Mygalin: An Acylpolyamine With Bactericidal Activity

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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...

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Detalles Bibliográficos
Autores: Espinoza-Culupu, Abraham, Mendes, Elizabeth, Vitorino, Hector Aguilar, da Silva Jr, Pedro Ismael, Borges, Monamaris Marques
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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network_acronym_str CONC
network_name_str CONCYTEC-Institucional
repository_id_str 4689
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
instname_str Consejo Nacional de Ciencia Tecnología e Innovación
instacron_str CONCYTEC
institution CONCYTEC
reponame_str CONCYTEC-Institucional
collection CONCYTEC-Institucional
repository.name.fl_str_mv 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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