Astichopus multifidus y Holothuria floridana de la costa yucateca como fuente potencial de agentes antifúngicos.

Autores/as

DOI:

https://doi.org/10.15649/2346075X.5093

Palabras clave:

Astichopus, Holothuria, Isostichopus, antifúngico, Yucatán

Resumen

Introducción. Las infecciones causadas por hongos patógenos representan un desafío persistente para la salud pública. Los invertebrados marinos, como los pepinos de mar (holoturias), son reconocidos por su alto contenido proteico y diversas propiedades medicinales. Además, actúan como reservorios de compuestos bioactivos. En las aguas territoriales de México, se encuentran seis especies de pepinos de mar, entre ellas Astichopus multifidus, Isostichopus badionotus y Holothuria floridana, distribuidas a lo largo de la península de Yucatán. Sin embargo, la sobreexplotación amenaza a estas especies, lo que podría reducir fuentes valiosas de agentes antimicrobianos. Objetivos. Este estudio tiene como objetivo evaluar la actividad antifúngica de extractos orgánicos de A. multifidus y H. floridana frente a diversas cepas fúngicas, mediante ensayos de concentración mínima inhibitoria (CMI) y concentración mínima fungicida (CMF). Materiales y métodos. Se obtuvieron extractos orgánicos de A. multifidus y H. floridana, los cuales fueron evaluados mediante el método de microdilución para determinar su actividad antifúngica. Se establecieron los valores de CMI y CMF frente a un panel de cepas fúngicas, incluyendo Trichophyton rubrum, Aspergillus niger y Cryptococcus neoformans. También se evaluaron extractos de Isostichopus badionotus. Resultados y discusión. Aproximadamente el 50 % de los extractos mostró actividad antifúngica. Los extractos butanólicos del cuerpo de A. multifidus y H. floridana presentaron los valores más bajos de CMI (15,6 µg/mL) frente a T. rubrum y A. niger, respectivamente. Además, estos extractos mostraron actividad antifúngica (31,2 µg/mL) contra C. neoformans. En contraste, los extractos de I. badionotus no presentaron actividad. Estos resultados sugieren que A. multifidus y H. floridana contienen compuestos bioactivos con potencial antifúngico. Conclusiones. Las propiedades antifúngicas de A. multifidus y H. floridana destacan su potencial como fuentes de nuevos agentes antifúngicos. Su uso sostenible podría contribuir al desarrollo de nuevos tratamientos antimicóticos

Referencias

1. Rodrigues ML, Nosanchuk JD. Recognition of fungal priority pathogens: What next? PLoS Negl Trop Dis. 2023;17(3):e0011136. https://doi.org/10.1371/journal.pntd.0011136

2. Kainz K, Bauer MA, Madeo F, Carmona-Gutierrez D. Fungal infections in humans: The silent crisis. Microb Cell. 2020;7(6):143-5. https://doi.org/10.15698/mic2020.06.718

3. Sousa NSO, Almeida JDR, Frickmann H, Lacerda MVG, Souza JVB. Searching for new antifungals for the treatment of cryptococcosis. Soc Bras Med Trop. 2023;56:e01212023. https://doi.org/10.1590/0037-8682-0121-2023

4. Chen Y, Shi ZW, Strickland AB, Shi M. Cryptococcus neoformans infection in the central nervous system: The battle between host and pathogen. J Fungi. 2022;8(8):1069. https://doi.org/10.3390/jof8101069

5. Maziarz EK, Perfect JR. Cryptococcosis. Infect Dis Clin North Am. 2016;30(1):179-206. https://doi.org/10.1016/j.idc.2015.10.006

6. Pasquier E, Kunda J, De Beaudrap P, Loyse A, Temfack E, Molloy SF, et al. Long-term mortality and disability in cryptococcal meningitis: A systematic literature review. Clin Infect Dis. 2018;66:1122-32. https://doi.org/10.1093/cid/cix870

7. Pappas P, Lionakis M, Arendrup M, Ostrosky‑Zeichner L, Kullberg BJ. Invasive candidiasis. Nat Rev Dis Primers. 2018;4:18026. https://doi.org/10.1038/nrdp.2018.26

8. Fang W, Wu J, Cheng M, Zhu X, Du M, Chen C, Liao W, Zhi K, Pan W. Diagnosis of invasive fungal infections: Challenges and recent developments. J Biomed Sci. 2023;30:42. https://doi.org/10.1186/s12929-023-00926-2

9. Arastehfar A, Carvalho A, Houbraken J, Lombardi L, Garcia-Rubio R, Jenks JD, Rivero-Menendez O, Aljohani R, Jacobsen ID, Berman J, Osherov N, Hedayati MT, Ilkit M, Armstrong-James D, Gabaldón T, Meletiadis J, Kostrzewa M, Pan W, Lass-Flörl C, Perlin DS, Hoenigl M. Aspergillus fumigatus and aspergillosis: From basics to clinics. Stud Mycol. 2021;100:100115. https://doi.org/10.1016/j.simyco.2021.100115

10. Kanaujia R, Singh S, Rudramurthy SM. Aspergillosis: An update on clinical spectrum, diagnostic schemes, and management. Curr Fungal Infect Rep. 2023;17:144-55. https://doi.org/10.1007/s12281-023-00461-5

11. Bandres MV, Modi P, Sharma S. Aspergillus fumigatus. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; January 2025. Available from: https://www.ncbi.nlm.nih.gov/books/NBK482464/

12. Rudramurthy SM, Paul RA, Chakrabarti A, Mouton JW, Meis JF. Invasive aspergillosis by Aspergillus flavus: Epidemiology, diagnosis, antifungal resistance, and management. J Fungi (Basel). 2019;5(2):55. https://doi.org/10.3390/jof5030055

13. Chanyachailert P, Leeyaphan C, Bunyaratavej S. Cutaneous fungal infections caused by dermatophytes and non-dermatophytes: An updated comprehensive review of epidemiology, clinical presentations, and diagnostic testing. J Fungi (Basel). 2023;9(6):669. https://doi.org/10.3390/jof9060669

14. McKeny PT, Nessel TA, Zito PM. Antifungal antibiotics. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023. Available from: https://www.ncbi.nlm.nih.gov/books/NBK538168

15. Mushtaq S, Abbasi BH, Uzair B, Abbasi R. Natural products as reservoirs of novel therapeutic agents. EXCLI J. 2018;17:420-51. https://doi.org/10.17179/excli2018-1174

16. Macedo MWFS, Cunha NBD, Carneiro JA, Costa RA, Alencar SA, Cardoso MH, Franco OL, Dias SC. Marine organisms as a rich source of biologically active peptides. Front Mar Sci. 2021;8:667764. https://doi.org/10.3389/fmars.2021.667764

17. Zhukova NV. Fatty acids of echinoderms: Diversity, current applications and future opportunities. Mar Drugs. 2022;21(1):21. https://doi.org/10.3390/md21010021

18. Pangestuti R, Arifin Z. Medicinal and health benefit effects of functional sea cucumbers. J Tradit Med Complement. 2017;8(3):341-51. https://doi.org/10.1016/j.jtcme.2017.06.007

19. Mashjoor S, Yousefzadi M. Cytotoxic effects of three Persian Gulf species of holothurians. Iran J Vet Res. 2019;20:19-26. https://pubmed.ncbi.nlm.nih.gov/31191695/

20. Khotimchenko Y. Pharmacological potential of sea cucumbers. Int J Mol Sci. 2018;19(5):1342. https://doi.org/10.3390/ijms19051342

21. Cheng X, Zhang R, Wen Z. Bioactive compounds and biological functions of sea cucumbers as potential functional foods. J Funct Foods. 2018;49:73-84. https://doi.org/10.1016/j.jff.2018.08.009

22. Hossain A, Dave D, Shahidi F. Antioxidant potential of sea cucumbers and their beneficial effects on human health. Mar Drugs. 2022;20:521. https://doi.org/10.3390/md20080521

23. Abdullah R, Putra MY, Yasman. Antibacterial and antioxidant activity of sea cucumber extracts collected from Lampung waters, Indonesia. K J S. 2023;50(4):615-21. https://doi.org/10.1016/j.kjs.2023.03.012

24. Zhong S, Qiao Y, Zhao L, Huang G, Liu Y, Huang L. Characterization and phylogenetic analysis of the complete mitochondrial genome of Actinopyga lecanora (Jaeger, 1833) (Holothuriida: Holothuriidae). Mitochondrial DNA B Resour. 2021;6(10):2801-2. https://doi.org/10.1080/23802359.2021.1970641

25. Ghanbari R, Ebrahimpour A, Abdul-Hamid A, Ismail A, Saari N. Actinopyga lecanora hydrolysates as natural antibacterial agents. Int J Mol Sci. 2012;13(12):16796-811. https://doi.org/10.3390/ijms131216796

26. Wang Z, Zhang H, Yuan W, Gong W, Tang H, Liu B, Yin S. Antifungal nortriterpene and triterpene glycosides from the sea cucumber Apostichopus japonicus Selenka. Food Chem. 2012;132:295-300. https://doi.org/10.1016/j.foodchem.2011.10.080

27. Keipour S, Emtyazjoo M, Ghaderian SMH, Araghi PE. Cytotoxic and antibacterial activities of Holothuria (Mertensiothuria) leucospilota extracts. Iran J Fish. 2023;22(1):138-55. https://doi.org/10.22092/ijfs.2023.128642

28. Omran NE, Khedr AM. Structure elucidation, protein profile and the antitumor effect of the biological active substance extracted from sea cucumber Holothuria polii. Toxicol Ind Health. 2015;31(1):1-8. https://doi.org/10.1177/0748233712466135

29. Mashjoor S, Yousefzadi M. Holothurians antifungal and antibacterial activity to human pathogens in the Persian Gulf. J Mycol Med. 2017;27(1):46-56. https://doi.org/10.1016/j.mycmed.2016.08.008

30. Careaga VP, Muniain C, Maier MS. Patagonicosides B and C, two antifungal sulfated triterpene glycosides from the sea cucumber Psolus patagonicus. Chem Biodivers. 2011;8(3):467-75. https://doi.org/10.1002/cbdv.201000044

31. Pedroza-Gutiérrez C, López-Rocha JA. Ungovernable systems: The strength of informal institutions in the sea cucumber fishery in Yucatán, México. PLoS ONE. 2021;16(3):e0249132. https://doi.org/10.1371/journal.pone.0249132

32. Hendler G. Collecting, preserving and archiving echinoderms. Nat Hist Los Angeles County. Los Angeles; 2004.

33. Clinical and Laboratory Standards Institute (CLSI). Reference method for broth dilution antifungal susceptibility testing of yeasts. Approved standard. 3rd ed. CLSI document M27-A3. Wayne, PA; 2008.

34. Clinical and Laboratory Standards Institute (CLSI). Reference method for broth dilution antifungal susceptibility testing of conidium-forming filamentous fungi. Approved standard. 2nd ed. CLSI document M38-A. Wayne, PA; 2002.

35. Cos P, Vlietinck A, Berghe D, Maes L. Anti-infective potential of natural products: How to develop a stronger in vitro ‘proof-of-concept’. J Ethnopharmacol. 2006;106:290-302. https://doi.org/10.1016/j.jep.2006.04.003

36. Zhang QW, Lin LG, Ye WC. Techniques for extraction and isolation of natural products: a comprehensive review. Chin Med. 2018;13(17):20. https://10.1186/s13020-018-0177-x

37. Bordbar S, Anwar F, Saari N. High-value components and bioactives from sea cucumbers for functional foods—a review. Mar Drugs. 2011;9(10):1761-1805. https://doi.org/10.3390/md9101761

38. Putra Y, Soffa FB, Firdaus M, Pangestuti R, Siahaan EA. Determination of fatty acid profiles and bioactive properties of body wall and viscera of Holothuria atra collected from Lombok Island, Indonesia. IOP Conf Ser Earth Environ Sci. 2022;1119:012052. https://10.1088/1755-1315/1119/1/012052

39. Carletti A, Cardoso C, Lobo-Arteaga J, Sales S, Juliao D, Ferreira I,. Antioxidant and anti-inflammatory extracts from sea cucumbers and tunicates induce a pro-osteogenic effect in zebrafish larvae. Front Nutr. 2022;9:888360. https://10.3389/fnut.2022.888360

40. Moguel-Salazar F, Ortiz-Vázquez E, Rodriguez-Canul R, Olivera Castillo L. Antimicrobial activity of aqueous extracts of sea cucumber (Isostichopus badionotus) from the coast of Yucatán, México. Afr J Microbiol Res. 2013;7:3621-3626. http://dx.doi.org/10.5897/AJMR12.860

41. Ereguero MG, Cordero MA, Rodelyn D, Tabugo S. Antifungal activity of selected sea cucumber species from Tukuran, Zamboanga del Sur, Mindanao, Philippines using modified SPOTi assay. Biodiversitas. 2022;23:6049-6045. http://dx.doi.org/10.13057/biodiv/d231160

42. Kumar R, Chaturvedi A, Shukla P, Lakshmi V. Antifungal activity in triterpene glycosides from the sea cucumber Actinopyga lecanora. Bioorg Med Chem Lett. 2007;17:4387-4391. https://doi.org/10.1016/j.bmcl.2006.12.052

43. Encarnacion-Dimayuga R, Murillo-Álvarez JI, Christophersen C, Chan-Bacab M, Reiriz MLG, Zacchino S. Leishmanicidal, antifungal, and cytotoxic activity of triterpenoid glycosides isolated from the sea cucumber Neothyone gibbosa. Nat Prod Commun. 2006;1(7). https://10.1177/1934578X0600100705

44. Husni A. Effect of extraction methods on antifungal activity of sea cucumber (Stichopus japonicus). Agritech. 2014;34:1-7. https://doi.org/10.22146/agritech.9515

45. Adibpour N, Nasr F, Nematpour F, Shakouri A, Ameri A. Antibacterial and antifungal activity of Holothuria leucospilota isolated from Persian Gulf and Oman Sea. Jundishapur J Microbiol. 2014;7(1):e8708. https://doi.org/10.5812/jjm.8708

46. Mohammadizadeh F, Ehsanpor M, Afkhami M, Mokhlesi A, Khazaali A, Montazeri S. Antibacterial, antifungal and cytotoxic effects of a sea cucumber Holothuria leucospilota, from the north coast of the Persian Gulf. J Mar Biol Assoc UK. 2013;93(5):1401-1405. https://doi.org/10.1017/S0025315412001889

47. Ismail H, Lemriss S, Aoun Z, Mhadhebi L, Dellai A, Kacem Y, Boiron P, Bouraoui A. Antifungal activity of aqueous and methanolic extracts from the Mediterranean sea cucumber, Holothuria polii. J Mycol Med. 2008;18:23-26. https://doi.org/10.1016/j.mycmed.2008.01.002

48. Dhinakaran DI, Lipton AP. Antitumor and antifungal activities of organic extracts of sea cucumber Holothuria atra from the southeast coast of India. J Ocean Univ China. 2015;14:185-189. https://doi.org/10.1007/s11802-015-2528-x

49. Ghadiri M, Kazemi S, Heidari B, Rassa M. Bioactivity of aqueous and organic extracts of sea cucumber Holothuria leucospilota (Brandt 1835) on pathogenic Candida and Streptococci. Int Aquat Res. 2018;10:31-43. https://doi.org/10.1007/s40071-017-0186-x

50. Shakouri A, Shoushizadeh MR, Nematpour F. Antimicrobial activity of sea cucumber (Stichopus variegatus) body wall extract in Chabahar Bay, Oman Sea. Jundishapur J Nat Pharm Prod. 2017;12(1):e32422. https://doi.org/10.5812/jjnpp.32422

51. Afkhami M, Ehsanpour M. Evaluation bioactivity of a sea cucumber, Stichopus hermanni from Persian Gulf. J Exp Biol. 2014;4:254-258. https://www.researchgate.net/publication/261760598_Evaluation_bioactivity_of_a_Sea_cucumber_Stichopus_hermanni_from_Persian_Gulf

52. Shaharuddin B. Antifungal effects of a sea cucumber (Stichopus chloronatus) on Aspergillus fumigatus-induced keratitis in rabbits. Int Med J. 2006;13:135-138. https://jglobal.jst.go.jp/en/detail?JGLOBAL_ID=200902255621957350

53. Omran NE, Allam NG. Screening of microbial contamination and antimicrobial activity of sea cucumber Holothuria polii. Toxicol Ind Health. 2013;29(10):944-954. https://doi.org/10.1177/0748233712448116

54. Kalinin V, Aminin S, Avilov A, Stonik V. Triterpene glycosides from sea cucumbers (Holothurioidea, Echinodermata). Biological activities and functions. In: Atta-ur-Rahman, editor. Studies in Natural Products Chemistry. Netherlands: Elsevier; 2008. p. 135-196.

55. Xianyou W, Mingzhu L, Yun B, Yaowu D, Shaofeng D. Non-holostane and holostane triterpene glycosides from spawn of sea cucumber Apostichopus japonicus Selenka. J Food Compos Anal. 2022;109:104492. https://doi.org/10.1016/j.jfca.2022.104492

56. Kalinin VI, Silchenko AS, Avilov SA, Stonik VA. Progress in the studies of triterpene glycosides from sea cucumbers (Holothuroidea, Echinodermata) between 2017 and 2021. Nat Prod Comm. 2021;16(10):1-24. https://doi.org/10.1177/1934578X211053934

57. Wang XH, Zou ZR, Yi YH, Han H, Li L, Pan MX. Variegatusides: new non-sulphated triterpene glycosides from the sea cucumber Stichopus variegatus Semper. Mar Drugs. 2014;12(4):2004-2018. https://doi.org/10.3390/md12042004

58. Thawabteh AM, Swaileh Z, Ammar M, Jaghama W, Yousef M, Karaman R, Bufo AS, Scrano L. Antifungal and antibacterial activities of isolated marine compounds. Toxins. 2023;15:93. https://doi.org/10.3390/toxins15020093

59. Solís-Marín F, Honey-Escandón M, Herrero-Perezrul M, Benitez-Villalobos F, Díaz-Martínez P, Buitrón-Sánchez E, Alvarado J, Solís-Marín F. The echinoderms of México: Biodiversity, distribution and current state of knowledge. In: Echinoderm Research and Diversity in Latin America. Berlin Heidelberg: Springer-Verlag; 2013. p. 11-65.

60. Stonik V, Maltsev I, Kalinovsky A, Konde K, Elyakov G. Glycosides of marine invertebrates. XI. Two new triterpene glycosides from sea cucumbers belonging to the family Stichopodidae. Khim Prirod Soedin. 1982;2:194-199.

61. Kitagawa I, Kobayashi M, Inamoto T, Yosuzawa T, Kyogoku Y. The structures of 6 antifungal oligoglycosides, stichloroside-A1, stichloroside-A2, stichloroside-B1, stichloroside-B2, stichloroside-C1, and stichloroside-C2, from the sea-cucumber Stichopus chloronotus (Brandt). Chem Pharm Bull. 1981;29:2387-2391. https://dx.doi.org/10.1248/cpb.29.2387

62. Elyakov G, Kuznetsova T, Conde C, Kalinovskaya N, Kalinovskii A, Smetanina O. Glycosides of marine invertebrates VIII. Steroid glycosides of the holothurian Isostichopus badionotus. Chem Nat Comp. 1979;15:706-708. https://link.springer.com/article/10.1007/BF00565567

63. Handayani S, Nurdiana N, Winarsih S, Endharti AT. Holothurin compound from sea cucumber (Holothuria sp.) as antifungal alternative against Candida infections. J Med Sci. 2022;10(A):470-474. https://doi.org/10.3889/oamjms.2022.8086

64. Ning Z, Wang P, Zuo Z, Tao X, Gao L, Xu C, Wang Z, Wu B, Gao N, Zha J. A fucan sulfate with pentasaccharide repeating units from the sea cucumber Holothuria floridana and its anticoagulant activity. Mar Drugs. 2022;20(6):377. https://doi.org/10.3390/md20060377

Descargas

Publicado

2025-09-19

Cómo citar

Padilla, N., León-Deniz, L., Salazar-Mendoza , J., Sabido-Graniel , M., Quijano, L., & Mena-Rejón , G. (2025). Astichopus multifidus y Holothuria floridana de la costa yucateca como fuente potencial de agentes antifúngicos. Innovaciencia, 13(1). https://doi.org/10.15649/2346075X.5093

Descargas

Los datos de descarga aún no están disponibles.

Número

Sección

Artículo original de investigación e innovacion