Regulatory effects of dexamethasone on NK and T cell immunity. Inflammopharmacology. (2018) 26:1331–8. doi: 10.1007/s10787-017-0418-0, PMID: PubMed DOI PMC

Witonsky SG, Gogal RM, Jr, Duncan RB, Lindsay DS. Immunopathologic effects associated with Sarcocystis neurona–infected interferon-gamma knockout mice. J Parasitol. (2003) 89:932–40. doi: 10.1645/GE-72R, PMID: PubMed DOI

Korpimäki E. Diet of breeding Tengmalm’s owls Aegolius funereus: long term changes and year to year variation under cyclic food conditions. Ornis Fennica. (1988) 65:21–30.

Korpimäki E, Hakkarainen H. The boreal owl: ecology, behaviour and conservation of a forest-dwelling predator. Cambridge: Cambridge University Press; (2012).

Hoogenboom I, Dijkstra C. Sarcocystis cernae: a parasite increasing the risk of predation of its intermediate host, Microtus arvalis. Oecologia. (1987) 74:86–92. doi: 10.1007/BF00377350, PMID: PubMed DOI

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...