An Overview of Angiostrongylus cantonensis (Nematoda: Angiostrongylidae), an Emerging Cause of Human Angiostrongylosis on the Indian Subcontinent

. 2023 Jun 20 ; 12 (6) : . [epub] 20230620

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

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid37375541

Grantová podpora
Grant No. 22-26136S GAČR Czech Science Foundation

Human angiostrongylosis is an emerging zoonosis caused by the larvae of three species of metastrongyloid nematodes of the genus Angiostrongylus, with Angiostrongylus cantonensis (Chen, 1935) being dominant across the world. Its obligatory heteroxenous life cycle includes rats as definitive hosts, mollusks as intermediate hosts, and amphibians and reptiles as paratenic hosts. In humans, the infection manifests as Angiostrongylus eosinophilic meningitis (AEM) or ocular form. Since there is no comprehensive study on the disease in the Indian subcontinent, our study aims at the growing incidence of angiostrongylosis in humans, alongside its clinical course and possible causes. A systematic literature search revealed 28 reports of 45 human cases from 1966 to 2022; eosinophilic meningitis accounted for 33 cases (75.5%), 12 cases were reported as ocular, 1 case was combined, and 1 case was unspecified. The presumed source of infection was reported in 5 cases only. Importantly, 22 AEM patients reported a history of eating raw monitor lizard (Varanus spp.) tissues in the past. As apex predators, monitor lizards accumulate high numbers of L3 responsible for acute illness in humans. For ocular cases, the source was not identified. Most cases were diagnosed based on nematode findings and clinical pathology (primarily eosinophilia in the cerebrospinal fluid). Only two cases were confirmed to be A. cantonensis, one by immunoblot and the other by q-PCR. Cases of angiostrongylosis have been reported in Delhi, Karnataka, Kerala, Maharashtra, Madhya Pradesh, Puducherry, Telangana, and West Bengal. With a population of more than 1.4 billion, India is one of the least studied areas for A. cantonensis. It is likely that many cases remain undetected/unreported. Since most cases have been reported from the state of Kerala, further research may focus on this region. Gastropods, amphibians, and reptiles are commonly consumed in India; however, typical preparation methods involve cooking, which kills the nematode larvae. In addition to studying rodent and mollusk hosts, monitor lizards can be used as effective sentinels. Sequence data are urgently needed to answer the question of the identity of Angiostrongylus-like metastrongylid nematodes isolated from all types of hosts. DNA-based diagnostic methods such as q-PCR and LAMP should be included in clinical diagnosis of suspected cases and in studies of genetic diversity and species identity of nematodes tentatively identified as A. cantonensis.

Zobrazit více v PubMed

Morgan E.R., Modry D., Paredes-Esquivel C., Foronda P., Traversa D. Angiostrongylosis in animals and humans in Europe. Pathogens. 2021;10:1236. doi: 10.3390/pathogens10101236. PubMed DOI PMC

Wang Q.-P., Lai D.-H., Zhu X.-Q., Chen X.-G., Lun Z.-R. Human angiostrongyliasis. Lancet Infect. Dis. 2008;8:621–630. doi: 10.1016/S1473-3099(08)70229-9. PubMed DOI

Eamsobhana P. Angiostrongyliasis in Thailand: Epidemiology and laboratory investigations. Hawaii J. Med. Public Health. 2013;72:28–32. PubMed PMC

Punyagupta S., Bunnag T., Juttijudata P., Rosen L. Eosinophilic meningitis in Thailand. Epidemiologic studies of 484 typical cases and the etiologic role of Angiostrongylus cantonensis. Am. J. Trop. Med. Hyg. 1970;19:950–958. doi: 10.4269/ajtmh.1970.19.950. PubMed DOI

Watthanakulpanich D., Jakkul W., Chanapromma C., Ketboonlue T., Dekumyoy P., Lv Z., Chan A.H.E., Thaenkham U., Chaisiri K. Co-occurrence of Angiostrongylus malaysiensis and Angiostrongylus cantonensis DNA in cerebrospinal fluid: Evidence from human eosinophilic meningitis after ingestion of raw snail dish in Thailand. Food Waterborne Parasitol. 2021;24:e00128. doi: 10.1016/j.fawpar.2021.e00128. PubMed DOI PMC

Parmeter S.N., Chowdhury A.B. Angiostrongylus cantonensis in India. Bull. Calcutta Sch. Trop. Med. 1966;14:38. PubMed

Turck H.C., Fox M.T., Cowie R.H. Paratenic hosts of Angiostrongylus cantonensis and their relation to human neuroangiostrongyliasis globally. One Health. 2022;15:100426. doi: 10.1016/j.onehlt.2022.100426. PubMed DOI PMC

Lecompte E., Aplin K., Denys C., Catzeflis F., Chades M., Chevret P. Phylogeny and biogeography of African Murinae based on mitochondrial and nuclear gene sequences, with a new tribal classification of the subfamily. BMC Evol. Biol. 2008;8:199. doi: 10.1186/1471-2148-8-199. PubMed DOI PMC

Chen H.-T. Un Nouveau nématode pulmonaire, Pulmonema cantonensis, n.g., n. sp. Ann. Parasitol. Hum. Comp. 1935;13:312–317. doi: 10.1051/parasite/1935134312. DOI

Alicata J.E. Biology and distribution of the Rat lungworm, Angiostrongylus cantonensis, and its relationship to eosinophilic meningoencephalitis and other neurological disorders of man and animals. Adv. Parasitol. 1965;3:223–248. doi: 10.1016/s0065-308x(08)60366-8. PubMed DOI

Walden H.D.S., Slapcinsky J.D., Roff S., Calle J.M., Goodwin Z.D., Stern J., Corlett R., Conway J., McIntosh A. Geographic distribution of Angiostrongylus cantonensis in wild rats (Rattus rattus) and terrestrial snails in Florida, USA. PLoS ONE. 2017;12:e0177910. doi: 10.1371/journal.pone.0177910. PubMed DOI PMC

Wallace G.D., Rosen L. Studies on eosinophilic meningitis: I. Observations on the geographic distribution of Angiostrongylus cantonensis in the Pacific area and its prevalence in wild rats. Am. J. Epidemiol. 1965;81:52–62. doi: 10.1093/oxfordjournals.aje.a120497. PubMed DOI

Mackerras M., Sandars D. The life history of the rat lung-worm, Angiostrongylus cantonensis (Chen) (Nematoda: Metastrongylidae) Aust. J. Zool. 1955;3:1–21. doi: 10.1071/ZO9550001. DOI

Červená B., Modrý D., Fecková B., Hrazdilová K., Foronda P., Alonso A.M., Lee R., Walker J., Niebuhr C.N., Malik R., et al. 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 Vectors. 2019;12:241. doi: 10.1186/s13071-019-3491-y. PubMed DOI PMC

Alicata J. The discovery of Angiostrongylus cantonensis as a cause of human eosinophilic meningitis. Parasitol. Today. 1991;7:151–153. doi: 10.1016/0169-4758(91)90285-V. PubMed DOI

Mason K.V., Prescott C.W., Kelly W.R., Waddell A.H. Granulomatous encephalomyelitis of puppies due to Angiostrongylus cantonensis. Aust. Vet. J. 1976;52:295. doi: 10.1111/j.1751-0813.1976.tb00124.x. PubMed DOI

Wright J., Kelly W., Hamilton J., Wadell A. Equine neural angiostrongylosis. Aust. Veter J. 1991;68:58–60. doi: 10.1111/j.1751-0813.1991.tb03131.x. PubMed DOI

Carlisle M.S., Prociv P., Grennan J., Pass M.A., Campbell G.L., Mudie A. Cerebrospinal angiostrongyliasis in five captive tamarins (Sanguinus spp.) Aust. Veter J. 1998;76:167–170. doi: 10.1111/j.1751-0813.1998.tb10121.x. PubMed DOI

Barrett J., Carlisle M., Prociv P. Neuro-angiostrongylosis in wild Black and Grey-headed flying foxes (Pteropus spp.) Aust. Vet. J. 2002;80:554–558. doi: 10.1111/j.1751-0813.2002.tb11039.x. PubMed DOI

Mason K.V. Canine neural angiostrongylosis: The clinical and therapeutic features of 55 natural cases. Aust. Vet. J. 1987;64:201–203. doi: 10.1111/j.1751-0813.1987.tb15181.x. PubMed DOI

Lunn J.A., Lee R., Smaller J., MacKay B.M., King T., Hunt G.B., Martin P., Krockenberger M.B., Spielman D., Malik R. Twenty two cases of canine neural angiostrongylosis in eastern Australia (2002–2005) and a review of the literature. Parasites Vectors. 2012;5:70. doi: 10.1186/1756-3305-5-70. PubMed DOI PMC

Kim J.R., Hayes K.A., Yeung N.W., Cowie R.H. Diverse gastropod hosts of Angiostrongylus cantonensis, the rat lungworm, globally and with a focus on the Hawaiian Islands. PLoS ONE. 2014;9:e94969. doi: 10.1371/journal.pone.0094969. PubMed DOI PMC

Thiengo S.C., Simões R.D.O., Fernandez M.A., Maldonado A. Angiostrongylus cantonensis and rat lungworm disease in Brazil. Hawaii J. Med. Public Health. 2013;72:18–22. PubMed PMC

Howe K., Kaluna L., Lozano A., Fischer B.T., Tagami Y., McHugh R., Jarvi S. Water transmission potential of Angiostrongylus cantonensis: Larval viability and effectiveness of rainwater catchment sediment filters. PLoS ONE. 2019;14:e0209813. doi: 10.1371/journal.pone.0209813. PubMed DOI PMC

Modrý D., Fecková B., Putnová B., Manalo S.M., Otranto D. Alternative pathways in Angiostrongylus cantonensis (Metastrongyloidea: Angiostrongylidae) transmission. Parasitology. 2021;148:167–173. doi: 10.1017/S0031182020001857. PubMed DOI PMC

Diao Z., Wang J., Qi H., Li X., Zheng X., Yin C. Human ocular angiostrongyliasis: A literature review. Trop. Doct. 2011;41:76–78. doi: 10.1258/td.2010.100294. PubMed DOI

Beaver P.C., Rosen L. Memorandum on the first report of Angiostrongylus in man, by Nomura and Lin, 1945. Am. J. Trop. Med. Hyg. 1964;13:589–590. doi: 10.4269/ajtmh.1964.13.589. PubMed DOI

Ansdell V., Wattanagoon Y. Angiostrongylus cantonensis in travelers: Clinical manifestations, diagnosis, and treatment. Curr. Opin. Infect. Dis. 2018;31:399–408. doi: 10.1097/QCO.0000000000000481. PubMed DOI

Kwon E., Ferguson T.M., Park S.Y., Manuzak A., Qvarnstrom Y., Morgan S., Ciminera P., Murphy G.S. A severe case of Angiostrongylus eosinophilic meningitis with encephalitis and neurologic sequelae in Hawa’i. Hawaii J. Med. Public Health. 2013;72:41–45. PubMed PMC

Murphy G.S., Johnson S. Clinical aspects of eosinophilic meningitis and meningoencephalitis caused by Angiostrongylus cantonensis, the rat lungworm. Hawaii J. Med. Public Health. 2013;72:35. PubMed PMC

Feng Y., Nawa Y., Sawanyavisuth K., Lv Z., Wu Z.-D. Comprehensive review of ocular angiostrongyliasis with special reference to optic neuritis. Korean J. Parasitol. 2013;51:613–619. doi: 10.3347/kjp.2013.51.6.613. PubMed DOI PMC

Kumar V., Kyprianou I., Keenan J.M. Ocular angiostrongyliasis: Removal of a live nematode from the anterior chamber. Eye. 2004;19:229–230. doi: 10.1038/sj.eye.6701442. PubMed DOI

Mattis A., Mowatt L., Lue A., Lindo J., Vaughan H. Ocular angiostrongyliasis—First case report from Jamaica. West Indian Med. J. 2009;58:383–385. PubMed

McCarthy K., Liu K., Kokame G.T., Merrill P.T., Gilca M., Cohen J. First case of subretinal ocular angiostrongyliasis associated with retinal detachment in the United States. Hawaii J. Health Soc. Welf. 2021;80:40. PubMed PMC

Sinawat S., Trisakul T., Choi S., Morley M., Sinawat S., Yospaiboon Y. Ocular angiostrongyliasis in Thailand: A retrospective analysis over two decades. Clin. Ophthalmol. 2019;13:1027–1031. doi: 10.2147/OPTH.S204380. PubMed DOI PMC

Baheti N.N., Sreedharan M., Krishnamoorthy T., Nair M.D., Radhakrishnan K. Eosinophilic meningitis and an ocular worm in a patient from Kerala, South India. Case Rep. 2009;2009:bcr2007122093. doi: 10.1136/bcr.2007.122093. PubMed DOI PMC

Sawanyawisuth K., Kitthaweesin K., Limpawattana P., Intapan P., Tiamkao S., Jitpimolmard S., Chotmongkol V. Intraocular angiostrongyliasis: Clinical findings, treatments and outcomes. Trans. R. Soc. Trop. Med. Hyg. 2007;101:497–501. doi: 10.1016/j.trstmh.2006.07.010. PubMed DOI

Sen P., Date A., Jain E., Mohan A. Angiostrongylus—A technique for removing a rare parasite from the cornea of a child. J. Am. Assoc. Pediatr. Ophthalmol. Strabismus. 2019;23:119–120. doi: 10.1016/j.jaapos.2018.11.005. PubMed DOI

Aishwarya A., Tiwari U.S., Gandhi S., Sisodia P. Angiostrongylus cantonensis in anterior chamber. Indian J. Ophthalmol. 2019;67:158–160. doi: 10.4103/ijo.IJO_843_18. PubMed DOI PMC

Renapurkar D.M., Bhopale M.K., Limaye L.S., Sharma K.D. Prevalence of Angiostrongylus cantonensis infection in commensal rats in Bombay. J. Helminthol. 1982;56:345–349. doi: 10.1017/S0022149X00034751. PubMed DOI

Thomas M., Thangavel M., Thomas R.P. Angiostrongylus cantonensis (Nematoda, Metastrongylidae) in bandicoot rats in Kerala, South India. Infect. Dis. 2015;8:324–326.

Mehta D.K., Arora R., Chauhan D., Shroff D., Narula R. Chemo-paralysis for the removal of a live intraocular worm in ocular angiostrongyliasis. Clin. Exp. Ophthalmol. 2006;34:493–495. doi: 10.1111/j.1442-9071.2006.01255.x. PubMed DOI

Malhotra S., Mehta D.K., Arora R., Chauhan D., Ray S., Jain M. Ocular angiostrongyliasis in a child—First case report from India. J. Trop. Pediatr. 2006;52:223–225. doi: 10.1093/tropej/fmi092. PubMed DOI

Rai S., Madi D., Pai S., Baliga S. Unusual larva in the CSF and unique MRI findings in a case of eosinophilic meningitis. J. Clin. Imaging Sci. 2014;4:76. doi: 10.4103/2156-7514.148303. PubMed DOI PMC

Hidelaratchi M.D.P., Riffsy M.T.M., Wijesekera J.C. A case of eosinophilic meningitis following monitor lizard meat consumption, exacerbated by anthelminthics. Ceylon Med. J. 2010;50:84–86. doi: 10.4038/cmj.v50i2.1577. PubMed DOI

Raveendrakumar A.G., Remadevi G.S., Eapen E.K., Vijayamma A.K.T. Eosinophilic meningitis in a toddler. Indian Pediatr. 2021;58:187–188. doi: 10.1007/s13312-021-2143-4. PubMed DOI

Shah I., Barot S., Madvariya M. Eosinophilic meningitis: A case series and review of literature of Angiostrongylus cantonensis and Gnathostoma spinigerum. Indian J. Med. Microbiol. 2015;33:154–158. doi: 10.4103/0255-0857.148430. PubMed DOI

Parameswaran K. Case series of eosinophilic meningoencephalitis from South India. Ann. Indian Acad. Neurol. 2006;9:217. doi: 10.4103/0972-2327.29203. DOI

Ianas V., Kuberski T. Eosinophilic meningitis due to Angiostrongylus cantonensis. Infect. Med. 2008;25:366–368.

Wang Q.-P., Wu Z.-D., Wei J., Owen R.L., Lun Z.-R. Human Angiostrongylus cantonensis: An update. Eur. J. Clin. Microbiol. Infect. Dis. 2012;31:389–395. doi: 10.1007/s10096-011-1328-5. PubMed DOI

Wilkins P.P., Qvarnstrom Y., Whelen A.C., Saucier C., Da Silva A.J., Eamsobhana P. The current status of laboratory diagnosis of Angiostrongylus cantonensis infections in humans using serologic and molecular methods. Hawaii J. Med. Public Health. 2013;72:55–57. PubMed PMC

de Melo L.C.V., de Souza F.C.R., Baccin A.D.O., Mota D.J.G.D., Pereira-Chioccola V.L., Pinto P.L.S. Immunoanalysis of different antigenic preparations of Angiostrongylus cantonensis for neuroangiostrongyliasis diagnosis improvement. Mem. Inst. Oswaldo Cruz. 2022;117:e220086. doi: 10.1590/0074-02760220086. PubMed DOI PMC

Qvarnstrom Y., Sullivan J.J., Bishop H.S., Hollingsworth R., Da Silva A.J. PCR-based detection of Angiostrongylus cantonensis in tissue and mucus secretions from molluscan hosts. Appl. Environ. Microbiol. 2007;73:1415–1419. doi: 10.1128/AEM.01968-06. PubMed DOI PMC

Qvarnstrom Y., Xayavong M., Chea N., da Silva A.C.A., Heng S., Park S.Y., Calimlim P.S., Johnson S., Whelen A.C., Fox L.M., et al. Real-time polymerase chain reaction detection of Angiostrongylus cantonensis DNA in cerebrospinal fluid from patients with eosinophilic meningitis. Am. J. Trop. Med. Hyg. 2016;94:176–181. doi: 10.4269/ajtmh.15-0146. PubMed DOI PMC

Maleewong W., Sombatsawat P., Intapan P.M., Wongkham C., Chotmongkol V. Immunoblot evaluation of the specificity of the 29-kDa antigen from young adult female worms Angiostrongylus cantonensis for immunodiagnosis of human angiostrongyliasis. Asian Pac. J. Allergy Immunol. 2001;19:267. PubMed

Eamsobhana P., Gan X., Ma A., Wang Y., Wanachiwanawin D., Yong H. Dot immunogold filtration assay (DIGFA) for the rapid detection of specific antibodies against the rat lungworm Angiostrongylus cantonensis (Nematoda: Metastrongyloidea) using purified 31-kDa antigen. J. Helminthol. 2014;88:396–401. doi: 10.1017/S0022149X13000321. PubMed DOI

Chen J.-X., Chen M.-X., Ai L., Chen J.-H., Chen S.-H., Zhang Y.-N., Cai Y.-C., Zhu X.-Q., Zhou X.-N. A protein microarray for the rapid screening of patients suspected of infection with various food-borne helminthiases. PLoS Negl. Trop. Dis. 2012;6:e1899. doi: 10.1371/journal.pntd.0001899. PubMed DOI PMC

Barratt J., Chan D., Sandaradura I., Malik R., Spielman D., Lee R., Marriott D., Harkness J., Ellis J., Stark D. Angiostrongylus cantonensis: A review of its distribution, molecular biology and clinical significance as a human pathogen. Parasitology. 2016;143:1087–1118. doi: 10.1017/S0031182016000652. PubMed DOI

Liu C.-Y., Song H.-Q., Zhang R.-L., Chen M.-X., Xu M.-J., Ai L., Chen X.-G., Zhan X.-M., Liang S.-H., Yuan Z.-G., et al. Specific detection of Angiostrongylus cantonensis in the snail Achatina fulica using a loop-mediated isothermal amplification (LAMP) assay. Mol. Cell. Probes. 2011;25:164–167. doi: 10.1016/j.mcp.2011.04.002. PubMed DOI

Sears W.J., Qvarnstrom Y., Nutman T.B. RPAcan3990: An ultrasensitive recombinase polymerase assay to detect Angiostrongylus cantonensis DNA. J. Clin. Microbiol. 2021;59:e01185-21. doi: 10.1128/JCM.01185-21. PubMed DOI PMC

Sears W.J., Qvarnstrom Y., Dahlstrom E., Snook K., Kaluna L., Baláž V., Feckova B., Šlapeta J., Modry D., Jarvi S. AcanR3990 qPCR: A novel, highly sensitive, bioinformatically-informed assay to detect Angiostrongylus cantonensis Infections. Clin. Infect. Dis. 2021;73:e1594–e1600. doi: 10.1093/cid/ciaa1791. PubMed DOI PMC

Jalal M.J.A., Varghese B., Menon M.K., Pratap T., Moheen A., Mathew J., Vijayan T.P., Tomy M.P. Eosinophilic meningitis: Report of three cases from a hilly area in Kerala. Ann. Indian Acad. Neurol. 2019;22:108–111. doi: 10.4103/aian.AIAN_254_18. PubMed DOI PMC

Nalini A., Ramakrishna A., Dekumoy P., Kumar R., Pakdee W., Saini J., Hegde V. Severe form of radiculo-myelo-neuropathy with meningo-encephalitis secondary to Angiostrongylus cantonensis infection: Unusual corpus callosal lesions and serial magnetic resonance imaging findings. Neurol. India. 2013;61:414–418. doi: 10.4103/0028-3886.117613. PubMed DOI

Pai S., Madi D., Achappa B., Mahalingam S., Kendambadi R. An interesting case of eosinophilic meningitis. J. Clin. Diagn. Res. 2013;7:734. doi: 10.7860/JCDR/2013/4743.2897. PubMed DOI PMC

Chaudhari J.P., Shenoy A.S., Goel N.A. Eosinophilic meningitis due to A. Cantonensis revealed at autopsy. Indian J. Pathol. Microbiol. 2022;65:420. PubMed

Panackel C., Vishad, Cherian G., Vijayakumar K., Sharma R. Eosinophilic meningitis due to Angiostrongylus cantonensis. Indian J. Med. Microbiol. 2006;24:220–221. doi: 10.1016/S0255-0857(21)02355-0. PubMed DOI

Hamide A., Johny J., Kumar A., Kolar V.V. Eosinophilic meningitis caused by consumption of meat of monitor lizard (Varanus bengalensis) Neurol. India. 2018;66:1166. doi: 10.4103/0028-3886.237031. PubMed DOI

Sharma K.D., Renapurkar D.M., Bhopale M.K., Nathan J., Boraskar A., Chotani S. Study of a focus of Angiostrongylus cantonensis in Greater Bombay. Bull Haffkine. 1981;9:38–46.

Purohit A.K., Dinakar I., Sundaram C., Ratnakar K.S. Angiostrongylus cantonensis abscess in the brain. J. Neurol. Neurosurg. Psychiatry. 1991;54:1015–1016. doi: 10.1136/jnnp.54.11.1015-a. PubMed DOI PMC

Joseph H.P. Clinical notes on the effects of a nematode larva in the eye. Ceylon J. Sci. Med. Sci. 1927;1:141.

Nicholls L. Note on a nematode larva removed from the eye of a man. Ceylon J. Sci. 1925;1:145.

Durette-Desset M.-C., Chabaud A.G., Cassim M.H.S., Ismail M.M., Premaratne U.N., Abeyewickreme W., Dissanaike A.S. On an infection of a human eye with Parastrongylus (=Angiostrongylus) sp. in Sri Lanka. J. Helminthol. 1993;67:69–72. doi: 10.1017/S0022149X00012876. PubMed DOI

Wariyapola D., Goonesinghe N., Priyamanna T.H., Fonseka C., Ismail M., Abeyewickreme W., Dissanaike A. Second case of ocular parastrongyliasis from Sri Lanka. Trans. R. Soc. Trop. Med. Hyg. 1998;92:64–65. doi: 10.1016/S0035-9203(98)90956-7. PubMed DOI

Alibhoy A.T., Senanayake B., Fernando M.A., Amarasekera H.S., Wijesekera J.C. A case of eosinophilic meningitis. Ceylon Med. J. 1999;44:173–174. PubMed

Dissanaike A.S., Ihalamulla R.L., Naotunne T.S., Senarathna T., Withana D.S. Third report of ocular parastrongyliasis (angiostrongyliasis) from Sri Lanka. Parassitologia. 2001;43:95–97. PubMed

Ilhalamulla R., Fernando S., Weerasena K., Cross J., Dissanaike A., Fonseka C. A further case of Parastrongyliasis (=Angiostrongyliasis) from the eye of a patient in Sri Lanka. Ceylon J. Med. Sci. 2008;50:15. doi: 10.4038/cjms.v50i1.118. DOI

Paul A., Pammal A.T. Ocular parasitosis: A rare cause of hypertensive uveitis. Indian J. Ophthalmol. 2008;56:501–502. doi: 10.4103/0301-4738.43369. PubMed DOI PMC

Sah R., Khatri A., Kharel R., Kc H., Rabaan A.A., Tiwari R., Dhama K., Malik Y.S., Donovan S., Rodriguez-Morales A.J., et al. Case report: Management of dead intraocular helminth parasites in asymptomatic patients. Am. J. Trop. Med. Hyg. 2020;103:719–722. doi: 10.4269/ajtmh.20-0218. PubMed DOI PMC

Peng J., He Z.-P., Zhang S., Lun Z.-R., Wu Z.-D., Fan C.-K., Brown C.L., Cheng P.-C., Peng S.-Y., Yang T.-B. Phylogeography of Angiostrongylus cantonensis (Nematoda: Angiostrongylidae) in southern China and some surrounding areas. PLoS Negl. Trop. Dis. 2017;11:e0005776. doi: 10.1371/journal.pntd.0005776. PubMed DOI PMC

Tokiwa T., Hashimoto T., Yabe T., Komatsu N., Akao N., Ohta N. First report of Angiostrongylus cantonensis (Nematoda: Angiostrongylidae) infections in invasive rodents from five islands of the Ogasawara Archipelago, Japan. PLoS ONE. 2013;8:e70729. doi: 10.1371/journal.pone.0070729. PubMed DOI PMC

Alicata J.E., McCarthy D.D. On the incidence and distribution of the rat lungworm Angiostrongylus cantonensis in the cook islands, with observations made in new zealand and western samoa. Can. J. Zool. 1964;42:605–611. doi: 10.1139/z64-052. DOI

Kliks M.M., Palumbo N.E. Eosinophilic meningitis beyond the Pacific Basin: The global dispersal of a peridomestic zoonosis caused by Angiostrongylus cantonensis, the nematode lungworm of rats. Soc. Sci. Med. 1992;34:199–212. doi: 10.1016/0277-9536(92)90097-A. PubMed DOI

Alicata J.E. The presence of Angiostrongylus cantonensis in islands of the Indian ocean and probable role of the giant African snail, achatina fulica, in dispersal of the parasite to the pacific islands. Can. J. Zool. 1966;44:1041–1049. doi: 10.1139/z66-111. PubMed DOI

Yousif F., Ibrahim A. The first record of Angiostrongylus cantonensis from Egypt. Parasitol. Res. 1978;56:73–80. doi: 10.1007/bf00925940. PubMed DOI

Aguiar P.H., Morera P., Pascual J. First record of Angiostrongylus cantonensis in Cuba. Am. J. Trop. Med. Hyg. 1981;30:963–965. doi: 10.4269/ajtmh.1981.30.963. PubMed DOI

Vargas M., JD G.P., Malek E.A. First record of Angiostrongylus cantonensis (Chen, 1935) (Nematoda: Metastrongylidae) in the Dominican Republic. Trop. Med. Parasitol. 1992;43:253–255. PubMed

Campbell B.G., Little M.D. The finding of Angiostrongylus cantonensis in rats in New Orleans. Am. J. Trop. Med. Hyg. 1988;38:568–573. doi: 10.4269/ajtmh.1988.38.568. PubMed DOI

Caldeira R.L., Mendonça C.L.G.F., Goveia C.O., Lenzi H.L., Graeff-Teixeira C., Lima W.S., Mota E.M., Pecora I.L., Medeiros A.M.Z.D., Carvalho O.D.S. First record of molluscs naturally infected with Angiostrongylus cantonensis (Chen, 1935) (Nematoda: Metastrongylidae) in Brazil. Mem. Inst. Oswaldo Cruz. 2007;102:887–889. doi: 10.1590/S0074-02762007000700018. PubMed DOI

Foronda P., López-González M., Miquel J., Torres J., Segovia M., Abreu-Acosta N., Casanova J.C., Valladares B., Mas-Coma S., Bargues M.D., et al. Finding of Parastrongylus cantonensis (Chen, 1935) in Rattus rattus in Tenerife, Canary Islands (Spain) Acta Trop. 2010;114:123–127. doi: 10.1016/j.actatropica.2010.02.004. PubMed DOI

Paredes-Esquivel C., Sola J., Delgado-Serra S., Riera M.P., Negre N., Miranda M.Á., Jurado-Rivera J.A. Angiostrongylus cantonensis in North African hedgehogs as vertebrate hosts, Mallorca, Spain, October 2018. Eurosurveillance. 2019;24:1900489. doi: 10.2807/1560-7917.ES.2019.24.33.1900489. PubMed DOI PMC

Mugisha L., Bwangamoi O., Cranfield M. Angiostrongylus cantonensis and other parasites infections of rodents of Budongo Forest Reserve, Uganda. Afr. J. Anim. Biomed. Sci. 2012;7:91–95.

Iwanowicz D.D., Sanders L.R., Schill W.B., Xayavong M.V., da Silva A.J., Qvarnstrom Y., Smith T. Spread of the rat lungworm (Angiostrongylus cantonensis) in giant African land snails (Lissachatina fulica) in Florida, USA. J. Wildl. Dis. 2015;51:749–753. doi: 10.7589/2014-06-160. PubMed DOI

Rizor J., Yanez R.A., Thaiwong T., Kiupel M. Angiostrongylus cantonensis in a red ruffed lemur at a zoo, Louisiana, USA. Emerg. Infect. Dis. 2022;28:1058. doi: 10.3201/eid2805.212287. PubMed DOI PMC

Dissanaike A.S., Cross J.H. Ocular parastrongyliasis (=angiostrongyliasis): Probable first report of human infection from a patient in Ceylon (Sri Lanka) Parassitologia. 2004;46:315–316. PubMed

Limaye L.S., Pradhan V.R., Bhopale M.K., Renapurkar D.M., Sharma K.D. Angiostrongylus cantonensis study of intermediate paratenic and definitive hosts in greater Bombay India. Helminthologia. 1988;25:31–35.

Limaye L.S., Bhopale M.K., Renapurkar D.M., Sharma K.D. The distribution of Angiostrongylus cantonensis (Chen) in the central nervous system of laboratory rats. Folia Parasitol. 1983;30:281–284. PubMed

Mahajan R., Almeida A., Sengupta S., Renapurkar D. Seasonal intensity of Angiostrongylus cantonensis in the intermediate host, Laevicaulis alte. Int. J. Parasitol. 1992;22:669–671. doi: 10.1016/0020-7519(92)90017-F. PubMed DOI

York E.M., Creecy J.P., Lord W.D., Caire W. Geographic range expansion for rat lungworm in North America. Emerg. Infect. Dis. 2015;21:1234–1236. doi: 10.3201/eid2107.141980. PubMed DOI PMC

Agrawal V.C. Taxonomic Studies on Indian Muridae and Hystricidae (Mammalia: Rodentia) Director, Zoological Survey of India; Calcutta, India: 2000. pp. 1–186. Rec. zool. Surv. India, Occasional Paper No. 180. i-viii.

Wilson D.E., Reeder D.M. Mammal Species of the World: A Taxonomic and Geographic Reference. 3rd ed. JHU Press; Baltimore, MA, USA: 2005.

Prakash I., Singh P., Nameer P., Ramesh D., Molur S. South asian muroids. Mamm. S. Asia. 2015;2:574–642.

Wilson D.E., Lacher T.E., Mittermeier R.A. Handbook of the Mammals of the World. Volume 7 Lynx Edicions; Barcelona, Spain: 2017. Rodents II.

Dissanaike A.S. The Proper Study of Mankind. Ceylon Association for the Advancement of Science; Colombo, Sri Lanka: 1968. pp. 115–142.

Yong H.S., Eamsobhana P. Definitive rodent hosts of the rat lungworm Angiostrongylus cantonensis. Raffles Bull. Zool. 2013;29:111–115.

Adhikari P., Han S.-H., Kim Y.-K., Kim T.-W., Thapa T.B., Subedi N., Kunwar A., Banjade M., Oh H.-S. New record of the Oriental house rat, Rattus tanezumi, in Nepal inferred from mitochondrial cytochrome B gene sequences. Mitochondrial DNA Part B. 2018;3:386–390. doi: 10.1080/23802359.2018.1436991. PubMed DOI PMC

Aplin K.P., Brown P.R., Jacob J., Krebs C.J., Singleton G.R. Field Methods for Rodent Studies in Asia and the Indo-Pacific. Australian Centre for International Agricultural Research; Melbourne Australia: 2003.

Bentley E., Bathard A. The rats of Addu Atoll, Maldive Islands. Ann. Mag. Nat. Hist. 1959;2:365–368. doi: 10.1080/00222935908655744. DOI

Cowie R.H. Biology, systematics, life cycle, and distribution of Angiostrongylus cantonensis, the cause of rat lungworm disease. Hawaii J. Med. Public Health. 2013;72:6. PubMed PMC

Lv S., Zhang Y., Liu H.-X., Hu L., Yang K., Steinmann P., Chen Z., Wang L.-Y., Utzinger J., Zhou X.-N. Invasive snails and an emerging infectious disease: Results from the first national survey on Angiostrongylus cantonensis in China. PLoS Negl. Trop. Dis. 2009;3:e368. doi: 10.1371/journal.pntd.0000368. PubMed DOI PMC

Richards C.S., Merritt J.W. Studies on Angiostrongylus cantonensis in molluscan intermediate hosts. J. Parasitol. 1967;53:382. doi: 10.2307/3276595. PubMed DOI

Tripathy B., Mukhopadhayay A. Aquatic Ecosystem: Biodiversity, Ecology and Conservation. Springer; New Delhi, India: 2015. Freshwater molluscs of India: An insight of into their diversity, distribution and conservation; pp. 163–195. DOI

Sen S., Ravikanth G., Aravind N. Land snails (Mollusca: Gastropoda) of India: Status, threats and conservation strategies. J. Threat. Taxa. 2012;4:3029–3037. doi: 10.11609/JoTT.o2722.3029-37. DOI

Boominathan M., Ravikumar G., Chandran M.D.S., Ramachandra T.V. Mangrove associated molluscs of India; Proceedings of the National Conference on Conservation and Management of Wetland Ecosystems; Kerala, India. 6–9 November 2012; pp. 1–11.

Ratnapala R. Ecology and Biogeography in Sri Lanka. Springer; Dordrecht, The Netherlands: 1984. Land snails: Distribution and notes on ecology; pp. 391–411. DOI

Strong E.E., Gargominy O., Ponder W., Bouchet P. Global diversity of gastropods (Gastropoda; Mollusca) in freshwater. Freshw. Anim. Divers. Assess. 2008;198:149–166. doi: 10.1007/s10750-007-9012-6. DOI

Mavinkurve R.G., Shanbhag S.P., Madhyastha N. Non-marine molluscs of Western Ghats: A status review. Zoos’ Print J. 2004;19:1708–1711. doi: 10.11609/JoTT.ZPJ.1160.1708-11. DOI

Thiengo S., Maldonado A., Mota E., Torres E., Caldeira R., Carvalho O., Oliveira A., Simões R., Fernandez M., Lanfredi R. The giant African snail Achatina fulica as natural intermediate host of Angiostrongylus cantonensis in Pernambuco, northeast Brazil. Acta Trop. 2010;115:194–199. doi: 10.1016/j.actatropica.2010.01.005. PubMed DOI

Wang Q.-P., Chen X.-G., Lun Z.-R. Invasive fresh water snail, China. Emerg. Infect. Dis. 2007;13:1119–1120. doi: 10.3201/eid1307.061360. PubMed DOI PMC

Cowie R.H. Angiostrongylus cantonensis: Agent of a sometimes fatal globally emerging infectious disease (rat lungworm disease) ACS Chem. Neurosci. 2017;8:2102–2104. doi: 10.1021/acschemneuro.7b00335. PubMed DOI

Eamsobhana P., Yong H.S., Prasartvit A., Wanachiwanawin D., Boonyong S. Geographical distribution and incidence of Angiostrongylus lungworms (Nematoda: Angiostrongylidae) and their rodent hosts in Thailand. Trop. Biomed. 2016;33:35–44. PubMed

Hamilton L.J., Tagami Y., Kaluna L., Jacob J., Jarvi S.I., Follett P. Demographics of the semi-slug Parmarion martensi, an intermediate host for Angiostrongylus cantonensis in Hawai‘i, during laboratory rearing. Parasitology. 2021;148:153–158. doi: 10.1017/S0031182020001353. PubMed DOI PMC

Kim J.R., Wong T.M., Curry P.A., Yeung N.W., Hayes K.A., Cowie R.H. Modelling the distribution in Hawaii of Angiostrongylus cantonensis (rat lungworm) in its gastropod hosts. Parasitology. 2019;146:42–49. doi: 10.1017/S0031182018001026. PubMed DOI

Tesana S., Srisawangwong T., Sithithaworn P., Laha T., Andrews R. Prevalence and intensity of infection with third stage larvae of Angiostrongylus cantonensis in mollusks from Northeast Thailand. Am. J. Trop. Med. Hyg. 2009;80:983–987. doi: 10.4269/ajtmh.2009.80.983. PubMed DOI

Xu Y., Wang W., Yao J., Yang M., Guo Y., Deng Z., Mao Q., Li S., Duan L. Comparative proteomics suggests the mode of action of a novel molluscicide against the invasive apple snail Pomacea canaliculata, intermediate host of Angiostrongylus cantonensis. Mol. Biochem. Parasitol. 2022;247:111431. doi: 10.1016/j.molbiopara.2021.111431. PubMed DOI

Yang T.-B., Wu Z.-D., Lun Z.-R. The apple snail Pomacea canaliculata, a novel vector of the rat lungworm, Angiostrongylus cantonensis: Its introduction, spread, and control in China. Hawaii J. Med. Public Health. 2013;72:23. PubMed PMC

Baloch W.A., Memon U.N., Burdi G.H., Soomro A.N., Tunio G.R., Khatian A.A. Invasion of channelled apple snail Pomacea canaliculata, Lamarck (Gastropoda: Ampullariidae) in Haleji Lake, Pakistan. Sindh Univ. Res. J. SURJ (Sci. Ser.) 2012;44:263–266.

Joshi R.C. Proceedings of the Area-Wide Control of Insect Pests: From Research to Field Implementation. Springer; Berlin/Heidelberg, Germany: 2007. Problems with the management of the golden apple snail Pomacea canaliculata: An important exotic pest of rice in Asia; pp. 257–264.

Rekha Sarma R., Munsi M., Neelavara Ananthram A. Effect of climate change on invasion risk of giant African snail (Achatina fulica Férussac, 1821: Achatinidae) in India. PLoS ONE. 2015;10:e0143724. doi: 10.1371/journal.pone.0143724. PubMed DOI PMC

Saha C., Pramanik S., Chakraborty J., Parveen S., Aditya G. Abundance and body size of the invasive snail Physa acuta occurring in Burdwan, West Bengal, India. J. Entomol. Zool. Stud. 2016;4:490–497.

Saha C., Parveen S., Chakraborty J., Pramanik S., Aditya G. Life table estimates of the invasive snail Physa acuta Draparnaud, 1805, occurring in India. Ekologia. 2017;36:60–68. doi: 10.1515/eko-2017-0006. DOI

Paul P., Aditya G. Invasion of the freshwater snail Physella acuta (Draparnaud, 1805) in selected ponds of North Dinajpur, India. J. Environ. Biol. 2021;42:577–581. doi: 10.22438/jeb/42/3/MRN-1628. DOI

Raut S.K., Mandal R.N. Natural history of the garden slug Laevicaulis alte. J. Bengal Nat. Hist. Soc. 1984;3:104–105.

Thakuri B., Acharya B.K., Sharma G. Population density and damage of invasive giant African snail Achatina fulica in organic farm in east Sikkim, India. Indian J. Ecol. 2019;46:631–635.

Sridhar V., Vinesh L.S., Jayashankar M. Mapping the potential distribution of Achatina fulica (Bowdich) (Stylommatophora: Achatinidae) in India using CLIMEX, a bioclimatic software. Pest Manag. Hortic. Ecosyst. 2014;20:14–21.

Husain A., Husain H.J., Hasan W., Kendra J.K.V. New records of tropical leather-leaf slug Laevicaulis alte (Ferussac, 1822) from Dehra Dun (Uttarakhand) and Jamshedpur (Jharkhand), India. Int. J. Agric. Appl. Sci. 2021;2:145–150. doi: 10.52804/ijaas2021.2222. DOI

Baghele M., Mishra S., Meyer-Rochow V.B., Jung C., Ghosh S. Utilization of snails as food and therapeutic agents by Baiga tribals of Baihar tehsil of Balaghat District, Madhya Pradesh, India. Int. J. Indust. Entomol. 2021;43:78–84.

Dhiman V., Pant D. Human health and snails. J Immunoassay Immunochem. 2021;42:211–235. doi: 10.1080/15321819.2020.1844751. PubMed DOI

Prabhakar A.K., Roy S. Ethno-medicinal uses of some shell fishes by people of Kosi river basin of North-Bihar, India. Stud. Ethno-Med. 2009;3:1–4. doi: 10.1080/09735070.2009.11886329. DOI

Sarkar T., Debnath S., Das B.K., Das M. Edible fresh water molluscs diversity in the different water bodies of Gangarampur Block, Dakshin Dinajpur, West Bengal. Eco. Env. Cons. 2021;27:S293–S296.

Baby R.L., Hasan I., Kabir K.A., Naser M.N. Nutrient analysis of some commercially important molluscs of Bangladesh. J. Sci. Res. 2010;2:390–396. doi: 10.3329/jsr.v2i2.3362. DOI

Rabha H.P., Mazumdar M., Baruah U.K. Indigenous technical knowledge on ethnic dishes of snail in Goalpara district of India. Sch. Acad. J. Biosci. 2014;2:307–317.

Borkakati R.N., Gogoi R., Borah B.K. Snail: From present perspective to the history of Assam. Asian Agrihist. 2009;13:227–234.

Ghosh S., Jung C., Meyer-Rochow V.B. Snail farming: An Indian perspective of a potential tool for food security. Ann. Aquac. Res. 2016;3:1024.

Bagde N., Jain S. Study of traditional man-animal relationship in Chhindwara district of Madhya Pradesh, India. J. Glob. Biosci. 2015;4:1456–1463.

Tsai H.-C., Lin H.-H., Wann S.-R., Liu Y.-C., Huang C.-K., Lai P.-H., Yen M.-Y., Kunin C.M., Ger L.-P., Lee S.S.-J., et al. Eosinophilic meningitis caused by Angiostrongylus cantonensis associated with eating raw snails: Correlation of brain magneticresonance imaging scans with clinical findings. Am. J. Trop. Med. Hyg. 2003;68:281–285. doi: 10.4269/ajtmh.2003.68.281. PubMed DOI

Alicata J.E. Effect of freezing and boiling on the infectivity of third-stage larvae of Angiostrongylus cantonensis present in and snails and freshwater prawns. J. Parasitol. 1967;53:1064. doi: 10.2307/3276839. PubMed DOI

Crook J.R., Fulton S.E., Supanwong K. The infectivity of third stage Angiostrongylus cantonensis larvae shed from drowned Achatina fulica snails and the effect of chemical agents on infectivity. Trans. R. Soc. Trop. Med. Hyg. 1971;65:602–605. doi: 10.1016/0035-9203(71)90043-5. PubMed DOI

Prasad S., Kumar M.U., Kumari A. Freshwater shellfish, Pila globosa (Gastropoda) favourable endeavour for rural nutrition. Agric. Lett. 2021;2:32–35.

Radomyos P., Tungtrongchitr A., Praewanich R. Experimental infection of yellow tree monitor (Varanus bengalensis) and related species with Angiostrongylus cantonensis. Southeast Asian J. Trop. Med. Public Health. 1992;23:167–168. PubMed

Böhme W. Checklist of the living monitor lizards of the world (Family Varanidae) Zool. Verh. 2003;341:4–43.

Pianka E., King D. Varanoid Lizards of the World. Indiana University Press; Bloomington, IN, USA: 2004.

Aengals R., Kumar V.S., Palot M.J., Ganesh S.R. A Checklist of Reptiles of India. Zoological Survey of India; Kolkata, India: 2018. p. 35.

Auffenberg W., Rahman H., Iffat F., Perveen Z. A study of Varanus flavescens (Hardwicke & Gray) (Sauria: Varanidae) J. Bombay Nat. Hist. Soc. 1989;86:286–307.

Wikramanayake E.D., Dryden G.L. Thermal ecology of habitat and microhabitat use by sympatric Varanus bengalensis and V. salvator in Sri Lanka. Copeia. 1993:709–714. doi: 10.2307/1447231. DOI

Radomyos P., Tungtrongchitr A., Praewanich R., Khewwatchan P., Kantangkul T., Junlananto P., Ayudhya S.I. Occurrence of the infective stage of Angiostrongylus cantonensis in the yellow tree monitor (Varanus bengalensis) in five Provinces of Thailand. Southeast Asian J. Trop. Med. Public Health. 1994;25:498–500. PubMed

Anettová L., Izquierdo-Rodriguez E., Foronda P., Baláž V., Novotný L., Modrý D. Endemic lizard Gallotia galloti is a paratenic host of invasive Angiostrongylus cantonensis in Tenerife, Spain. Parasitology. 2022;149:934–939. doi: 10.1017/S0031182022000336. PubMed DOI PMC

Yang L., Darasavath C., Chang K., Vilay V., Sengduangphachanh A., Adsamouth A., Vongsouvath M., Keolouangkhot V., Robinson M.T. Cluster of angiostrongyliasis cases following consumption of raw monitor lizard in the Lao People’s Democratic Republic and review of the literature. Trop. Med. Infect. Dis. 2021;6:107. doi: 10.3390/tropicalmed6030107. PubMed DOI PMC

Ash L.R. The Occurrence of Angiostrongylus cantonensis in frogs of New Caledonia with observations on paratenic hosts of metastrongyles. J. Parasitol. 1968;54:432. doi: 10.2307/3277060. PubMed DOI

Chellappandian M., Pandikumar P., Mutheeswaran S., Paulraj M.G., Prabakaran S., Duraipandiyan V., Ignacimuthu S., Al-Dhabi N. Documentation and quantitative analysis of local ethnozoological knowledge among traditional healers of Theni district, Tamil Nadu, India. J. Ethnopharmacol. 2014;154:116–130. doi: 10.1016/j.jep.2014.03.028. PubMed DOI

Jugli S., Chakravorty J., Meyer-Rochow V.B. Zootherapeutic uses of animals and their parts: An important element of the traditional knowledge of the Tangsa and Wancho of Eastern Arunachal Pradesh, North-East India. Environ. Dev. Sustain. 2020;22:4699–4734. doi: 10.1007/s10668-019-00404-6. DOI

Chakravorty J., Meyer-Rochow V.B., Ghosh S. Vertebrates used for medicinal purposes by members of the Nyishi and Galo tribes in Arunachal Pradesh (North-East India) J. Ethnobiol. Ethnomed. 2011;7:13. doi: 10.1186/1746-4269-7-13. PubMed DOI PMC

Das K.S., Choudhury S., Nonglait K.C.L. Zootherapy among the ethnic groups of north eastern region of india-a critical review. J. Crit. Rev. 2017;4:1–9. doi: 10.22159/jcr.2017v4i2.14698. DOI

Mahawar M.M., Jaroli D.P. Animals and their products utilized as medicines by the inhabitants surrounding the Ranthambhore National Park, India. J. Ethnobiol. Ethnomed. 2006;2:46. doi: 10.1186/1746-4269-2-46. PubMed DOI PMC

Verma A.K., Prasad S.B., Rongpi T., Arjun J. Traditional healing with animals (zootherapy) by the major ethnic group of Karbi Anglong district of Assam, India. Int. J. Pharm. Pharm. Sci. 2014;6:593–600.

Borah M.P., Prasad S.B. Ethnozoological study of animals based medicine used by traditional healers and indigenous inhabitants in the adjoining areas of Gibbon Wildlife Sanctuary, Assam, India. J. Ethnobiol. Ethnomed. 2017;13:39. doi: 10.1186/s13002-017-0167-6. PubMed DOI PMC

Betlu A.L.S. Indigenous knowledge of zootherapeutic use among the Biate tribe of Dima Hasao District, Assam, Northeastern India. J. Ethnobiol. Ethnomed. 2013;9:56. doi: 10.1186/1746-4269-9-56. PubMed DOI PMC

Oku Y., Katakura K., Kamiya M. Tadpole of the clawed frog, Xenopus Laevis, as an experimental intermediate host of Angiostrongylus cantonensis. Am. J. Trop. Med. Hyg. 1980;29:316–318. doi: 10.4269/ajtmh.1980.29.316. PubMed DOI

Niebuhr C.N., Jarvi S.I., Kaluna L., Fischer B.L.T., Deane A.R., Leinbach I.L., Siers S.R. Occurrence of rat lungworm (Angiostrongylus cantonensis) in invasive coqui frogs (Eleutherodactylus coqui) and other hosts in Hawaii, USA. J. Wildl. Dis. 2020;56:203. doi: 10.7589/2018-12-294. PubMed DOI

Asato R., Sato Y., Otsuru M. The occurrence of Angiostrongylus cantonensis in toads and frogs in Okinawa Prefecture, Japan. Jpn J. Parasitol. 1978;27:1–8.

Mahawar M.M., Jaroli D. Traditional zootherapeutic studies in India: A review. J. Ethnobiol. Ethnomed. 2008;4:17. doi: 10.1186/1746-4269-4-17. PubMed DOI PMC

Shah K.B., Gire M.K. Some Amphibians and Their Local Uses in Arun Basin. J. Nat. Hist. Museum. 1992;13:9–17.

Pradhan S., Mishra D., Sahu K.R. Herpetofauna used as traditional medicine by tribes of Gandhamardan Hills Range, Western Orissa, India. Int. J. Res. Zool. 2014;4:32–35.

Pandian T.J., Marian M.P. Production and utilization of frogs: An ecological view. Proc. Anim. Sci. 1986;95:289–301. doi: 10.1007/BF03179365. DOI

Kawlni L., Lalronunga S., Manral U., Das A. Uchang-Sa: A report on frog consumption around Dampa Tiger Reserve, Mizoram, Northeast India. Hamadryad. 2022;39:30–36.

Talukdar S., Sengupta S. Edible frog species of Nagaland. J. Environ. Biol. 2020;41:927–930. doi: 10.22438/jeb/4(SI)/MS_1918. DOI

Talukdar S., Sengupta S., Konyak M., Rizwan M. Cooking methods and medicinal uses of frog species among the Naga tribes in Dimapur. World News Nat. Sci. 2020;30:144–149.

Thomas A., Biju S.D. Tadpole consumption is a direct threat to the endangered purple frog, Nasikabatrachus Sahyadrensis. Salamandra. 2015;51:252–258.

Yong H.-S., Eamsobhana P., Song S.-L., Prasartvit A., Lim P.-E. Molecular phylogeography of Angiostrongylus cantonensis (Nematoda: Angiostrongylidae) and genetic relationships with congeners using cytochrome b gene marker. Acta Trop. 2015;148:66–71. doi: 10.1016/j.actatropica.2015.04.020. PubMed DOI

Yong H.-S., Song S.-L., Eamsobhana P., Goh S.-Y., Lim P.-E. Complete mitochondrial genome reveals genetic diversity of Angiostrongylus cantonensis (Nematoda: Angiostrongylidae) Acta Trop. 2015;152:157–164. doi: 10.1016/j.actatropica.2015.09.001. PubMed DOI

Vitta A., Srisongcram N., Thiproaj J., Wongma A., Polsut W., Fukruksa C., Yimthin T., Mangkit B., Thanwisai A., Dekumyoy P. Phylogeny of Angiostrongylus cantonensis in Thailand based on cytochrome c oxidase subunit I gene sequence. Southeast Asian J. Trop. Med. Public Health. 2016;47:377–386. PubMed

Dumidae A., Subkrasae C., Ardpairin J., Thanwisai A., Vitta A. Genetic analysis of a 66-kDa protein-encoding gene of Angiostrongylus cantonensis and Angiostrongylus malaysiensis. Parasitology. 2023;150:98–114. doi: 10.1017/S0031182022001573. PubMed DOI PMC

Rodpai R., Intapan P.M., Thanchomnang T., Sanpool O., Sadaow L., Laymanivong S., Aung W.P., Phosuk I., Laummaunwai P., Maleewong W. Angiostrongylus cantonensis and A. malaysiensis broadly overlap in Thailand, Lao PDR, Cambodia and Myanmar: A molecular survey of larvae in land snails. PLoS ONE. 2016;11:e0161128. doi: 10.1371/journal.pone.0161128. PubMed DOI PMC

Chan A.H.E., Chaisiri K., Dusitsittipon S., Jakkul W., Charoennitiwat V., Komalamisra C., Thaenkham U. Mitochondrial ribosomal genes as novel genetic markers for discrimination of closely related species in the Angiostrongylus cantonensis lineage. Acta Trop. 2020;211:105645. doi: 10.1016/j.actatropica.2020.105645. PubMed DOI

Eamsobhana P., Lim P., Yong H. Phylogenetics and systematics of Angiostrongylus lungworms and related taxa (Nematoda: Metastrongyloidea) inferred from the nuclear small subunit (SSU) ribosomal DNA sequences. J. Helminthol. 2014;89:317–325. doi: 10.1017/S0022149X14000108. PubMed DOI

Eamsobhana P., Song S.-L., Yong H.-S., Prasartvit A., Boonyong S., Tungtrongchitr A. Cytochrome c oxidase subunit I haplotype diversity of Angiostrongylus cantonensis (Nematoda: Angiostrongylidae) Acta Trop. 2017;171:141–145. doi: 10.1016/j.actatropica.2017.03.020. PubMed DOI

Eamsobhana P., Yong H.-S., Song S.-L., Gan X.-X., Prasartvit A., Tungtrongchitr A. Molecular phylogeography and genetic diversity of Angiostrongylus cantonensis and A. malaysiensis (Nematoda: Angiostrongylidae) based on 66-kDa protein gene. Parasitol. Int. 2019;68:24–30. doi: 10.1016/j.parint.2018.09.006. PubMed DOI

Mishra N., Panda T. Zootherapeutical Uses of Animal Diversity in Coastal District of Orissa, India. Br. J. Pharmacol. Toxicol. 2011;2:154–158.

Joshi N., Pandey S. Meat Demand-Snailed It: A Comprehensive Review on Snail Rearing, to Meet the Meat Demand in Future India. J. Entomol. Zool. Stud. 2019;7:396–400.

MESHRAM L., HUSAIN N. Use of Animals as Traditional Medicine in Chhattisgarh, India. Indian J. Sci. Res. 2017;12:26–29.

Raja L., Matheswaran P., Anbalagan M., Sureshkumar V., Ganesan D., Gani S.B. Ethnozoological Study of Animal-Based Products Practices among the Tribal Inhabitants in Kolli Hills Namakkal District, Tamil Nadu, India. World J. Pharm. Pharm. Sci. 2018;7:785–797.

Debnath C., Sahoo L., Haldar A., Datta M., Yadav G.S., Singha A., Bhattacharjee J. Proximate and Mineral Composition of Freshwater Snails of Tripura, North-East India. Fish. Technol. 2016;53:307–312.

Chinlampianga M., Singh R.K., Shukla A.C. Ethnozoological Diversity of Northeast India: Empirical Learning with Traditional Knowledge Holders of Mizoram and Arunachal Pradesh. NISCAIR-CSIR; Delhi, India: 2013.

Singh R.K., Kumar A., Singh A., Singhal P. Evidence That Cultural Food Practices of Adi Women in Arunachal Pradesh, India, Improve Social-Ecological Resilience: Insights for Sustainable Development Goals. Ecol. Process. 2020;9:1–19. doi: 10.1186/s13717-020-00232-x. DOI

Jadhav A., Das N.K., Aravind N.A. Edible Freshwater Molluscs from Northeast India. Tentacle. 2020;28:1–4.

Bhattacharya S., Chakraborty M., Bose M., Mukherjee D., Roychoudhury A., Dhar P., Mishra R. Indian Freshwater Edible Snail Bellamya Bengalensis Lipid Extract Prevents T Cell Mediated Hypersensitivity and Inhibits LPS Induced Macrophage Activation. J. Ethnopharmacol. 2014;157:320–329. doi: 10.1016/j.jep.2014.09.009. PubMed DOI

Gomes A., Sarkar A., Ghosh S., Saha K., Saha P.P. Edible Fresh Water Snail Viviparous Bengalensis Purified Flesh Protein VB-P4 Induced Toxicities and Its Protection by Heat Treatment. J. Toxins. 2015;2:3.

Dhakal P., Chettri B., Lepcha S., Acharya B.K. Rich yet Undocumented Ethnozoological Practices of Socio-Culturally Diverse Indigenous Communities of Sikkim Himalaya, India. J. Ethnopharmacol. 2020;249:112386. doi: 10.1016/j.jep.2019.112386. PubMed DOI

Patel R., Pal M.C. Exploring Ethnozoological Observations Among The Tribal Inhabitants In ‘Bajag’ Forest Range Of Dindori District Of Central India. Int. J. Aquat. Sci. 2021;12:4513–4538.

Vyas N., Mahawar M.M., Jaroli D.P. Traditional Medicines Derived from Domestic Animals Used by Rebari Community of Rajasthan, India. Nature. 1970;7:129–138. doi: 10.3126/on.v7i1.2560. DOI

Solavan A., Paulmurugan R., Wilsanand V., Sing A.J. Traditional Therapeutic Uses of Animals among Tribal Population of Tamil Nadu. CSIR; Lucknow, India: 2004.

Haq S.M., Calixto E.S., Yaqoob U., Ahmed R., Mahmoud A.H., Bussmann R.W., Mohammed O.B., Ahmad K., Abbasi A.M. Traditional Usage of Wild Fauna among the Local Inhabitants of Ladakh, Trans-Himalayan Region. Animals. 2020;10:2317. doi: 10.3390/ani10122317. PubMed DOI PMC

Imkongwapang R., Jyrwa D.B., Lal P., Tandon V. A Checklist of Helminth Parasite Fauna in Anuran Amphibia (Frogs) of Nagaland, Northeast India. J. Parasit. Dis. 2014;38:85–100. doi: 10.1007/s12639-012-0180-6. PubMed DOI PMC

Hassan M., Haq S.M., Amjad M.S., Ahmad R., Bussmann R.W., de la Lastra J.M.P. Invertebrates and Herptiles for Livelihoods—Ethnozoological Use among Different Ethnic Communities in Jammu and Kashmir (Indian Himalayas) Front. Pharmacol. 2023;13:1043155. doi: 10.3389/fphar.2022.1043155. PubMed DOI PMC

Narzary J., Bordoloi S. Ethnozoological Practices on Frogs of Bodo Tribe from Kokrajhar District, Assam, India. Am. J. Ethnomedicine. 2014;1:368–370.

Vijayakumar S., Yabesh J.E.M., Prabhu S., Ayyanar M., Damodaran R. Ethnozoological Study of Animals Used by Traditional Healers in Silent Valley of Kerala, India. J. Ethnopharmacol. 2015;162:296–305. doi: 10.1016/j.jep.2014.12.055. PubMed DOI

Joseph J., Sreeedharan S., George S., Antony M.M. The Complete Mitochondrial Genome of an Endemic Cichlid Etroplus Canarensis from Western Ghats, India (Perciformes: Cichlidae) and Molecular Phylogenetic Analysis. Mol. Biol. Rep. 2022;49:3033–3044. doi: 10.1007/s11033-022-07130-9. PubMed DOI

Esakkimuthu S., Sylvester Darvin S., Mutheeswaran S., Gabriel Paulraj M., Pandikumar P., Ignacimuthu S., Al-Dhabi N.A. A Study on Food-Medicine Continuum among the Non-Institutionally Trained Siddha Practitioners of Tiruvallur District, Tamil Nadu, India. J. Ethnobiol. Ethnomed. 2018;14:45. doi: 10.1186/s13002-018-0240-9. PubMed DOI PMC

Kumar Kiran S., Anoop V.S., Sivakumar K.C., Dinesh R., Mano J.P., Kaushik D., Sanil G. An Additional Record of Fejervarya Manoharani Garg and Biju from the Western Ghats with a Description of Its Complete Mitochondrial Genome. Zootaxa. 2017;4277:491–502. doi: 10.11646/zootaxa.4277.4.2. PubMed DOI

Anoop V.S., George S. Population Genetic Structure and Evolutionary Demographic Patterns of Phrynoderma Karaavali, an Edible Frog Species of Kerala, India. J. Genet. 2023;102:8. doi: 10.1007/s12041-022-01407-5. PubMed DOI

Chettri B., Bhupathy S., Acharya B.K. Biodiversity of Sikkim: Exploring and Conserving a Global Hotspot. Information and Public Relations Department, Government of Sikkim; Gangtok, India: 2011. An Overview of the Herpetofauna of Sikkim with Emphasis on the Elevational Distribution Pattern and Threats and Conservation Issues; pp. 233–254.

Jaroli D.P., Mahawar M.M., Vyas N. An Ethnozoological Study in the Adjoining Areas of Mount Abu Wildlife Sanctuary, India. J. Ethnobiol. Ethnomed. 2010;6:6. doi: 10.1186/1746-4269-6-6. PubMed DOI PMC

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...