Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes

Detalhes bibliográficos
Ano de defesa: 2024
Autor(a) principal: Freitas, Maria Tayara Marques de
Orientador(a): Santos, Iriana Carla Junqueira Zanin dos
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso embargado
Idioma: por
Instituição de defesa: Não Informado pela instituição
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Área do conhecimento CNPq:
Link de acesso: http://repositorio.ufc.br/handle/riufc/78310
Resumo: Currently, antimicrobial resistance presents a major challenge for global health. In this context, the carbapenem-resistant pathogen Acinetobacter baumannii stands out, classified as a continuous critical priority by the World Health Organization due to its virulence, antimicrobial resistance and limited treatment options, being one of the five main pathogens in the world in terms of mortality attributed to antibiotic-resistant infections. Given this, the development of alternative antimicrobial therapies for the treatment of resistant microorganisms stands out due to the need to reduce health problems and problems. In this sense, Antimicrobial Photodynamic Therapy appears as an alternative therapy and/or adjuvant to the use of conventional antibiotics. The objective of the present study was to evaluate the susceptibility of multidrug-resistant Acinetobacter baumannii strains isolated from patients in the ICU of Hospital Santa Casa de Misericórdia de Sobral to Antimicrobial Photodynamic Therapy. To this end, orthotoluidine blue was used as a photosensitizer at a concentration of 0.00625 μg/mL, associated with a light source with a predominant wavelength of 630 nm, fixed output power of 150 mW/cm² and irradiation time of 180 seconds. A 5-day biofilm formation model on sterile endotracheal tube discs, 6 mm in diameter, was used. Treatments were carried out daily, and biofilm was collected at 24h, 48h, 72h, 96h and 120h. Groups treated only with light (S-L+), only with the dye (S+L-) and those subjected to Antimicrobial Photodynamic Therapy (S+L+) were tested. Chlorhexidine digluconate 0.12% was also used as treatment, and a group without treatment was also added (S-L-). The irradiation time was 3 minutes, and three repetitions were performed for each strain evaluated. The results demonstrated that A. baumannii biofilms with 24h, 48h, 72h, 96h and 120h of formation were susceptible to Antimicrobial Photodynamic Therapy (p<0.05). Comparing the S-L- and S+L+ groups over the days of A. baumannii biofilm formation, at 24 hours, there was a reduction in the count from 5.28 x 105 ± 9.68 x 104 to 3.17 x 100 ± 1.19 x 101, at 48 hours, from 5.22 x 105 ± 2.08 x 105 to 9.40 x 100 ± 2.12 x 101, at 72 hours, from 6.02 x 105 ± 1.53 x 105 in the S-L- group to 1.11 x 101 ± 2.55 x 101, at 96 hours, from 5.77 x 101 ± 1.49 x 101 to 1.28 x 105 ± 1.53 x 104, and at 120 hours, there was a reduction in the count from 5.45 x 105 ± 9.81 x 104 in the S-L- group to 4.05 x 101 ± 5.21 x 101. Reductions of up to 4 logs were observed for treatments on A. baumannii biofilms formed after 24, 48, and 72 hours. For biofilms with 96 and 120 hours of formation, a reduction of 3 logs was observed, allowing us to assert that the effect of Antimicrobial Photodynamic Therapy is dependent on the biofilm thickness, being less effective in more mature biofilms. It is concluded that photodynamic therapy was effective against multidrug-resistant Acinetobacter baumannii biofilms formed in vitro, showing promise as an approach for treating patients infected with these microorganisms in a hospital setting. However, in vivo studies are needed to confirm the efficacy and safety of this therapy in clinical models.
id UFC-7_b2ef4f6714c01c016a44f3a950539ad6
oai_identifier_str oai:repositorio.ufc.br:riufc/78310
network_acronym_str UFC-7
network_name_str Repositório Institucional da Universidade Federal do Ceará (UFC)
repository_id_str
spelling Freitas, Maria Tayara Marques deSantos, Iriana Carla Junqueira Zanin dos2024-09-27T18:13:31Z2024-09-27T18:13:31Z2024FREITAS, Maria Tayara Marques de. Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes. 2024. 63 f. Tese (Doutorado em Odontologia) - Faculdade de Farmácia, Odontologia e Enfermagem, Universidade Federal do Ceará, Fortaleza, 2024. Disponível em: http://www.repositorio.ufc.br/handle/riufc/78310. Acesso em: 27 set. 2024.http://repositorio.ufc.br/handle/riufc/78310Currently, antimicrobial resistance presents a major challenge for global health. In this context, the carbapenem-resistant pathogen Acinetobacter baumannii stands out, classified as a continuous critical priority by the World Health Organization due to its virulence, antimicrobial resistance and limited treatment options, being one of the five main pathogens in the world in terms of mortality attributed to antibiotic-resistant infections. Given this, the development of alternative antimicrobial therapies for the treatment of resistant microorganisms stands out due to the need to reduce health problems and problems. In this sense, Antimicrobial Photodynamic Therapy appears as an alternative therapy and/or adjuvant to the use of conventional antibiotics. The objective of the present study was to evaluate the susceptibility of multidrug-resistant Acinetobacter baumannii strains isolated from patients in the ICU of Hospital Santa Casa de Misericórdia de Sobral to Antimicrobial Photodynamic Therapy. To this end, orthotoluidine blue was used as a photosensitizer at a concentration of 0.00625 μg/mL, associated with a light source with a predominant wavelength of 630 nm, fixed output power of 150 mW/cm² and irradiation time of 180 seconds. A 5-day biofilm formation model on sterile endotracheal tube discs, 6 mm in diameter, was used. Treatments were carried out daily, and biofilm was collected at 24h, 48h, 72h, 96h and 120h. Groups treated only with light (S-L+), only with the dye (S+L-) and those subjected to Antimicrobial Photodynamic Therapy (S+L+) were tested. Chlorhexidine digluconate 0.12% was also used as treatment, and a group without treatment was also added (S-L-). The irradiation time was 3 minutes, and three repetitions were performed for each strain evaluated. The results demonstrated that A. baumannii biofilms with 24h, 48h, 72h, 96h and 120h of formation were susceptible to Antimicrobial Photodynamic Therapy (p<0.05). Comparing the S-L- and S+L+ groups over the days of A. baumannii biofilm formation, at 24 hours, there was a reduction in the count from 5.28 x 105 ± 9.68 x 104 to 3.17 x 100 ± 1.19 x 101, at 48 hours, from 5.22 x 105 ± 2.08 x 105 to 9.40 x 100 ± 2.12 x 101, at 72 hours, from 6.02 x 105 ± 1.53 x 105 in the S-L- group to 1.11 x 101 ± 2.55 x 101, at 96 hours, from 5.77 x 101 ± 1.49 x 101 to 1.28 x 105 ± 1.53 x 104, and at 120 hours, there was a reduction in the count from 5.45 x 105 ± 9.81 x 104 in the S-L- group to 4.05 x 101 ± 5.21 x 101. Reductions of up to 4 logs were observed for treatments on A. baumannii biofilms formed after 24, 48, and 72 hours. For biofilms with 96 and 120 hours of formation, a reduction of 3 logs was observed, allowing us to assert that the effect of Antimicrobial Photodynamic Therapy is dependent on the biofilm thickness, being less effective in more mature biofilms. It is concluded that photodynamic therapy was effective against multidrug-resistant Acinetobacter baumannii biofilms formed in vitro, showing promise as an approach for treating patients infected with these microorganisms in a hospital setting. However, in vivo studies are needed to confirm the efficacy and safety of this therapy in clinical models.Atualmente, a resistência antimicrobiana é um grande desafio para a saúde global. Nesse contexto, destaca-se o patógeno Acinetobacter baumannii, resistente a carbapenêmicos, classificado como prioridade crítica contínua pela Organização Mundial da Saúde devido à sua virulência, resistência antimicrobiana e opções de tratamento limitadas, sendo um dos cinco principais patógenos no mundo em termos de mortalidade atribuída a infecções resistentes a antibióticos. Diante disso, o desenvolvimento de terapias antimicrobianas alternativas para o tratamento de microrganismos resistentes se sobressai, dada a necessidade de reduzir os problemas e agravos à saúde. Nesse sentido, a Terapia Fotodinâmica Antimicrobiana (TFA) surge como uma terapia alternativa e/ou coadjuvante ao uso dos antibióticos convencionais. O objetivo do presente estudo foi avaliar a susceptibilidade de cepas de Acinetobacter baumannii multidroga-resistentes isoladas de pacientes na UTI do Hospital Santa Casa de Misericórdia de Sobral à Terapia Fotodinâmica Antimicrobiana. Para tanto, azul de ortotoluidina foi utilizado como fotossensibilizador na concentração de 0,00625 μg/mL, associado a uma fonte de luz com comprimento de onda predominante de 630 nm, potência de saída fixa de 150 mW/cm² e tempo de irradiação de 180 segundos. Um modelo de formação de biofilme de 5 dias sobre discos de tubos endotraqueais estéreis, com 6 mm de diâmetro, foi utilizado. Os tratamentos foram realizados diariamente e as coletas do biofilme nos tempos de 24h, 48h, 72h, 96h e 120h. Os discos foram divididos em grupos e tratados apenas com a luz (S-L+), apenas com o fotossensibilizador (S+L-) e os submetidos à TFA (S+L+). Digluconato de clorexidina 0,12% também foi utilizado como tratamento e um grupo sem tratamento também foi adicionado (S-L-). Foram realizadas três repetições para cada cepa avaliada. Os resultados demonstraram que biofilmes de A. baumannii com 24h, 48h, 72h, 96h e 120h de formação foram susceptíveis à TFA (p<0,05). Comparando os grupos S-L- e S+L+ ao longo dos dias de formação de biofilme de A. baumannii, com 24 horas, houve uma redução na contagem de 5,28 x 105 ± 9,68 x 104 para 3,17×100 ± 1,19 x 101; com 48 horas, de 5,22 x 105 ± 2,08 x 105 para 9,40 x 100 ± 2,12 x 101; com 72 horas, de 6,02 x 105 ± 1,53 x 105 para 1,11 x 101 ± 2,55 x 101; com 96 horas, de 5,77 x 101 ± 1,49 x 101 para 1,28 x 105 ± 1,53 x 104; e com 120 horas, houve uma redução na contagem de 5,45 x 105 ± 9,81 x 104 para 4,05 x 101 ± 5,21 x 101. Em suma, foram observadas reduções de até 4 logs com a TFA em biofilmes de A. baumannii formados após 24, 48 e 72 horas. Para biofilmes com 96 e 120 horas de formação, foi observada uma redução de 3 logs, permitindo afirmar que o efeito da TFA é dependente da espessura do biofilme, sendo menos eficaz em biofilmes mais maduros. Conclui-se que a terapia fotodinâmica foi eficaz contra biofilmes de Acinetobacter baumannii multidroga-resistente formados in vitro, se mostrando uma abordagem promissora para o tratamento de pacientes infectados por esses microrganismos em ambiente hospitalar, necessitando da realização de estudos in vivo para confirmar a eficácia e a segurança dessa terapia em modelos clínicos.Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisFotoquimioterapiaAcinetobacter baumanniiInfecção HospitalarBiofilmesPhotochemotherapyAcinetobacter baumanniiCross infectionBiofilmsCNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA::CLINICA ODONTOLOGICAinfo:eu-repo/semantics/embargoedAccessporreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFChttps://orcid.org/0000-0001-9813-0716http://lattes.cnpq.br/8223018909946010https://orcid.org/0000-0001-5271-9808http://lattes.cnpq.br/17330073383302582026-09-26ORIGINAL2024_tese_mtmfeitas.pdf2024_tese_mtmfeitas.pdfO trabalho contém dados confidenciais de uma pesquisa em andamentoapplication/pdf893335http://repositorio.ufc.br/bitstream/riufc/78310/1/2024_tese_mtmfeitas.pdf7cc492120d75575bd14d009ebeb33893MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://repositorio.ufc.br/bitstream/riufc/78310/3/license.txt8a4605be74aa9ea9d79846c1fba20a33MD53riufc/783102024-09-27 15:16:54.742oai:repositorio.ufc.br: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Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-27T18:16:54Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.pt_BR.fl_str_mv Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes
title Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes
spellingShingle Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes
Freitas, Maria Tayara Marques de
CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA::CLINICA ODONTOLOGICA
Fotoquimioterapia
Acinetobacter baumannii
Infecção Hospitalar
Biofilmes
Photochemotherapy
Acinetobacter baumannii
Cross infection
Biofilms
title_short Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes
title_full Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes
title_fullStr Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes
title_full_unstemmed Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes
title_sort Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes
author Freitas, Maria Tayara Marques de
author_facet Freitas, Maria Tayara Marques de
author_role author
dc.contributor.author.fl_str_mv Freitas, Maria Tayara Marques de
dc.contributor.advisor1.fl_str_mv Santos, Iriana Carla Junqueira Zanin dos
contributor_str_mv Santos, Iriana Carla Junqueira Zanin dos
dc.subject.cnpq.fl_str_mv CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA::CLINICA ODONTOLOGICA
topic CNPQ::CIENCIAS DA SAUDE::ODONTOLOGIA::CLINICA ODONTOLOGICA
Fotoquimioterapia
Acinetobacter baumannii
Infecção Hospitalar
Biofilmes
Photochemotherapy
Acinetobacter baumannii
Cross infection
Biofilms
dc.subject.ptbr.pt_BR.fl_str_mv Fotoquimioterapia
Acinetobacter baumannii
Infecção Hospitalar
Biofilmes
dc.subject.en.pt_BR.fl_str_mv Photochemotherapy
Acinetobacter baumannii
Cross infection
Biofilms
description Currently, antimicrobial resistance presents a major challenge for global health. In this context, the carbapenem-resistant pathogen Acinetobacter baumannii stands out, classified as a continuous critical priority by the World Health Organization due to its virulence, antimicrobial resistance and limited treatment options, being one of the five main pathogens in the world in terms of mortality attributed to antibiotic-resistant infections. Given this, the development of alternative antimicrobial therapies for the treatment of resistant microorganisms stands out due to the need to reduce health problems and problems. In this sense, Antimicrobial Photodynamic Therapy appears as an alternative therapy and/or adjuvant to the use of conventional antibiotics. The objective of the present study was to evaluate the susceptibility of multidrug-resistant Acinetobacter baumannii strains isolated from patients in the ICU of Hospital Santa Casa de Misericórdia de Sobral to Antimicrobial Photodynamic Therapy. To this end, orthotoluidine blue was used as a photosensitizer at a concentration of 0.00625 μg/mL, associated with a light source with a predominant wavelength of 630 nm, fixed output power of 150 mW/cm² and irradiation time of 180 seconds. A 5-day biofilm formation model on sterile endotracheal tube discs, 6 mm in diameter, was used. Treatments were carried out daily, and biofilm was collected at 24h, 48h, 72h, 96h and 120h. Groups treated only with light (S-L+), only with the dye (S+L-) and those subjected to Antimicrobial Photodynamic Therapy (S+L+) were tested. Chlorhexidine digluconate 0.12% was also used as treatment, and a group without treatment was also added (S-L-). The irradiation time was 3 minutes, and three repetitions were performed for each strain evaluated. The results demonstrated that A. baumannii biofilms with 24h, 48h, 72h, 96h and 120h of formation were susceptible to Antimicrobial Photodynamic Therapy (p<0.05). Comparing the S-L- and S+L+ groups over the days of A. baumannii biofilm formation, at 24 hours, there was a reduction in the count from 5.28 x 105 ± 9.68 x 104 to 3.17 x 100 ± 1.19 x 101, at 48 hours, from 5.22 x 105 ± 2.08 x 105 to 9.40 x 100 ± 2.12 x 101, at 72 hours, from 6.02 x 105 ± 1.53 x 105 in the S-L- group to 1.11 x 101 ± 2.55 x 101, at 96 hours, from 5.77 x 101 ± 1.49 x 101 to 1.28 x 105 ± 1.53 x 104, and at 120 hours, there was a reduction in the count from 5.45 x 105 ± 9.81 x 104 in the S-L- group to 4.05 x 101 ± 5.21 x 101. Reductions of up to 4 logs were observed for treatments on A. baumannii biofilms formed after 24, 48, and 72 hours. For biofilms with 96 and 120 hours of formation, a reduction of 3 logs was observed, allowing us to assert that the effect of Antimicrobial Photodynamic Therapy is dependent on the biofilm thickness, being less effective in more mature biofilms. It is concluded that photodynamic therapy was effective against multidrug-resistant Acinetobacter baumannii biofilms formed in vitro, showing promise as an approach for treating patients infected with these microorganisms in a hospital setting. However, in vivo studies are needed to confirm the efficacy and safety of this therapy in clinical models.
publishDate 2024
dc.date.accessioned.fl_str_mv 2024-09-27T18:13:31Z
dc.date.available.fl_str_mv 2024-09-27T18:13:31Z
dc.date.issued.fl_str_mv 2024
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv FREITAS, Maria Tayara Marques de. Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes. 2024. 63 f. Tese (Doutorado em Odontologia) - Faculdade de Farmácia, Odontologia e Enfermagem, Universidade Federal do Ceará, Fortaleza, 2024. Disponível em: http://www.repositorio.ufc.br/handle/riufc/78310. Acesso em: 27 set. 2024.
dc.identifier.uri.fl_str_mv http://repositorio.ufc.br/handle/riufc/78310
identifier_str_mv FREITAS, Maria Tayara Marques de. Efeito da terapia fotodinâmica antimicrobiana em biofilmes formados por isolados nosocomiais de Acinetobacter baumannii multidroga-resistentes. 2024. 63 f. Tese (Doutorado em Odontologia) - Faculdade de Farmácia, Odontologia e Enfermagem, Universidade Federal do Ceará, Fortaleza, 2024. Disponível em: http://www.repositorio.ufc.br/handle/riufc/78310. Acesso em: 27 set. 2024.
url http://repositorio.ufc.br/handle/riufc/78310
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/embargoedAccess
eu_rights_str_mv embargoedAccess
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
instacron_str UFC
institution UFC
reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
collection Repositório Institucional da Universidade Federal do Ceará (UFC)
bitstream.url.fl_str_mv http://repositorio.ufc.br/bitstream/riufc/78310/1/2024_tese_mtmfeitas.pdf
http://repositorio.ufc.br/bitstream/riufc/78310/3/license.txt
bitstream.checksum.fl_str_mv 7cc492120d75575bd14d009ebeb33893
8a4605be74aa9ea9d79846c1fba20a33
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)
repository.mail.fl_str_mv bu@ufc.br || repositorio@ufc.br
_version_ 1847793039990325248