INFORMAZIONI SU QUESTO ARTICOLO

Cita

Bébéar C. Les Mycoplasmes. Aspects biologiques, diagnostiques etthérapeutiques. In: Bébéar Ch, editor. Mycoplasmes et Chlamydiae. Paris (France): Elsevier; 2002. p. 37–47.BébéarC. Les Mycoplasmes. Aspects biologiques, diagnostiques etthérapeutiques. In: BébéarCh, editor. Mycoplasmes et Chlamydiae. Paris (France): Elsevier; 2002. p. 3747.Search in Google Scholar

Bergin SM, Mendis SM, Young B, Binti Izharuddin E. Postoperative Mycoplasma hominis brain abscess: keep it in mind! BMJ Case Rep. 2017 Jan 9;2017:bcr2016218022. https://doi.org/10.1136/bcr-2016-218022BerginSMMendisSMYoungBBinti IzharuddinE. Postoperative Mycoplasma hominis brain abscess: keep it in mind!BMJ Case Rep. 2017Jan9;2017:bcr2016218022. https://doi.org/10.1136/bcr-2016-218022525554428069785Search in Google Scholar

Biernat-Sudolska M, Rojek-Zakrzewska D, Bilska-Wilkosz A. In vitro activity of lipoic acid against Ureaplasma urealyticum and Ureaplasma parvum isolated from women with infections of the urogenital tract. A pilot study. Acta Biochim Pol. 2020 Dec 17;67(4):623–628. https://doi.org/10.18388/abp.2020_5413Biernat-SudolskaMRojek-ZakrzewskaDBilska-WilkoszA. In vitro activity of lipoic acid against Ureaplasma urealyticum and Ureaplasma parvum isolated from women with infections of the urogenital tract. A pilot study. Acta Biochim Pol. 2020Dec17;67(4):623628. https://doi.org/10.18388/abp.2020_541333332062Search in Google Scholar

Biernat-Sudolska M, Rojek-Zakrzewska D, Lauterbach R. Assessment of various diagnostic methods of ureaplasma respiratory tract infections in newborns. Acta Biochim Pol. 2006 Oct 01;53(3):609–612. https://doi.org/10.18388/abp.2006_3335Biernat-SudolskaMRojek-ZakrzewskaDLauterbachR. Assessment of various diagnostic methods of ureaplasma respiratory tract infections in newborns. Acta Biochim Pol. 2006Oct01;53(3):609612. https://doi.org/10.18388/abp.2006_3335Search in Google Scholar

Bilska A, Dudek M, Iciek M, Kwiecień I, Sokołowska-Jezewicz M, Filipek B, Włodek L. Biological actions of lipoic acid associated with sulfane sulfur metabolism. Pharmacol Rep. 2008 Mar-Apr; 60(2): 225–232.BilskaADudekMIciekMKwiecieńISokołowska-JezewiczMFilipekBWłodekL. Biological actions of lipoic acid associated with sulfane sulfur metabolism. Pharmacol Rep. 2008Mar-Apr; 60(2): 225232.Search in Google Scholar

Bilska-Wilkosz A, Iciek M, Kowalczyk-Pachel D, Górny M, Sokołowska-Jeżewicz M, Włodek L. Lipoic acid as a possible pharmacological source of hydrogen sulfide/sulfane sulfur. Molecules. 2017 Mar 02;22(3):388. https://doi.org/10.3390/molecules22030388Bilska-WilkoszAIciekMKowalczyk-PachelDGórnyMSokołowska-JeżewiczMWłodekL. Lipoic acid as a possible pharmacological source of hydrogen sulfide/sulfane sulfur. Molecules. 2017Mar02;22(3):388. https://doi.org/10.3390/molecules22030388615542728257119Search in Google Scholar

Eremeeva ME, Silverman DJ. Rickettsia rickettsii infection of the EA.hy 926 endothelial cell line: morphological response to infection and evidence for oxidative injury. Microbiology. 1998 Aug 01; 144(8):2037–2048. https://doi.org/10.1099/00221287-144-8-2037EremeevaMESilvermanDJ. Rickettsia rickettsii infection of the EA.hy 926 endothelial cell line: morphological response to infection and evidence for oxidative injury. Microbiology. 1998Aug01; 144(8):20372048. https://doi.org/10.1099/00221287-144-8-20379720025Search in Google Scholar

Hou N, Yan Z, Fan K, Li H, Zhao R, Xia Y, Xun L, Liu H. OxyR senses sulfane sulfur and activates the genes for its removal in Escherichia coli. Redox Biol. 2019 Sep;26:101293. https://doi.org/10.1016/j.redox.2019.101293HouNYanZFanKLiHZhaoRXiaYXunLLiuH. OxyR senses sulfane sulfur and activates the genes for its removal in Escherichia coli. Redox Biol. 2019Sep;26:101293. https://doi.org/10.1016/j.redox.2019.101293683187531421411Search in Google Scholar

Iciek M, Górny M, Bilska-Wilkosz A, Kowalczyk-Pachel D. Is aldehyde dehydrogenase inhibited by sulfur compounds? In vitro and in vivo studies. Acta Biochim Pol. 2018 May 27;65(1):125–132. https://doi.org/10.18388/abp.2017_2324IciekMGórnyMBilska-WilkoszAKowalczyk-PachelD. Is aldehyde dehydrogenase inhibited by sulfur compounds? In vitro and in vivo studies. Acta Biochim Pol. 2018May27;65(1):125132. https://doi.org/10.18388/abp.2017_232429518171Search in Google Scholar

Jariwalla RJ, Lalezari J, Cenko D, Mansour SE, Kumar A, Gangapurkar B, Nakamura D. Restoration of blood total glutathione status and lymphocyte function following α-lipoic acid supplementation in patients with HIV infection. J Altern Complement Med. 2008 Mar;14(2):139–146. https://doi.org/10.1089/acm.2006.6397JariwallaRJLalezariJCenkoDMansourSEKumarAGangapurkarBNakamuraD. Restoration of blood total glutathione status and lymphocyte function following α-lipoic acid supplementation in patients with HIV infection. J Altern Complement Med. 2008Mar;14(2):139146. https://doi.org/10.1089/acm.2006.639718315507Search in Google Scholar

Kafkewitz D, Fava F, Armenante PM. Effect of vitamins on the aerobic degradation of 2-chlorophenol, 4-chlorophenol, and 4-chlorobiphenyl. Appl Microbiol Biotechnol. 1996 Nov;46(4):414–421. https://doi.org/10.1007/BF00166239KafkewitzDFavaFArmenantePM. Effect of vitamins on the aerobic degradation of 2-chlorophenol, 4-chlorophenol, and 4-chlorobiphenyl. Appl Microbiol Biotechnol. 1996Nov;46(4):414421. https://doi.org/10.1007/BF001662398987730Search in Google Scholar

Koch A, Bilina A, Teodorowicz L, Stary A. Mycoplasma hominis and Ureaplasma urealyticum in patients with sexually transmitted diseases. Wien Klin Wochenschr. 1997 Aug 8;109(14–15):584–589.KochABilinaATeodorowiczLStaryA. Mycoplasma hominis and Ureaplasma urealyticum in patients with sexually transmitted diseases. Wien Klin Wochenschr. 1997Aug8;109(14–15):584589.Search in Google Scholar

Krijnen MR, Hekker T, Algra J, Wuisman PI, Van Royen BJ. Mycoplasma hominis deep wound infection after neuromuscular scoliosis surgery: the use of real-time polymerase chain reaction (PCR). Eur Spine J. 2006 Oct;15 Suppl 5(Suppl 5):599–603. https://doi.org/10.1007/s00586-005-0055-yKrijnenMRHekkerTAlgraJWuismanPIVan RoyenBJ. Mycoplasma hominis deep wound infection after neuromuscular scoliosis surgery: the use of real-time polymerase chain reaction (PCR). Eur Spine J. 2006Oct;15Suppl 5(Suppl 5):599603. https://doi.org/10.1007/s00586-005-0055-y160219116429284Search in Google Scholar

Le Guern R, Loïez C, Loobuyck V, Rousse N, Courcol R, Wallet F. A new case of Mycoplasma hominis mediastinitis and sternal osteitis after cardiac surgery. Int J Infect Dis. 2015 Feb;31:53–55. https://doi.org/10.1016/j.ijid.2014.12.028Le GuernRLoïezCLoobuyckVRousseNCourcolRWalletF. A new case of Mycoplasma hominis mediastinitis and sternal osteitis after cardiac surgery. Int J Infect Dis. 2015Feb;31:5355. https://doi.org/10.1016/j.ijid.2014.12.02825532483Search in Google Scholar

Li WR, Ma YK, Shi QS, Xie XB, Sun TL, Peng H, Huang XM. Diallyl disulfide from garlic oil inhibits Pseudomonas aeruginosa virulence factors by inactivating key quorum sensing genes. Appl Microbiol Biotechnol. 2018 Sep;102(17):7555–7564. https://doi.org/10.1007/s00253-018-9175-2LiWRMaYKShiQSXieXBSunTLPengHHuangXM. Diallyl disulfide from garlic oil inhibits Pseudomonas aeruginosa virulence factors by inactivating key quorum sensing genes. Appl Microbiol Biotechnol. 2018Sep;102(17):75557564. https://doi.org/10.1007/s00253-018-9175-229951860Search in Google Scholar

Luki N, Lebel P, Boucher M, Doray B, Turgeon J, Brousseau R. Comparison of polymerase chain reaction assay with culture for detection of genital mycoplasmas in perinatal infections. Eur J Clin Microbiol Infect Dis. 1998 Apr;17(4):255–263. https://doi.org/10.1007/BF01699982LukiNLebelPBoucherMDorayBTurgeonJBrousseauR. Comparison of polymerase chain reaction assay with culture for detection of genital mycoplasmas in perinatal infections. Eur J Clin Microbiol Infect Dis. 1998Apr;17(4):255263. https://doi.org/10.1007/BF016999829707308Search in Google Scholar

Meyer RD, Clough W. Extragenital Mycoplasma hominis infections in adults: emphasis on immunosuppression. Clin Infect Dis. 1993 Aug;17 Suppl 1:S243–S249. https://doi.org/10.1093/clinids/17.supplement_1.s243MeyerRDCloughW. Extragenital Mycoplasma hominis infections in adults: emphasis on immunosuppression. Clin Infect Dis. 1993Aug;17Suppl 1:S243S249. https://doi.org/10.1093/clinids/17.supplement_1.s2438399923Search in Google Scholar

Miranda C, Camacho E, Reina G, Turiño J, Rodríguez-Granger J, Yeste R, Bautista MF, García M, Alados JC, De la Rosa M. Isolation of Mycoplasma hominis from extragenital cultures. Eur J Clin Microbiol Infect Dis. 2005 May;24(5):334–337. https://doi.org/10.1007/s10096-005-1326-6MirandaCCamachoEReinaGTuriñoJRodríguez-GrangerJYesteRBautistaMFGarcíaMAladosJCDe la RosaM. Isolation of Mycoplasma hominis from extragenital cultures. Eur J Clin Microbiol Infect Dis. 2005May;24(5):334337. https://doi.org/10.1007/s10096-005-1326-615868155Search in Google Scholar

Qiu HJ, Lu WP, Li M, Wang ZM, Du QY, Wang AM, Xiong Y. The infection of Mycoplasma hominis after total knee replacement: Case report and literature review. Chin J Traumatol. 2017 Aug; 20(4):243–245. https://doi.org/10.1016/j.cjtee.2017.04.005QiuHJLuWPLiMWangZMDuQYWangAMXiongY. The infection of Mycoplasma hominis after total knee replacement: Case report and literature review. Chin J Traumatol. 2017Aug; 20(4):243245. https://doi.org/10.1016/j.cjtee.2017.04.005555524428711272Search in Google Scholar

Ran M, Wang T, Shao M, Chen Z, Liu H, Xia Y, Xun L. Sensitive method for reliable quantification of sulfane sulfur in biological samples. Anal Chem. 2019 Sep 17;91(18):11981–11986. https://doi.org/10.1021/acs.analchem.9b02875RanMWangTShaoMChenZLiuHXiaYXunL. Sensitive method for reliable quantification of sulfane sulfur in biological samples. Anal Chem. 2019Sep17;91(18):1198111986. https://doi.org/10.1021/acs.analchem.9b0287531436086Search in Google Scholar

Reed LJ, DeBusk BG, Gunsalus IC, Hornberger CS Jr. Crystalline α-lipoic acid; a catalytic agent associated with pyruvate dehydrogenase. Science. 1951 Jul 27;114(2952):93–94. https://doi.org/10.1126/science.114.2952.93ReedLJDeBuskBGGunsalusICHornbergerCSJr. Crystalline α-lipoic acid; a catalytic agent associated with pyruvate dehydrogenase. Science. 1951Jul27;114(2952):9394. https://doi.org/10.1126/science.114.2952.9314854913Search in Google Scholar

Rodwell AW. A defined medium for Mycoplasma strain Y. J Gen Microbiol. 1969 Sep;58(1):39–47. https://doi.org/10.1099/00221287-58-1-39RodwellAW. A defined medium for Mycoplasma strain Y. J Gen Microbiol. 1969Sep;58(1):3947. https://doi.org/10.1099/00221287-58-1-394243269Search in Google Scholar

Salehi B, Berkay Yılmaz Y, Antika G, Boyunegmez Tumer T, Fawzi Mahomoodally M, Lobine D, Akram M, Riaz M, Capanoglu E, Sharopov F, et al. Insights on the use of α-lipoic acid for therapeutic purposes. Biomolecules. 2019;9(8):356. https://doi.org/10.3390/biom9080356SalehiBBerkay YılmazYAntikaGBoyunegmez TumerTFawzi MahomoodallyMLobineDAkramMRiazMCapanogluESharopovF. Insights on the use of α-lipoic acid for therapeutic purposes. Biomolecules. 2019;9(8):356. https://doi.org/10.3390/biom9080356672318831405030Search in Google Scholar

Shi C, Sun Y, Zhang X, Zheng Z, Yang M, Ben H, Song K, Cao Y, Chen Y, Liu X, et al. Antimicrobial effect of lipoic acid against Cronobacter sakazakii. Food Control. 2016 Jan;59:352–358. https://doi.org/10.1016/j.foodcont.2015.05.041ShiCSunYZhangXZhengZYangMBenHSongKCaoYChenYLiuX. Antimicrobial effect of lipoic acid against Cronobacter sakazakii. Food Control. 2016Jan;59:352358. https://doi.org/10.1016/j.foodcont.2015.05.041Search in Google Scholar

Spalding MD, Prigge ST. Lipoic acid metabolism in microbial pathogens. Microbiol Mol Biol Rev. 2010 Jun;74(2):200–228. https://doi.org/10.1128/MMBR.00008-10SpaldingMDPriggeST. Lipoic acid metabolism in microbial pathogens. Microbiol Mol Biol Rev. 2010Jun;74(2):200228. https://doi.org/10.1128/MMBR.00008-10288441220508247Search in Google Scholar

Waites KB, Schelonka RL, Xiao L, Grigsby PL, Novy MJ. Congenital and opportunistic infections: Ureaplasma species and Mycoplasma hominis. Semin Fetal Neonatal Med. 2009 Aug;14(4):190–199. https://doi.org/10.1016/j.siny.2008.11.009WaitesKBSchelonkaRLXiaoLGrigsbyPLNovyMJ. Congenital and opportunistic infections: Ureaplasma species and Mycoplasma hominis. Semin Fetal Neonatal Med. 2009Aug;14(4):190199. https://doi.org/10.1016/j.siny.2008.11.00919109084Search in Google Scholar

Whitson WJ, Ball PA, Lollis SS, Balkman JD, Bauer DF. Postoperative Mycoplasma hominis infections after neurosurgical intervention. J Neurosurg Pediatr. 2014 Aug;14(2):212–218. https://doi.org/10.3171/2014.4.PEDS13547WhitsonWJBallPALollisSSBalkmanJDBauerDF. Postoperative Mycoplasma hominis infections after neurosurgical intervention. J Neurosurg Pediatr. 2014Aug;14(2):212218. https://doi.org/10.3171/2014.4.PEDS1354724856879Search in Google Scholar

Xuan G, Lv C, Xu H, Li K, Liu H, Xia Y, Xun L. Sulfane sulfur regulates LasR-mediated quorum sensing and virulence in Pseudomonas aeruginosa PAO1. Antioxidants. 2021 Sep 21;10(9):1498. https://doi.org/10.3390/antiox10091498XuanGLvCXuHLiKLiuHXiaYXunL. Sulfane sulfur regulates LasR-mediated quorum sensing and virulence in Pseudomonas aeruginosa PAO1. Antioxidants. 2021Sep21;10(9):1498. https://doi.org/10.3390/antiox10091498846961034573130Search in Google Scholar

Zhao G, Hu C, Xue Y. In vitro evaluation of chitosan-coated liposome containing both coenzyme Q10 and alpha-lipoic acid: Cytotoxicity, antioxidant activity, and antimicrobial activity. J Cosmet Dermatol. 2018 Apr;17(2):258–262. https://doi.org/10.1111/jocd.12369ZhaoGHuCXueY. In vitro evaluation of chitosan-coated liposome containing both coenzyme Q10 and alpha-lipoic acid: Cytotoxicity, antioxidant activity, and antimicrobial activity. J Cosmet Dermatol. 2018Apr;17(2):258262. https://doi.org/10.1111/jocd.1236928722258Search in Google Scholar

Zhong M, Sun A, Xiao T, Yao G, Sang L, Zheng X, Zhang J, Jin X, Xu L, Yang W, et al. A randomized, single-blind, group sequential, active-controlled study to evaluate the clinical efficacy and safety of α-lipoic acid for critically ill patients with coronavirus disease 2019 (COVID-19). MedRxiv, 2020. https://doi.org/10.1101/2020.04.15.20066266ZhongMSunAXiaoTYaoGSangLZhengXZhangJJinXXuLYangW. A randomized, single-blind, group sequential, active-controlled study to evaluate the clinical efficacy and safety of α-lipoic acid for critically ill patients with coronavirus disease 2019 (COVID-19). MedRxiv, 2020. https://doi.org/10.1101/2020.04.15.20066266Search in Google Scholar

Zhou M, Wang P, Chen S, Du B, Du J, Wang F, Xiao M, Kong F, Xu Y. Meningitis in a Chinese adult patient caused by Mycoplasma hominis: a rare infection and literature review. BMC Infect Dis. 2016 Oct 12;16(1):557. https://doi.org/10.1186/s12879-016-1885-4ZhouMWangPChenSDuBDuJWangFXiaoMKongFXuY. Meningitis in a Chinese adult patient caused by Mycoplasma hominis: a rare infection and literature review. BMC Infect Dis. 2016Oct12;16(1):557. https://doi.org/10.1186/s12879-016-1885-4505990127729031Search in Google Scholar

Zhou W, Du Y, Li X, Yao C. Lipoic acid modified antimicrobial peptide with enhanced antimicrobial properties. Bioorg Med Chem. 2020 Oct 1;28(19):115682. https://doi.org/10.1016/j.bmc.2020.115682ZhouWDuYLiXYaoC. Lipoic acid modified antimicrobial peptide with enhanced antimicrobial properties. Bioorg Med Chem. 2020Oct1;28(19):115682. https://doi.org/10.1016/j.bmc.2020.11568232912428Search in Google Scholar

Zorzoli A, Grayczyk JP, Alonzo F 3rd. Staphylococcus aureus tissue infection during sepsis is supported by differential use of bacterial or host-derived lipoic acid. PLoS Pathog. 2016 Oct 4;12(10):e1005933. https://doi.org/10.1371/journal.ppat.1005933ZorzoliAGrayczykJPAlonzoF3rd. Staphylococcus aureus tissue infection during sepsis is supported by differential use of bacterial or host-derived lipoic acid. PLoS Pathog. 2016Oct4;12(10):e1005933. https://doi.org/10.1371/journal.ppat.1005933504984927701474Search in Google Scholar

eISSN:
2544-4646
Lingua:
Inglese
Frequenza di pubblicazione:
4 volte all'anno
Argomenti della rivista:
Life Sciences, Microbiology and Virology