S. Batterman, J. Eisenberg, R. Hardin, M. E. Kruk, M. C. Lemos et al., Sustainable control of water-related infectious diseases: a review and proposal for interdisciplinary health-based systems research, Environ Health Perspect, vol.117, pp.1023-1055, 2009.

. Who-w, Field use of molluscicides in schistosomiasis control programmes: an operational manual for programme managers, 2018.

L. Savioli, S. Stansfield, D. A. Bundy, A. Mitchell, R. Bhatia et al., Schistosomiasis and soil-transmitted helminth infections: forging control efforts, Trans R Soc Trop Med Hyg, vol.96, pp.577-586, 2002.

L. Savioli, M. Albonico, D. Engels, and A. Montresor, Progress in the prevention and control of schistosomiasis and soil-transmitted helminthiasis, Parasitol Int, vol.53, pp.103-116, 2004.

R. C. Augusto, D. Duval, and C. Grunau, Effects of the environment on developmental plasticity and infection success of Schistosoma parasites-an epigenetic perspective, Front Microbiol, vol.10, p.1475, 2019.
URL : https://hal.archives-ouvertes.fr/hal-02178309

C. Shiff, Why reinvent the wheel? Lessons in schistosomiasis control from the past, PLoS Negl Trop Dis, vol.11, p.5812, 2017.

M. Parker and T. Allen, Does mass drug administration for the integrated treatment of neglected tropical diseases really work? Assessing evidence for the control of schistosomiasis and soil-transmitted helminths in Uganda, Health Res Policy Syst, vol.9, p.3, 2011.

P. Lamberton, C. L. Faust, and J. P. Webster, Praziquantel decreases fecundity in Schistosoma mansoni adult worms that survive treatment: evidence from a laboratory life-history trade-offs selection study, Infect Dis Poverty, vol.6, p.110, 2017.

P. He, W. Wang, B. Sanogo, X. Zeng, X. Sun et al., Molluscicidal activity and mechanism of toxicity of a novel salicylanilide ester derivative against Biomphalaria species, Parasit Vectors, vol.10, p.383, 2017.

B. Sures, M. Nachev, C. Selbach, and D. J. Marcogliese, Parasite responses to pollution: what we know and where we go in ?Environmental Parasitology?, Parasit Vectors, vol.10, p.65, 2017.

E. C. Oliveira-filho and F. J. Paumgartten, Toxicity of Euphorbia milii latex and niclosamide to snails and nontarget aquatic species, Ecotoxicol Environ Saf, vol.46, pp.342-50, 2000.

J. R. Dai, Y. Z. Li, W. Wang, Y. T. Xing, G. L. Qu et al., Resistance to niclosamide in Oncomelania hupensis, the intermediate host of Schistosoma japonicum: should we be worried?, Parasitology, vol.142, pp.332-372, 2015.

A. R. De-carvalho, M. Silva, and C. C. , Phytochemical molluscicides and schistosomiasis: what we know and what we still need to learn, Vet Sci, vol.5, p.94, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01914813

T. W. Jia, W. Wang, L. P. Sun, S. Lv, K. Yang et al., Molluscicidal effectiveness of Luo-Wei, a novel plant-derived molluscicide, against Oncomelania hupensis, Biomphalaria alexandrina and Bulinus truncatus, Infect Dis Poverty, vol.8, p.27, 2019.

H. Li and W. Wang, Apropos: critical analysis of molluscicide application in schistosomiasis control programs in Brazil, Infect Dis Poverty, vol.6, p.54, 2017.

J. L. Matos, K. R. Da-silva, L. A. De-lima-paula, W. R. Cunha, S. B. Ramos et al., Molluscicidal and cercaricidal activities of curcumin on Biomphalaria glabrata and Schistosoma mansoni cercariae Molluscicidal and cercaricidal activities of curcumin, Pest Manag Sci, vol.76, pp.1228-1262, 2020.

H. Silva, J. Sa, W. N. Siqueira, M. V. Lima, M. Martins et al., Toxicological effects of Ramalina aspera (lichen) on Biomphalaria glabrata snails and Schistosoma mansoni cercariae, Acta Trop, vol.196, pp.172-181, 2019.

A. M. Ibrahim and S. I. Ghoname, Molluscicidal impacts of Anagallis arvensis aqueous extract on biological, hormonal, histological and molecular aspects of Biomphalaria alexandrina snails, Exp Parasitol, vol.192, pp.36-41, 2018.

B. Mandefro, S. T. Mereta, Y. Tariku, and A. Ambelu, Molluscicidal effect of Achyranthes aspera L. (Amaranthaceae) aqueous extract on adult snails of Biomphalaria pfeifferi and Lymnaea natalensis, Infect Dis Poverty, vol.6, p.133, 2017.

F. Bouzergoune, M. L. Ciavatta, F. Bitam, M. Carbone, M. C. Aberkane et al., Phytochemical study of Eryngium triquetrum: isolation of polyacetylenes and lignans, Planta Med, vol.82, pp.1438-1483, 2016.

S. D. Nusair and M. I. Ahmad, Toxicity of Vipera palaestinae venom and antagonistic effects of methanolic leaf extract of Eryngium creticum lam, Toxicon, vol.166, pp.1-8, 2019.

G. Paun, E. Neagu, V. Moroeanu, C. Albu, S. Savin et al., Chemical and bioactivity evaluation of Eryngium planum and Cnicus benedictus polyphenolic-rich extracts, Biomed Res Int, p.3692605, 2019.

A. Medbouhi, N. Merad, A. Khadir, M. Bendahou, N. Djabou et al., Chemical composition and biological investigations of Eryngium triquetrum essential oil from Algeria, Chem Biodivers, vol.15, p.1700343, 2018.

A. Medbouhi, A. Tintaru, C. Beaufay, J. V. Naubron, N. Djabou et al., Structural elucidation and cytotoxicity of a new 17-membered ring lactone from Algerian Eryngium campestre, Molecules, vol.23, p.3250, 2018.
URL : https://hal.archives-ouvertes.fr/hal-02091874

A. Sadiq, S. Ahmad, R. Ali, F. Ahmad, A. Zeb et al., Antibacterial and antifungal potentials of the solvents extracts from Eryngium caeruleum, Notholirion thomsonianum and Allium consanguineum, BMC Complement Altern Med, vol.16, p.478, 2016.

E. Co, European Pharmacopoeia, 1997.

R. P. Adams, Identification of essential oil components by gas chromatography/mass spectrometry, 2007.

, NIST. PC Version 1.7 of the NIST/EPA/NIH Mass Spectral Library, 1999.

P. Rubiolo, E. Liberto, B. Sgorbini, R. Russo, J. L. Veuthey et al., Fast-GCconventional quadrupole mass spectrometry in essential oil analysis, J Sep Sci, vol.31, pp.1074-84, 2008.

N. Djabou, J. Paolini, J. Desjobert, H. Allali, N. Baldovini et al., Qualitative and quantitative analysis of volatile components of Teucrium massiliense L.-identification of 6-methyl-3-heptyl acetate as a new natural product, Flavour Fragrance J, vol.25, pp.475-87, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00592394

, Guidelines for laboratory and field testing of molluscicides for control of schistosomiasis. Geneva: World Health Organization, 2019.

Y. Mone, G. Mitta, D. Duval, and B. Gourbal, Effect of amphotericin B on the infection success of Schistosoma mansoni in Biomphalaria glabrata, Exp Parasitol, vol.125, pp.70-75, 2010.
URL : https://hal.archives-ouvertes.fr/halsde-00495366

D. J. Finney, Probit analysis, 1971.

A. Zerlotini, E. R. Aguiar, F. Yu, H. Xu, Y. Li et al., SchistoDB: an updated genome resource for the three key schistosomes of humans, Nucleic Acids Res, vol.41, pp.728-759, 2013.

C. M. Adema, L. W. Hillier, C. S. Jones, E. S. Loker, M. Knight et al., Whole genome analysis of a schistosomiasis-transmitting freshwater snail, Nat Commun, vol.8, p.15451, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01523953

D. O. Famakinde, Treading the path towards genetic control of snail resistance to schistosome infection, Trop Med Infect Dis, vol.3, p.86, 2018.

A. De-carvalho, Parasites Vectors (2020) 13:486 ? fast, convenient online submission ? thorough peer review by experienced researchers in your field ? rapid publication on acceptance ? support for research data, including large and complex data types ? gold Open Access which fosters wider collaboration and increased citations maximum visibility for your research: over

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T. Maier, N. J. Wheeler, E. Namigai, J. Tycko, R. E. Grewelle et al., Gene drives for schistosomiasis transmission control, PLoS Negl Trop Dis, vol.13, p.7833, 2019.

T. A. Adekiya, R. T. Aruleba, B. E. Oyinloye, K. O. Okosun, and A. P. Kappo, The effect of climate change and the snail-schistosome cycle in transmission and biocontrol of schistosomiasis in sub-Saharan Africa, Int J Environ Res Public Health, vol.17, p.181, 2019.

A. S. Stensgaard, P. Vounatsou, M. E. Sengupta, J. Utzinger, and . Schistosomes, snails and climate change: current trends and future expectations, Acta Trop, vol.190, pp.257-68, 2019.

L. Govic, Y. Kincaid-smith, J. Allienne, J. F. Rey, O. De-gentile et al., Schistosoma haematobium-Schistosoma mansoni hybrid parasite in migrant boy, Emerg Infect Dis, vol.25, pp.365-372, 2017.
URL : https://hal.archives-ouvertes.fr/hal-02483187

M. Ismail, S. Botros, A. Metwally, S. William, A. Farghally et al., Resistance to praziquantel: direct evidence from Schistosoma mansoni isolated from Egyptian villagers, Am J Trop Med Hyg, vol.60, pp.932-937, 1999.

V. Da-silva, B. Campos, J. F. De-oliveira, J. L. Decout, and M. Do-carmo-alves-de-lima, Medicinal chemistry of antischistosomal drugs: praziquantel and oxamniquine, Bioorg Med Chem, vol.25, pp.3259-77, 2017.

P. Coelho and R. L. Caldeira, Critical analysis of molluscicide application in schistosomiasis control programs in Brazil, Infect Dis Poverty, vol.5, p.57, 2016.

C. H. King, L. J. Sutherland, and D. Bertsch, Systematic review and meta-analysis of the impact of chemical-based mollusciciding for control of Schistosoma mansoni and S. haematobium transmission, PLoS Negl Trop Dis, vol.9, p.4290, 2015.

A. D. Harrison, The effects of Bayluscid on gastropod snails and other aquatic fauna in Rhodesia, Hydrobiologia, vol.28, pp.371-84, 1966.

C. P. Souza, Molluscicide control of snail vectors of schistosomiasis, Mem Inst Oswaldo Cruz, vol.90, pp.165-173, 1995.

A. F. Santos, D. P. De-azevedo, S. Mata-rda, C. De-mendonça, D. I. Sant?ana et al., The lethality of Euphorbia conspicua to adults of Biomphalaria glabrata, cercaria of Schistosoma mansoni and larvae of Artemia salina, Bioresour Technol, vol.98, pp.135-144, 2007.

L. Pereira, C. N. Dias, M. V. Miranda, W. Firmo, C. Rosa et al., Molluscicidal effect of Euphorbia umbellata (Pax) Bruyns latex on Biomphalaria glabrata, Schistosoma mansoni host snail, Rev Inst Med Trop Sao Paulo, vol.59, p.85, 2017.

P. Jurberg, C. Neto, J. B. Schall, and V. T. , Molluscicide activity of the "avelós" plant (Euphorbia tirucalli L.) on Biomphalaria glabrata, the mollusc vector of schistosomiasis, Mem Inst Oswaldo Cruz, vol.80, pp.423-430, 1985.

M. C. De-vasconcellos and A. De-amorim, Christ?s Crown") (Euphorbiaceae) against Lymnaea columella (Say, 1817) (Pulmonata: Lymnaeidae), intermediate host of Fasciola hepatica Linnaeus, 1758 (Trematode: Fasciolidae): 1-test in laboratory, Mem Inst Oswaldo Cruz, vol.98, pp.557-63, 2003.

A. A. Pereira-filho, C. R. Franca, S. Oliveira-dda, R. J. Mendes, G. Jde et al., Evaluation of the molluscicidal potential of hydroalcoholic extracts of Jatropha gossypiifolia Linnaeus, 1753 on Biomphalaria glabrata (Say, 1818), Rev Inst Med Trop Sao Paulo, vol.56, pp.505-515, 2014.

A. M. Ibrahim and A. M. Abdalla, Impact of Moringa oleifera seed aqueous extract on some biological, biochemical, and histological aspects of Biomphalaria alexandrina snails, Environ Sci Pollut Res Int, vol.24, pp.28072-28080, 2017.

A. F. Santos, S. A. Fonseca, F. A. Cesar, M. C. De-azevedo-albuquerque, J. V. Santana et al., A penta-substituted pyridine alkaloid from the rhizome of Jatropha elliptica (Pohl) Muell. Arg. is active against Schistosoma mansoni and Biomphalaria glabrata, Parasitol Res, vol.113, pp.1077-84, 2014.

M. A. Radwan, S. R. El-zemity, S. A. Mohamed, and S. M. Sherby, Potential of some monoterpenoids and their new N-methyl carbamate derivatives against schistosomiasis snail vector, Biomphalaria alexandrina, Ecotoxicol Environ Saf, vol.71, pp.889-94, 2008.

L. Pereira, E. Ribeiro, M. Brito, D. Silveira, F. Araruna et al., Essential oils as molluscicidal agents against schistosomiasis transmitting snails-a review, Acta Trop, vol.209, p.105489, 2020.

M. Lahlou, R. Berrada, and M. Hmamouchi, Molluscicidal activity of thirty essential oils on Bulinus truncatus, Therapie, vol.56, pp.71-73, 2001.

D. K. Rai, N. P. Brunton, A. Koidis, A. Rawson, P. Mcloughlin et al., Characterisation of polyacetylenes isolated from carrot (Daucus carota) extracts by negative ion tandem mass spectrometry, Rapid Commun Mass Spectrom, vol.25, pp.2231-2240, 2011.

A. Medbouhi, F. Benbelaid, N. Djabou, C. Beaufay, M. Bendahou et al., Essential oil of Algerian Eryngium campestre: chemical variability and evaluation of biological activities, Molecules, vol.24, p.2575, 2019.
URL : https://hal.archives-ouvertes.fr/hal-02491500

A. Landoulsi, T. Hennebelle, J. Bero, C. Rivière, S. Sahpaz et al., Antimicrobial and light-enhanced antimicrobial activities, cytotoxicity and chemical variability of all Tunisian Eryngium species, Chem Biodivers, vol.17, p.1900543, 2020.
URL : https://hal.archives-ouvertes.fr/hal-02955241

M. Kikowska, D. Kalemba, J. Dlugaszewska, and B. Thiem, Chemical composition of essential oils from rare and endangered species-Eryngium maritimum L. and E. alpinum L. Plants (Basel), vol.9, p.417, 2020.

B. Thiem, M. Kikowska, A. Kurowska, and D. Kalemba, Essential oil composition of the different parts and in vitro shoot culture of Eryngium planum L, Molecules, vol.16, pp.7115-7139, 2011.

M. Kobaek-larsen, G. Baatrup, M. Khataeinotabi, R. B. El-houri, E. Pipó-ollé et al., Dietary polyacetylenic oxylipins falcarinol and falcarindiol prevent inflammation and colorectal neoplastic transformation: a mechanistic and dose-response study in a rat model, Nutrients, vol.11, p.2223, 2019.

S. M. Zhang, S. K. Buddenborg, C. M. Adema, J. T. Sullivan, and E. S. Loker, Altered gene expression in the Schistosome-transmitting snail Biomphalaria glabrata following exposure to niclosamide, the active ingredient in the widely used molluscicide Bayluscide, PLoS Negl Trop Dis, vol.9, p.4131, 2015.

A. El-ansary, E. M. Sammour, M. S. Soliman, and F. A. Gawish, In vivo, attenuation of schistosome cercarial development and disturbance of egg laying capacity in Biomphalaria alexandrina using sublethal concentrations of plant molluscicides, J Egypt Soc Parasitol, vol.31, pp.657-69, 2001.

K. A. Rodrigues, C. N. Dias, F. M. Do-amaral, D. F. Moraes, M. Filho et al., Molluscicidal and larvicidal activities and essential oil composition of Cymbopogon winterianus, Pharm Biol, vol.51, pp.1293-1300, 2013.

A. F. Santos, S. A. Fonseca, F. A. César, M. C. De-azevedo-albuquerque, J. V. Santana et al., A penta-substituted pyridine alkaloid from the rhizome of Jatropha elliptica (Pohl) Muell. Arg. is active against Schistosoma mansoni and Biomphalaria glabrata, Parasitol Res, vol.113, pp.1077-84, 2014.

A. M. Ibrahim, M. M. Abdel-gawad, H. A. El-nahas, and N. S. Osman, Studies on the molluscicidal activity of Agave angustifolia and Pittosporum tobira on schistosomiasis transmitting snails, J Egypt Soc Parasitol, vol.45, pp.133-174, 2015.

R. C. Augusto, G. Tetreau, P. Chan, M. L. Walet-balieu, C. C. Mello-silva et al., Double impact: natural molluscicide for schistosomiasis vector control also impedes development of Schistosoma mansoni cercariae into adult parasites, PLoS Negl Trop Dis, vol.11, p.5789, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01598383

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