Factors affecting probiotic adhesion in vitro and to skin keratinocytes
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Tipo de documento: | Dissertação |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.14/34665 |
Resumo: | Probiotics are defined as "live microorganisms, which when administrated in adequate amounts confer a health benefit in the host". Although its main application is the digestive system, over the last years several benefits that come from its topical use, have been investigated. Several studies have reported beneficial effects on different skin disorders such as atopic dermatitis, acne, eczema, psoriasis, wound healing, skin aging and reactive skin. Its main action is assigned to the inhibition of skin colonization by pathogens. In order to understand the factors that affect the probiotic adhesion to skin keratinocytes, firstly the growth of three probiotic strains was evaluated (Lactobacillus rhamnosus, Lactobacillus delbrueckii subsp. bulgaricus and Propioniferax innocua) in vitro in the presence of abiotic factors similar to those found in skin, namely UV radiation, temperature, pH, NaCl and fatty acids. Then invasion and adhesion assays were performed on the three probiotics, in the presence of pathogenic bacteria (Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli). For that, Cell Culture studies were performed with HaCaT cells, counting later the bacteria through plate counting method using the culture media de Man, Rogosa and Sharp (MRS) and Brain Heart Infusion (BHI), for probiotic and pathogenic bacteria, respectively. As a result, E. coli showed no capacity to invade the keratinocytes, presenting a non-significant viable bacterial count (0.47 ± 0.62 log CFU/mL, while P. aeruginosa (2.19 ± 0.65 log CFU/mL) and S. aureus (2.74 ± 0.40 log CFU/mL) revealed higher invasive bacterial cell values and in invasion tests without the presence of probiotics. In contrast, in the adhesion assays, a considerable number (4.64 ± 0.13 log CFU / mL) of adherent bacteria was obtained. This value is close to those obtained for the remaining pathogenic bacteria: 4.77 ± 0.28 and 5.18 ± 0.04 log CFU/mL for P. aeruginosa and S. aureus, respectively, indicating that the bacterium E. coli does not have the capacity to invade keratinocytes, but rather to adhere to them. The remaining pathogenic bacteria invaded the keratinocytes, although the probiotics of the genus Lactobacillus showed a higher value of viable bacteria in invasion tests alone, demonstrating that these probiotics are more effective in the invasion of HaCaT cells than P. aeruginosa or S. aureus; in these assays the probiotics L. rhamnosus and L. delbrueckii showed approximately 2 more logs of viable bacterial cells in the interior than the pathogenic bacteria. In pathogen adhesion, E. coli adhered less to cells in the presence of probiotics; in competition assay with P. innocua (less 1.96 log CFU/mL) and L. rhamnosus (less 1.77 log CFU/mL), and in substitution assays with all probiotics, while P. aeruginosa only showed vi reduced adhesion ability in competition assays with the bacteria P. innocua (less 1.39 log CFU/mL) and L. rhamnosus (less 1.41 log CFU/mL). Lastly, S. aureus showed reduced adhesion capacity in substitution experiments with L. rhamnosus (less 1.59 log CFU/mL) and competition with P. innocua (less 1.12 log CFU/mL). The mechanisms responsible for the adhesion of probiotics to keratinocytes were investigated, verifying that this may occur through carbohydrates or proteins, as was the case for S. aureus. In ex-vivo assays, using human skin equivalents, the bacterium S. aureus adhered less (1.35 log CFU/mL) in the presence of L. rhamnosus, whereas the probiotic adhered similarly in the model with the presence of the pathogen and without it. The macroscopic analysis showed improvements (tissue regeneration, less exudate and white halo less evident) in wound healing on the model infected by L. rhamnosus and S. aureus suggesting that the utilized probiotic may be benefic in wound healing, inhibiting S. aureus colonization. |
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Factors affecting probiotic adhesion in vitro and to skin keratinocytesProbioticsKeratinocytesSkinAdhesionHaCaTProbióticosQueratinócitosPeleAdesãoDomínio/Área Científica::Ciências Naturais::Ciências BiológicasProbiotics are defined as "live microorganisms, which when administrated in adequate amounts confer a health benefit in the host". Although its main application is the digestive system, over the last years several benefits that come from its topical use, have been investigated. Several studies have reported beneficial effects on different skin disorders such as atopic dermatitis, acne, eczema, psoriasis, wound healing, skin aging and reactive skin. Its main action is assigned to the inhibition of skin colonization by pathogens. In order to understand the factors that affect the probiotic adhesion to skin keratinocytes, firstly the growth of three probiotic strains was evaluated (Lactobacillus rhamnosus, Lactobacillus delbrueckii subsp. bulgaricus and Propioniferax innocua) in vitro in the presence of abiotic factors similar to those found in skin, namely UV radiation, temperature, pH, NaCl and fatty acids. Then invasion and adhesion assays were performed on the three probiotics, in the presence of pathogenic bacteria (Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli). For that, Cell Culture studies were performed with HaCaT cells, counting later the bacteria through plate counting method using the culture media de Man, Rogosa and Sharp (MRS) and Brain Heart Infusion (BHI), for probiotic and pathogenic bacteria, respectively. As a result, E. coli showed no capacity to invade the keratinocytes, presenting a non-significant viable bacterial count (0.47 ± 0.62 log CFU/mL, while P. aeruginosa (2.19 ± 0.65 log CFU/mL) and S. aureus (2.74 ± 0.40 log CFU/mL) revealed higher invasive bacterial cell values and in invasion tests without the presence of probiotics. In contrast, in the adhesion assays, a considerable number (4.64 ± 0.13 log CFU / mL) of adherent bacteria was obtained. This value is close to those obtained for the remaining pathogenic bacteria: 4.77 ± 0.28 and 5.18 ± 0.04 log CFU/mL for P. aeruginosa and S. aureus, respectively, indicating that the bacterium E. coli does not have the capacity to invade keratinocytes, but rather to adhere to them. The remaining pathogenic bacteria invaded the keratinocytes, although the probiotics of the genus Lactobacillus showed a higher value of viable bacteria in invasion tests alone, demonstrating that these probiotics are more effective in the invasion of HaCaT cells than P. aeruginosa or S. aureus; in these assays the probiotics L. rhamnosus and L. delbrueckii showed approximately 2 more logs of viable bacterial cells in the interior than the pathogenic bacteria. In pathogen adhesion, E. coli adhered less to cells in the presence of probiotics; in competition assay with P. innocua (less 1.96 log CFU/mL) and L. rhamnosus (less 1.77 log CFU/mL), and in substitution assays with all probiotics, while P. aeruginosa only showed vi reduced adhesion ability in competition assays with the bacteria P. innocua (less 1.39 log CFU/mL) and L. rhamnosus (less 1.41 log CFU/mL). Lastly, S. aureus showed reduced adhesion capacity in substitution experiments with L. rhamnosus (less 1.59 log CFU/mL) and competition with P. innocua (less 1.12 log CFU/mL). The mechanisms responsible for the adhesion of probiotics to keratinocytes were investigated, verifying that this may occur through carbohydrates or proteins, as was the case for S. aureus. In ex-vivo assays, using human skin equivalents, the bacterium S. aureus adhered less (1.35 log CFU/mL) in the presence of L. rhamnosus, whereas the probiotic adhered similarly in the model with the presence of the pathogen and without it. The macroscopic analysis showed improvements (tissue regeneration, less exudate and white halo less evident) in wound healing on the model infected by L. rhamnosus and S. aureus suggesting that the utilized probiotic may be benefic in wound healing, inhibiting S. aureus colonization.Os probióticos são definidos como “organismos vivos, que quando administrados em quantidades adequadas conferem benefícios para a saúde do hospedeiro”. Apesar da sua principal aplicação ser o sistema digestivo, ao longo dos últimos anos, vários benefícios que advêm do seu uso tópico, têm sido investigados. Diferentes estudos relataram efeitos benéficos em diferentes distúrbios da pele como a dermatite atópica, acne, eczemas, psoríase, cicatrização de feridas, envelhecimento da pele e pele reativa. A sua principal ação é atribuída à inibição da colonização da pele por agentes patogénicos. Tendo como objetivo compreender os fatores que afetam a adesão dos probióticos aos queratinócitos da pele, primeiramente avaliou-se o crescimento de três espécies de probióticos (Lactobacillus rhamnosus, Lactobacillus delbrueckii subsp. bulgaricus e Propioniferax innocua) in vitro na presença de fatores abióticos semelhantes aos encontrados na pele, nomeadamente radiação UV, temperatura, pH, NaCl e ácidos gordos. Posteriormente, procedeu-se a ensaios de invasão e adesão dos três probióticos, na presença de bactérias patogénicas (Pseudomonas aeruginosa, Staphylococcus aureus e Escherichia coli). Para tal, foram realizados ensaios de Cultura Celular com células HaCaT, contabilizando posteriormente as bactérias por método de contagem em placa utilizando os meios de cultura de Man, Rogosa e Sharp (MRS) e Brain Heart Infusion (BHI), para probióticos e patogénicos, respetivamente. Como resultado realça-se que a bactéria E. coli não mostrou capacidade de invadir os queratinócitos da pele, apresentando uma contagem de bactérias viáveis não significante (0.47 ± 0.62 log CFU/mL), enquanto a P. aeruginosa (2.19 ± 0.65 log CFU/mL) e S. aureus (2.74 ± 0.40 log CFU/mL) mostraram valores de células bacterianas invasoras superiores nos ensaios de invasão sem a presença de probióticos. Contrariamente, nos ensaios de adesão obteve-se um valor próximo (4.64 ± 0.13 log CFU/mL) dos valores obtidos para os restantes patógenos (4.77 ± 0.28 e 5.18 ± 0.04 log CFU/mL, para a P. aeruginosa e S. aureus respetivamente), indicando que a bactéria E. coli não possui capacidade de invadir os queratinócitos, mas sim de aderir aos mesmos. As restantes bactérias patogénicas invadiram os queratinócitos, embora os probióticos do género Lactobacillus tenham apresentado um valor significativamente superior de bactérias viáveis nos ensaios de invasão sozinhas, demonstrando que estes probióticos serão mais eficazes na invasão das células HaCaT do que P. aeruginosa ou o S. aureus; nestes ensaios os probióticos L. rhamnosus e L. delbrueckii apresentaram aproximadamente mais 2 logs de células bacterianas viáveis no interior do que as bactérias patogénicas. iv Quanto à adesão das bactérias patogénicas, a E. coli aderiu menos às células em ensaios de competição na presença de P. innocua (menos 1.96 log CFU/mL) e L. rhamnosus (menos 1.77 log CFU/mL), e substituição com todos os probióticos, enquanto P. aeruginosa apenas mostrou menor capacidade de adesão nos ensaios de competição com as bactérias P. innocua (menos 1.39 log CFU/mL) e L. rhamnosus (menos 1.41 log CFU/mL). Por último, o S. aureus mostrou adesão mais reduzida em ensaios de substituição com L. rhamnosus (menos 1.59 log CFU/mL) e de competição com P. innocua (menos 1.12 log CFU/mL). Os mecanismos responsáveis pela adesão dos probióticos aos queratinócitos foram investigados, verificando-se que esta poderá ocorrer através de carboidratos ou de proteínas, como foi o caso para S. aureus. Em ensaios ex-vivo, utilizando modelos de pele humana, a bactéria S. aureus aderiu menos 1.35 log CFU/mL na presença de L. rhamnosus, já o probiótico aderiu de forma semelhante no modelo com a presença do patogénico e sem o mesmo. A análise macroscópica mostrou melhorias (regeneração do tecido, exsudado em menor quantidade e halo branco menos evidente) na cicatrização das feridas no modelo infetado com L. rhamnosus e S. aureus, sugerindo que o probiótico utilizado poderá ser benéfico na cicatrização de feridas, inibindo a colonização por S. aureus.Tavaria, Freni KekhasharúVeritati - Repositório Institucional da Universidade Católica PortuguesaLizardo, Mariana Valente Palla2022-09-07T00:30:25Z2021-06-082021-052021-06-08T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10400.14/34665TID:202755401enginfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-12T17:40:10Zoai:repositorio.ucp.pt:10400.14/34665Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:28:06.076531Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Factors affecting probiotic adhesion in vitro and to skin keratinocytes |
title |
Factors affecting probiotic adhesion in vitro and to skin keratinocytes |
spellingShingle |
Factors affecting probiotic adhesion in vitro and to skin keratinocytes Lizardo, Mariana Valente Palla Probiotics Keratinocytes Skin Adhesion HaCaT Probióticos Queratinócitos Pele Adesão Domínio/Área Científica::Ciências Naturais::Ciências Biológicas |
title_short |
Factors affecting probiotic adhesion in vitro and to skin keratinocytes |
title_full |
Factors affecting probiotic adhesion in vitro and to skin keratinocytes |
title_fullStr |
Factors affecting probiotic adhesion in vitro and to skin keratinocytes |
title_full_unstemmed |
Factors affecting probiotic adhesion in vitro and to skin keratinocytes |
title_sort |
Factors affecting probiotic adhesion in vitro and to skin keratinocytes |
author |
Lizardo, Mariana Valente Palla |
author_facet |
Lizardo, Mariana Valente Palla |
author_role |
author |
dc.contributor.none.fl_str_mv |
Tavaria, Freni Kekhasharú Veritati - Repositório Institucional da Universidade Católica Portuguesa |
dc.contributor.author.fl_str_mv |
Lizardo, Mariana Valente Palla |
dc.subject.por.fl_str_mv |
Probiotics Keratinocytes Skin Adhesion HaCaT Probióticos Queratinócitos Pele Adesão Domínio/Área Científica::Ciências Naturais::Ciências Biológicas |
topic |
Probiotics Keratinocytes Skin Adhesion HaCaT Probióticos Queratinócitos Pele Adesão Domínio/Área Científica::Ciências Naturais::Ciências Biológicas |
description |
Probiotics are defined as "live microorganisms, which when administrated in adequate amounts confer a health benefit in the host". Although its main application is the digestive system, over the last years several benefits that come from its topical use, have been investigated. Several studies have reported beneficial effects on different skin disorders such as atopic dermatitis, acne, eczema, psoriasis, wound healing, skin aging and reactive skin. Its main action is assigned to the inhibition of skin colonization by pathogens. In order to understand the factors that affect the probiotic adhesion to skin keratinocytes, firstly the growth of three probiotic strains was evaluated (Lactobacillus rhamnosus, Lactobacillus delbrueckii subsp. bulgaricus and Propioniferax innocua) in vitro in the presence of abiotic factors similar to those found in skin, namely UV radiation, temperature, pH, NaCl and fatty acids. Then invasion and adhesion assays were performed on the three probiotics, in the presence of pathogenic bacteria (Pseudomonas aeruginosa, Staphylococcus aureus and Escherichia coli). For that, Cell Culture studies were performed with HaCaT cells, counting later the bacteria through plate counting method using the culture media de Man, Rogosa and Sharp (MRS) and Brain Heart Infusion (BHI), for probiotic and pathogenic bacteria, respectively. As a result, E. coli showed no capacity to invade the keratinocytes, presenting a non-significant viable bacterial count (0.47 ± 0.62 log CFU/mL, while P. aeruginosa (2.19 ± 0.65 log CFU/mL) and S. aureus (2.74 ± 0.40 log CFU/mL) revealed higher invasive bacterial cell values and in invasion tests without the presence of probiotics. In contrast, in the adhesion assays, a considerable number (4.64 ± 0.13 log CFU / mL) of adherent bacteria was obtained. This value is close to those obtained for the remaining pathogenic bacteria: 4.77 ± 0.28 and 5.18 ± 0.04 log CFU/mL for P. aeruginosa and S. aureus, respectively, indicating that the bacterium E. coli does not have the capacity to invade keratinocytes, but rather to adhere to them. The remaining pathogenic bacteria invaded the keratinocytes, although the probiotics of the genus Lactobacillus showed a higher value of viable bacteria in invasion tests alone, demonstrating that these probiotics are more effective in the invasion of HaCaT cells than P. aeruginosa or S. aureus; in these assays the probiotics L. rhamnosus and L. delbrueckii showed approximately 2 more logs of viable bacterial cells in the interior than the pathogenic bacteria. In pathogen adhesion, E. coli adhered less to cells in the presence of probiotics; in competition assay with P. innocua (less 1.96 log CFU/mL) and L. rhamnosus (less 1.77 log CFU/mL), and in substitution assays with all probiotics, while P. aeruginosa only showed vi reduced adhesion ability in competition assays with the bacteria P. innocua (less 1.39 log CFU/mL) and L. rhamnosus (less 1.41 log CFU/mL). Lastly, S. aureus showed reduced adhesion capacity in substitution experiments with L. rhamnosus (less 1.59 log CFU/mL) and competition with P. innocua (less 1.12 log CFU/mL). The mechanisms responsible for the adhesion of probiotics to keratinocytes were investigated, verifying that this may occur through carbohydrates or proteins, as was the case for S. aureus. In ex-vivo assays, using human skin equivalents, the bacterium S. aureus adhered less (1.35 log CFU/mL) in the presence of L. rhamnosus, whereas the probiotic adhered similarly in the model with the presence of the pathogen and without it. The macroscopic analysis showed improvements (tissue regeneration, less exudate and white halo less evident) in wound healing on the model infected by L. rhamnosus and S. aureus suggesting that the utilized probiotic may be benefic in wound healing, inhibiting S. aureus colonization. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-06-08 2021-05 2021-06-08T00:00:00Z 2022-09-07T00:30:25Z |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/masterThesis |
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masterThesis |
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