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Volume 31, Number 10—October 2025
Research Letter
Angiostrongylus cantonensis Lungworms in Definitive and Intermediate Hosts, Madagascar, 2024
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Abstract
We assessed the prevalence of the rat lungworm, Angiostrongylus cantonensis, in rats and snails in Toamasina, Madagascar, using molecular techniques. Although no human cases of neuroangiostrongyliasis have been reported in Madagascar, the pathogen’s presence in definitive hosts (2.5%, 2/78) and intermediate hosts (26.9%, 35/130) reveals active circulation and potential zoonotic risk.
The rat lungworm, Angiostrongylus cantonensis (Strongylida: Angiostrongylidae), first identified and described in China in 1935 (1), is responsible for neuroangiostrongyliasis, which can cause neurologic damage, such as eosinophilic meningitis or encephalitis, in humans. The life cycle of this parasitic nematode involves rats as definitive host and snails and slugs as intermediate hosts; humans act as incidental hosts only in this system (2).
Neuroangiostrongyliasis is a foodborne disease, contracted by humans through accidental ingestion of the A. cantonensis infective larvae; several thousand human cases have been documented worldwide (3). The infective larva can be found not only in intermediate hosts but also in paratenic hosts (e.g., crustaceans, frogs), on contaminated vegetables, and in water (2,4).
In Madagascar, A. cantonensis worms were first sampled in 1964 (5) in rats from Ambavaniasy, Alaotra Mangoro Region, and later confirmed in Rattus spp. rats (6). The parasite was reported in rats captured in Antananarivo in 1982 (7); prevalence was 12% during the rainy season and 5% during the dry season. Human cases of neuroangiostrongyliasis on the neighboring islands of Mayotte and La Reunion have been reported (2). In addition, human breeding and consumption of intermediate hosts of this parasite, specifically snails of the genus Achatina, are still taking place on the island; however, data on the potential role of this snail as a carrier of A. cantonensis worms are currently unavailable. In this context, the aim of this study was to update the occurrence of A. cantonensis worms in rats and investigate their presence in snails.
We trapped rats and collected snails in March 2024 in 3 communes in Toamasina district: Fanandrana, Antetezambaro, and Ankirihiry (Appendix). Further, we collected snails of the genus Achatina (Figure 1, panel A) and sampled and preserved a portion of the foot of each snail for molecular screening for the presence of A. cantonensis worms. After DNA extraction, we performed conventional PCR targeting the cytochrome c gene to confirm the identity of adult lungworms (Appendix). Further, we performed molecular screening of A. cantonensis worms using TaqMan quantitative PCR (ThermoFisher Scientific, https://www.thermofisher.com) targeting the internal transcribed spacer gene (Appendix). We used the χ2 test to compare the statistical differences in intermediate host infection by localities.
We captured a total of 78 individual rats of 2 species, 76 Rattus rattus rats and 2 R. norvegicus rats; 61.5% (48/78) were male and 38.4% (30/78) were female, and the age distribution was 55.1% (43/78) juvenile and 44.8% (35/78) adult (Table 2; Appendix). Two R. norvegicus rats captured in Ankirihiry harbored 12 adult lungworms; 8 were isolated from a pregnant female rat and 4 from a juvenile male rat (Figure 1, panel B). We amplified and sequenced 2 adult lungworms from each of the 2 rats (GenBank accession nos. PV185895, PV185896). Those sequences showed 100% similarity with a partial genome sequence of an isolate from Spain (accession no. PP748576) and clustered with nucleotide sequences from Spain, Australia, the United States, Japan, and Brazil (Figure 2). The overall prevalence of infection in rats was 2.5% (2/78).
For the intermediate host, we collected 130 snails of the Achatina genus. A total of 35 individual snails tested positive by quantitative PCR, reaching an overall prevalence of 26.9% (35/130); rates of prevalence were 51.5% (17/33) in Ankirihiry, 29.6% (16/54) in Antetezambaro, and 4.6% (2/43) in Fanandrana. Statistical analysis revealed a significant difference in prevalence of A. cantonensis worms in Achatina snails collected in those localities (χ2 = 38.343, degrees of freedom = 2; p<0.0001).
Our data report an overall prevalence of 26.9% of A. cantonensis worms in Achatina snails from the east coast of Madagascar, which is higher than in other A. cantonensis–endemic regions such as China (21.5%) (8), Brazil (21.7%) (9), and Ecuador (15.2%) (10). The high prevalence of A. cantonensis worms in the Achatina genus demonstrates their involvement in the life cycle of this zoonotic parasite in Madagascar. Furthermore, 2 R. norvegicus rats (a juvenile male and pregnant female) caught in Ankirihiry were parasitized by A. cantonensis worms. The presence of this lungworm in R. norvegicus rats and snails in Ankirihiry suggest an active circulation of this parasite and a potential risk for human neuroangiostrongyliasis on the east coast of Madagascar because of the abundance of hosts (intermediate or definitive) and the consumption of either infected snails or food contaminated by infective larva. Properly boiling water to cook snail meat thoroughly before consumption is critical to avoid infection. Because Rattus spp. rats are found everywhere in Madagascar, future research should investigate other locations to survey the prevalence of A. cantonensis worms in rats, as well as the distribution of Achatina spp. snails and the prevalence of the parasite in those and other snail species to implement surveillance. Although no human infections have been reported in Madagascar, our findings indicate active circulation of the A. cantonensis rat lungworm, posing a potential zoonotic risk.
Mr. Maminirina is a PhD student working on zoonotic microorganisms of public health importance in Madagascar. He also conducts ecoepidemiological surveys on small mammals to investigate host–parasite interactions.
Acknowledgment
Financial support to conduct this research was given by Institut Pasteur de Paris through ACIP ORACAN (ACIP no. 569-2022).
References
- Chen HT. A new lungworm, Pulmonema cantonensis [in French]. Ann Parasitol Hum Comp. 1935;13:312–7. DOIGoogle Scholar
- Wang QP, Lai DH, Zhu XQ, Chen XG, Lun ZR. Human angiostrongyliasis. Lancet Infect Dis. 2008;8:621–30. DOIPubMedGoogle Scholar
- Cowie RH. Angiostrongylus cantonensis: agent of a sometimes fatal globally emerging infectious disease (rat lungworm disease). ACS Chem Neurosci. 2017;8:2102–4. DOIPubMedGoogle Scholar
- Howe K, Kaluna L, Lozano A, Torres Fischer B, Tagami Y, McHugh R, et al. Water transmission potential of Angiostrongylus cantonensis: Larval viability and effectiveness of rainwater catchment sediment filters. PLoS One. 2019;14:
e0209813 . DOIPubMedGoogle Scholar - Brygoo ER, Chabaud AG. Presence of Angiostrongylus cantonensis in Madagascar. Ann Parasitol Hum Comp. 1964;39:793–5.
- Alicata JE. Occurrence of Angiostrongylus cantonensis in Madagascar, Mauritius, Ceylon, and Sarawak. J Parasitol. 1965;51:937. DOIPubMedGoogle Scholar
- Song L, Wang X, Yang Z, Lv Z, Wu Z. Angiostrongylus cantonensis in the vector snails Pomacea canaliculata and Achatina fulica in China: a meta-analysis. Parasitol Res. 2016;115:913–23. DOIPubMedGoogle Scholar
- Guerino LR, Pecora IL, Miranda MS, Aguiar-Silva C, Carvalho OD, Caldeira RL, et al. Prevalence and distribution of Angiostrongylus cantonensis (Nematoda, Angiostrongylidae) in Achatina fulica (Mollusca, Gastropoda) in Baixada Santista, São Paulo, Brazil. Rev Soc Bras Med Trop. 2017;50:92–8. DOIPubMedGoogle Scholar
- Solórzano-Alava L, Sánchez-Amador F, Valverde T. Angiostrongylus (Parastrongylus) cantonensis on intermediate and definitive hosts in Ecuador, 2014-2017. [in Spanish]. Biomedica. 2019;39:370–84. DOIPubMedGoogle Scholar
Figures
Suggested citation for this article: Maminirina LA, Bodoarison ZI, Rajerison M, Ferdinand S, Ramasindrazana B. Angiostrongylus cantonensis lungworms in definitive and intermediate hosts, Madagascar, 2024. Emerg Infect Dis. 2025 Oct [date cited]. https://doi.org/10.3201/eid3110.241741
Original Publication Date: August 26, 2025
1These authors contributed equally to this article.
Table of Contents – Volume 31, Number 10—October 2025
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Beza Ramasindrazana, Unité Peste, Institut Pasteur de Madagascar, BP 1274 Ambatofotsikely, Antananarivo, Madagascar
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