Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape

Detalhes bibliográficos
Ano de defesa: 2024
Autor(a) principal: SANTOS, Pâmela Gomes lattes
Orientador(a): GUERRA, Rosane Nassar Meireles lattes
Banca de defesa: GUERRA, Rosane Nassar Meireles lattes, MONTEIRO NETO, Valério lattes, RIBEIRO, Rachel Melo lattes, OLIVEIRA, Aluísio da Silva lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal do Maranhão
Programa de Pós-Graduação: PROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS DA SAÚDE/CCBS
Departamento: COBI - COORDENAÇÃO DO CURSO DE BIOLOGIA/CCCH
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://tedebc.ufma.br/jspui/handle/tede/5864
Resumo: The bioprospection of natural products, with antimicrobial action and therapeutic purpose, has been gaining much prominence worldwide, especially considering the high number of microorganisms resistant to conventional treatments. In this context, products derived from Anacardium occidentale, a species native to Brazil and known as the cashew tree, emerge as a promising alternative due to their antimicrobial potential. The present study evaluated the effect of ethanolic extract of A. occidentale (EAO) flowers in vitro, considering the action on the adhesion and biofilm formation of ESKAPE’s bacteria group, as well as on lethal Staphylococcus aureus infection induced in Tenebrio molitor larvae. HPLC and LC- MS determined the chemical composition of the extract. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) determined the antibacterial activity on standard strains of Staphylococcus aureus (ATCC 25923) and Enterococcus faecalis (ATCC 29212), Escherichia coli (ATCC 29922), Klebsiella pneumoniae (ATCC 700603) and in multidrug-resistant clinical strains of S. aureus (MRSA 240016969961 and MRSA 240016969962). The effects of EAO were also evaluated on the viability and biomass of adhesion and preformed and formed biofilms. For the in vivo assays, T. molitor larvae were used to determine the toxicity of EAO, standardize the lethal inoculum of S. aureus, and evaluate the EAO effect after lethal infection with S. aureus. The animals were divided into six groups (N=10) to determine their survival during the lethal infection. Sham: without infection or treatment, and five groups lethally infected with S. aureus (105 CFU/μL), intracelomic and treated with EAO or CIPRO by the same route. Groups EAO1/2: treated EAO in a concentration corresponding to 1/2 MIC (3.12 mg/mL), EAOCIM: EAO in MIC concentration (6.25 mg/mL) and EAO2: treated with EAO corresponding to 2x MIC concentration (12.5 mg/mL). Negative control: received phosphate-balanced salt solution (PBS), CiPro: treated with ciprofloxacin (1,56 μg/mL), The major compounds identified were: shikimic acid, gallic acid, quercetin, isoquercetin, galloyl glucose, digaloyglucose, isomer 1 and isomer 2 of tetragalloylglucose. The MIC values ranged from 6.25 to 50 mg/mL for the strains, with the best activity for S. aureus (MIC=6.25 mg/mL) and the MRSA strains (MIC 12.5 mg/mL). The EAO had bactericidal action according to CBM/CIM. The extract reduced the biomass and viability of adhesion- preformed and formed biofilms of S. aureus. EAO showed low toxicity to T. molitor. Treatment with EAO increased the larvae's survival after lethal infection with S. aureus in a dose-dependent way. In conclusion, EAO prolonged the survival of larvae lethally infected by S. aureus, possibly due to its antibacterial action and its effects on adhesion and biofilms.
id UFMA_dc503cdfccd07a6e892d4070a6f4df25
oai_identifier_str oai:tede2:tede/5864
network_acronym_str UFMA
network_name_str Biblioteca Digital de Teses e Dissertações da UFMA
repository_id_str
spelling GUERRA, Rosane Nassar Meireleshttp://lattes.cnpq.br/2316192786452127GUERRA, Rosane Nassar Meireleshttp://lattes.cnpq.br/2316192786452127MONTEIRO NETO, Valériohttp://lattes.cnpq.br/5476942147520772RIBEIRO, Rachel Melohttp://lattes.cnpq.br/4752952470368965OLIVEIRA, Aluísio da Silvahttp://lattes.cnpq.br/2751713874701874http://lattes.cnpq.br/7818949201806939SANTOS, Pâmela Gomes2025-02-05T16:32:57Z2024-11-29SANTOS, Pâmela Gomes. Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape. 2024. 70 f. Dissertação (Programa de Pós-Graduação em Ciências da Saúde/CCBS) - Universidade Federal do Maranhão, São Luís, 2024.https://tedebc.ufma.br/jspui/handle/tede/5864The bioprospection of natural products, with antimicrobial action and therapeutic purpose, has been gaining much prominence worldwide, especially considering the high number of microorganisms resistant to conventional treatments. In this context, products derived from Anacardium occidentale, a species native to Brazil and known as the cashew tree, emerge as a promising alternative due to their antimicrobial potential. The present study evaluated the effect of ethanolic extract of A. occidentale (EAO) flowers in vitro, considering the action on the adhesion and biofilm formation of ESKAPE’s bacteria group, as well as on lethal Staphylococcus aureus infection induced in Tenebrio molitor larvae. HPLC and LC- MS determined the chemical composition of the extract. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) determined the antibacterial activity on standard strains of Staphylococcus aureus (ATCC 25923) and Enterococcus faecalis (ATCC 29212), Escherichia coli (ATCC 29922), Klebsiella pneumoniae (ATCC 700603) and in multidrug-resistant clinical strains of S. aureus (MRSA 240016969961 and MRSA 240016969962). The effects of EAO were also evaluated on the viability and biomass of adhesion and preformed and formed biofilms. For the in vivo assays, T. molitor larvae were used to determine the toxicity of EAO, standardize the lethal inoculum of S. aureus, and evaluate the EAO effect after lethal infection with S. aureus. The animals were divided into six groups (N=10) to determine their survival during the lethal infection. Sham: without infection or treatment, and five groups lethally infected with S. aureus (105 CFU/μL), intracelomic and treated with EAO or CIPRO by the same route. Groups EAO1/2: treated EAO in a concentration corresponding to 1/2 MIC (3.12 mg/mL), EAOCIM: EAO in MIC concentration (6.25 mg/mL) and EAO2: treated with EAO corresponding to 2x MIC concentration (12.5 mg/mL). Negative control: received phosphate-balanced salt solution (PBS), CiPro: treated with ciprofloxacin (1,56 μg/mL), The major compounds identified were: shikimic acid, gallic acid, quercetin, isoquercetin, galloyl glucose, digaloyglucose, isomer 1 and isomer 2 of tetragalloylglucose. The MIC values ranged from 6.25 to 50 mg/mL for the strains, with the best activity for S. aureus (MIC=6.25 mg/mL) and the MRSA strains (MIC 12.5 mg/mL). The EAO had bactericidal action according to CBM/CIM. The extract reduced the biomass and viability of adhesion- preformed and formed biofilms of S. aureus. EAO showed low toxicity to T. molitor. Treatment with EAO increased the larvae's survival after lethal infection with S. aureus in a dose-dependent way. In conclusion, EAO prolonged the survival of larvae lethally infected by S. aureus, possibly due to its antibacterial action and its effects on adhesion and biofilms.A bioprospecção de produtos naturais, com ação antimicrobiana e finalidade terapêutica, vem ganhando bastante destaque no mundo, sobretudo considerando o elevado número de microrganismos resistentes aos tratamentos convencionais. Nesse contexto, os produtos derivados de Anacardium occidentale, espécie nativa do Brasil e popularmente conhecida como cajueiro, surgem como uma promissora alternativa, devido ao seu potencial antimicrobiano. O presente estudo avaliou o efeito do extrato etanólico das flores de A. occidentale (EAO) in vitro, considerando a ação sobre a adesão e formação de biofilme de bactérias do grupo ESKAPE, bem como os efeitos do extrato na infecção letal ocasionada por Staphylococcus aureus em larvas de Tenebrio molitor. A composição química do extrato foi analisada por HPLC e LC-MS. A ação antimicrobiana in vitro foi avaliada pelo ensaio de microdiluição em caldo para determinar a concentração inibitória mínima (CIM) e concentração bactericida mínima (CBM) sobre cepas padrão S. aureus (ATCC 25923), Enterococcus. faecalis (ATCC 29212), Escherichia coli (ATCC 25922); Klebsiella pneumoniae (ATCC 700603) e em linhagens clínicas multirresistentes (MRSA 240016969961 e MRSA 240016969962). Os efeitos do EAO também foram avaliados sobre a viabilidade e biomassa da adesão e biofilmes pré-formados e formados. Os ensaios in vivo com as larvas de T. molitor determinaram a toxicidade do EAO, e os efeitos do extrato na infecção letal induzida por S. aureus. As larvas foram divididas em seis grupos (N=10), sendo um Sham, sem infecção ou tratamento e cinco grupos infectados, letalmente, com S. aureus (105 UFC/μL), por via intracelômica (ic.) e tratados pela mesma via. Os três grupos tratados com diferentes concentrações do extrato: EAO1/2: extrato na concentração correspondente a 1/2 MIC (3,12 mg/mL), EAOCIM: EAO no valor de MIC (6,25 mg/mL) e EAO2: Tratado com EAO no valor de 2x MIC (12,5 mg/mL). Esses grupos foram comparados ao grupo Controle: recebeu solução salina balanceada com fostato (PBS) e ao grupo CiPro: recebeu ciprofloxacina (1,56 μg/mL). No EAO foram identificados como compostos majoritários: ácido chiquímico, ácido gálico, quercetina, isoquercetina, galoil glucose, digaloilglucose, isômero 1 e isômero 2 de tetragaloilglucose. Os valores de CIM variaram entre 6,25 e 50 mg/mL, sendo a melhor atividade para S. aureus (ATCC 25923) (CIM=6,25 mg/mL) e para as linhagens de MRSA (CIM 12,5 mg/mL). A ação do EAO foi bactericida de acordo com a relação CBM/CIM. O extrato reduziu a biomassa e a viabilidade da adesão e dos biofilmes pré-formados e formados de S. aureus, E. coli e MRSA. In vivo os resultados mostraram baixa toxicidade para T. molitor, para a maioria das concentrações testadas. O tratamento com EAO aumentou a sobrevida das larvas letalmente infectadas com S. aureus, tendo efeito dose dependente. Em conclusão, o EAO prolongou a sobrevida de larvas letalmente infectadas por S. aureus, possivelmente devido sua ação antibacteriana e seus efeitos sobre a adesão e os biofilmes bacterianos.Submitted by Jonathan Sousa de Almeida (jonathan.sousa@ufma.br) on 2025-02-05T16:32:57Z No. of bitstreams: 1 PÂMELAGOMESSANTOS.pdf: 2013406 bytes, checksum: a9b3c1f68c33d6f13fdb761e24598f26 (MD5)Made available in DSpace on 2025-02-05T16:32:57Z (GMT). No. of bitstreams: 1 PÂMELAGOMESSANTOS.pdf: 2013406 bytes, checksum: a9b3c1f68c33d6f13fdb761e24598f26 (MD5) Previous issue date: 2024-11-29CAPESapplication/pdfporUniversidade Federal do MaranhãoPROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS DA SAÚDE/CCBSUFMABrasilCOBI - COORDENAÇÃO DO CURSO DE BIOLOGIA/CCCHantibiótico;antivirulência;Staphylococcus aureus;MRSA.antibiotic;anti-virulence;Staphylococcus aureus;MRSA.Ciências da SaúdeAtividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskapeActividad antibacteriana de Anacardium occidentale contra bacterias del grupo eskapeinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UFMAinstname:Universidade Federal do Maranhão (UFMA)instacron:UFMAORIGINALPÂMELAGOMESSANTOS.pdfPÂMELAGOMESSANTOS.pdfapplication/pdf2013406http://tedebc.ufma.br:8080/bitstream/tede/5864/2/P%C3%82MELAGOMESSANTOS.pdfa9b3c1f68c33d6f13fdb761e24598f26MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-82255http://tedebc.ufma.br:8080/bitstream/tede/5864/1/license.txt97eeade1fce43278e63fe063657f8083MD51tede/58642025-02-05 13:32:57.502oai:tede2: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Biblioteca Digital de Teses e Dissertaçõeshttps://tedebc.ufma.br/jspui/PUBhttp://tedebc.ufma.br:8080/oai/requestrepositorio@ufma.br||repositorio@ufma.bropendoar:21312025-02-05T16:32:57Biblioteca Digital de Teses e Dissertações da UFMA - Universidade Federal do Maranhão (UFMA)false
dc.title.por.fl_str_mv Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape
dc.title.alternative.eng.fl_str_mv Actividad antibacteriana de Anacardium occidentale contra bacterias del grupo eskape
title Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape
spellingShingle Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape
SANTOS, Pâmela Gomes
antibiótico;
antivirulência;
Staphylococcus aureus;
MRSA.
antibiotic;
anti-virulence;
Staphylococcus aureus;
MRSA.
Ciências da Saúde
title_short Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape
title_full Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape
title_fullStr Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape
title_full_unstemmed Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape
title_sort Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape
author SANTOS, Pâmela Gomes
author_facet SANTOS, Pâmela Gomes
author_role author
dc.contributor.advisor1.fl_str_mv GUERRA, Rosane Nassar Meireles
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/2316192786452127
dc.contributor.referee1.fl_str_mv GUERRA, Rosane Nassar Meireles
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/2316192786452127
dc.contributor.referee2.fl_str_mv MONTEIRO NETO, Valério
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/5476942147520772
dc.contributor.referee3.fl_str_mv RIBEIRO, Rachel Melo
dc.contributor.referee3Lattes.fl_str_mv http://lattes.cnpq.br/4752952470368965
dc.contributor.referee4.fl_str_mv OLIVEIRA, Aluísio da Silva
dc.contributor.referee4Lattes.fl_str_mv http://lattes.cnpq.br/2751713874701874
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/7818949201806939
dc.contributor.author.fl_str_mv SANTOS, Pâmela Gomes
contributor_str_mv GUERRA, Rosane Nassar Meireles
GUERRA, Rosane Nassar Meireles
MONTEIRO NETO, Valério
RIBEIRO, Rachel Melo
OLIVEIRA, Aluísio da Silva
dc.subject.por.fl_str_mv antibiótico;
antivirulência;
Staphylococcus aureus;
MRSA.
topic antibiótico;
antivirulência;
Staphylococcus aureus;
MRSA.
antibiotic;
anti-virulence;
Staphylococcus aureus;
MRSA.
Ciências da Saúde
dc.subject.eng.fl_str_mv antibiotic;
anti-virulence;
Staphylococcus aureus;
MRSA.
dc.subject.cnpq.fl_str_mv Ciências da Saúde
description The bioprospection of natural products, with antimicrobial action and therapeutic purpose, has been gaining much prominence worldwide, especially considering the high number of microorganisms resistant to conventional treatments. In this context, products derived from Anacardium occidentale, a species native to Brazil and known as the cashew tree, emerge as a promising alternative due to their antimicrobial potential. The present study evaluated the effect of ethanolic extract of A. occidentale (EAO) flowers in vitro, considering the action on the adhesion and biofilm formation of ESKAPE’s bacteria group, as well as on lethal Staphylococcus aureus infection induced in Tenebrio molitor larvae. HPLC and LC- MS determined the chemical composition of the extract. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) determined the antibacterial activity on standard strains of Staphylococcus aureus (ATCC 25923) and Enterococcus faecalis (ATCC 29212), Escherichia coli (ATCC 29922), Klebsiella pneumoniae (ATCC 700603) and in multidrug-resistant clinical strains of S. aureus (MRSA 240016969961 and MRSA 240016969962). The effects of EAO were also evaluated on the viability and biomass of adhesion and preformed and formed biofilms. For the in vivo assays, T. molitor larvae were used to determine the toxicity of EAO, standardize the lethal inoculum of S. aureus, and evaluate the EAO effect after lethal infection with S. aureus. The animals were divided into six groups (N=10) to determine their survival during the lethal infection. Sham: without infection or treatment, and five groups lethally infected with S. aureus (105 CFU/μL), intracelomic and treated with EAO or CIPRO by the same route. Groups EAO1/2: treated EAO in a concentration corresponding to 1/2 MIC (3.12 mg/mL), EAOCIM: EAO in MIC concentration (6.25 mg/mL) and EAO2: treated with EAO corresponding to 2x MIC concentration (12.5 mg/mL). Negative control: received phosphate-balanced salt solution (PBS), CiPro: treated with ciprofloxacin (1,56 μg/mL), The major compounds identified were: shikimic acid, gallic acid, quercetin, isoquercetin, galloyl glucose, digaloyglucose, isomer 1 and isomer 2 of tetragalloylglucose. The MIC values ranged from 6.25 to 50 mg/mL for the strains, with the best activity for S. aureus (MIC=6.25 mg/mL) and the MRSA strains (MIC 12.5 mg/mL). The EAO had bactericidal action according to CBM/CIM. The extract reduced the biomass and viability of adhesion- preformed and formed biofilms of S. aureus. EAO showed low toxicity to T. molitor. Treatment with EAO increased the larvae's survival after lethal infection with S. aureus in a dose-dependent way. In conclusion, EAO prolonged the survival of larvae lethally infected by S. aureus, possibly due to its antibacterial action and its effects on adhesion and biofilms.
publishDate 2024
dc.date.issued.fl_str_mv 2024-11-29
dc.date.accessioned.fl_str_mv 2025-02-05T16:32:57Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv SANTOS, Pâmela Gomes. Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape. 2024. 70 f. Dissertação (Programa de Pós-Graduação em Ciências da Saúde/CCBS) - Universidade Federal do Maranhão, São Luís, 2024.
dc.identifier.uri.fl_str_mv https://tedebc.ufma.br/jspui/handle/tede/5864
identifier_str_mv SANTOS, Pâmela Gomes. Atividade antibacteriana de Anacardium occidentale frente a bactérias do grupo eskape. 2024. 70 f. Dissertação (Programa de Pós-Graduação em Ciências da Saúde/CCBS) - Universidade Federal do Maranhão, São Luís, 2024.
url https://tedebc.ufma.br/jspui/handle/tede/5864
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal do Maranhão
dc.publisher.program.fl_str_mv PROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS DA SAÚDE/CCBS
dc.publisher.initials.fl_str_mv UFMA
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv COBI - COORDENAÇÃO DO CURSO DE BIOLOGIA/CCCH
publisher.none.fl_str_mv Universidade Federal do Maranhão
dc.source.none.fl_str_mv reponame:Biblioteca Digital de Teses e Dissertações da UFMA
instname:Universidade Federal do Maranhão (UFMA)
instacron:UFMA
instname_str Universidade Federal do Maranhão (UFMA)
instacron_str UFMA
institution UFMA
reponame_str Biblioteca Digital de Teses e Dissertações da UFMA
collection Biblioteca Digital de Teses e Dissertações da UFMA
bitstream.url.fl_str_mv http://tedebc.ufma.br:8080/bitstream/tede/5864/2/P%C3%82MELAGOMESSANTOS.pdf
http://tedebc.ufma.br:8080/bitstream/tede/5864/1/license.txt
bitstream.checksum.fl_str_mv a9b3c1f68c33d6f13fdb761e24598f26
97eeade1fce43278e63fe063657f8083
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da UFMA - Universidade Federal do Maranhão (UFMA)
repository.mail.fl_str_mv repositorio@ufma.br||repositorio@ufma.br
_version_ 1853508042739417088