Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?

Autores:
Correa Jiménez, Oscar
Reyes, Niradiz
Tipo de recurso:
Article of journal
Fecha de publicación:
2014
Institución:
Universidad de Cartagena
Repositorio:
Repositorio Universidad de Cartagena
Idioma:
spa
OAI Identifier:
oai:repositorio.unicartagena.edu.co:11227/13123
Acceso en línea:
https://hdl.handle.net/11227/13123
https://doi.org/10.32997/rcb-2014-2894
Palabra clave:
Factores de virulencia
Patogenicidad
Toxinas bacterianas
Citotoxinas
Staphylococcus aureus.
Rights
openAccess
License
Revista Ciencias Biomédicas - 2020
id UCART2_c71e814ac05287155f929d50524065c0
oai_identifier_str oai:repositorio.unicartagena.edu.co:11227/13123
network_acronym_str UCART2
network_name_str Repositorio Universidad de Cartagena
repository_id_str
dc.title.spa.fl_str_mv Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
dc.title.translated.eng.fl_str_mv Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
title Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
spellingShingle Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
Factores de virulencia
Patogenicidad
Toxinas bacterianas
Citotoxinas
Staphylococcus aureus.
title_short Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
title_full Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
title_fullStr Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
title_full_unstemmed Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
title_sort Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?
dc.creator.fl_str_mv Correa Jiménez, Oscar
Reyes, Niradiz
dc.contributor.author.spa.fl_str_mv Correa Jiménez, Oscar
Reyes, Niradiz
dc.subject.spa.fl_str_mv Factores de virulencia
Patogenicidad
Toxinas bacterianas
Citotoxinas
Staphylococcus aureus.
topic Factores de virulencia
Patogenicidad
Toxinas bacterianas
Citotoxinas
Staphylococcus aureus.
publishDate 2014
dc.date.accessioned.none.fl_str_mv 2014-01-15 00:00:00
dc.date.available.none.fl_str_mv 2014-01-15 00:00:00
dc.date.issued.none.fl_str_mv 2014-01-15
dc.type.spa.fl_str_mv Artículo de revista
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.version.spa.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.coarversion.spa.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.content.spa.fl_str_mv Text
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
dc.type.local.eng.fl_str_mv Journal article
format http://purl.org/coar/resource_type/c_6501
status_str publishedVersion
dc.identifier.issn.none.fl_str_mv 2215-7840
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/11227/13123
dc.identifier.doi.none.fl_str_mv 10.32997/rcb-2014-2894
dc.identifier.eissn.none.fl_str_mv 2389-7252
dc.identifier.url.none.fl_str_mv https://doi.org/10.32997/rcb-2014-2894
identifier_str_mv 2215-7840
10.32997/rcb-2014-2894
2389-7252
url https://hdl.handle.net/11227/13123
https://doi.org/10.32997/rcb-2014-2894
dc.language.iso.spa.fl_str_mv spa
language spa
dc.relation.ispartofjournal.spa.fl_str_mv Revista Ciencias Biomédicas
dc.relation.bitstream.none.fl_str_mv https://revistas.unicartagena.edu.co/index.php/cbiomedicas/article/download/2894/2437
dc.relation.citationedition.spa.fl_str_mv Núm. 1 , Año 2014
dc.relation.citationendpage.none.fl_str_mv 115
dc.relation.citationissue.spa.fl_str_mv 1
dc.relation.citationstartpage.none.fl_str_mv 107
dc.relation.citationvolume.spa.fl_str_mv 5
dc.relation.references.spa.fl_str_mv David MZ, Daum RS. Community-associated methicillin-resistant Staphylococcus aureus: epidemiology and clinical consequences of an emerging epidemic. Clin Microbiol Rev. 2010;23(3):616-687.
Castillo JS, Leal AL, Cortes JA, Álvarez CA, Sánchez R, Buitrago G, Barrero LI, et al. Mortality among critically ill patients with methicillin-resistant Staphylococcus aureus bacteremia: a multicenter cohort study in Colombia. Rev Panam Salud Pública. 2012 ;32(5):343-50.
Thompson RL, Cabezudo I, Wenzel RP. Epidemiology of nosocomial infections caused by methicillin-resistant Staphylococcus aureus. Ann Intern Med. 1982;97(3):309-317.
Miller LG, Kaplan SL. Staphylococcus aureus: a community pathogen. Infect Dis Clin North Am. 2009;23(1):35-52.
Naimi TS, LeDell KH, Como-Sabetti K, Borchardt SM, Boxrud DJ, Etienne J, et al. Comparison of community- and health care-associated methicillin-resistant Staphylococcus aureus infection. JAMA. 2003;290(22):2976-84.
Ochoa TJ, Mohr J, Wanger A, Murphy JR, Heresi GP. Community-associated methicillinresistant Staphylococcus aureus in pediatric patients. Emerg Infect Dis. 2005;11(6):966-8.
Zetola N, Francis JS, Nuermberger EL, Bishai WR. Community-acquired meticillin-resistant Staphylococcus aureus: an emerging threat. Lancet Infect Dis. 2005;5(5):275-286.
Von Eiff C, Becker K, Machka K, Stammer H, Peters G. Nasal carriage as a source of Staphylococcus aureus bacteremia. Study Group. N Engl J Med. 2001;344(1):11-16.
Bettin A, Suárez P, Bedoya A, Reyes N. Staphylococcus aureus in residents from a nursinghome in Cartagena. Rev Salud Publica. 2008;10(4):650-657.
Correa O, Delgado K, Rangel C, Bello A, Reyes N. Nasal and vaginal colonization of methicillin-resistant Staphylococcus aureus in pregnant women in Cartagena, Colombia. Colombia Médica. 2012;43(1):19-27.
Rebollo-Pérez J, Ordonez-Tapia C, Herazo-Herazo C, Reyes-Ramos N. Nasal carriage of Panton Valentine leukocidin-positive methicillin-resistant Staphylococcus aureus in healthy preschool children. Rev Salud Pública. 2011;13(5):824-832.
Bettin A, Causil C, Reyes N. Molecular identification and antimicrobial susceptibility of Staphylococcus aureus nasal isolates from medical students in Cartagena, Colombia. Braz J Infect Dis. 2012;16(4):329-334.
del Rio A, Cervera C, Moreno A, Moreillon P, Miró JM. Patients at risk of complications of Staphylococcus aureus bloodstream infection. Clin Infect Dis. 2009;48(Suppl 4):S246-253.
Sollid JU, Furberg AS, Hanssen AM, Johannessen M. Staphylococcus aureus: determinants of human carriage. Infect Genet Evol. 2013;21:531-41.
Nygaard TK, DeLeo FR, Voyich JM. Community-associated methicillin-resistant Staphylo-coccus aureus skin infections: advances toward identifying the key virulence factors. Curr Opin Infect Dis. 2008;21(2):147-152.
Holmes A, Ganner M, McGuane S, Pitt TL, Cookson BD, Kearns AM. Staphylococcus aureus isolates carrying Panton-Valentine leucocidin genes in England and Wales: frequency, characterization, and association with clinical disease. J Clin Microbiol. 2005;43(5):2384-90.
Cercenado E, Cuevas O, Marin M, Bouza E, Trincado P, Boquete T, et al. Communityacquired methicillin-resistant Staphylococcus aureus in Madrid, Spain: transcontinental importation and polyclonal emergence of Panton-Valentine leukocidin-positive isolates. Diagn Microbiol Infect Dis. 2008;61(2):143-149.
Villaruz AE, Bubeck Wardenburg J, Khan BA, Whitney AR, Sturdevant DE, Gardner DJ, et al. A point mutation in the agr locus rather than expression of the Panton-Valentine leukocidin caused previously reported phenotypes in Staphylococcus aureus pneumonia and gene regulation. J Infect Dis. 2009;200(5):724-734.
Li M, Cheung GY, Hu J, Wang D, Joo HS, Deleo FR, et al. Comparative analysis of virulence and toxin expression of global community-associated methicillin-resistant Staphylococcus aureus strains. J Infect Dis. 2010;202(12):1866-76.
Wang R, Braughton KR, Kretschmer D, Bach TH, Queck SY, Li M, et al. Identification of novel cytolytic peptides as key virulence determinants for community-associated MRSA. Nat Med. 2007;13(12):1510-14.
Mehlin C, Headley CM, Klebanoff SJ. An inflammatory polypeptide complex from Staphylococcus epidermidis: isolation and characterization. J Exp Med. 1999;189(6):907-918.
Rautenberg M, Joo HS, Otto M, Peschel A. Neutrophil responses to staphylococcal pathogens and commensals via the formyl peptide receptor 2 relates to phenol-soluble modulin release and virulence. FASEB J. 2011;25(4):1254-1263.
Arias CA, Rincon S, Chowdhury S, Martínez E, Coronell W, Reyes J, et al. MRSA USA300 clone and VREF--a U.S.-Colombian connection? N Engl J Med. 2008;359(20):2177-9.
Diep BA, Otto M. The role of virulence determinants in community-associated MRSA pathogenesis. Trends Microbiol. 2008;16(8):361-9.
Otto M. Basis of virulence in community-associated methicillin-resistant Staphylococcus aureus. Annu Rev Microbiol. 2010;64:143-162.
Grumann D, Nübel U, Bröker BM. Staphylococcus aureus toxins - Their functions and genetics. Infect Genet Evol. 2014;21:583-92.
Queck SY, Khan BA, Wang R, Bach TH, Kretschmer D, Chen L, et al. Mobile genetic element-encoded cytolysin connects virulence to methicillin resistance in MRSA. PLoS Pathog. 2009;5(7):e1000533.
Chatterjee SS, Chen L, Joo HS, Cheung GY, Kreiswirth BN, Otto M. Distribution and regulation of the mobile genetic element-encoded phenol-soluble modulin PSM-mec in methicillin-resistant Staphylococcus aureus. PLoS One. 2011;6(12):e28781.
Monecke S, Engelmann I, Archambault M, Coleman DC, Coombs GW, Cortez de Jackel S, et al. Distribution of SCCmec-associated phenol-soluble modulin in staphylococci. Mol Cell Probes. 2012;26(2):99-103.
Gonzalez DJ, Okumura CY, Hollands A, Kersten R, Akong-Moore K, Pence MA, et al. Novel phenol-soluble modulin derivatives in community-associated methicillin-resistant Staphylococcus aureus identified through imaging mass spectrometry. J Biol Chem. 2012;287(17):13889-98.
Schwartz K, Syed AK, Stephenson RE, Rickard AH, Boles BR. Functional amyloids composed of phenol soluble modulins stabilize Staphylococcus aureus biofilms. PLoS Pathog. 2012;8(6):e1002744.
Queck SY, Jameson-Lee M, Villaruz AE, Bach TH, Khan BA, Sturdevant DE, et al. RNAIIIindependent target gene control by the agr quorum-sensing system: insight into the evolution of virulence regulation in Staphylococcus aureus. Mol Cell. 2008;32(1):150-8.
Kaito C, Saito Y, Nagano G, Ikuo M, Omae Y, Hanada Y, et al. Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence. PLoS Pathog. 2011;7(2):e1001267.
Kaito C, Saito Y, Ikuo M, Omae Y, Mao H, Nagano G, et al. Mobile genetic element SCCmec-encoded psm-mec RNA suppresses translation of agrA and attenuates MRSA virulence. PLoS Pathog. 2013;9(4):e1003269.
Chatterjee SS, Joo HS, Duong AC, Dieringer TD, Tan VY, Song Y, et al. Essential Staphylococcus aureus toxin export system. Nat Med.2013;19(3):364-7.
Kretschmer D, Nikola N, Durr M, Otto M, Peschel A. The virulence regulator Agr controls the staphylococcal capacity to activate human neutrophils via the formyl peptide receptor 2. J Innate Immun. 2012;4(2):201-12.
Forsman H, Christenson K, Bylund J, Dahlgren C. Receptor-dependent and -independent immunomodulatory effects of phenol-soluble modulin peptides from Staphylococcus aureus on human neutrophils are abrogated through peptide inactivation by reactive oxygen species. Infect Immun. 2012;80(6):1987-1995.
Kobayashi SD, Malachowa N, Whitney AR, Braughton KR, Gardner DJ, Long D, et al. Comparative analysis of USA300 virulence determinants in a rabbit model of skin and soft tissue infection. J Infect Dis. 2011;204(6):937-41.
Hongo I, Baba T, Oishi K, Morimoto Y, Ito T, Hiramatsu K. Phenol-soluble modulin alpha 3 enhances the human neutrophil lysis mediated by Panton-Valentine leukocidin. J Infect Dis. 2009;200(5):715-723.
Liles WC, Thomsen AR, O’Mahony DS, Klebanoff SJ. Stimulation of human neutrophils and monocytes by staphylococcal phenol-soluble modulin. J Leukoc Biol. 2001;70(1):96-102.
Kretschmer D, Gleske AK, Rautenberg M, Wang R, Koberle M, Bohn E, et al. Human formyl peptide receptor 2 senses highly pathogenic Staphylococcus aureus. Cell Host Microbe. 2010;7(6):463-73.
Schreiner J, Kretschmer D, Klenk J, Otto M, Buhring HJ, Stevanovic S, et al. Staphylococcus aureus phenol-soluble modulin peptides modulate dendritic cell functions and increase in vitro priming of regulatory T cells. J Immunol. 2013;190(7):3417-26.
Hajjar AM, O’Mahony DS, Ozinsky A, Underhill DM, Aderem A, Klebanoff SJ, et al. Cutting edge: functional interactions between toll-like receptor (TLR) 2 and TLR1 or TLR6 in response to phenol-soluble modulin. J Immunol.2001;166(1):15-19.
Joo HS, Cheung GY, Otto M. Antimicrobial activity of community-associated methicillinresistant Staphylococcus aureus is caused by phenol-soluble modulin derivatives. J Biol Chem. 2011;286(11):8933-40.
Periasamy S, Joo HS, Duong AC, Bach TH, Tan VY, Chatterjee SS, et al. How Staphylococcus aureus biofilms develop their characteristic structure. PNAS. 2012;109(4):1281-6.
Tsompanidou E, Denham EL, Becher D, de Jong A, Buist G, van Oosten M, et al. Distinct roles of phenol-soluble modulins in spreading of Staphylococcus aureus on wet surfaces. Appl Environ Microbiol. 2013;79(3):886-95.
Johannessen M, Sollid JE, Hanssen AM. Host- and microbe determinants that may influence the success of S. aureus colonization. Front Cell Infect Microbiol. 2012;2:56.
Krismer B, Peschel A. Does Staphylococcus aureus nasal colonization involve biofilm formation? Future Microbiol. 2011 May;6(5):489-93.
Otto M, Echner H, Voelter W, Gotz F. Pheromone cross-inhibition between Staphylococcus aureus and Staphylococcus epidermidis. Infect Immun. 2001;69(3):1957-1960.
Cogen AL, Yamasaki K, Sánchez KM, Dorschner RA, Lai Y, MacLeod DT, et al. Selective antimicrobial action is provided by phenol-soluble modulins derived from Staphylococcus epidermidis, a normal resident of the skin. J Invest Dermatol. 2010;130(1):192-200.
Cogen AL, Yamasaki K, Muto J, Sánchez KM, Crotty Alexander L, Tanios J, et al. Staphylococcus epidermidis antimicrobial delta-toxin (phenol-soluble modulin-gamma) cooperates with host antimicrobial peptides to kill group A Streptococcus. PLoS One. 2010;5(1):e8557.
Yamaki J, Synold T, Wong-Beringer A. Antivirulence potential of TR-700 and clindamycin on clinical isolates of Staphylococcus aureus producing phenol-soluble modulins. Antimicrob Agents Chemother. 2011;55(9):4432-35.
Joo HS, Chan JL, Cheung GY, Otto M. Subinhibitory concentrations of protein synthesisinhibiting antibiotics promote increased expression of the agr virulence regulator and production of phenol-soluble modulin cytolysins in community-associated methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 2010;54(11):4942-44.
dc.rights.spa.fl_str_mv Revista Ciencias Biomédicas - 2020
dc.rights.uri.spa.fl_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rights.coar.spa.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.accessrights.spa.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv Revista Ciencias Biomédicas - 2020
https://creativecommons.org/licenses/by-nc-sa/4.0/
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Universidad de Cartagena
dc.source.spa.fl_str_mv https://revistas.unicartagena.edu.co/index.php/cbiomedicas/article/view/2894
institution Universidad de Cartagena
bitstream.url.fl_str_mv https://repositorio.unicartagena.edu.co/bitstreams/6bba267e-586e-451e-bbf8-0d58ab6cc331/download
bitstream.checksum.fl_str_mv 26f8fd4f9eccced2671228bdf7bc171e
bitstream.checksumAlgorithm.fl_str_mv MD5
repository.name.fl_str_mv Biblioteca Digital Universidad de Cartagena
repository.mail.fl_str_mv bdigital@metabiblioteca.com
_version_ 1818153112101191680
spelling Correa Jiménez, OscarReyes, Niradiz2014-01-15 00:00:002014-01-15 00:00:002014-01-152215-7840https://hdl.handle.net/11227/1312310.32997/rcb-2014-28942389-7252https://doi.org/10.32997/rcb-2014-2894application/pdfspaUniversidad de CartagenaRevista Ciencias Biomédicashttps://revistas.unicartagena.edu.co/index.php/cbiomedicas/article/download/2894/2437Núm. 1 , Año 201411511075David MZ, Daum RS. Community-associated methicillin-resistant Staphylococcus aureus: epidemiology and clinical consequences of an emerging epidemic. Clin Microbiol Rev. 2010;23(3):616-687.Castillo JS, Leal AL, Cortes JA, Álvarez CA, Sánchez R, Buitrago G, Barrero LI, et al. Mortality among critically ill patients with methicillin-resistant Staphylococcus aureus bacteremia: a multicenter cohort study in Colombia. Rev Panam Salud Pública. 2012 ;32(5):343-50.Thompson RL, Cabezudo I, Wenzel RP. Epidemiology of nosocomial infections caused by methicillin-resistant Staphylococcus aureus. Ann Intern Med. 1982;97(3):309-317.Miller LG, Kaplan SL. Staphylococcus aureus: a community pathogen. Infect Dis Clin North Am. 2009;23(1):35-52.Naimi TS, LeDell KH, Como-Sabetti K, Borchardt SM, Boxrud DJ, Etienne J, et al. Comparison of community- and health care-associated methicillin-resistant Staphylococcus aureus infection. JAMA. 2003;290(22):2976-84.Ochoa TJ, Mohr J, Wanger A, Murphy JR, Heresi GP. Community-associated methicillinresistant Staphylococcus aureus in pediatric patients. Emerg Infect Dis. 2005;11(6):966-8.Zetola N, Francis JS, Nuermberger EL, Bishai WR. Community-acquired meticillin-resistant Staphylococcus aureus: an emerging threat. Lancet Infect Dis. 2005;5(5):275-286.Von Eiff C, Becker K, Machka K, Stammer H, Peters G. Nasal carriage as a source of Staphylococcus aureus bacteremia. Study Group. N Engl J Med. 2001;344(1):11-16.Bettin A, Suárez P, Bedoya A, Reyes N. Staphylococcus aureus in residents from a nursinghome in Cartagena. Rev Salud Publica. 2008;10(4):650-657.Correa O, Delgado K, Rangel C, Bello A, Reyes N. Nasal and vaginal colonization of methicillin-resistant Staphylococcus aureus in pregnant women in Cartagena, Colombia. Colombia Médica. 2012;43(1):19-27.Rebollo-Pérez J, Ordonez-Tapia C, Herazo-Herazo C, Reyes-Ramos N. Nasal carriage of Panton Valentine leukocidin-positive methicillin-resistant Staphylococcus aureus in healthy preschool children. Rev Salud Pública. 2011;13(5):824-832.Bettin A, Causil C, Reyes N. Molecular identification and antimicrobial susceptibility of Staphylococcus aureus nasal isolates from medical students in Cartagena, Colombia. Braz J Infect Dis. 2012;16(4):329-334.del Rio A, Cervera C, Moreno A, Moreillon P, Miró JM. Patients at risk of complications of Staphylococcus aureus bloodstream infection. Clin Infect Dis. 2009;48(Suppl 4):S246-253.Sollid JU, Furberg AS, Hanssen AM, Johannessen M. Staphylococcus aureus: determinants of human carriage. Infect Genet Evol. 2013;21:531-41.Nygaard TK, DeLeo FR, Voyich JM. Community-associated methicillin-resistant Staphylo-coccus aureus skin infections: advances toward identifying the key virulence factors. Curr Opin Infect Dis. 2008;21(2):147-152.Holmes A, Ganner M, McGuane S, Pitt TL, Cookson BD, Kearns AM. Staphylococcus aureus isolates carrying Panton-Valentine leucocidin genes in England and Wales: frequency, characterization, and association with clinical disease. J Clin Microbiol. 2005;43(5):2384-90.Cercenado E, Cuevas O, Marin M, Bouza E, Trincado P, Boquete T, et al. Communityacquired methicillin-resistant Staphylococcus aureus in Madrid, Spain: transcontinental importation and polyclonal emergence of Panton-Valentine leukocidin-positive isolates. Diagn Microbiol Infect Dis. 2008;61(2):143-149.Villaruz AE, Bubeck Wardenburg J, Khan BA, Whitney AR, Sturdevant DE, Gardner DJ, et al. A point mutation in the agr locus rather than expression of the Panton-Valentine leukocidin caused previously reported phenotypes in Staphylococcus aureus pneumonia and gene regulation. J Infect Dis. 2009;200(5):724-734.Li M, Cheung GY, Hu J, Wang D, Joo HS, Deleo FR, et al. Comparative analysis of virulence and toxin expression of global community-associated methicillin-resistant Staphylococcus aureus strains. J Infect Dis. 2010;202(12):1866-76.Wang R, Braughton KR, Kretschmer D, Bach TH, Queck SY, Li M, et al. Identification of novel cytolytic peptides as key virulence determinants for community-associated MRSA. Nat Med. 2007;13(12):1510-14.Mehlin C, Headley CM, Klebanoff SJ. An inflammatory polypeptide complex from Staphylococcus epidermidis: isolation and characterization. J Exp Med. 1999;189(6):907-918.Rautenberg M, Joo HS, Otto M, Peschel A. Neutrophil responses to staphylococcal pathogens and commensals via the formyl peptide receptor 2 relates to phenol-soluble modulin release and virulence. FASEB J. 2011;25(4):1254-1263.Arias CA, Rincon S, Chowdhury S, Martínez E, Coronell W, Reyes J, et al. MRSA USA300 clone and VREF--a U.S.-Colombian connection? N Engl J Med. 2008;359(20):2177-9.Diep BA, Otto M. The role of virulence determinants in community-associated MRSA pathogenesis. Trends Microbiol. 2008;16(8):361-9.Otto M. Basis of virulence in community-associated methicillin-resistant Staphylococcus aureus. Annu Rev Microbiol. 2010;64:143-162.Grumann D, Nübel U, Bröker BM. Staphylococcus aureus toxins - Their functions and genetics. Infect Genet Evol. 2014;21:583-92.Queck SY, Khan BA, Wang R, Bach TH, Kretschmer D, Chen L, et al. Mobile genetic element-encoded cytolysin connects virulence to methicillin resistance in MRSA. PLoS Pathog. 2009;5(7):e1000533.Chatterjee SS, Chen L, Joo HS, Cheung GY, Kreiswirth BN, Otto M. Distribution and regulation of the mobile genetic element-encoded phenol-soluble modulin PSM-mec in methicillin-resistant Staphylococcus aureus. PLoS One. 2011;6(12):e28781.Monecke S, Engelmann I, Archambault M, Coleman DC, Coombs GW, Cortez de Jackel S, et al. Distribution of SCCmec-associated phenol-soluble modulin in staphylococci. Mol Cell Probes. 2012;26(2):99-103.Gonzalez DJ, Okumura CY, Hollands A, Kersten R, Akong-Moore K, Pence MA, et al. Novel phenol-soluble modulin derivatives in community-associated methicillin-resistant Staphylococcus aureus identified through imaging mass spectrometry. J Biol Chem. 2012;287(17):13889-98.Schwartz K, Syed AK, Stephenson RE, Rickard AH, Boles BR. Functional amyloids composed of phenol soluble modulins stabilize Staphylococcus aureus biofilms. PLoS Pathog. 2012;8(6):e1002744.Queck SY, Jameson-Lee M, Villaruz AE, Bach TH, Khan BA, Sturdevant DE, et al. RNAIIIindependent target gene control by the agr quorum-sensing system: insight into the evolution of virulence regulation in Staphylococcus aureus. Mol Cell. 2008;32(1):150-8.Kaito C, Saito Y, Nagano G, Ikuo M, Omae Y, Hanada Y, et al. Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence. PLoS Pathog. 2011;7(2):e1001267.Kaito C, Saito Y, Ikuo M, Omae Y, Mao H, Nagano G, et al. Mobile genetic element SCCmec-encoded psm-mec RNA suppresses translation of agrA and attenuates MRSA virulence. PLoS Pathog. 2013;9(4):e1003269.Chatterjee SS, Joo HS, Duong AC, Dieringer TD, Tan VY, Song Y, et al. Essential Staphylococcus aureus toxin export system. Nat Med.2013;19(3):364-7.Kretschmer D, Nikola N, Durr M, Otto M, Peschel A. The virulence regulator Agr controls the staphylococcal capacity to activate human neutrophils via the formyl peptide receptor 2. J Innate Immun. 2012;4(2):201-12.Forsman H, Christenson K, Bylund J, Dahlgren C. Receptor-dependent and -independent immunomodulatory effects of phenol-soluble modulin peptides from Staphylococcus aureus on human neutrophils are abrogated through peptide inactivation by reactive oxygen species. Infect Immun. 2012;80(6):1987-1995.Kobayashi SD, Malachowa N, Whitney AR, Braughton KR, Gardner DJ, Long D, et al. Comparative analysis of USA300 virulence determinants in a rabbit model of skin and soft tissue infection. J Infect Dis. 2011;204(6):937-41.Hongo I, Baba T, Oishi K, Morimoto Y, Ito T, Hiramatsu K. Phenol-soluble modulin alpha 3 enhances the human neutrophil lysis mediated by Panton-Valentine leukocidin. J Infect Dis. 2009;200(5):715-723.Liles WC, Thomsen AR, O’Mahony DS, Klebanoff SJ. Stimulation of human neutrophils and monocytes by staphylococcal phenol-soluble modulin. J Leukoc Biol. 2001;70(1):96-102.Kretschmer D, Gleske AK, Rautenberg M, Wang R, Koberle M, Bohn E, et al. Human formyl peptide receptor 2 senses highly pathogenic Staphylococcus aureus. Cell Host Microbe. 2010;7(6):463-73.Schreiner J, Kretschmer D, Klenk J, Otto M, Buhring HJ, Stevanovic S, et al. Staphylococcus aureus phenol-soluble modulin peptides modulate dendritic cell functions and increase in vitro priming of regulatory T cells. J Immunol. 2013;190(7):3417-26.Hajjar AM, O’Mahony DS, Ozinsky A, Underhill DM, Aderem A, Klebanoff SJ, et al. Cutting edge: functional interactions between toll-like receptor (TLR) 2 and TLR1 or TLR6 in response to phenol-soluble modulin. J Immunol.2001;166(1):15-19.Joo HS, Cheung GY, Otto M. Antimicrobial activity of community-associated methicillinresistant Staphylococcus aureus is caused by phenol-soluble modulin derivatives. J Biol Chem. 2011;286(11):8933-40.Periasamy S, Joo HS, Duong AC, Bach TH, Tan VY, Chatterjee SS, et al. How Staphylococcus aureus biofilms develop their characteristic structure. PNAS. 2012;109(4):1281-6.Tsompanidou E, Denham EL, Becher D, de Jong A, Buist G, van Oosten M, et al. Distinct roles of phenol-soluble modulins in spreading of Staphylococcus aureus on wet surfaces. Appl Environ Microbiol. 2013;79(3):886-95.Johannessen M, Sollid JE, Hanssen AM. Host- and microbe determinants that may influence the success of S. aureus colonization. Front Cell Infect Microbiol. 2012;2:56.Krismer B, Peschel A. Does Staphylococcus aureus nasal colonization involve biofilm formation? Future Microbiol. 2011 May;6(5):489-93.Otto M, Echner H, Voelter W, Gotz F. Pheromone cross-inhibition between Staphylococcus aureus and Staphylococcus epidermidis. Infect Immun. 2001;69(3):1957-1960.Cogen AL, Yamasaki K, Sánchez KM, Dorschner RA, Lai Y, MacLeod DT, et al. Selective antimicrobial action is provided by phenol-soluble modulins derived from Staphylococcus epidermidis, a normal resident of the skin. J Invest Dermatol. 2010;130(1):192-200.Cogen AL, Yamasaki K, Muto J, Sánchez KM, Crotty Alexander L, Tanios J, et al. Staphylococcus epidermidis antimicrobial delta-toxin (phenol-soluble modulin-gamma) cooperates with host antimicrobial peptides to kill group A Streptococcus. PLoS One. 2010;5(1):e8557.Yamaki J, Synold T, Wong-Beringer A. Antivirulence potential of TR-700 and clindamycin on clinical isolates of Staphylococcus aureus producing phenol-soluble modulins. Antimicrob Agents Chemother. 2011;55(9):4432-35.Joo HS, Chan JL, Cheung GY, Otto M. Subinhibitory concentrations of protein synthesisinhibiting antibiotics promote increased expression of the agr virulence regulator and production of phenol-soluble modulin cytolysins in community-associated methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 2010;54(11):4942-44.Revista Ciencias Biomédicas - 2020https://creativecommons.org/licenses/by-nc-sa/4.0/http://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccesshttps://revistas.unicartagena.edu.co/index.php/cbiomedicas/article/view/2894Factores de virulenciaPatogenicidadToxinas bacterianasCitotoxinasStaphylococcus aureus.Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?Modulinas solubles en fenol: ¿actores principales en la patogénesis del staphylococcus aureus?Artículo de revistainfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1Textinfo:eu-repo/semantics/articleJournal articlePublicationOREORE.xmltext/xml2566https://repositorio.unicartagena.edu.co/bitstreams/6bba267e-586e-451e-bbf8-0d58ab6cc331/download26f8fd4f9eccced2671228bdf7bc171eMD5111227/13123oai:repositorio.unicartagena.edu.co:11227/131232024-09-05 15:30:31.155https://creativecommons.org/licenses/by-nc-sa/4.0/Revista Ciencias Biomédicas - 2020metadata.onlyhttps://repositorio.unicartagena.edu.coBiblioteca Digital Universidad de Cartagenabdigital@metabiblioteca.com