Pro & Postbiotics play a role in disruptive relationships between yeast and bacterias
Pró & Pós-biótico desempenham um papel nas relações disruptivas entre leveduras e bactérias
Palavras-chave:
Candida, Lactobacillus, Probiotics, PrebioticsResumo
Antimicrobial resistance is an inevitable evolutionary event. Pathogenic strains of Candida spp. have been increasing in a number of cases, so candidiasis has become a serious public health problem. Alternative therapeutic approaches are gaining "space" and attention in the treatment of fungal diseases. This study is a systematic review, using the identification, selection, inclusion, and exclusion criteria of the PRISMA method. Works were selected and separated in 5 tables. The Lactobacillus spp. causing opposite effects against several pathogenic microorganisms, being considered one of the probiotic that play essential functions of immunomodulation in the intestinal mucosa, with beneficial effects, restores and promotes the maintenance of vaginal microbiota. It is clear from the data investigated that the use of Lactobacillus may be an alternative therapeutic approach for the treatment or control of the spread of Candida species responsible for candidiasis.
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Alves, R., Kastora, S. L., Gomes-Gonçalves, A., Azevedo, N., Rodrigues, C. F., Silva, S., Demuyser, L., Van Dijck, P., Casal, M., Brown, A. J. P., Henriques, M., & Paiva, S. (2020). Transcriptional responses of Candida glabrata biofilm cells to fluconazole are modulated by the carbon source. Npj Biofilms and Microbiomes, 6(1), 4. https://doi.org/10.1038/s41522-020-0114-5
Beyer, R., Jandric, Z., Zutz, C., Gregori, C., Willinger, B., Jacobsen, I. D., Kovarik, P., Strauss, J., & Schüller, C. (2018). Competition of Candida glabrata against Lactobacillus is Hog1 dependent. Cellular Microbiology, 20(12), e12943. https://doi.org/10.1111/cmi.12943
Bottery, M. J., Pitchford, J. W., & Friman, V.-P. (2021). Ecology and evolution of antimicrobial resistance in bacterial communities. The ISME Journal, 15(4), 939–948. https://doi.org/10.1038/s41396-020-00832-7
Brandão, F. A., Derengowski, L. S., Albuquerque, P., Nicola, A. M., Silva-Pereira, I., & Poças-Fonseca, M. J. (2015). Histone deacetylases inhibitors effects on Cryptococcus neoformans major virulence phenotypes. Virulence, 6(6), 618–630. https://doi.org/10.1080/21505594.2015.1038014
Buggio, L., Somigliana, E., Borghi, A., & Vercellini, P. (2019). Probiotics and vaginal microecology: Fact or fancy? BMC Women’s Health, 19(1), 25. https://doi.org/10.1186/s12905-019-0723-4
Cavalcante, J. P., Paulino, G. V. B., Broetto, L., Morais, T. M. de L., Ferreira, S. M. S., Valente, P., & Landel, M. F. (2020). Prevalence, antifungal susceptibility and virulence determinants of oral yeast species isolated from immunodeficient patients in Northeastern Brazil. 8. https://www.redalyc.org/journal/5704/570468605007/570468605007.pdf
Ceccarani, C., Foschi, C., Parolin, C., D’Antuono, A., Gaspari, V., Consolandi, C., Laghi, L., Camboni, T., Vitali, B., Severgnini, M., & Marangoni, A. (2019). Diversity of vaginal microbiome and metabolome during genital infections. Scientific Reports, 9(1), 14095. https://doi.org/10.1038/s41598-019-50410-x
Chew, S. Y., Cheah, Y. K., Seow, H. F., Sandai, D., & Than, L. T. L. (2015). Probiotic L actobacillus rhamnosus GR ‐1 and L actobacillus reuteri RC ‐14 exhibit strong antifungal effects against vulvovaginal candidiasis‐causing C andida glabrata isolates. Journal of Applied Microbiology, 118(5), 1180–1190. https://doi.org/10.1111/jam.12772
Davies, J., & Davies, D. (2010). Origins and Evolution of Antibiotic Resistance. Microbiology and Molecular Biology Reviews, 74(3), 417–433. https://doi.org/10.1128/MMBR.00016-10
De Gregorio, P. R., Parolin, C., Abruzzo, A., Luppi, B., Protti, M., Mercolini, L., Silva, J. A., Giordani, B., Marangoni, A., Nader-Macías, M. E. F., & Vitali, B. (2020). Biosurfactant from vaginal Lactobacillus crispatus BC1 as a promising agent to interfere with Candida adhesion. Microbial Cell Factories, 19(1), 133. https://doi.org/10.1186/s12934-020-01390-5
Deorukhkar, S. C., Saini, S., & Mathew, S. (2014). Non- albicans Candida Infection: An Emerging Threat. Interdisciplinary Perspectives on Infectious Diseases, 2014, 1–7. https://doi.org/10.1155/2014/615958
Galvão, T. F., Pansani, T. de S. A., & Harrad. (2015). Principais itens para relatar Revisões sistemáticas e Meta-análises: A recomendação PRISMA. Epidemiologia e Serviços de Saúde, 24(2), 335–342. https://doi.org/10.5123/S1679-49742015000200017
Gómez-Gaviria, M., Ramírez-Sotelo, U., & Mora-Montes, H. M. (2022). Non-albicans Candida Species: Immune Response, Evasion Mechanisms, and New Plant-Derived Alternative Therapies. Journal of Fungi, 9(1), 11. https://doi.org/10.3390/jof9010011
Hellstein, J. W., & Marek, C. L. (2019). Candidiasis: Red and White Manifestations in the Oral Cavity. Head and Neck Pathology, 13(1), 25–32. https://doi.org/10.1007/s12105-019-01004-6
Interagency Coordination Group on Antimicrobial Resistance. (2019). No Time To Wait: Securing The Future From Drug-Resistant Infections. https://www.who.int/docs/default-source/documents/no-time-to-wait-securing-the-future-from-drug-resistant-infections-en.pdf
Ji, J., Shu, D., Zheng, M., Wang, J., Luo, C., Wang, Y., Guo, F., Zou, X., Lv, X., Li, Y., Liu, T., & Qu, H. (2016). Microbial metabolite butyrate facilitates M2 macrophage polarization and function. Scientific Reports, 6(1), 24838. https://doi.org/10.1038/srep24838
MacAlpine, J., Daniel-Ivad, M., Liu, Z., Yano, J., Revie, N. M., Todd, R. T., Stogios, P. J., Sanchez, H., O’Meara, T. R., Tompkins, T. A., Savchenko, A., Selmecki, A., Veri, A. O., Andes, D. R., Fidel, P. L., Robbins, N., Nodwell, J., Whitesell, L., & Cowen, L. E. (2021). A small molecule produced by Lactobacillus species blocks Candida albicans filamentation by inhibiting a DYRK1-family kinase. Nature Communications, 12(1), 6151. https://doi.org/10.1038/s41467-021-26390-w
Martin Lopez, J. E. (2015). Candidiasis (vulvovaginal). BMJ Clinical Evidence, 2015, 0815.
McKloud, E., Delaney, C., Sherry, L., Kean, R., Williams, S., Metcalfe, R., Thomas, R., Richardson, R., Gerasimidis, K., Nile, C. J., Williams, C., & Ramage, G. (2021). Recurrent Vulvovaginal Candidiasis: A Dynamic Interkingdom Biofilm Disease of Candida and Lactobacillus. MSystems, 6(4), e00622-21. https://doi.org/10.1128/mSystems.00622-21
Mundula, T., Ricci, F., Barbetta, B., Baccini, M., & Amedei, A. (2019). Effect of Probiotics on Oral Candidiasis: A Systematic Review and Meta-Analysis. Nutrients, 11(10), 2449. https://doi.org/10.3390/nu11102449
Nguyen, L. N., Lopes, L. C. L., Cordero, R. J. B., & Nosanchuk, J. D. (2011). Sodium butyrate inhibits pathogenic yeast growth and enhances the functions of macrophages. Journal of Antimicrobial Chemotherapy, 66(11), 2573–2580. https://doi.org/10.1093/jac/dkr358
Nocua-Báez, L. C., Uribe-Jerez, P., Tarazona-Guaranga, L., Robles, R., & Cortés, J. A. (2020). Azoles de antes y ahora: Una revisión. Revista Chilena de Infectología, 37(3), 219–230. https://doi.org/10.4067/s0716-10182020000300219
Oliveira, L. de C. (2012). Efeito de Drogas Moduladoras da estrutura da cromatina sobre a interação entre Macrófagos Murinos e Paracoccidioides brasiliensis. https://repositorio.unb.br/bitstream/10482/12370/1/2012_LuanaCastroOliveira.pdf
Pais, P., Califórnia, R., Galocha, M., Viana, R., Ola, M., Cavalheiro, M., Takahashi-Nakaguchi, A., Chibana, H., Butler, G., & Teixeira, M. C. (2020). Candida glabrata Transcription Factor Rpn4 Mediates Fluconazole Resistance through Regulation of Ergosterol Biosynthesis and Plasma Membrane Permeability. Antimicrobial Agents and Chemotherapy, 64(9), e00554-20. https://doi.org/10.1128/AAC.00554-20
Paladine, H. L., & Desai, U. A. (2018). Vaginitis: Diagnosis and Treatment. American Family Physician, 97(5), 321–329. https://www.aafp.org/pubs/afp/issues/2018/0301/p321.html
Paniágua, A. L., Correia, A. F., Pereira, L. C., de Alencar, B. M., Silva, F. B. A., Almeida, R. M., & de Medeiros Nóbrega, Y. K. (2021). Inhibitory effects of Lactobacillus casei Shirota against both Candida auris and Candida spp. Isolates that cause vulvovaginal candidiasis and are resistant to antifungals. BMC Complementary Medicine and Therapies, 21(1), 237. https://doi.org/10.1186/s12906-021-03405-z
Parolin, C., Croatti, V., Giordani, B., & Vitali, B. (2022). Vaginal Lactobacillus Impair Candida Dimorphic Switching and Biofilm Formation. Microorganisms, 10(10), 2091. https://doi.org/10.3390/microorganisms10102091
Pereira, L. C., Correia, A. F., da Silva, Z. D. L., de Resende, C. N., Brandão, F., Almeida, R. M., & de Medeiros Nóbrega, Y. K. (2021). Vulvovaginal candidiasis and current perspectives: New risk factors and laboratory diagnosis by using MALDI TOF for identifying species in primary infection and recurrence. European Journal of Clinical Microbiology & Infectious Diseases, 40(8), 1681–1693. https://doi.org/10.1007/s10096-021-04199-1
Pericolini, E., Gabrielli, E., Ballet, N., Sabbatini, S., Roselletti, E., Cayzeele Decherf, A., Pélerin, F., Luciano, E., Perito, S., Jüsten, P., & Vecchiarelli, A. (2017). Therapeutic activity of a Saccharomyces cerevisiae -based probiotic and inactivated whole yeast on vaginal candidiasis. Virulence, 8(1), 74–90. https://doi.org/10.1080/21505594.2016.1213937
Pristov, K. E., & Ghannoum, M. A. (2019). Resistance of Candida to azoles and echinocandins worldwide. Clinical Microbiology and Infection, 25(7), 792–798. https://doi.org/10.1016/j.cmi.2019.03.028
Quindos, G., Gil-Alonso, S., Marcos-Arias, C., Sevillano, E., Mateo, E., Jauregizar, N., & Eraso, E. (2019). Therapeutic tools for oral candidiasis: Current and new antifungal drugs. Medicina Oral Patología Oral y Cirugia Bucal, 0–0. https://doi.org/10.4317/medoral.22978
Rocha-Ramírez, L. M., Pérez-Solano, R. A., Castañón-Alonso, S. L., Moreno Guerrero, S. S., Ramírez Pacheco, A., García Garibay, M., & Eslava, C. (2017). Probiotic Lactobacillus Strains Stimulate the Inflammatory Response and Activate Human Macrophages. Journal of Immunology Research, 2017, 1–14. https://doi.org/10.1155/2017/4607491
Rodrigues, C., Rodrigues, M., Silva, S., & Henriques, M. (2017). Candida glabrata Biofilms: How Far Have We Come? Journal of Fungi, 3(1), 11. https://doi.org/10.3390/jof3010011
Rodríguez-Cerdeira, C., Martínez-Herrera, E., Carnero-Gregorio, M., López-Barcenas, A., Fabbrocini, G., Fida, M., El-Samahy, M., & González-Cespón, J. L. (2020). Pathogenesis and Clinical Relevance of Candida Biofilms in Vulvovaginal Candidiasis. Frontiers in Microbiology, 11, 544480. https://doi.org/10.3389/fmicb.2020.544480
Salari, S., & Ghasemi Nejad Almani, P. (2020). Antifungal effects of Lactobacillus acidophilus and Lactobacillus plantarum against different oral Candida species isolated from HIV/ AIDS patients: An in vitro study. Journal of Oral Microbiology, 12(1), 1769386. https://doi.org/10.1080/20002297.2020.1769386
Sampaio, R., & Mancini, M. (2007). Estudos de revisão sistemática: Um guia para síntese criteriosa da evidência científica. Revista Brasileira de Fisioterapia, 11(1), 83–89. https://doi.org/10.1590/S1413-35552007000100013
Schluter, D. (2001). Ecology and the origin of species. Trends in Ecology & Evolution, 16(7), 372–380. https://doi.org/10.1016/S0169-5347(01)02198-X
Smith, W. L., & Edlind, T. D. (2002). Histone Deacetylase Inhibitors Enhance Candida albicans Sensitivity to Azoles and Related Antifungals: Correlation with Reduction in CDR and ERG Upregulation. Antimicrobial Agents and Chemotherapy, 46(11), 3532–3539. https://doi.org/10.1128/AAC.46.11.3532-3539.2002
Spaggiari, L., Sala, A., Ardizzoni, A., De Seta, F., Singh, D. K., Gacser, A., Blasi, E., & Pericolini, E. (2022). Lactobacillus acidophilus, L. plantarum, L. rhamnosus, and L. reuteri Cell-Free Supernatants Inhibit Candida parapsilosis Pathogenic Potential upon Infection of Vaginal Epithelial Cells Monolayer and in a Transwell Coculture System In Vitro. Microbiology Spectrum, 10(3), e02696-21. https://doi.org/10.1128/spectrum.02696-21
Timmermans, B., De Las Peñas, A., Castaño, I., & Van Dijck, P. (2018). Adhesins in Candida glabrata. Journal of Fungi, 4(2), 60. https://doi.org/10.3390/jof4020060
Vila, T., Sultan, A. S., Montelongo-Jauregui, D., & Jabra-Rizk, M. A. (2020). Oral Candidiasis: A Disease of Opportunity. Journal of Fungi, 6(1), 15. https://doi.org/10.3390/jof6010015
Wall, G., Montelongo-Jauregui, D., Vidal Bonifacio, B., Lopez-Ribot, J. L., & Uppuluri, P. (2019). Candida albicans biofilm growth and dispersal: Contributions to pathogenesis. Current Opinion in Microbiology, 52, 1–6. https://doi.org/10.1016/j.mib.2019.04.001
Wang, Y., Gu, Y., Fang, K., Mao, K., Dou, J., Fan, H., Zhou, C., & Wang, H. (2018). Lactobacillus acidophilus and Clostridium butyricum ameliorate colitis in murine by strengthening the gut barrier function and decreasing inflammatory factors. Beneficial Microbes, 9(5), 775–787. https://doi.org/10.3920/BM2017.0035
Xie, H. Y., Feng, D., Wei, D. M., Mei, L., Chen, H., Wang, X., & Fang, F. (2017). Probiotics for vulvovaginal candidiasis in non-pregnant women. Cochrane Database of Systematic Reviews, 2017(11). https://doi.org/10.1002/14651858.CD010496.pub2
Yano, J., Sobel, J. D., Nyirjesy, P., Sobel, R., Williams, V. L., Yu, Q., Noverr, M. C., & Fidel, P. L. (2019). Current patient perspectives of vulvovaginal candidiasis: Incidence, symptoms, management and post-treatment outcomes. BMC Women’s Health, 19(1), 48. https://doi.org/10.1186/s12905-019-0748-8
Zangl, I., Pap, I.-J., Aspöck, C., & Schüller, C. (2020). The role of Lactobacillus species in the control of Candida via biotrophic interactions. Microbial Cell, 7(1), 1–14. https://doi.org/10.15698/mic2020.01.702