Mygalin: An Acylpolyamine With Bactericidal Activity
Descripción del Articulo
Inappropriate use of antibiotics favors the selection and spread of resistant bacteria. To reduce the spread of these bacteria, finding new molecules with activity is urgent and necessary. Several polyamine analogs have been constructed and used to control microorganisms and tumor cells. Mygalin is...
| Autores: | , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2020 |
| Institución: | Consejo Nacional de Ciencia Tecnología e Innovación |
| Repositorio: | CONCYTEC-Institucional |
| Lenguaje: | inglés |
| OAI Identifier: | oai:repositorio.concytec.gob.pe:20.500.12390/2892 |
| Enlace del recurso: | https://hdl.handle.net/20.500.12390/2892 https://doi.org/10.3389/fmicb.2019.02928 |
| Nivel de acceso: | acceso abierto |
| Materia: | Microbiology (medical) Microbiology http://purl.org/pe-repo/ocde/ford#1.06.01 |
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| dc.title.none.fl_str_mv |
Mygalin: An Acylpolyamine With Bactericidal Activity |
| title |
Mygalin: An Acylpolyamine With Bactericidal Activity |
| spellingShingle |
Mygalin: An Acylpolyamine With Bactericidal Activity Espinoza-Culupu, Abraham Microbiology (medical) Microbiology http://purl.org/pe-repo/ocde/ford#1.06.01 |
| title_short |
Mygalin: An Acylpolyamine With Bactericidal Activity |
| title_full |
Mygalin: An Acylpolyamine With Bactericidal Activity |
| title_fullStr |
Mygalin: An Acylpolyamine With Bactericidal Activity |
| title_full_unstemmed |
Mygalin: An Acylpolyamine With Bactericidal Activity |
| title_sort |
Mygalin: An Acylpolyamine With Bactericidal Activity |
| author |
Espinoza-Culupu, Abraham |
| author_facet |
Espinoza-Culupu, Abraham Mendes, Elizabeth Vitorino, Hector Aguilar da Silva Jr, Pedro Ismael Borges, Monamaris Marques |
| author_role |
author |
| author2 |
Mendes, Elizabeth Vitorino, Hector Aguilar da Silva Jr, Pedro Ismael Borges, Monamaris Marques |
| author2_role |
author author author author |
| dc.contributor.author.fl_str_mv |
Espinoza-Culupu, Abraham Mendes, Elizabeth Vitorino, Hector Aguilar da Silva Jr, Pedro Ismael Borges, Monamaris Marques |
| dc.subject.none.fl_str_mv |
Microbiology (medical) |
| topic |
Microbiology (medical) Microbiology http://purl.org/pe-repo/ocde/ford#1.06.01 |
| dc.subject.es_PE.fl_str_mv |
Microbiology |
| dc.subject.ocde.none.fl_str_mv |
http://purl.org/pe-repo/ocde/ford#1.06.01 |
| description |
Inappropriate use of antibiotics favors the selection and spread of resistant bacteria. To reduce the spread of these bacteria, finding new molecules with activity is urgent and necessary. Several polyamine analogs have been constructed and used to control microorganisms and tumor cells. Mygalin is a synthetic acylpolyamine, which are analogs of spermidine, derived from the hemolymph of the spider Acanthoscurria gomesiana. The effective activity of polyamines and their analogs has been associated with their structure. The presence of two acyl groups in the Mygalin structure may give this molecule a specific antibacterial activity. The aim of this study was to identify the mechanisms involved in the interaction of Mygalin with Escherichia coli to clarify its antimicrobial action. The results indicated that Mygalin exhibits intense dose and time-dependent bactericidal activity. Treatment of E. coli with this molecule caused membrane rupture, inhibition of DNA synthesis, DNA damage, and morphological changes. The esterase activity increased along with the intracellular production of reactive oxygen species (ROS) after treatment of the bacteria with Mygalin. In addition, this molecule was able to sequester iron and bind to LPS. We have shown that Mygalin has bactericidal activity with underlying mechanisms involving ROS generation and chelation of iron ions that are necessary for bacterial metabolism, which may contribute to its microbicidal activity. Taken together, our data suggest that Mygalin can be explored as a new alternative drug with antimicrobial potential against Gram-negative bacteria or other infectious agents. |
| publishDate |
2020 |
| dc.date.accessioned.none.fl_str_mv |
2024-05-30T23:13:38Z |
| dc.date.available.none.fl_str_mv |
2024-05-30T23:13:38Z |
| dc.date.issued.fl_str_mv |
2020 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/20.500.12390/2892 |
| dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.3389/fmicb.2019.02928 |
| url |
https://hdl.handle.net/20.500.12390/2892 https://doi.org/10.3389/fmicb.2019.02928 |
| dc.language.iso.none.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartof.none.fl_str_mv |
FRONTIERS IN MICROBIOLOGY |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.publisher.none.fl_str_mv |
Frontiers Media SA |
| publisher.none.fl_str_mv |
Frontiers Media SA |
| dc.source.none.fl_str_mv |
reponame:CONCYTEC-Institucional instname:Consejo Nacional de Ciencia Tecnología e Innovación instacron:CONCYTEC |
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Consejo Nacional de Ciencia Tecnología e Innovación |
| instacron_str |
CONCYTEC |
| institution |
CONCYTEC |
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CONCYTEC-Institucional |
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CONCYTEC-Institucional |
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Repositorio Institucional CONCYTEC |
| repository.mail.fl_str_mv |
repositorio@concytec.gob.pe |
| _version_ |
1844883125509816320 |
| spelling |
Publicationrp08054600rp08057600rp08055600rp08053600rp08056600Espinoza-Culupu, AbrahamMendes, ElizabethVitorino, Hector Aguilarda Silva Jr, Pedro IsmaelBorges, Monamaris Marques2024-05-30T23:13:38Z2024-05-30T23:13:38Z2020https://hdl.handle.net/20.500.12390/2892https://doi.org/10.3389/fmicb.2019.02928Inappropriate use of antibiotics favors the selection and spread of resistant bacteria. To reduce the spread of these bacteria, finding new molecules with activity is urgent and necessary. Several polyamine analogs have been constructed and used to control microorganisms and tumor cells. Mygalin is a synthetic acylpolyamine, which are analogs of spermidine, derived from the hemolymph of the spider Acanthoscurria gomesiana. The effective activity of polyamines and their analogs has been associated with their structure. The presence of two acyl groups in the Mygalin structure may give this molecule a specific antibacterial activity. The aim of this study was to identify the mechanisms involved in the interaction of Mygalin with Escherichia coli to clarify its antimicrobial action. The results indicated that Mygalin exhibits intense dose and time-dependent bactericidal activity. Treatment of E. coli with this molecule caused membrane rupture, inhibition of DNA synthesis, DNA damage, and morphological changes. The esterase activity increased along with the intracellular production of reactive oxygen species (ROS) after treatment of the bacteria with Mygalin. In addition, this molecule was able to sequester iron and bind to LPS. We have shown that Mygalin has bactericidal activity with underlying mechanisms involving ROS generation and chelation of iron ions that are necessary for bacterial metabolism, which may contribute to its microbicidal activity. Taken together, our data suggest that Mygalin can be explored as a new alternative drug with antimicrobial potential against Gram-negative bacteria or other infectious agents.Fondo Nacional de Desarrollo Científico y Tecnológico - FondecytengFrontiers Media SAFRONTIERS IN MICROBIOLOGYinfo:eu-repo/semantics/openAccessMicrobiology (medical)Microbiology-1http://purl.org/pe-repo/ocde/ford#1.06.01-1Mygalin: An Acylpolyamine With Bactericidal Activityinfo:eu-repo/semantics/articlereponame:CONCYTEC-Institucionalinstname:Consejo Nacional de Ciencia Tecnología e Innovacióninstacron:CONCYTEC#PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE#20.500.12390/2892oai:repositorio.concytec.gob.pe:20.500.12390/28922024-05-30 15:26:02.81http://purl.org/coar/access_right/c_14cbinfo:eu-repo/semantics/closedAccessmetadata only accesshttps://repositorio.concytec.gob.peRepositorio Institucional CONCYTECrepositorio@concytec.gob.pe#PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE#<Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="731f8642-afe7-41cb-ab3a-1b0c5c6009af"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>Mygalin: An Acylpolyamine With Bactericidal Activity</Title> <PublishedIn> <Publication> <Title>FRONTIERS IN MICROBIOLOGY</Title> </Publication> </PublishedIn> <PublicationDate>2020</PublicationDate> <DOI>https://doi.org/10.3389/fmicb.2019.02928</DOI> <Authors> <Author> <DisplayName>Espinoza-Culupu, Abraham</DisplayName> <Person id="rp08054" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Mendes, Elizabeth</DisplayName> <Person id="rp08057" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Vitorino, Hector Aguilar</DisplayName> <Person id="rp08055" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>da Silva Jr, Pedro Ismael</DisplayName> <Person id="rp08053" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Borges, Monamaris Marques</DisplayName> <Person id="rp08056" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Frontiers Media SA</DisplayName> <OrgUnit /> </Publisher> </Publishers> <Keyword>Microbiology (medical)</Keyword> <Keyword>Microbiology</Keyword> <Abstract>Inappropriate use of antibiotics favors the selection and spread of resistant bacteria. To reduce the spread of these bacteria, finding new molecules with activity is urgent and necessary. Several polyamine analogs have been constructed and used to control microorganisms and tumor cells. Mygalin is a synthetic acylpolyamine, which are analogs of spermidine, derived from the hemolymph of the spider Acanthoscurria gomesiana. The effective activity of polyamines and their analogs has been associated with their structure. The presence of two acyl groups in the Mygalin structure may give this molecule a specific antibacterial activity. The aim of this study was to identify the mechanisms involved in the interaction of Mygalin with Escherichia coli to clarify its antimicrobial action. The results indicated that Mygalin exhibits intense dose and time-dependent bactericidal activity. Treatment of E. coli with this molecule caused membrane rupture, inhibition of DNA synthesis, DNA damage, and morphological changes. The esterase activity increased along with the intracellular production of reactive oxygen species (ROS) after treatment of the bacteria with Mygalin. In addition, this molecule was able to sequester iron and bind to LPS. We have shown that Mygalin has bactericidal activity with underlying mechanisms involving ROS generation and chelation of iron ions that are necessary for bacterial metabolism, which may contribute to its microbicidal activity. Taken together, our data suggest that Mygalin can be explored as a new alternative drug with antimicrobial potential against Gram-negative bacteria or other infectious agents.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication> -1 |
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13.394457 |
Nota importante:
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).