The recent introduction of Angiostrongylus cantonensis and its intermediate host Achatina fulica into Guadeloupe detected by phylogenetic analyses.


Journal

Parasites & vectors
ISSN: 1756-3305
Titre abrégé: Parasit Vectors
Pays: England
ID NLM: 101462774

Informations de publication

Date de publication:
10 Aug 2023
Historique:
received: 20 01 2023
accepted: 06 07 2023
medline: 14 8 2023
pubmed: 11 8 2023
entrez: 10 8 2023
Statut: epublish

Résumé

Angiostrongylus cantonensis (rat lungworm) is the main pathogen responsible for eosinophilic meningitis in humans. One of its intermediate snail hosts, Achatina fulica, was already present in many countries around the world before it appeared in the West Indies in the late 1980s. In the French territories in the Caribbean and northern South America, the first cases of human neuroangiostrongyliasis were reported in Martinique, Guadeloupe and French Guiana in 2002, 2013 and 2017, respectively. In order to better characterize angiostrongyliasis in Guadeloupe, particularly its geographical origin and route of introduction, we undertook molecular characterization of adult worms of Angiostrongylus cantonensis and its intermediate host Achatina fulica. Genomic DNA of adult Angiostrongylus cantonensis and Achatina fulica was extracted and amplified by polymerase chain reaction (PCR) targeting the mitochondrial genes cytochrome B and C for A. cantonensis and 16S ribosomal RNA for A. fulica. The PCR products were sequenced and studied by phylogenetic analysis. Cytochrome B and cytochrome C molecular markers indicate a monophyletic lineage of A. cantonensis adult worms in Guadeloupe. Two sequences of A. fulica were identified. These results confirm the recent introduction of both Angiostrongylus cantonensis and Achatina fulica into Guadeloupe. Achatina fulica in Guadeloupe shares a common origin with those in Barbados and New Caledonia, while Angiostrongylus cantonensis in Guadeloupe shares a common origin with those in Brazil, Hawaii and Japan.

Sections du résumé

BACKGROUND BACKGROUND
Angiostrongylus cantonensis (rat lungworm) is the main pathogen responsible for eosinophilic meningitis in humans. One of its intermediate snail hosts, Achatina fulica, was already present in many countries around the world before it appeared in the West Indies in the late 1980s. In the French territories in the Caribbean and northern South America, the first cases of human neuroangiostrongyliasis were reported in Martinique, Guadeloupe and French Guiana in 2002, 2013 and 2017, respectively. In order to better characterize angiostrongyliasis in Guadeloupe, particularly its geographical origin and route of introduction, we undertook molecular characterization of adult worms of Angiostrongylus cantonensis and its intermediate host Achatina fulica.
METHODS METHODS
Genomic DNA of adult Angiostrongylus cantonensis and Achatina fulica was extracted and amplified by polymerase chain reaction (PCR) targeting the mitochondrial genes cytochrome B and C for A. cantonensis and 16S ribosomal RNA for A. fulica. The PCR products were sequenced and studied by phylogenetic analysis.
RESULTS RESULTS
Cytochrome B and cytochrome C molecular markers indicate a monophyletic lineage of A. cantonensis adult worms in Guadeloupe. Two sequences of A. fulica were identified.
CONCLUSIONS CONCLUSIONS
These results confirm the recent introduction of both Angiostrongylus cantonensis and Achatina fulica into Guadeloupe. Achatina fulica in Guadeloupe shares a common origin with those in Barbados and New Caledonia, while Angiostrongylus cantonensis in Guadeloupe shares a common origin with those in Brazil, Hawaii and Japan.

Identifiants

pubmed: 37563598
doi: 10.1186/s13071-023-05872-4
pii: 10.1186/s13071-023-05872-4
pmc: PMC10416417
doi:

Substances chimiques

Cytochromes b 9035-37-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

276

Subventions

Organisme : European Regional Development Fund
ID : 2018-FED-1084

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

Références

Appl Environ Microbiol. 2010 Aug;76(15):5287-9
pubmed: 20543049
Eur J Clin Microbiol Infect Dis. 2012 Apr;31(4):389-95
pubmed: 21725905
PLoS Negl Trop Dis. 2016 May 04;10(5):e0004635
pubmed: 27144645
3 Biotech. 2017 Aug;7(4):252
pubmed: 28721680
Emerg Infect Dis. 2015 Jul;21(7):1234-6
pubmed: 26079818
Am J Trop Med Hyg. 2004 Apr;70(4):425-8
pubmed: 15100458
Mol Biol Evol. 2013 Apr;30(4):772-80
pubmed: 23329690
J Helminthol. 2019 Jul;93(4):389-423
pubmed: 31064435
Arq Neuropsiquiatr. 2009 Dec;67(4):1093-6
pubmed: 20069226
Bioinformatics. 2014 May 1;30(9):1312-3
pubmed: 24451623
PLoS One. 2017 Dec 18;12(12):e0189458
pubmed: 29252992
Am J Trop Med Hyg. 1988 May;38(3):568-73
pubmed: 3275136
Lancet Infect Dis. 2008 Oct;8(10):621-30
pubmed: 18922484
Hawaii J Med Public Health. 2013 Jun;72(6 Suppl 2):6-9
pubmed: 23901372
Nucleic Acids Res. 2021 Jul 2;49(W1):W293-W296
pubmed: 33885785
Z Parasitenkd. 1978 Jul 3;56(1):73-80
pubmed: 706552
Bioinform Adv. 2022 Feb 18;2(1):vbac010
pubmed: 36699379
Ann Parasitol Hum Comp. 1964 Jan-Feb;39:69-94
pubmed: 14152068
Soc Sci Med. 1992 Jan;34(2):199-212
pubmed: 1738873
Am J Trop Med Hyg. 1981 Sep;30(5):963-5
pubmed: 7283015
Parasitol Int. 2014 Jun;63(3):544-9
pubmed: 24583335
J Helminthol. 2015 Sep;89(5):545-51
pubmed: 24933508
PLoS One. 2014 Sep 09;9(9):e105151
pubmed: 25203830
Parasite. 2020;27:31
pubmed: 32394891
Can J Zool. 1966 Nov;44(6):1041-9
pubmed: 5981486
Hawaii J Med Public Health. 2013 Jun;72(6 Suppl 2):28-32
pubmed: 23901379
Trans R Soc Trop Med Hyg. 2008 May;102(5):485-92
pubmed: 18358508
Emerg Infect Dis. 2018 Jun;24(6):1153-1155
pubmed: 29774852
Acta Trop. 2015 Jan;141(Pt A):46-53
pubmed: 25312338
Parasit Vectors. 2019 May 16;12(1):241
pubmed: 31097040
One Health. 2022 Aug 06;15:100426
pubmed: 36277113
N Engl J Med. 2002 Feb 28;346(9):668-75
pubmed: 11870244
Rev Bras Parasitol Vet. 2020 Feb 10;29(1):e018119
pubmed: 32049148
Asian Pac J Trop Med. 2011 Aug;4(8):597-9
pubmed: 21914534

Auteurs

Gelixa Gamiette (G)

Réservoir et Diversité des Pathogènes, Unité Transmission, Institut Pasteur de Guadeloupe, Pointe-à-Pitre, France. ggamiette@pasteur-guadeloupe.fr.

Séverine Ferdinand (S)

Réservoir et Diversité des Pathogènes, Unité Transmission, Institut Pasteur de Guadeloupe, Pointe-à-Pitre, France.

David Couvin (D)

Réservoir et Diversité des Pathogènes, Unité Transmission, Institut Pasteur de Guadeloupe, Pointe-à-Pitre, France.

Céline Dard (C)

Institute for Advanced Biosciences, Team Host-Pathogen Interactions and Immunity to Infection, INSERM U1209-CNRS UMR5309, Université Grenoble Alpes, Grenoble, France.

Antoine Talarmin (A)

Réservoir et Diversité des Pathogènes, Unité Transmission, Institut Pasteur de Guadeloupe, Pointe-à-Pitre, France.

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Classifications MeSH