Gastropod-Borne Helminths: A Look at the Snail–Parasite Interplay

Trends in Parasitology - Tập 32 - Trang 255-264 - 2016
Alessio Giannelli1, Cinzia Cantacessi2, Vito Colella1, Filipe Dantas-Torres1,3, Domenico Otranto1
1Dipartimento di Medicina Veterinaria, Università degli Studi di Bari, Valenzano 70010, Italy
2Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK
3Departamento de Imunologia, Centro de Pesquisas Aggeu Magalhães (Fiocruz-PE), Recife, Pernambuco, Brazil

Tài liệu tham khảo

Bouchet, 2005, Classification and nomenclator of gastropod families, Malacologia, 47, 1 Adema, 2012, Will all scientists working on snails and the diseases they transmit please stand up?, PLoS Negl. Trop. Dis., 6, e1835, 10.1371/journal.pntd.0001835 Kim, 2014, Diverse gastropod hosts of Angiostrongylus cantonensis, the rat lungworm, globally and with a focus on the Hawaiian Islands, PLoS ONE, 9, e94969, 10.1371/journal.pone.0094969 Kostadinova, 2014, Systematics of the Trematoda in digenetic trematodes, Vol. 766, 21 Grewal, 2003, Parasitism of molluscs by nematodes: types of associations and evolutionary trends, J. Nematol., 35, 146 2015 Knubben-Schweizer, 2015, Bovine fasciolosis: control strategies based on the location of Galba truncatula habitats on farms, Vet. Parasitol., 208, 77, 10.1016/j.vetpar.2014.12.019 Morgan, 2012, Parasite epidemiology in a changing world: can molecular phylogeography help us tell the wood from the trees?, Parasitology, 139, 1924, 10.1017/S0031182012001060 Beugnet, 2014, Parasites of domestic owned cats in Europe: co-infestations and risk factors, Parasit. Vectors, 7, 291, 10.1186/1756-3305-7-291 Knight, 2014, Schistosomes and snails: a molecular encounter, Front. Genet., 5, 230, 10.3389/fgene.2014.00230 Huang, 2012, Genomics and molecular genetics of Clonorchis sinensis: current status and perspectives, Parasitol. Int., 61, 71, 10.1016/j.parint.2011.06.008 Chen, 2013, Development and evaluation of loop-mediated isothermal amplification (LAMP) for rapid detection of Clonorchis sinensis from its first intermediate hosts, freshwater snails, Parasitology, 140, 1377, 10.1017/S0031182013000498 York, 2014, Global decline in suitable habitat for Angiostrongylus (=Parastrongylus) cantonensis: the role of climate change, PLoS ONE, 9, e103831, 10.1371/journal.pone.0103831 Romero-Alegría, 2014, Angiostrongylus costaricensis: systematic review of case reports, Adv. Infect. Dis., 4, 36, 10.4236/aid.2014.41007 2001 Morley, 2010, Aquatic molluscs as auxiliary hosts for terrestrial nematode parasites: implications for pathogen transmission in a changing climate, Parasitology, 137, 1041, 10.1017/S0031182010000016 Negrão-Corrêa, 2007, Molluscan response to parasite Biomphalaria and Schistosoma mansoni interaction, Invert. S. urviv. J., 4, 101 Coustau, 2015, Advances in gastropod immunity from the study of the interaction between the snail Biomphalaria glabrata and its parasites: a review of research progress over the last decade, Fish Shellfish Immunol., 46, 5, 10.1016/j.fsi.2015.01.036 Gordy, 2015, The role of fibrinogen-related proteins in the gastropod immune response, Fish Shellfish Immunol., 46, 39, 10.1016/j.fsi.2015.03.005 Hotez, 2014, The global burden of disease study 2010: interpretation and implications for the neglected tropical diseases, PLoS Negl. Trop. Dis., 8, e2865, 10.1371/journal.pntd.0002865 Elmorshedy, 2015, Can human schistosomiasis mansoni control be sustained in high-risk transmission foci in Egypt?, Parasit. Vectors, 8, 372, 10.1186/s13071-015-0983-2 He, 2001, Host–parasite relationships of Schistosoma japonicum in mammalian hosts, Trends Parasitol., 17, 320, 10.1016/S1471-4922(01)01904-3 Hotez, 2006, Helminth infections: soil-transmitted helminth infections and schistosomiasis, 467 Gordon, 2012, High prevalence of Schistosoma japonicum infection in Carabao from Samar Province, the Philippines: implications for transmission and control, PLoS Negl. Trop. Dis., 6, e1778, 10.1371/journal.pntd.0001778 Attwood, 2015, Comparative phylogenetic studies on Schistosoma japonicum and its snail intermediate host Oncomelania hupensis: origins, dispersal and coevolution, PLoS Negl. Trop. Dis., 9, e0003935, 10.1371/journal.pntd.0003935 McCreesh, 2013, Challenges in predicting the effects of climate change on Schistosoma mansoni and Schistosoma haematobium transmission potential, Trends Parasitol., 29, 548, 10.1016/j.pt.2013.08.007 Rollinson, 2001, Interactions between intermediate snail hosts of the genus Bulinus and schistosomes of the Schistosoma haematobium group, Parasitology, 123, S245, 10.1017/S0031182001008046 Attwood, 2013, A population growth trend analysis for Neotricula aperta, the snail intermediate host of Schistosoma mekongi, after construction of the Pak-Mun dam, PLoS Negl. Trop. Dis., 7, e2539, 10.1371/journal.pntd.0002539 Fukuhara, 2011, Analysis of the effectiveness of control measures against Schistosoma mekongi using an intra- and inter-village model in Champasak Province Lao PDR, Parasitol. Int., 60, 452, 10.1016/j.parint.2011.07.017 Scholte, 2012, Spatial distribution of Biomphalaria spp., the intermediate host snails of Schistosoma mansoni, in Brazil, Geospat. Health, 6, S95, 10.4081/gh.2012.127 Abou-El-Naga, 2015, Impact of the age of Biomphalaria alexandrina snails on Schistosoma mansoni transmission: modulation of the genetic outcome and the internal defence system of the snail, Mem. Inst. Oswaldo Cruz, 110, 585, 10.1590/0074-02760150016 McCreesh, 2015, Predicting the effects of climate change on Schistosoma mansoni transmission in eastern Africa, Parasit. Vectors, 8, 4, 10.1186/s13071-014-0617-0 Zein-Eddine, 2014, Phylogeny of seven Bulinus species originating from endemic areas in three African countries, in relation to the human blood fluke Schistosoma haematobium, BMC Evol. Biol., 14, 271, 10.1186/s12862-014-0271-3 Jørgensen, 2007, Molecular phylogenetic investigations of Bulinus (Gastropoda: Planorbidae) in Lake Malawi with comments on the topological incongruence between DNA loci, Zoolog. Scripta, 36, 577, 10.1111/j.1463-6409.2007.00298.x Faro, 2013, Biological, biochemical and histopathological features related to parasitic castration of Biomphalaria glabrata infected by Schistosoma mansoni, Exp. Parasitol., 134, 228, 10.1016/j.exppara.2013.03.020 Alberto-Silva, 2015, Changes in the locomotory and reproductive behavior of Biomphalaria glabrata infected with Schistosoma mansoni, Exp. Parasitol., 153, 68, 10.1016/j.exppara.2015.03.004 Brant, 2013, Discovery-based studies of schistosome diversity stimulate new hypotheses about parasite biology, Trends Parasitol., 29, 449, 10.1016/j.pt.2013.06.004 Adema, 2015, Digenean–gastropod host associations inform on aspects of specific immunity in snails, Dev. Comp. Immunol., 48, 275, 10.1016/j.dci.2014.06.014 Negrão-Corrêa, 2012, Interaction of Schistosoma mansoni sporocysts and hemocytes of Biomphalaria, J. Parasitol. Res., 2012, 743920, 10.1155/2012/743920 Sorensen, 2001, Snail–trematode life history interactions: past trends and future directions, Parasitology, 123, S3, 10.1017/S0031182001007843 Lafferty, 2009, Parasitic castration: the evolution and ecology of body snatchers, Trends Parasitol., 25, 564, 10.1016/j.pt.2009.09.003 Théron, 1992, Spatial and energy compromise between host and parasite: the Biomphalaria glabrata–Schistosoma mansoni system, Int. J. Parasitol., 22, 91, 10.1016/0020-7519(92)90084-X de Jong-Brink, 1992, The anti-gonadotropic neuropeptide schistosomin interferes with peripheral and central neuroendocrine mechanisms involved in the regulation of reproduction and growth in the schistosome-infected snail Lymnaea stagnalis, Prog. Brain Res., 92, 385, 10.1016/S0079-6123(08)61191-7 Zhang, 2009, Schistosomin from the snail Biomphalaria glabrata: expression studies suggest no involvement in trematode-mediated castration, Mol. Biochem. Parasitol., 165, 79, 10.1016/j.molbiopara.2009.01.006 Lv, 2009, Invasive snails and an emerging infectious disease: results from the first national survey on Angiostrongylus cantonensis in China, PLoS Negl. Trop. Dis., 3, e368, 10.1371/journal.pntd.0000368 Wang, 2012, Human Angiostrongylus cantonensis: an update, Eur. J. Clin. Microbiol. Infect. Dis., 31, 389, 10.1007/s10096-011-1328-5 Yong, 2015, Molecular phylogeography of Angiostrongylus cantonensis (Nematoda: Angiostrongylidae) and genetic relationships with congeners using cytochrome b gene marker, Acta Trop., 148, 66, 10.1016/j.actatropica.2015.04.020 Graeff-Teixeira, 2009, Update on eosinophilic meningoencephalitis and its clinical relevance, Clin. Microbiol. Rev., 22, 322, 10.1128/CMR.00044-08 Chan, 2015, The prevalence of Angiostrongylus cantonensis/mackerrasae complex in molluscs from the Sydney region, PLoS ONE, 10, e0128128, 10.1371/journal.pone.0128128 Iwanowicz, 2015, Spread of the rat lungworm (Angiostrongylus cantonensis) in giant African land snails (Lissachatina fulica) in Florida, USA, J. Wildl. Dis., 51, 749, 10.7589/2014-06-160 Martin-Alonso, 2015, Intermediate hosts of Angiostrongylus cantonensis in Tenerife, Spain, PLoS ONE, 10, e0120686, 10.1371/journal.pone.0120686 Stockdale-Walden, 2015, Angiostrongylus cantonensis in introduced gastropods in Southern Florida, J. Parasitol., 101, 156, 10.1645/14-553.1 Wang, 2007, Invasive freshwater snail, China, Emerg. Infect. Dis., 13, 1119, 10.3201/eid1307.061360 Harris, 1975, The encapsulation process in Biomphalaria glabrata experimentally infected with the metastrongylid Angiostrongylus cantonensis: light microscopy, Int. J. Parasitol., 5, 521, 10.1016/0020-7519(75)90044-2 Tunholi-Alves, 2014, Activation of anaerobic metabolism in Biomphalaria glabrata (Mollusca: Gastropoda) experimentally infected by Angiostrongylus cantonensis (Nematoda Metastrongylidae) by high-performance liquid chromatography, Parasitol. Int., 63, 64, 10.1016/j.parint.2013.09.004 Tunholi-Alves, 2012, Effects of infection by larvae of Angiostrongylus cantonensis (Nematoda Metastrongylidae) on the metabolism of the experimental intermediate host Biomphalaria glabrata, Exp. Parasitol., 131, 143, 10.1016/j.exppara.2012.03.003 dos Santos Bonfim, 2014, Biochemical and histopathological alterations in Biomphalaria glabrata due to co-infection by Angiostrongylus cantonensis and Echinostoma paraensei, J. Invertebr. Pathol., 115, 80, 10.1016/j.jip.2013.10.005 Cantacessi, 2013, Coming out of the shell: building the molecular infrastructure for research on parasite-harbouring snails, PLoS Negl. Trop. Dis., 7, e2284, 10.1371/journal.pntd.0002284 Giannelli, 2015, Release of lungworm larvae from snails in the environment: potential for alternative transmission pathways, PloS Negl. Trop. Dis., 9, e0003722, 10.1371/journal.pntd.0003722 Colella, 2015, Feline lungworms unlock a novel mode of parasite transmission, Sci. Rep., 5, 13105, 10.1038/srep13105 Yoshino, 2013, Molluscan cells in culture: primary cell cultures and cell lines, Can. J. Zool., 91, 6, 10.1139/cjz-2012-0258 Berriman, 2009, The genome of the blood fluke Schistosoma mansoni, Nature, 460, 352, 10.1038/nature08160 Young, 2012, Whole-genome sequence of Schistosoma haematobium, Nat. Genet., 44, 221, 10.1038/ng.1065 2009, Schistosoma japonicum Genome Sequencing and Functional Analysis Consortium The Schistosoma japonicum genome reveals features of host–parasite interplay, Nature, 460, 345, 10.1038/nature08140 Lin, 2013, Angiostrongylus cantonensis (Nematode: Metastrongiloidea): in vitro cultivation of infective third-stage larvae to fourth-stage larvae, PLoS ONE, 8, e72084, 10.1371/journal.pone.0072084 Rollinson, 2013, Time to set the agenda for schistosomiasis elimination, Acta Trop., 128, 423, 10.1016/j.actatropica.2012.04.013 King, 2015, Historical perspective: snail control to prevent schistosomiasis, PLoS Negl. Trop. Dis., 9, e0003657, 10.1371/journal.pntd.0003657 2012, Elimination of Schistosomiasis, 36 Coelho, 2008, Transmission control of schistosomiasis mansoni by introduction of a resistant strain of Biomphalaria tenagophila in areas where transmission is maintained by this species, Acta Trop., 108, 245, 10.1016/j.actatropica.2008.05.028 Richards, 1970, Genetics of a molluscan vector of schistosomiasis, Nature, 227, 806, 10.1038/227806a0 Berg, 1973, Biological control of snail-borne diseases: a review, Exp. Parasitol., 33, 318, 10.1016/0014-4894(73)90036-2 Chernin, 1960, Daubaylia potomaca, a nematode parasite of Helisoma trivolvis, transmissible to Australorbis glabratus, J. Parasitol., 46, 599, 10.2307/3274944 Zimmermann, 2011, The unusual life cycle of Daubaylia potomaca, a nematode parasite of Helisoma anceps, J. Parasitol., 97, 430, 10.1645/GE-2604.1 Duval, 2015, A novel bacterial pathogen of Biomphalaria glabrata: a potential weapon for schistosomiasis control?, PLoS Negl. Trop. Dis., 9, e0003489, 10.1371/journal.pntd.0003489 Sokolow, 2015, Reduced transmission of human schistosomiasis after restoration of a native river prawn that preys on the snail intermediate host, Proc. Natl. Acad. Sci. U.S.A., 112, 9650, 10.1073/pnas.1502651112 Donaghy, 2010, First characterisation of the populations and immune-related activities of hemocytes from two edible gastropod species, the disk abalone Haliotis discus discus and the spiny top shell, Turbo cornutus, Fish Shellfish Immunol., 28, 87e97, 10.1016/j.fsi.2009.10.006 Hanington, 2010, The primary role of fibrinogen-related proteins in invertebrates is defense, not coagulation, J. Innate. Immun., 3, 17, 10.1159/000321882 Hanington, 2012, A somatically diversified defense factor FREP3, is a determinant of snail resistance to schistosome infection, PLoS Negl. Trop. Dis., 6, e1591, 10.1371/journal.pntd.0001591 Baeza Garcia, 2010, Involvement of the cytokine MIF in the snail host immune response to the parasite Schistosoma mansoni, PLoS Pathog., 6, e1001115, 10.1371/journal.ppat.1001115 Galinier, 2013, Biomphalysin, a new β pore-forming toxin involved in Biomphalaria glabrata immune defense against Schistosoma mansoni, PLoS Pathog., 9, e1003216, 10.1371/journal.ppat.1003216 Knight, 2015, Susceptibility of snails to infection with schistosomes is influenced by temperature and expression of heat shock proteins, Epidemiology, 5, 189 Tennessen, 2015, Hyperdiverse gene cluster in snail host conveys resistance to human schistosome parasites, PLoS Genet., 11, e1005067, 10.1371/journal.pgen.1005067 Théron, 2005, Are Biomphalaria snails resistant to Schistosoma mansoni?, J. Helminthol., 79, 187, 10.1079/JOH2005299 Marques, 2014, Reduced susceptibility of a Biomphalaria tenagophila population to Schistosoma mansoni after introducing the resistant Taim/RS strain of B. tenagophila into Herivelton Martins stream, PLoS ONE, 9, e99573, 10.1371/journal.pone.0099573 Richards, 1992, Genetics of Biomphalaria glabrata and its effect on the outcome of Schistosoma mansoni infection, Parasitol. Today, 8, 171, 10.1016/0169-4758(92)90015-T Lie, 1979, Specificity of natural resistance to trematode infections in Biomphalaria glabrata, Int. J. Parasitol., 9, 529, 10.1016/0020-7519(79)90008-0