Alternative pathways in Angiostrongylus cantonensis (Metastrongyloidea: Angiostrongylidae) transmission

. 2021 Feb ; 148 (2) : 167-173. [epub] 20200928

Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid32981541

In order to elucidate the infection pathways of third stage larvae (L3) of Angiostrongylus cantonensis, we performed experiments to assess: (i) the shedding of L3 from two species of experimental veronicellid slugs drowned in water and the ratio of emerged larvae, (ii) the transmission of viable L3 from drowned terrestrial gastropods to aquatic snails, and (iii) the transmission of viable L3 between terrestrial snails. Molluscs were experimentally infected by first stage larvae (L1) of A. cantonensis. Significantly more L3 larvae were released from Veronicella cubensis than from Veronicella sloanei. Numerous L3 were observed in the muscular foot, and also in the connective tissue between internal organs. Experimental exposure of P. maculata to L3 of A. cantonensis liberated from other gastropod species led to their infection and the infectivity of larvae after intermediesis was demonstrated by infection of laboratory rats (Rattus norvegicus). The transmission of L3 was observed in three out of four experiment replications and L3 were retrieved from 6 out of 24 Subulina octona snails. The infected synanthropic molluscs represent a key component in the epidemiology of human infections by A. cantonensis. Escape of L3 larvae from bodies of dead snails or slugs and their ability to infect further gastropod hosts (intermediesis) represents a public health risk. Thus, control of molluscs living in peri-domestic environment is an essential part of prevention of human infections.

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Anderson RC (2000) Nematode Parasites of Vertebrates. Their Development and Transmission, 2nd Edn. Wallingford, Oxon (UK): CABI Publishing, 650 pp.

Barratt J, Chan D, Sandaradura I, Malik R, Spielman D, Lee R, Mariott D, Harkness J, Ellis J and Stark D (2016) Angiostrongylus cantonensis: a review of its distribution, molecular biology and clinical significance as a human pathogen. Parasitology 143, 1087–1118. PubMed

Campbell BG and Little MD (1988) The finding of Angiostrongylus cantonensis in rats in new Orleans. American Journal of Tropical Medicine and Hygiene 38, 568–573. PubMed

Červená B, Modrý D, Fecková B, Hrazdilová K, Foronda P, Alonso AM, Lee R, Walker J, Niebuhr CN, Malik R and Šlapeta J (2019) Low diversity of Angiostrongylus cantonensis complete mitochondrial DNA sequences from Australia, Hawaii, French Polynesia and the Canary Islands revealed using whole genome next-generation sequencing. Parasites and Vectors 12, 241. PubMed PMC

Cheng TC and Alicata JE (1964) Possible role of water in the transmission of Angiostrongylus cantonensis (Nematoda: Metastrongylidae). The Journal of Parasitology 50, 39–40.

Colella V, Giannelli A, Brianti E, Ramos RAN, Cantacessi C, Dantas-Torres F and Otranto D (2015) Feline lungworms unlock a novel mode of parasite transmission. Scientific Reports 5, 13105. PubMed PMC

Conboy G, Guselle N and Schaper R (2017) Spontaneous shedding of metastrongyloid third-stage larvae by experimentally infected Limax maximus. Parasitology Research 116, 41–54. PubMed

Cowie RH (2013a) Biology, systematics, life cycle, and distribution of Angiostrongylus cantonensis, the cause of rat lungworm disease. Hawai'i Journal of Medicine & Public Health: A Journal of Asia Pacific Medicine & Public Health 72, 6–9. PubMed PMC

Cowie RH (2013b) Pathways for transmission of angiostrongyliasis and the risk of disease associated with them. Hawai'i Journal of Medicine & Public Health: A Journal of Asia Pacific Medicine & Public Health 72, 70–74. PubMed PMC

Crook JR, Fulton SE and Supanwong K (1971) The infectivity of third stage Angiostrongylus cantonensis larvae shed from drowned Achatina fulica snails and the effect of chemical agents on infectivity. Transactions of the Royal Society of Tropical Medicine and Hygiene 65, 602–605. PubMed

Dard C, Tessier E, Nguyen D, Epelboin L, Harrois D, Swale C, Cabié A, de Meuron K, Miossec C and Desbois-Nogard N (2020) First cases of Angiostrongylus cantonensis infection reported in Martinique 2002–2017. Parasite 27, 31. PubMed PMC

Epelboin L, Blondé R, Chamouine A, Chrisment A, Diancourt L, Villemant N, Atale A, Cadix C, Caro V, Malvy D and Collet L (2016) Angiostrongylus cantonensis infection on Mayotte Island, Indian Ocean, 2007–2012. PLoS Neglected Tropical Diseases 10, e0004635. PubMed PMC

Giannelli A, Colella V, Abramo F, do Nascimento Ramos RA, Falsone L, Brianti E, Varcasia A, Dantas-Torres F, Knaus M, Fox MT and Otranto D (2015) Release of lungworm larvae from snails in the environment: potential for alternative transmission pathways. PLoS Neglected Tropical Diseases 9, e0003722. PubMed PMC

Grewal PS, Grewal SK, Tan L and Adams BJ (2003) Parasitism of molluscs by nematodes: types of associations and evolutionary trends. Journal of Nematology 35, 146–156. PubMed PMC

Hollingsworth RG, Howe K and Jarvi SI (2013) Control measures for slug and snail hosts of Angiostrongylus cantonensis, with special reference to the semi-slug Parmarion martensi. Hawai'i Journal of Medicine & Public Health: A Journal of Asia Pacific Medicine & Public Health 72, 75–80. PubMed PMC

Howe K, Kaluna L, Lozano A, Torres Fischer B, Tagami Y, McHugh R and Jarvi S (2019) Water transmission potential of Angiostrongylus cantonensis: larval viability and effectiveness of rainwater catchment sediment filters. PLoS ONE 14, e0209813. PubMed PMC

Jarvi SI, Farias MEM, Howe K, Jacquier S, Hollingsworth R and Pitt W (2012) Quantitative PCR estimates Angiostrongylus cantonensis (rat lungworm) infection levels in semi-slugs (Parmarion martensi). Molecular and Biochemical Parasitology 185, 174–176. 10.1016/j.molbiopara.2012.08.002. PubMed DOI PMC

Kim JR, Hayes KA, Yeung NW and Cowie RH (2014) Diverse gastropod hosts of Angiostrongylus cantonensis, the rat lungworm, globally and with a focus on the Hawaiian islands. PLoS ONE 9, e94969. PubMed PMC

Kim JR, Hayes KA, Yeung NW and Cowie RH (2016) Identity and distribution of introduced slugs (Veronicellidae) in the Hawaiian and Samoan Islands. Pacific Science 70, 477–493.

Kramer K, Posner J and Gosnell W (2018) The role of gastropod mucus in the transmission of Angiostrongylus cantonensis, a potentially serious neurological infection. ACS Chemical Neuroscience 9, 629–632. PubMed

Mendoza-Roldan JA, Modrý D and Otranto D (2020) Zoonotic parasites of reptiles: a crawling threat. Trends in Parasitology 36, 677–687. PubMed PMC

Morley N (2010) Aquatic molluscs as auxiliary hosts for terrestrial nematode parasites: implications for pathogen transmission in a changing climate. Parasitology 137, 1041–1056. PubMed

Noda S, Uchikawa R, Matayoshi S, Watanabe Y and Sato A (1987) Observations on the transmission of Angiostrongylus cantonensis from snail to rodent. Journal of Helminthology 61, 241–246. PubMed

Rachford FW (1976) Host-parasite relationship of Angiostrongylus cantonensis in Lymnaea palustris. II. Histopathology. Experimental Parasitology 39, 382–392. PubMed

Richards CS and Merritt JW (1967) Studies on Angiostrongylus cantonensis In molluscan intermediate hosts. The Journal of Parasitology 53, 382. PubMed

Thomé JW (1972) Redescrição dos tipos de Veronicellidae (Mollusca, Gastropoda) neotropicais: VIII. Espécies depositadas no ‘Institut für Spezielle Zoologie und zoologisches Museum’ de Berlim, Alemanha Oriental. Arquivos de Zoologia 21, 235–281.

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