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
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
ID2017010092
"Proyectos I + D de la Consejeria de Economía, Industria, Comercio y Conocimiento de la Comunidad Autónoma de Canarias" and FEDER 2014-2020
RD16/0027/0001
Red de Investigación de Centros de Enfermedades Tropicales-RICET, ISCIIISubdirección General de Redes y Centros de Investigación Cooperativa RETICS, Ministry of Health and Consumption, Spain
CZ02.2.69/0.0/0.0/16_027/0008027
International Collaboration in ecological and evolutionary biology of vertebrates
123/2018/FVL
Internal Grant agency of UVPS
CEITEC 2020 (LQ1601)
Ministerstvo Školství, Mládeže a Tělovýchovy
PubMed
31097040
PubMed Central
PMC6524341
DOI
10.1186/s13071-019-3491-y
PII: 10.1186/s13071-019-3491-y
Knihovny.cz E-zdroje
- Klíčová slova
- Genetic diversity, Invasive species, Mitochondrial genome, Next-generation sequencing, Rat lungworm, Rattus, cox1,
- MeSH
- Angiostrongylus cantonensis genetika MeSH
- cyklooxygenasa 1 genetika MeSH
- fylogeneze MeSH
- genetická variace * MeSH
- genom mitochondriální * MeSH
- genom u helmintů MeSH
- infekce hlísticemi řádu Strongylida parazitologie MeSH
- krysa rodu Rattus MeSH
- mitochondriální DNA * MeSH
- sekvenční analýza DNA MeSH
- sekvenování celého genomu MeSH
- vysoce účinné nukleotidové sekvenování MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Austrálie MeSH
- Havajské ostrovy MeSH
- Polynésie MeSH
- Španělsko MeSH
- Názvy látek
- cyklooxygenasa 1 MeSH
- mitochondriální DNA * MeSH
BACKGROUND: Rats (Rattus spp.) invaded most of the world as stowaways including some that carried the rat lungworm, Angiostrongylus cantonensis, the cause of eosinophilic meningoencephalitis in humans and other warm-blooded animals. A high genetic diversity of A. cantonensis based on short mitochondrial DNA regions is reported from Southeast Asia. However, the identity of invasive A. cantonensis is known for only a minority of countries. The affordability of next-generation sequencing for characterisation of A. cantonensis genomes should enable new insights into rat lung worm invasion and parasite identification in experimental studies. METHODS: Genomic DNA from morphologically verified A. cantonensis (two laboratory-maintained strains and two field isolates) was sequenced using low coverage whole genome sequencing. The complete mitochondrial genome was assembled and compared to published A. cantonensis and Angiostrongylus malaysiensis sequences. To determine if the commonly sequenced partial cox1 can unequivocally identify A. cantonensis genetic lineages, the diversity of cox1 was re-evaluated in the context of the publicly available cox1 sequences and the entire mitochondrial genomes. Published experimental studies available in Web of Science were systematically reviewed to reveal published identities of A. cantonensis used in experimental studies. RESULTS: New A. cantonensis mitochondrial genomes from Sydney (Australia), Hawaii (USA), Canary Islands (Spain) and Fatu Hiva (French Polynesia), were assembled from next-generation sequencing data. Comparison of A. cantonensis mitochondrial genomes from outside of Southeast Asia showed low genetic diversity (0.02-1.03%) within a single lineage of A. cantonensis. Both cox1 and cox2 were considered the preferred markers for A. cantonensis haplotype identification. Systematic review revealed that unequivocal A. cantonensis identification of strains used in experimental studies is hindered by absence of their genetic and geographical identity. CONCLUSIONS: Low coverage whole genome sequencing provides data enabling standardised identification of A. cantonensis laboratory strains and field isolates. The phenotype of invasive A. cantonensis, such as the capacity to establish in new territories, has a strong genetic component, as the A. cantonensis found outside of the original endemic area are genetically uniform. It is imperative that the genotype of A. cantonensis strains maintained in laboratories and used in experimental studies is unequivocally characterised.
Centre for Veterinary Education University of Sydney Sydney NSW 2006 Australia
Institute of Vertebrate Biology Czech Academy of Sciences Květná 8 603 65 Brno Czech Republic
Manaaki Whenua Landcare Research PO Box 69040 Lincoln 7608 New Zealand
Sydney School of Veterinary Science University of Sydney Sydney NSW 2006 Australia
USDA APHIS WS National Wildlife Research Center Hawaii Field Station PO Box 10880 Hilo HI 96721 USA
Westmead Clinical School University of Sydney Sydney NSW 2145 Australia
Zobrazit více v PubMed
Pysek P, Richardson DM. Invasive species, environmental change and management, and health. Annu Rev Env Resour. 2010;35:25–55. doi: 10.1146/annurev-environ-033009-095548. DOI
Simberloff D, Martin JL, Genovesi P, Maris V, Wardle DA, Aronson J, et al. Impacts of biological invasions: whatʼs what and the way forward. Trends Ecol Evol. 2013;28:58–66. doi: 10.1016/j.tree.2012.07.013. PubMed DOI
Hulme PE. Trade, transport and trouble: managing invasive species pathways in an era of globalization. J Appl Ecol. 2009;46:10–18. doi: 10.1111/j.1365-2664.2008.01600.x. DOI
Pejchar L, Mooney HA. Invasive species, ecosystem services and human well-being. Trends Ecol Evol. 2009;24:497–504. doi: 10.1016/j.tree.2009.03.016. PubMed DOI
Hoberg EP. Invasive processes, mosaics and the structure of helminth parasite faunas. Rev Sci Tech. 2010;29:255–272. doi: 10.20506/rst.29.2.1972. PubMed DOI
Ehrenfeld JG. Ecosystem consequences of biological invasions. Annu Rev Ecol Evol S. 2010;41:59–80. doi: 10.1146/annurev-ecolsys-102209-144650. DOI
Audoin-Rouzeau F, Vigne J-D. La colonisation de l’Europe par le rat noir (Rattus rattus) Rev Paléobiol. 1994;13:125–145.
Morand S, Bordes F, Chen HW, Claude J, Cosson JF, Galan M, et al. Global parasite and Rattus rodent invasions: the consequences for rodent-borne diseases. Integr Zool. 2015;10:409–423. doi: 10.1111/1749-4877.12143. PubMed DOI
Kosoy M, Khlyap L, Cosson JF, Morand S. Aboriginal and invasive rats of genus Rattus as hosts of infectious agents. Vector-Borne Zoonotic Dis. 2015;15:3–12. doi: 10.1089/vbz.2014.1629. PubMed DOI
Barratt J, Chan D, Sandaradura I, Malik R, Spielman D, Lee R, et al. 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
Rosen L, Chappell R, Laqueur GL, Wallace GD, Weinstein PP. Eosinophilic meningoencephalitis caused by a metastrongylid lung-worm of rats. JAMA. 1962;179:620–624. doi: 10.1001/jama.1962.03050080032007. PubMed DOI
Rosen L, Laigret J, Bories S. Observations on an outbreak of eosinophilic meningitis on Tahiti, French Polynesia. Am J Hyg. 1961;74:26–42. PubMed
Chen HT. Un noveau nématode pulmonaire, Pulmonema cantonensis n.g., n.sp. des rats de Canton. Ann Parasitol Hum Comp. 1935;13:312–317. doi: 10.1051/parasite/1935134312. DOI
Beaver PC, 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
Bhaibulaya M. Comparative studies on the life history of Angiostrongylus mackerrasae Bhaibulaya, 1968 and Angiostrongylus cantonensis (Chen, 1935) Int J Parasitol. 1975;5:7–20. doi: 10.1016/0020-7519(75)90091-0. PubMed DOI
Wallace GD, Rosen L. Studies on eosinophilic meningitis. II. Experimental infection of shrimp and crabs with Angiostrongylus cantonensis. Am J Epidemiol. 1966;84:120–131. doi: 10.1093/oxfordjournals.aje.a120617. PubMed DOI
Kim JR, Hayes KA, Yeung NW, Cowie RH. 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
Lunn JA, Lee R, Smaller J, MacKay BM, King T, Hunt GB, et al. Twenty two cases of canine neural angiostronglyosis in eastern Australia (2002–2005) and a review of the literature. Parasit Vectors. 2012;5:70. doi: 10.1186/1756-3305-5-70. PubMed DOI PMC
Ma GM, Dennis M, Rose K, Spratt D, Spielman D. Tawny frogmouths and brushtail possums as sentinels for Angiostrongylus cantonensis, the rat lungworm. Vet Parasitol. 2013;192:158–165. doi: 10.1016/j.vetpar.2012.11.009. PubMed DOI
Walker AG, Spielman D, Malik R, Graham K, Ralph E, Linton M, et al. Canine neural angiostrongylosis: a case-control study in Sydney dogs. Aust Vet J. 2015;93:195–199. doi: 10.1111/avj.12332. PubMed DOI
Alicata JE. 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
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
Wallace GD, 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
Foronda P, Lopez-Gonzalez M, Miquel J, Torres J, Segovia M, Abreu-Acosta N, 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
Mugisha L, Bwangamoi O, Cranfield MR. Angiostrongylus cantonensis and other parasites infections of rodents of Budongo Forest Reserve, Uganda. AJABS. 2012;7:91–95.
York EM, Creecy JP, Lord WD, Caire W. Geographic range expansion for the rat lungworm in North America. Emerg Infect Dis. 2015;21:1234–1236. doi: 10.3201/eid2107.141980. PubMed DOI PMC
Dusitsittipon S, Criscione CD, Morand S, Komalamisra C, Thaenkham U. Cryptic lineage diversity in the zoonotic pathogen Angiostrongylus cantonensis. Mol Phylogenet Evol. 2017;107:404–414. doi: 10.1016/j.ympev.2016.12.002. PubMed DOI
Dusitsittipon S, Thaenkham U, Watthanakulpanich D, Adisakwattana P, Komalamisra C. Genetic differences in the rat lungworm, Angiostrongylus cantonensis (Nematoda: Angiostrongylidae), in Thailand. J Helminthol. 2015;89:545–551. doi: 10.1017/S0022149X14000388. PubMed DOI
Eamsobhana P, Lim PE, Solano G, Zhang HM, Gan XX, Sen Yong H. Molecular differentiation of Angiostrongylus taxa (Nematoda: Angiostrongylidae) by cytochrome c oxidase subunit I (COI) gene sequences. Acta Trop. 2010;116:152–156. doi: 10.1016/j.actatropica.2010.07.005. PubMed DOI
Eamsobhana P, Song SL, Yong HS, 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
Lv S, Guo YH, Nguyen HM, Sinuon M, Sayasone S, Lo NC, et al. Invasive Pomacea snails as important intermediate hosts of Angiostrongylus cantonensis in Laos, Cambodia and Vietnam: Implications for outbreaks of eosinophilic meningitis. Acta Trop. 2018;183:32–35. doi: 10.1016/j.actatropica.2018.03.021. PubMed DOI
Rodpai R, Intapan PM, Thanchomnang T, Sanpool O, Sadaow L, Laymanivong S, et al. 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
Tokiwa T, Harunari T, Tanikawa T, Komatsu N, Koizumi N, Tung KC, et al. Phylogenetic relationships of rat lungworm, Angiostrongylus cantonensis, isolated from different geographical regions revealed widespread multiple lineages. Parasitol Int. 2012;61:431–436. doi: 10.1016/j.parint.2012.02.005. PubMed DOI
Vitta A, Srisongcram N, Thiproaj J, Wongma A, Polsut W, Fukruksa C, et al. 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
Yong HS, Eamsobhana P, Song SL, Prasartvit A, Lim PE. 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
Dusitsittipon S, Criscione CD, Morand S, Komalamisra C, Thaenkham U. Hurdles in the evolutionary epidemiology of Angiostrongylus cantonensis: pseudogenes, incongruence between taxonomy and DNA sequence variants, and cryptic lineages. Evol Appl. 2018;11:1257–1269. doi: 10.1111/eva.12621. PubMed DOI PMC
Dalton MF, Fenton H, Cleveland CA, Elsmo EJ, Yabsley MJ. Eosinophilic meningoencephalitis associated with rat lungworm (Angiostrongylus cantonensis) migration in two nine-banded armadillos (Dasypus novemcinctus) and an opossum (Didelphis virginiana) in the southeastern United States. Int J Parasitol Parasites Wildl. 2017;6:131–134. doi: 10.1016/j.ijppaw.2017.05.004. PubMed DOI PMC
Monte TCC, Simoes RO, Oliveira APM, Novaes CF, Thiengo SC, Silva AJ, et al. Phylogenetic relationship of the Brazilian isolates of the rat lungworm Angiostrongylus cantonensis (Nematoda: Metastrongylidae) employing mitochondrial COI gene sequence data. Parasit Vectors. 2012;5:248. doi: 10.1186/1756-3305-5-248. PubMed DOI PMC
Moreira VLC, Giese EG, Melo FTV, Simoes RO, Thiengo SC, Maldonado A, et al. Endemic angiostrongyliasis in the Brazilian Amazon: natural parasitism of Angiostrongylus cantonensis in Rattus rattus and R. norvegicus, and sympatric giant African land snails, Achatina fulica. Acta Trop. 2013;125:90–97. doi: 10.1016/j.actatropica.2012.10.001. PubMed DOI
Simões RO, Monteiro FA, Sanchez E, Thiengo SC, Garcia JS, Costa-Neto SF, et al. Endemic angiostrongyliasis, Rio de Janeiro, Brazil. Emerg Infect Dis. 2011;17:1331–1333. doi: 10.3201/eid1707.101822. PubMed DOI PMC
Monte TC, Gentile R, Garcia J, Mota E, Santos JN, Maldonado A. Brazilian Angiostrongylus cantonensis haplotypes, ac8 and ac9, have two different biological and morphological profiles. Mem Inst Oswaldo Cruz. 2014;109:1057–1063. doi: 10.1590/0074-0276130378. PubMed DOI PMC
Bhaibulaya M. A new species of Angiostrongylus in an Australian rat Rattus fuscipes. Parasitology. 1968;58:789–799. doi: 10.1017/S0031182000069572. DOI
Lv S, Zhang Y, Zhang L, Liu Q, Liu HX, Hu L, et al. The complete mitochondrial genome of the rodent intra-arterial nematodes Angiostrongylus cantonensis and Angiostrongylus costaricensis. Parasitol Res. 2012;111:115–123. doi: 10.1007/s00436-011-2807-4. PubMed DOI
Yong HS, Song SL, Eamsobhana P, Lim PE. Complete mitochondrial genome of Angiostrongylus malaysiensis lungworm and molecular phylogeny of metastrongyloid nematodes. Acta Trop. 2016;161:33–40. doi: 10.1016/j.actatropica.2016.05.002. PubMed DOI
Mackerras MJ, Sandars DF. The life history of the rat lung-worm, Angiostrongylus cantonensis (Chen) (Nematoda: Metastrongylidae) Aust J Zool. 1955;3:1–25. doi: 10.1071/ZO9550001. DOI
Prociv P, Carlisle MS. The spread of Angiostrongylus cantonensis in Australia. Southeast Asian J Trop Med Public Health. 2001;32:126–128. PubMed
Verneau O, Catzeflis F, Furano AV. Determining and dating recent rodent speciation events by using L1 (LINE-1) retrotransposons. Proc Natl Acad Sci USA. 1998;95:11284–11289. doi: 10.1073/pnas.95.19.11284. PubMed DOI PMC
Maldonado Junior A, Zeitone BK, Amado LA, Rosa IF, Machado-Silva JR, Lanfredi RM. Biological variation between two Brazilian geographical isolates of Echinostoma paraensei. J Helminthol. 2005;79:345–351. doi: 10.1079/JOH2005293. PubMed DOI
Gharamah AA, Rahman WA, Azizah MNS. Morphological variation between isolates of the nematode Haemonchus contortus from sheep and goat populations in Malaysia and Yemen. J Helminthol. 2014;88:82–88. doi: 10.1017/S0022149X12000776. PubMed DOI
Lee JD, Chung LY, Wang LC, Lin RJ, Wang JJ, Tu HP, et al. Sequence analysis in partial genes of five isolates of Angiostrongylus cantonensis from Taiwan and biological comparison in infectivity pathogenicity between two strains. Acta Trop. 2014;133:26–34. doi: 10.1016/j.actatropica.2014.01.010. PubMed DOI
Yong HS, Eamsobhana P, Lim PE, Razali R, Aziz FA, Rosli NSM, et al. Draft genome of neurotropic nematode parasite Angiostrongylus cantonensis, causative agent of human eosinophilic meningitis. Acta Trop. 2015;148:51–57. doi: 10.1016/j.actatropica.2015.04.012. PubMed DOI
Bhaibulaya M, Cross JH. Angiostrongylus malaysiensis (Nematoda: Metastrongylidae), a new species of rat lung-worm from Malaysia. Southeast Asian J Trop Med Public Health. 1971;2:527–533. PubMed
Yokogawa S. A new species of nematode found in the lungs of rats Haemostrongylus ratti sp. nov. Trans Nat Hist Soc Formosa. 1937;27:247–250.
Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol. 1994;3:294–299. PubMed
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990;215:403–410. doi: 10.1016/S0022-2836(05)80360-2. PubMed DOI
Hahn C, Bachmann L, Chevreux B. Reconstructing mitochondrial genomes directly from genomic next-generation sequencing reads-a baiting and iterative mapping approach. Nucl Acids Res. 2013;41:e129. doi: 10.1093/nar/gkt371. PubMed DOI PMC
Bernt M, Donath A, Juhling F, Externbrink F, Florentz C, Fritzsch G, et al. MITOS: improved de novo metazoan mitochondrial genome annotation. Mol Phylogenet Evol. 2013;69:313–319. doi: 10.1016/j.ympev.2012.08.023. PubMed DOI
Kumar S, Stecher G, Li M, Knyaz C, Tamura K. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol. 2018;35:1547–1549. doi: 10.1093/molbev/msy096. PubMed DOI PMC
Nei M, Kumar S. Molecular evolution and phylogenetics. New York: Oxford University Press; 2000.
Tamura K, Nei M. Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol. 1993;10:512–526. PubMed
Jones DT, Taylor WR, Thornton JM. The rapid generation of mutation data matrices from protein sequences. Comput Appl Biosci. 1992;8:275–282. PubMed
Release of Angiostrongylus cantonensis larvae from live intermediate hosts under stress
Angiostrongylosis in Animals and Humans in Europe
Pathology of Angiostrongylus cantonensis infection in two model avian hosts