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Journal of Complementary and Integrative Medicine

Editor-in-Chief: Lui, Edmund

Ed. by Ko, Robert / Leung, Kelvin Sze-Yin / Saunders, Paul / Suntres, PH. D., Zacharias


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Antimicrobial properties of terrestrial snail and slug mucus

Giovanni Cilia / Filippo Fratini
  • Corresponding author
  • Department of Veterinary Sciences, University of Pisa, Viale delle Piagge 2, Pisa, Italy
  • Interdepartmental Research Center “Nutraceuticals and Food for Health”, University of Pisa, Via del Borghetto 80, Pisa, Italy
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Published Online: 2018-03-27 | DOI: https://doi.org/10.1515/jcim-2017-0168

Abstract

Snail and slug mucus is a viscous-elastic substance secreted by specific glands with adhesive and lubricants properties that allows them to adhere tenaciously to many different surfaces. It has been used since ancient times for care and human health and it is still very important in traditional and folkloristic medicine. Recently, mucus from snail and slugs and its protein and components have been subjected to some investigations on their antibacterial, antiviral and antifungal activity due to extensive traditional uses and for a future application in medicine. Antimicrobial activities of crude mucus, and its components, against different microorganism have been reported, showing antimicrobial activities that lead their potential employment in several fields as natural additives. The purpose of this Review is to summarize the results of antimicrobial studies of snail and slug mucus and its compounds from the first scientific applications to the isolation of the single components in order to better understand its application and propose an employment in future studies as a natural antimicrobial agent.

Keywords: antibacterial activity; antifungal activity; antiviral activity; mucus; slug; terrestrial snails

Introduction

Slugs and snails are terrestrial molluscs, belonging to the order Pulmonata, class Gastropoda, phylum Mollusca, characterized by a similar morphology.

The main difference between snails and slugs is the fact that the snails are provided of shells. Snails usually have a spiral-shaped shell which is wound around a spindle. This is the snail shell which they retract their soft bodies into when they detect danger [1].The spiral direction is species-specific.

Slugs are snails-like animals without shell. Not having a shell to protect them, slugs have a very thick slime which makes them disgusting to predators [2].

Both slugs and snails are able to produce a viscous-elastic substance named slime or mucus, with adhesive and lubricant properties that allows them to adhere tenaciously to many different surfaces. The mucus has also other functions: hindering the molluscs dehydration and making slugs and snails unattractive to potential predators [1, 2].

Moreover, snail mucus has the ability to facilitate wound healing and to prevent its infections thanks to its many bioactive compounds [3, 4].

Over the few last years, numerous studies on mucus composition have clarified many aspects of its properties, although much remains to be investigated on its antibacterial activity.

Recently, several researches carried out on snail secretion composition have confirmed that the Helix aspersa mucus contains a great amount of natural substances with beneficial and therapeutic properties for human skin such as allantoin and glycolic acid [5].

This review aims to represent an organic collection of the results obtained from the few studies until today carried out to test the snail mucus antibacterial activity and its main components against various microorganisms.

Historic background

Although the use of many gastropods including snails for food has been demonstrated by numerous archeological discoveries, it is much more difficult to prove their use in therapy and medicine [6]. The brown garden snail, Helix aspersa, has been used in human medicine since ancient times; the earliest application of snail mucus secretions in medicine dates back to the Ancient Greeks. Hippocrates was reported to have used crushed snails to alleviate inflammatory skin conditions. Moreover, the father of Western medicine recommended snail mucus for the treatment of protocoele. Celse claimed that the crude snail with its shell had remarkable healing properties, while after boiling it also acquired emollient capacity. Pliny stated that snail preparations could be employed in every type of wound, such as burns, abscesses and nosebleeds. Galien recommended snails mucus against hydrops foetalis [7].

Dermatological preparation with snail mucus was employed during the eighteenth century to treat dermatological disorders and symptoms associated with tuberculosis and nephritis. In the nineteenth century there was renewed interest in the pharmaceutical and medical use of snails with more and more preparations. This interest in snails continued into the next century with the acquisition of new analytical data on mucus components. Recently, anecdotal reports of generic skin regeneration properties of the mucus from Helix aspersa have been explored; this has resulted in the commercial production of a topical preparation claimed to have “wound healing” as well as anti-ageing properties. These preparations were tested on burn patients and while they noted that a range of pathogenic bacteria were isolated from the wounds before treatment, this was not followed up with culture of post-treatment specimens [8].

Composition of snail mucus

Snail mucus composition varies according to species and according to its role, trail or adhesion function and for these functions, typically, consists of between 90% and 99.7 % water by weight [9]. The remaining part of mucus without water consists of a mixture of proteoglycans, glycosaminoglycans, glycoprotein enzymes, hyaluronic acid, copper peptides, antimicrobial peptides, and metal ions [10, 11, 12, 13]. Atomic absorption spectrometry showed that glue from the slug Arion subfuscus contains substantial quantities of zinc, iron, copper and manganese. Experimentally it was shown that the addition of iron or copper to dissolved slug glue causes the proteins to precipitate rapidly but the addition of zinc had no effect, suggesting that some metal ions play an important role in gel formation [14].

The snail mucus principally contains allantoin, collagen, elastin and glycolic acid.

Allantoin, or 5-Ureidohydantoin, derives from the uric acid transformation by the enzyme uricase. It is known for its desquamating action, its promotion of cell proliferation and wound healing [15, 16, 17].

Glycolic acid, or alfa-Hydroxyacetic acid, has an excellent capability to penetrate skin and is capable to increase collagen synthesis [18, 19, 20].

Another study evidenced that snail mucus can be used, potentially, in regenerating and repairing bone and teeth, because it increased the expression of osteopontin and NF-κB and induced the expression of some inflammatory genes in dental pulp cells [21].

Furthermore, glycoproteins and mucopolysaccharides, physiologically active bio-macromolecular structures are present in snail mucus [9, 22]. Mucin glycoproteins are the major macromolecular constituents of epithelial mucus and have long been implicated in health and disease [12, 23, 24]. The glycoproteins, such as achacin, are, probably, the components involved in antimicrobial activity of snail mucus. Indeed, achacin, other than inhibit bacteria growth, also appeared to attack the bacterial plasma membranes [25]. However, the achacin has the ability to catalyze oxidative deamination producing ketoacids, hydrogen peroxide and ammonia [26]. The antibacterial activity of achacin was found to be dependent on H2O2 production which is produced by the oxidative deamination reaction. These data illustrate that achacin may attack pathogens during other growth phases too by increasing the local concentration of H2O2 so as not to harm neighboring host cells [23, 25, 26].

Scientific evidence provides some credible basis for the possible use of mucus in wound management [27]. The mucus from Cryptomphalus aspersa (also known as Helix aspersa or the common garden snail) contains antioxidant superoxide dismutase (SOD) and Glutathione-S-Transferase activity (GST) activities. Antioxidants are substances that may protect cells from the damage caused by unstable molecules known as free radicals or reactive oxygen species. SODs act as antioxidants and protect cellular components from being oxidized by reactive oxygen species [27]. Furthermore, the Cryptomphalus aspersa mucus stimulated fibroblast proliferation, extracellular matrix assembly and the regulation of metalloproteinase activities and concluded that these effects together provided an array of molecular mechanisms underlying the secretion’s induced cellular regeneration, thereby supporting its possible use in repair of wounded tissues [27]. In a subsequent study it was also demonstrated that the mucus increased migration and increased the expression of cell-cell and cell-substrate adhesion molecules in mammalian fibroblast and keratinocyte cells [28].

It should be noted that some of these properties are analogous to claims made for some modern wound management materials.

Antimicrobial activity

The antibacterial activity of snail mucus was evaluated for the first time with a sample from Achatina fulica Fèrussac, the African giant snail [29]. In this study two different fractions of snail mucus were examined: the water-soluble fraction and the mucin fraction, contained proteins. Both fractions showed a positive antibacterial activity against Gram positive bacteria, such as Bacillus subtilis and Staphylococcus aureus, and Gram negative strains, like Escherichia coli and Pseudomonas aeruginosa. Furthermore, the mucin fraction resulted more effective against bacteria compared to water-soluble fraction [29].

Another antibacterial factor was isolated from the Achatina fulica mucus [30]. This unnamed antibacterial effect showed great inhibition activity against Staphylococcus aureus, followed, with high concentration, by Bacillus subtilis and Pseudomonas aeruginosa and, finally, by Escherichia coli [30].

An N-Acetylneuraminic Acid-Specific Lectin, called Achatinin, isolated from the African giant snail body-surface mucus showed an antibacterial activity against Staphylococcus aureus and Escherichia coli only a concentration of 50 µg/ml [31].

As reported in Table 1, the mucus extracted from various species of land snail exhibited an inhibition action against Gram positive and Gram negative bacteria strains.

Table 1:

Antibacterial activity of snail slime and its antimicrobial compounds.

The Achatina fulica mucus showed a great antibacterial activity against Staphylococcus aureus and Streptococcus epidermidis with high inhibition diameter, expressed in mm [33].

Archachatina marginata mucus was investigated in relationship with the different variety of this snail species, as reported in Table 1. The Archachatina marginata var. saturalis showed different antibacterial activity compared to Archachatina marginata var. ovum [34]. Staphylococcus spp. was inhibited mostly by var. saturalis, while Pseudomonas spp. and Streptococcus spp. resulted more susceptible to var. ovum [34], data showed in Table 1. Another interesting comparison was performed with Archachatina marginata normal skinned and albino skinned mucus samples [35]. The mucus collected from the normal skinned snail showed a more effective antibacterial activity against Staphylococcus spp. and Pseudomonas spp. than the albino skinned snail. Different trends were reported for Escherichia coli and Salmonella spp.; Escherichia coli resulted more susceptible with the albino skinned snail mucus, while Salmonella spp. with the normal skinned snail mucus [35], data reported in Table 1.

The Helix aspersa mucus showed efficient antibacterial activity against two different Pseudomonas aeruginosa strains [36]. The mucus from the same snail also resulted incisive against Streptococcus pyogenes, while no inhibition diameters were evaluated for other tested strains [36]. The Helix aspersa mucus purification was improved by Bortolotti et al. (2016). The mucus extracted showed the same antibacterial activity confirming the data previously evidenced by Pitt et al. (2015).

Achacin [23, 26, 37], Achatin CRP (C-reactive protein) [38] and Mytimacin-AF [39] and Hemocyanin β c-HaH [40] are antimicrobial peptide isolated from Achatina fulica and Helix aspersa mucus, respectively.

Achacin from African giant snail mucus inhibited the growth of Escherichia coli and Staphylococcus aures spp [26]., while the MIC50 value resulted effective against Streptococcus agalactiae and Methicillin-Resistant Staphylococcus aureus (MRSA) [37], as reported in Table 1.

The C-reactive protein Achatin from Achatina fulica mucus showed effective antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, Streptococcus epidermidis and Pantoea ananatis with MIC values, with 100 µg of protein, ranging from 11 to 12 mm, while the most resistant bacteria strain resulted in Bacillus subtilis (18 mm) followed by Salmonella thyphimurium (15 mm) [38].

Two unknown and undefined compounds isolated on TLC (Thin Layer Chromatography) from Achatina fulica mucus showed an inhibition to Escherichia coli and Vibrio cholerae growth [41]. Unfortunately, these antibacterial compounds have not been identified, but it is interesting to continue this research line.

Staphylococcus aureus resulted in the most sensitive bacteria strain subject to antibacterial activity of Mytimacin-AF, a protein from African giant snail mucus, followed by Bacillus pyocyaneus and Bacillus dysenteriae [39]. Bacillus megatherium and Klebsiella pneumoniae showed high resistance to peptide Mytimacin-AF [39], data reported in Table 1.

Hemocyanin β c-HaH from Helix aspersa mucus inhibited the growth of Escherichia coli, Staphylococcus aureus and Staphylococcus epidermidis, while Pseudomonas aeruginosa and Enterococcus faecium have grown unconditionally with the presence of the antimicrobial peptide [40].

Two glycosilated peptides with mass of 4021.04 and 6403.73 Da, isolated from Fraction B of Helix aspersa and Helix lucorum mucus showed inhibition of Propionibacterium acnes, Escherichia coli and Helicobacter pylori growth [42].

Unfortunately, lectin isolated from the Achatina fulica mucus did not show an inhibition activity against Staphylococcus aureus and Escherichia coli even though an hemagglutinating activity was evidenced from the same investigation [43].

Mytimacin-AF showed also an antifungal activity against Candida albicans with a MIC value of 7.5 µg/ml [39], while the Helix aspersa mucus did not show inhibition action against the same yeast [36].

The fraction 39 and fraction 50 from Phyllocaulis boraceiensis, tropical leatherleaf slug, mucus was analyzed using Fourier Transform Infrared Spectrometry (FT-IR) and tested against Measles virus (MV), a single-stranded, negative-sense, enveloped RNA virus of the genus Morbillivirus [44]. The antiviral action could be correlated to polyunsaturated fatty acids in fraction 39, in detail the most active fatty acids against MV were hydroxy-tritriacontapentaenoic acid and hydroxy-pentatriacontapentaenoic acid. Furthermore, the fraction 50 showed a lower antiviral activity against tested virus [44].

Conclusions

From available literature snail and slug mucus and its derivate components, such as achacin, achatina CRP and mytimacin-AF, showed a high activity against Gram positive and Gram negative bacteria, virus and yeast. Moreover, several studies could be carried out on its antimicrobial activity against other microorganisms, especially against multidrug resistant bacteria, such as MRSA (methicillin-resistant Staphylococcus aureus). This is particularly important since one of the major public health problems is currently represented right from the onset by an increasing number of antibiotic resistant bacteria. The indiscriminate use of antibiotics has led to the selection of resistant clones many for which an adequate therapy is often not provided. Multidrug resistant bacteria management requires increasing attention towards the antibacterial molecules or products used. For this reason, researches in recent years has been directed towards the discovery of new antimicrobial substances, particularly natural substances such as plant extracts, essential oils and antimicrobial peptides isolated from many different animals. Based on the results obtained by several studies on the antimicrobial properties of snail and slug mucus, it seems clear that this natural product could be a potential subject of further investigations. The new findings regarding its active components, their inner mechanisms of action and the possibility of isolation and purification of the pure substances, represent a starting point for the formulation of new products for therapeutic and pharmacological uses as an alternative to conventional antibiotics. Natural peptides, as like those extracted from the snail and slug mucus, could be considered as potential alternatives in therapy.

Acknowledgments

We wish to thank Dr Anna Paola Biagi for the indispensable linguistic assistance provided.

References

  • [1]

    HäMäLäInen EM, Järvinen S. Snails: biology, ecology, and conservation. Hauppauge, NY: Nova Science Publisher’s, 2012. Google Scholar

  • [2]

    South A. Terrestrial slugs: biology, ecology, and control. London: Chapman & Hall, 1992. Google Scholar

  • [3]

    Adikwu MU, Alozie BU. Application of snail mucin dispersed in detarium gum gel in wound healing. Sci Res Essay. 2007;2:195–98. Google Scholar

  • [4]

    Adikwu MU, Enebeke TC. Evaluation of snail mucin dispersed in brachystegia gum gel as a wound healing agent. Anim Res Int. 2008;4:685–97. Google Scholar

  • [5]

    El Mubarak MA, Lamari FN, Kontoyannis C. Simultaneous determination of allantoin and glycolic acid in snail mucus and cosmetic creams with high performance liquid chromatography and ultraviolet detection. J Chromatogr A. 2013;1322:49–53. CrossrefPubMedWeb of ScienceGoogle Scholar

  • [6]

    Meyer-Rochow VB. Therapeutic arthropods and other, largely terrestrial, folk-medicinally important invertebrates: a comparative survey and review. J Ethnobiol Ethnomed. 2017;13:9. Web of SciencePubMedCrossrefGoogle Scholar

  • [7]

    Bonnemain B. Helix and drugs: snails for Western health care from antiquity to the present. Evid Based Complement Alternat Med. 2005;2:25–28. PubMedCrossrefGoogle Scholar

  • [8]

    Tsoutsos D, Kakagia D, Tamparopoulos K. The efficacy of Helix aspersa Müller extract in the healing of partial thickness burns: a novel treatment for open burn management protocols. J Dermatolog Treat. 2009;20:219–22. CrossrefGoogle Scholar

  • [9]

    Denny M. Molecular biomechanics of molluscan mucous secretions. In: Metabolic biochemistry and molecular biomechanics. Amsterdam: Elsevier, 1983:431–65. Google Scholar

  • [10]

    Gabriel UI, Mirela S, Ionel J. Quantification of mucoproteins (glycoproteins) from snails mucus, Helix aspersa and Helix Pomatia. J Agroaliment Process Technol. 2011;17:410–13. Google Scholar

  • [11]

    Skingley D. Investigation of mucus using Fourier transform infrared spectroscopy. Spectrosc Eur. 2010;22:10–13. Google Scholar

  • [12]

    Sallam AA, El-Massry SA, Nasr IN. Archives of phytopathology and plant protection chemical analysis of mucus from certain land snails under Egyptian conditions chemical analysis of mucus from certain land snails under Egyptian conditions. Arch Phytopathol Plant Prot. 2009;42:874–81. CrossrefGoogle Scholar

  • [13]

    Greistorfer S, Klepal W, Cyran N, Gugumuck A, Rudoll L, Suppan J, et al. Snail mucus − glandular origin and composition in Helix pomatia. Zoology. 2017;122:126–38. Web of ScienceCrossrefGoogle Scholar

  • [14]

    Werneke SW, Swann C, Farquharson LA, Hamilton KS, Smith AM. The role of metals in molluscan adhesive gels. J Exp Biol. 2007;210:2137–45. Web of ScienceCrossrefPubMedGoogle Scholar

  • [15]

    Thornfeldt C. Cosmeceuticals containing herbs: fact, fiction, and future. Dermatologic Surg. 2005;31:873–80. Google Scholar

  • [16]

    Veraldi S, De Micheli P, Schianchi R, Lunardon L. Treatment of pruritus in mild-to-moderate atopic dermatitis with a topical non-steroidal agent. J Drugs Dermatol. 2009;8:537–39. PubMedGoogle Scholar

  • [17]

    Araújo LU, Grabe-Guimarães A, Mosqueira VC, Carneiro CM, Silva-Barcellos NM. Profile of wound healing process induced by allantoin. Acta Cir Bras. 2010;25:460–66. CrossrefWeb of SciencePubMedGoogle Scholar

  • [18]

    Kim SJ, Park JH, Kim DH, Won YH, Maibach HI. Increased in vivo collagen synthesis and in vitro cell proliferative effect of glycolic acid. Dermatologic Surg. 1998;24:1054–58. CrossrefGoogle Scholar

  • [19]

    Bernstein EF, Lee J, Brown DB, Yu R, Van Scott E. Glycolic acid treatment increases type I Collagen mRNA and hyaluronic acid content of human skin. Dermatologic Surg. 2001;27:429–33. Google Scholar

  • [20]

    Inan S, Oztukcan S, Vatansever S, Ermertcan AT, Zeybek D, Oksal A, et al. Histopathological and ultrastructural effects of glycolic acid on rat skin. Acta Histochem. 2006;108:37–47. PubMedCrossrefGoogle Scholar

  • [21]

    Kantawong F, Thaweenan P, Mungkala S, Tamang S, Manaphan R, Wanachantararak P, et al. Mucus of Achatina fulica stimulates mineralization and inflammatory response in dental pulp cells. Turkish J Biol. 2016;40:353–59. CrossrefWeb of ScienceGoogle Scholar

  • [22]

    Deyrup-Olsen I, Luchtel DL, Martin AW. Components of mucus of terrestrial slugs (Gastropoda). Am J Physiol. 1983;245:R448–R4452. Google Scholar

  • [23]

    Otsuka-Fuchino H, Watanabe Y, Hirakawa C, Tamiya T, Matsumoto JJ, Tsuchiya T. Bactericidal action of a glycoprotein from the body surface mucus of giant African snail. Comp Biochem Physiol C. 1992;101:607–13. CrossrefPubMedGoogle Scholar

  • [24]

    Shabelnikov S, Kiselev A. Cysteine-rich atrial secretory protein from the Snail Achatina achatina: purification and structural characterization. PLoS One. 2015;10:e0138787. Web of ScienceGoogle Scholar

  • [25]

    Otsuka-Fuchino H, Watanabe Y, Hirakawa C, Takeda J, Tamiya T, Matsumoto JJ, et al. Morphological aspects of Achacin-treated bacteria. Comp Biochem Physiol C. 1993;104:37–42. PubMedCrossrefGoogle Scholar

  • [26]

    Ehara T, Kitajima S, Kanzawa N, Tamiya T, Tsuchiya T. Antimicrobial action of achacin is mediated by L-amino acid oxidase activity. FEBS Lett. 2002;531:509–12. CrossrefPubMedGoogle Scholar

  • [27]

    Brieva A, Philips N, Tejedor R, Guerrero A, Pivel JP, Alonso-Lebrero JL, et al. Molecular basis for the regenerative properties of a secretion of the Mollusk Cryptomphalus aspersa. Skin Pharmacol Physiol. 2008;21:15–22. Web of ScienceCrossrefPubMedGoogle Scholar

  • [28]

    Iglesias-de la Cruz MC, Sanz-Rodríguez F, Zamarrón A, Reyes E, Carrasco E, González S, et al. A secretion of the mollusc Cryptomphalus aspersa promotes proliferation, migration and survival of keratinocytes and dermal fibroblasts in vitro. Int J Cosmet Sci. 2012;34:183–89. PubMedCrossrefGoogle Scholar

  • [29]

    Iguchi SM, Aikawa T, Matsumoto JJ. Antibacterial activity of snail mucus mucin. Comp Biochem Physiol A. 1982;72:571–74. CrossrefGoogle Scholar

  • [30]

    Kubota Y, Watanabe Y, Otsuka H, Tamiya T, Tsuchiya T, Matsumoto JJ. Purification and characterization of an antibacterial factor from snail mucus. Comp Biochem Physiol C. 1985;82:345–48. PubMedCrossrefGoogle Scholar

  • [31]

    Iguchi SM, Momoi T, Egawa E, Matsumoto JJ. An N-acetylneuraminic acid-specific lectin from the body surface mucus of African giant snail. Comp Biochem Physiol B. 1985;81:897–900. CrossrefGoogle Scholar

  • [32]

    Bortolotti D, Trapella C, Bernardi T, Rizzo R. Letter to the editor: antimicrobial properties of mucus from the brown garden snail Helix aspersa. Br J Biomed Sci. 2016;73:49–50. PubMedWeb of ScienceCrossrefGoogle Scholar

  • [33]

    Santana WA, de Melo CM, Cardoso JC, Pereira-Filho RN, Rabelo AS, Reis FP, et al. Assessment of antimicrobial activity and healing potential of mucous secretion of Achatina fulica. Int J Morphol. 2012;30:365–73. CrossrefWeb of ScienceGoogle Scholar

  • [34]

    Etim L, Aleruchi C, Obande G. Antibacterial properties of snail mucus on bacteria isolated from patients with wound infection. Br Microbiol Res J. 2016;11:1–9. Google Scholar

  • [35]

    Abiona J, Akinduti A, Osinowo O, Onagbesan O. Comparative evaluation of inhibitory activity of epiphgram from albino and normal skinned giant African land snail (Archachatina marginata) against selected bacteria isolates. Ethiop J Environ Stud Manag. 2013;6:177–81. Google Scholar

  • [36]

    Pitt SJ, Graham MA, Dedi CG, Taylor-Harris PM, Gunn A. Antimicrobial properties of mucus from the brown garden snail Helix aspersa. Br J Biomed Sci. 2015;72:174–81. PubMedWeb of ScienceCrossrefGoogle Scholar

  • [37]

    Pereira AE, Rey A, Lopez JP, Castro JP, Uribe N. Caracterización físico-química y actividad antimicrobiana de la secreción mucosa de Achatina fulica. Rev Univ Ind Santander Salud. 2016;48:188–95. Google Scholar

  • [38]

    Mukherjee S, Barman S, Mandal NC, Bhattacharya S. Anti-bacterial activity of Achatina CRP and its mechanism of action. Indian J Exp Biol. 2014;52:692–704. PubMedGoogle Scholar

  • [39]

    Zhong J, Wang W, Yang X, Yan X, Liu R. A novel cysteine-rich antimicrobial peptide from the mucus of the snail of Achatina fulica. Peptides. 2013;39:1–5. CrossrefPubMedWeb of ScienceGoogle Scholar

  • [40]

    Dolashka P, Dolashki A, Van Beeumen J, Floetenmeyer M, Velkova L, Stevanovic S, et al. Antimicrobial activity of molluscan hemocyanins from Helix and Rapana Snails. Curr Pharm Biotechnol. 2016;17:263–70. CrossrefPubMedWeb of ScienceGoogle Scholar

  • [41]

    Zodape GV. A study on presence of bioactive compounds in snail Achantina fulica. J Appl Nat Sci. 2010;2:266–68. CrossrefGoogle Scholar

  • [42]

    Dolashka P, Dolashki A, Velkova L, Stevanovic S, Molin L, Traldi P, et al. Bioactive compounds isolated from garden snails. J Biosci Biotechnol. 2015;SE:147–55. Google Scholar

  • [43]

    Ito S, Shimizu M, Nagatsuka M, Kitajima S, Honda M, Tsuchiya T, et al. High molecular weight lectin isolated from the mucus of the Giant African snail Achatina fulica. Biosci Biotechnol Biochem. 2011;75:20–25. CrossrefPubMedWeb of ScienceGoogle Scholar

  • [44]

    de Toledo-Piza AR, Figueiredo CA, de Oliveira MI, Negri G, Namiyama G, Tonelotto M, et al. The antiviral effect of mollusk mucus on measles virus. Antiviral Res. 2016;134:172–81. CrossrefWeb of SciencePubMedGoogle Scholar

About the article

Received: 2017-12-07

Accepted: 2018-03-12

Published Online: 2018-03-27


Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

Research funding: None declared.

Employment or leadership: None declared.

Honorarium: None declared.

Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.


Citation Information: Journal of Complementary and Integrative Medicine, Volume 15, Issue 3, 20170168, ISSN (Online) 1553-3840, DOI: https://doi.org/10.1515/jcim-2017-0168.

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