Tigecycline antibacterial activity, clinical effectiveness, and mechanisms and epidemiology of resistance: narrative review

. 2022 Jul ; 41 (7) : 1003-1022. [epub] 20210105

Jazyk angličtina Země Německo Médium print-electronic

Typ dokumentu časopisecké články, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid33403565
Odkazy

PubMed 33403565
PubMed Central PMC7785128
DOI 10.1007/s10096-020-04121-1
PII: 10.1007/s10096-020-04121-1
Knihovny.cz E-zdroje

Tigecycline is unique glycylcycline class of semisynthetic antimicrobial agents developed for the treatment of polymicrobial infections caused by multidrug-resistant Gram-positive and Gram-negative pathogens. Tigecycline evades the main tetracycline resistance genetic mechanisms, such as tetracycline-specific efflux pump acquisition and ribosomal protection, via the addition of a glycyclamide moiety to the 9-position of minocycline. The use of the parenteral form of tigecycline is approved for complicated skin and skin structure infections (excluding diabetes foot infection), complicated intra-abdominal infections, and community-acquired bacterial pneumonia in adults. New evidence also suggests the effectiveness of tigecycline for the treatment of severe Clostridioides difficile infections. Tigecycline showed in vitro susceptibility to Coxiella spp., Rickettsia spp., and multidrug-resistant Neisseria gonnorrhoeae strains which indicate the possible use of tigecycline in the treatment of infections caused by these pathogens. Except for intrinsic, or often reported resistance in some Gram-negatives, tigecycline is effective against a wide range of multidrug-resistant nosocomial pathogens. Herein, we summarize the currently available data on tigecycline pharmacokinetics and pharmacodynamics, its mechanism of action, the epidemiology of tigecycline resistance, and its clinical effectiveness.

Zobrazit více v PubMed

Ventola CL. The antibiotic resistance crisis: part 1: causes and threats. Pharmacy and therapeutics. 2015;40(4):277. PubMed PMC

Tasina E, Haidich A-B, Kokkali S, Arvanitidou M. Efficacy and safety of tigecycline for the treatment of infectious diseases: a meta-analysis. Lancet Infect Dis. 2011;11(11):834–844. doi: 10.1016/S1473-3099(11)70177-3. PubMed DOI

Guay DR. Oritavancin and tigecycline: investigational antimicrobials for multidrug-resistant bacteria. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy. 2004;24(1):58–68. doi: 10.1592/phco.24.1.58.34808. PubMed DOI

Stein GE, Babinchak T. Tigecycline: an update. Diagn Microbiol Infect Dis. 2013;75(4):331–336. doi: 10.1016/j.diagmicrobio.2012.12.004. PubMed DOI

FDA U FDA drug safety communication: increased risk of death with Tygacil (tigecycline) compared to other antibiotics used to treat similar infections (1 September 2010).

Food Administration D (2017) FDA drug safety communication: FDA warns of increased risk of death with IV antibacterial Tygacil (tigecycline) and approves new boxed warning. US Food and Drug Administration, Silver Spring, MD

Lauf L, Ozsvár Z, Mitha I, Regöly-Mérei J, Embil JM, Cooper A, Sabol MB, Castaing N, Dartois N, Yan JJDM, disease i (2014) Phase 3 study comparing tigecycline and ertapenem in patients with diabetic foot infections with and without osteomyelitis. 78(4):469–480 PubMed

Kechagias KS, Chorepsima S, Triarides NA, Falagas ME (2020) Tigecycline for the treatment of patients with Clostridium difficile infection: an update of the clinical evidence. Eur J Clin Microbiol Infect Dis:1–6 PubMed

Marot J-C, Jonckheere S, Munyentwali H, Belkhir L, Vandercam B, Yombi JC. Tigecycline-induced acute pancreatitis: about two cases and review of the literature. Acta Clin Belg. 2012;67(3):229–232. PubMed

Finch RG, Greenwood D, Whitley RJ, Norrby SR. Antibiotic and chemotherapy e-book. 2010.

Mukker JK, Singh RP, Derendorf HJJOPS (2014) Determination of atypical nonlinear plasma–protein-binding behavior of tigecycline using an in vitro microdialysis technique. 103 (3):1013-1019 PubMed

Bennett JE, Dolin R, Blaser MJ (2014) Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases: 2-Volume Set. Elsevier Health Sciences

DE ROSA FG, Corcione S, Di Perri G, Scaglione F (2015) Re-defining tigecycline therapy. PubMed

Cai Y, Bai N, Liu X, Liang B, Wang J, Wang R. Tigecycline: Alone or in combination? Infectious Diseases. 2016;48(7):491–502. doi: 10.3109/23744235.2016.1155735. PubMed DOI

Stein GE, Smith CL, Missavage A, Saunders JP, Nicolau DP, Battjes SM, Kepros JP. Tigecycline penetration into skin and soft tissue. Surg Infect. 2011;12(6):465–467. doi: 10.1089/sur.2011.022. PubMed DOI

Tombs N (1999) Tissue distribution of GAR-936, a broad spectrum antibiotic in male rats. Program and abstracts of the Thirty-ninth Interscience Conference on Antimicrobial Agents and Chemotherapy, pp 26-29

Postier RG, Green SL, Klein SR, Ellis-Grosse E, Loh E, Group TS Results of a multicenter, randomized, open-label efficacy and safety study of two doses of tigecycline for complicated skin and skin-structure infections in hospitalized patients. Clin Ther. 2004;26(5):704–714. doi: 10.1016/S0149-2918(04)90070-7. PubMed DOI

Rodvold KA, Gotfried MH, Cwik M, Korth-Bradley JM, Dukart G, Ellis-Grosse EJ. Serum, tissue and body fluid concentrations of tigecycline after a single 100 mg dose. J Antimicrob Chemother. 2006;58(6):1221–1229. doi: 10.1093/jac/dkl403. PubMed DOI

Bhattacharya I, Gotfried MH, Ji AJ, Saunders JP, Gourley I, Diehl A, Korth-Bradley JM. Reassessment of tigecycline bone concentrations in volunteers undergoing elective orthopedic procedures. J Clin Pharmacol. 2014;54(1):70–74. doi: 10.1002/jcph.201. PubMed DOI

Meagher A, Passarell J, Cirincione B, Van Wart S, Liolios K, Babinchak T, Ellis-Grosse E, Ambrose P. Exposure-response analyses of tigecycline efficacy in patients with complicated skin and skin-structure infections. Antimicrob Agents Chemother. 2007;51(6):1939–1945. doi: 10.1128/AAC.01084-06. PubMed DOI PMC

Passarell J, Meagher A, Liolios K, Cirincione B, Van Wart S, Babinchak T, Ellis-Grosse E, Ambrose P. Exposure-response analyses of tigecycline efficacy in patients with complicated intra-abdominal infections. Antimicrob Agents Chemother. 2008;52(1):204–210. doi: 10.1128/AAC.00813-07. PubMed DOI PMC

Townsend ML, Pound MW, Drew RH. Tigecycline in the treatment of complicated intra-abdominal and complicated skin and skin structure infections. Ther Clin Risk Manag. 2007;3(6):1059. PubMed PMC

Petersen PJ, Bradford PA, Weiss WJ, Murphy TM, Sum P, Projan SJ. In vitro and in vivo activities of tigecycline (GAR-936), daptomycin, and comparative antimicrobial agents against glycopeptide-intermediate Staphylococcus aureus and other resistant gram-positive pathogens. Antimicrob Agents Chemother. 2002;46(8):2595–2601. doi: 10.1128/AAC.46.8.2595-2601.2002. PubMed DOI PMC

Van Ogtrop M, Andes D, Stamstad T, Conklin B, Weiss W, Craig W, Vesga OJAA, chemotherapy (2000) In vivo pharmacodynamic activities of two glycylcyclines (GAR-936 and WAY 152,288) against various gram-positive and gram-negative bacteria 44 (4):943-949 PubMed PMC

Rello J (2005) Pharmacokinetics, pharmacodynamics, safety and tolerability of tigecycline. Journal of chemotherapy 17 (sup1):12-22 PubMed

Muralidharan G, Micalizzi M, Speth J, Raible D, Troy S. Pharmacokinetics of tigecycline after single and multiple doses in healthy subjects. Antimicrob Agents Chemother. 2005;49(1):220–229. doi: 10.1128/AAC.49.1.220-229.2005. PubMed DOI PMC

Kaewpoowat Q, Ostrosky-Zeichner L. Tigecycline: a critical safety review. Expert Opin Drug Saf. 2015;14(2):335–342. doi: 10.1517/14740338.2015.997206. PubMed DOI

Korth-Bradley JM, Baird-Bellaire SJ, Patat AA, Troy SM, Böhmer GM, Gleiter CH, Buecheler R, Morgan MY. Pharmacokinetics and safety of a single intravenous dose of the antibiotic tigecycline in patients with cirrhosis. J Clin Pharmacol. 2011;51(1):93–101. doi: 10.1177/0091270010363477. PubMed DOI

Greer ND (2006) Tigecycline (Tygacil): the first in the glycylcycline class of antibiotics. Baylor University Medical Center Proceedings. Taylor & Francis, pp 155-161 PubMed PMC

CLSI C (2019) Performance standards for antimicrobial susceptibility testing. Clinical Lab Standards Institute

Testing ECOAS. European Committee on Antimicrobial Susceptibility Testing Breakpoint tables for interpretation of MICs and zone diameters European Committee on Antimicrobial Susceptibility Testing Breakpoint tables for interpretation of MICs and zone diameters. Sweden: Växjö; 2019.

Wyeth P. Tygacil (tigecycline) for injection. Philadelphia, PA: Wyeth Pharmaceuticals Inc; 2010.

Nathwani D (2018) British Society for Antimicrobial Chemotherapy. Antimicrobial stewardship: from principles to practice

Hawkey P, Finch R. Tigecycline: in-vitro performance as a predictor of clinical efficacy. Clin Microbiol Infect. 2007;13(4):354–362. doi: 10.1111/j.1469-0691.2006.01621.x. PubMed DOI

Seiffert SN, Marschall J, Perreten V, Carattoli A, Furrer H, Endimiani A. Emergence of Klebsiella pneumoniae co-producing NDM-1, OXA-48, CTX-M-15, CMY-16, QnrA and ArmA in Switzerland. Int J Antimicrob Agents. 2014;44(3):260–262. doi: 10.1016/j.ijantimicag.2014.05.008. PubMed DOI

Kumarasamy KK, Toleman MA, Walsh TR, Bagaria J, Butt F, Balakrishnan R, Chaudhary U, Doumith M, Giske CG, Irfan S. Emergence of a new antibiotic resistance mechanism in India, Pakistan, and the UK: a molecular, biological, and epidemiological study. Lancet Infect Dis. 2010;10(9):597–602. doi: 10.1016/S1473-3099(10)70143-2. PubMed DOI PMC

Hidalgo L, Hopkins KL, Gutierrez B, Ovejero CM, Shukla S, Douthwaite S, Prasad KN, Woodford N, Gonzalez-Zorn B. Association of the novel aminoglycoside resistance determinant RmtF with NDM carbapenemase in Enterobacteriaceae isolated in India and the UK. J Antimicrob Chemother. 2013;68(7):1543–1550. doi: 10.1093/jac/dkt078. PubMed DOI

Du X, He F, Shi Q, Zhao F, Xu J, Fu Y, Yu Y. The Rapid Emergence of Tigecycline Resistance in blaKPC–2 Harboring Klebsiella pneumoniae, as Mediated in Vivo by Mutation in tetA During Tigecycline Treatment. Front Microbiol. 2018;9:648. doi: 10.3389/fmicb.2018.00648. PubMed DOI PMC

Alhashem F, Tiren-Verbeet NL, Alp E, Doganay M. Treatment of sepsis: What is the antibiotic choice in bacteremia due to carbapenem resistant Enterobacteriaceae? World J Clin Cases. 2017;5(8):324. doi: 10.12998/wjcc.v5.i8.324. PubMed DOI PMC

Iovleva A, Doi Y. Carbapenem-resistant enterobacteriaceae. Clin Lab Med. 2017;37(2):303–315. doi: 10.1016/j.cll.2017.01.005. PubMed DOI PMC

Horiyama T, Nikaido E, Yamaguchi A, Nishino K. Roles of Salmonella multidrug efflux pumps in tigecycline resistance. J Antimicrob Chemother. 2010;66(1):105–110. doi: 10.1093/jac/dkq421. PubMed DOI

Gales AC, Jones RN, Andrade SS, Pereira AS, Sader HS. In vitro activity of tigecycline, a new glycylcycline, tested against 1,326 clinical bacterial strains isolated from Latin America. Braz J Infect Dis. 2005;9(5):348–356. doi: 10.1590/S1413-86702005000500001. PubMed DOI

Y-y Z, Zhou L, Zhu D-m, Wu P-c, Hu F-p, Wu W-h, Wang F. In vitro activities of tigecycline against clinical isolates from Shanghai, China. Diagn Microbiol Infect Dis. 2004;50(4):267–281. doi: 10.1016/j.diagmicrobio.2004.08.007. PubMed DOI

Lee H, Kim H, Seo YH, Yong D, Jeong SH, Lee K, Chong Y. In vitro activity of tigecycline alone and antimicrobial combinations against clinical Neisseria gonorrhoeae isolates. Diagn Microbiol Infect Dis. 2017;87(2):160–162. doi: 10.1016/j.diagmicrobio.2016.10.022. PubMed DOI

Blanton LS, Wilson NM, Quade BR, Walker DH. Susceptibility of Rickettsia rickettsii to Tigecycline in a Cell Culture Assay and Animal Model for Rocky Mountain Spotted Fever. The American Journal of Tropical Medicine and Hygiene. 2019;101(5):1091–1095. doi: 10.4269/ajtmh.19-0445. PubMed DOI PMC

Spyridaki I, Psaroulaki A, Vranakis I, Tselentis Y, Gikas A. Bacteriostatic and bactericidal activities of tigecycline against Coxiella burnetii and comparison with those of six other antibiotics. Antimicrob Agents Chemother. 2009;53(6):2690–2692. doi: 10.1128/AAC.01424-08. PubMed DOI PMC

Lee S-M, Kwon H-Y, Im J-H, Baek JH, Hwang S-S, Kang J-S, Chung M-H, Lee J-S. In vitro activity of tigecycline against Orientia tsutsugamushi. Yonsei Med J. 2016;57(4):1034–1037. doi: 10.3349/ymj.2016.57.4.1034. PubMed DOI PMC

Freeman J, Vernon J, Pilling S, Morris K, Nicolson S, Shearman S, Clark E, Palacios-Fabrega JA, Wilcox MJEJoCM, Diseases I (2020) Five-year Pan-European, longitudinal surveillance of Clostridium difficile ribotype prevalence and antimicrobial resistance: the extended ClosER study 39 (1):169-177 PubMed PMC

Wu J, Sun L, Chen X, Du F, Shi H, Chen C, Chen ZJ. Cyclic GMP-AMP is an endogenous second messenger in innate immune signaling by cytosolic DNA. Science. 2013;339(6121):826–830. doi: 10.1126/science.1229963. PubMed DOI PMC

Kechagias KS, Chorepsima S, Triarides NA, Falagas MEJEJoCM, Diseases I (2020) Tigecycline for the treatment of patients with Clostridium difficile infection: an update of the clinical evidence.1-6 PubMed

Bauer G, Berens C, Projan SJ, Hillen W. Comparison of tetracycline and tigecycline binding to ribosomes mapped by dimethylsulphate and drug-directed Fe2+ cleavage of 16S rRNA. J Antimicrob Chemother. 2004;53(4):592–599. doi: 10.1093/jac/dkh125. PubMed DOI

Jenner L, Starosta AL, Terry DS, Mikolajka A, Filonava L, Yusupov M, Blanchard SC, Wilson DN, Yusupova G. Structural basis for potent inhibitory activity of the antibiotic tigecycline during protein synthesis. Proc Natl Acad Sci. 2013;110(10):3812–3816. doi: 10.1073/pnas.1216691110. PubMed DOI PMC

Olson MW, Ruzin A, Feyfant E, Rush TS, O'Connell J, Bradford PA. Functional, biophysical, and structural bases for antibacterial activity of tigecycline. Antimicrob Agents Chemother. 2006;50(6):2156–2166. doi: 10.1128/AAC.01499-05. PubMed DOI PMC

Pournaras S, Koumaki V, Gennimata V, Kouskouni E, Tsakris A (2015) In vitro activity of tigecycline against Acinetobacter baumannii: global epidemiology and resistance mechanisms. Advances in Microbiology, Infectious Diseases and Public Health. Springer, pp 1-14 PubMed

Pournaras S, Koumaki V, Spanakis N, Gennimata V, Tsakris A. Current perspectives on tigecycline resistance in Enterobacteriaceae: susceptibility testing issues and mechanisms of resistance. Int J Antimicrob Agents. 2016;48(1):11–18. doi: 10.1016/j.ijantimicag.2016.04.017. PubMed DOI

Gordon N, Wareham D. A review of clinical and microbiological outcomes following treatment of infections involving multidrug-resistant Acinetobacter baumannii with tigecycline. J Antimicrob Chemother. 2009;63(4):775–780. doi: 10.1093/jac/dkn555. PubMed DOI

Linkevicius M, Sandegren L, Andersson DI. Potential of tetracycline resistance proteins to evolve tigecycline resistance. Antimicrob Agents Chemother. 2016;60(2):789–796. doi: 10.1128/AAC.02465-15. PubMed DOI PMC

Deng M, Zhu M-H, Li J-J, Bi S, Sheng Z-K, Hu F-S, Zhang J-J, Chen W, Xue X-W, Sheng J-F. Molecular epidemiology and mechanisms of tigecycline resistance in clinical isolates of Acinetobacter baumannii from a Chinese university hospital. Antimicrob Agents Chemother. 2014;58(1):297–303. doi: 10.1128/AAC.01727-13. PubMed DOI PMC

Moore IF, Hughes DW, Wright GD. Tigecycline is modified by the flavin-dependent monooxygenase TetX. Biochemistry. 2005;44(35):11829–11835. doi: 10.1021/bi0506066. PubMed DOI

Leski TA, Bangura U, Jimmy DH, Ansumana R, Lizewski SE, Stenger DA, Taitt CR, Vora GJ. Multidrug-resistant tet (X)-containing hospital isolates in Sierra Leone. Int J Antimicrob Agents. 2013;42(1):83–86. doi: 10.1016/j.ijantimicag.2013.04.014. PubMed DOI

Hentschke M, Christner M, Sobottka I, Aepfelbacher M, Rohde H. Combined ramR mutation and presence of a Tn1721-associated tet (A) variant in a clinical isolate of Salmonella enterica serovar Hadar resistant to tigecycline. Antimicrob Agents Chemother. 2010;54(3):1319–1322. doi: 10.1128/AAC.00993-09. PubMed DOI PMC

Veleba M, De Majumdar S, Hornsey M, Woodford N, Schneiders T. Genetic characterization of tigecycline resistance in clinical isolates of Enterobacter cloacae and Enterobacter aerogenes. J Antimicrob Chemother. 2013;68(5):1011–1018. doi: 10.1093/jac/dks530. PubMed DOI

Keeney D, Ruzin A, Bradford PA. RamA, a transcriptional regulator, and AcrAB, an RND-type efflux pump, are associated with decreased susceptibility to tigecycline in Enterobacter cloacae. Microb Drug Resist. 2007;13(1):1–6. doi: 10.1089/mdr.2006.9990. PubMed DOI

Ni W, Cai X, Liang B, Cai Y, Cui J, Wang R. Effect of proton pump inhibitors on in vitro activity of tigecycline against several common clinical pathogens. PloS one. 2014;9(1):e86715. doi: 10.1371/journal.pone.0086715. PubMed DOI PMC

Montana S, Vilacoba E, Traglia GM, Almuzara M, Pennini M, Fernandez A, Sucari A, Centrón D, Ramirez MS. Genetic variability of AdeRS two-component system associated with tigecycline resistance in XDR-Acinetobacter baumannii isolates. Curr Microbiol. 2015;71(1):76–82. doi: 10.1007/s00284-015-0829-3. PubMed DOI

Sun J-R, Perng C-L, Lin J-C, Yang Y-S, Chan M-C, Chang T-Y, Lin F-M, Chiueh T-S. AdeRS combination codes differentiate the response to efflux pump inhibitors in tigecycline-resistant isolates of extensively drug-resistant Acinetobacter baumannii. Eur J Clin Microbiol Infect Dis. 2014;33(12):2141–2147. doi: 10.1007/s10096-014-2179-7. PubMed DOI

Yoon E-J, Courvalin P, Grillot-Courvalin C. RND-type efflux pumps in multidrug-resistant clinical isolates of Acinetobacter baumannii: major role for AdeABC overexpression and AdeRS mutations. Antimicrob Agents Chemother. 2013;57(7):2989–2995. doi: 10.1128/AAC.02556-12. PubMed DOI PMC

Sun J-R, Perng C-L, Chan M-C, Morita Y, Lin J-C, Su C-M, Wang W-Y, Chang T-Y, Chiueh T-S. A truncated AdeS kinase protein generated by ISAba1 insertion correlates with tigecycline resistance in Acinetobacter baumannii. PLoS One. 2012;7(11):e49534. doi: 10.1371/journal.pone.0049534. PubMed DOI PMC

Lin M-F, Lin Y-Y, Yeh H-W, Lan C-Y. Role of the BaeSR two-component system in the regulation of Acinetobacter baumannii adeAB genes and its correlation with tigecycline susceptibility. BMC Microbiol. 2014;14(1):119. doi: 10.1186/1471-2180-14-119. PubMed DOI PMC

Chen Q, Li X, Zhou H, Jiang Y, Chen Y, Hua X, Yu Y. Decreased susceptibility to tigecycline in Acinetobacter baumannii mediated by a mutation in trm encoding SAM-dependent methyltransferase. J Antimicrob Chemother. 2013;69(1):72–76. doi: 10.1093/jac/dkt319. PubMed DOI

Rumbo C, Gato E, López M, de Alegría CR, Fernández-Cuenca F, Martínez-Martínez L, Vila J, Pachón J, Cisneros JM, Rodríguez-Baño J. Contribution of efflux pumps, porins, and β-lactamases to multidrug resistance in clinical isolates of Acinetobacter baumannii. Antimicrob Agents Chemother. 2013;57(11):5247–5257. doi: 10.1128/AAC.00730-13. PubMed DOI PMC

Ruzin A, Keeney D, Bradford PA. AcrAB efflux pump plays a role in decreased susceptibility to tigecycline in Morganella morganii. Antimicrob Agents Chemother. 2005;49(2):791–793. doi: 10.1128/AAC.49.2.791-793.2005. PubMed DOI PMC

He F, Fu Y, Chen Q, Ruan Z, Hua X, Zhou H, Yu Y. Tigecycline susceptibility and the role of efflux pumps in tigecycline resistance in KPC-producing Klebsiella pneumoniae. PLoS One. 2015;10(3):e0119064. doi: 10.1371/journal.pone.0119064. PubMed DOI PMC

Pérez A, Poza M, Aranda J, Latasa C, Medrano FJ, Tomás M, Romero A, Lasa I, Bou G. Effect of transcriptional activators SoxS, RobA, and RamA on expression of multidrug efflux pump AcrAB-TolC in Enterobacter cloacae. Antimicrob Agents Chemother. 2012;56(12):6256–6266. doi: 10.1128/AAC.01085-12. PubMed DOI PMC

Wang X, Chen H, Zhang Y, Wang Q, Zhao C, Li H, He W, Zhang F, Wang Z, Li S. Genetic characterisation of clinical Klebsiella pneumoniae isolates with reduced susceptibility to tigecycline: Role of the global regulator RamA and its local repressor RamR. Int J Antimicrob Agents. 2015;45(6):635–640. doi: 10.1016/j.ijantimicag.2014.12.022. PubMed DOI

Falagas ME, Tansarli GS, Karageorgopoulos DE, Vardakas KZ. Deaths attributable to carbapenem-resistant Enterobacteriaceae infections. Emerg Infect Dis. 2014;20(7):1170. doi: 10.3201/eid2007.121004. PubMed DOI PMC

Villa L, Feudi C, Fortini D, García-Fernández A, Carattoli A. Genomics of KPC-producing Klebsiella pneumoniae sequence type 512 clone highlights the role of RamR and ribosomal S10 protein mutations in conferring tigecycline resistance. Antimicrob Agents Chemother. 2014;58(3):1707–1712. doi: 10.1128/AAC.01803-13. PubMed DOI PMC

Hirata T, Saito A, Nishino K, Tamura N, Yamaguchi A. Effects of efflux transporter genes on susceptibility of Escherichia coli to tigecycline (GAR-936) Antimicrob Agents Chemother. 2004;48(6):2179–2184. doi: 10.1128/AAC.48.6.2179-2184.2004. PubMed DOI PMC

Elkins CA, Nikaido H. Substrate specificity of the RND-type multidrug efflux pumps AcrB and AcrD of Escherichia coli is determined predominately by two large periplasmic loops. J Bacteriol. 2002;184(23):6490–6498. doi: 10.1128/JB.184.23.6490-6499.2002. PubMed DOI PMC

Chollet R, Chevalier J, Bollet C, Pages J-M, Davin-Regli A. RamA is an alternate activator of the multidrug resistance cascade in Enterobacter aerogenes. Antimicrob Agents Chemother. 2004;48(7):2518–2523. doi: 10.1128/AAC.48.7.2518-2523.2004. PubMed DOI PMC

Alekshun MN, Levy SB. Regulation of chromosomally mediated multiple antibiotic resistance: the mar regulon. Antimicrob Agents Chemother. 1997;41(10):2067. doi: 10.1128/AAC.41.10.2067. PubMed DOI PMC

Barbosa TM, Levy SB. Differential expression of over 60 chromosomal genes in Escherichia coli by constitutive expression of MarA. J Bacteriol. 2000;182(12):3467–3474. doi: 10.1128/JB.182.12.3467-3474.2000. PubMed DOI PMC

Keeney D, Ruzin A, McAleese F, Murphy E, Bradford PA. MarA-mediated overexpression of the AcrAB efflux pump results in decreased susceptibility to tigecycline in Escherichia coli. J Antimicrob Chemother. 2007;61(1):46–53. doi: 10.1093/jac/dkm397. PubMed DOI

Linkevicius M, Sandegren L, Andersson DI. Mechanisms and fitness costs of tigecycline resistance in Escherichia coli. J Antimicrob Chemother. 2013;68(12):2809–2819. doi: 10.1093/jac/dkt263. PubMed DOI

Pérez A, Poza M, Fernández A, del Carmen FM, Mallo S, Merino M, Rumbo-Feal S, Cabral MP, Bou G. Involvement of the AcrAB-TolC efflux pump in the resistance, fitness, and virulence of Enterobacter cloacae. Antimicrob Agents Chemother. 2012;56(4):2084–2090. doi: 10.1128/AAC.05509-11. PubMed DOI PMC

Ruzin A, Immermann FW, Bradford PA. Real-time PCR and statistical analyses of acrAB and ramA expression in clinical isolates of Klebsiella pneumoniae. Antimicrob Agents Chemother. 2008;52(9):3430–3432. doi: 10.1128/AAC.00591-08. PubMed DOI PMC

Ruzin A, Visalli MA, Keeney D, Bradford PA. Influence of transcriptional activator RamA on expression of multidrug efflux pump AcrAB and tigecycline susceptibility in Klebsiella pneumoniae. Antimicrob Agents Chemother. 2005;49(3):1017–1022. doi: 10.1128/AAC.49.3.1017-1022.2005. PubMed DOI PMC

Zhong X, Xu H, Chen D, Zhou H, Hu X, Cheng G. First emergence of acrAB and oqxAB mediated tigecycline resistance in clinical isolates of Klebsiella pneumoniae pre-dating the use of tigecycline in a Chinese hospital. PLoS One. 2014;9(12):e115185. doi: 10.1371/journal.pone.0115185. PubMed DOI PMC

Roy S, Datta S, Viswanathan R, Singh AK, Basu S. Tigecycline susceptibility in Klebsiella pneumoniae and Escherichia coli causing neonatal septicaemia (2007–10) and role of an efflux pump in tigecycline non-susceptibility. J Antimicrob Chemother. 2013;68(5):1036–1042. doi: 10.1093/jac/dks535. PubMed DOI

Rosenblum R, Khan E, Gonzalez G, Hasan R, Schneiders T. Genetic regulation of the ramA locus and its expression in clinical isolates of Klebsiella pneumoniae. Int J Antimicrob Agents. 2011;38(1):39–45. doi: 10.1016/j.ijantimicag.2011.02.012. PubMed DOI PMC

De Majumdar S, Veleba M, Finn S, Fanning S, Schneiders T. Elucidating the regulon of multidrug resistance regulator RarA in Klebsiella pneumoniae. Antimicrob Agents Chemother. 2013;57(4):1603–1609. doi: 10.1128/AAC.01998-12. PubMed DOI PMC

Sheng Z-K, Hu F, Wang W, Guo Q, Chen Z, Xu X, Zhu D, Wang M. Mechanisms of tigecycline resistance among Klebsiella pneumoniae clinical isolates. Antimicrob Agents Chemother. 2014;58(11):6982–6985. doi: 10.1128/AAC.03808-14. PubMed DOI PMC

Hentschke M, Wolters M, Sobottka I, Rohde H, Aepfelbacher M. ramR mutations in clinical isolates of Klebsiella pneumoniae with reduced susceptibility to tigecycline. Antimicrob Agents Chemother. 2010;54(6):2720–2723. doi: 10.1128/AAC.00085-10. PubMed DOI PMC

Nielsen LE, Snesrud EC, Onmus-Leone F, Kwak YI, Avilés R, Steele ED, Sutter DE, Waterman PE, Lesho EP. IS5 element integration, a novel mechanism for rapid in vivo emergence of tigecycline nonsusceptibility in Klebsiella pneumoniae. Antimicrob Agents Chemother. 2014;58(10):6151–6156. doi: 10.1128/AAC.03053-14. PubMed DOI PMC

Lat A, Clock SA, Wu F, Whittier S, Della-Latta P, Fauntleroy K, Jenkins SG, Saiman L, Kubin CJ. Comparison of polymyxin B, tigecycline, cefepime, and meropenem MICs for KPC-producing Klebsiella pneumoniae by broth microdilution, Vitek 2, and Etest. J Clin Microbiol. 2011;49(5):1795–1798. doi: 10.1128/JCM.02534-10. PubMed DOI PMC

Pharmaceutics W. Tygacil®(package insert) Philadelphia, PA: Wyeth Pharmaceutics; 2009.

Chiu S-K, Huang L-Y, Chen H, Tsai Y-K, Liou C-H, Lin J-C, Siu LK, Chang F-Y, Yeh K-M. Roles of ramR and tet (A) mutations in conferring tigecycline resistance in carbapenem-resistant Klebsiella pneumoniae clinical isolates. Antimicrob Agents Chemother. 2017;61(8):e00391–e00317. doi: 10.1128/AAC.00391-17. PubMed DOI PMC

Hornsey M, Ellington MJ, Doumith M, Hudson S, Livermore DM, Woodford N. Tigecycline resistance in Serratia marcescens associated with up-regulation of the SdeXY-HasF efflux system also active against ciprofloxacin and cefpirome. J Antimicrob Chemother. 2010;65(3):479–482. doi: 10.1093/jac/dkp475. PubMed DOI

Hornsey M, Ellington MJ, Doumith M, Scott G, Livermore DM, Woodford N. Emergence of AcrAB-mediated tigecycline resistance in a clinical isolate of Enterobacter cloacae during ciprofloxacin treatment. Int J Antimicrob Agents. 2010;35(5):478–481. doi: 10.1016/j.ijantimicag.2010.01.011. PubMed DOI

Zheng B, Li A, Jiang X, Hu X, Yao J, Zhao L, Ji J, Ye M, Xiao Y, Li L. Genome sequencing and genomic characterization of a tigecycline-resistant Klebsiella pneumoniae strain isolated from the bile samples of a cholangiocarcinoma patient. Gut Pathogens. 2014;6(1):40. doi: 10.1186/s13099-014-0040-2. PubMed DOI PMC

Abouzeed YM, Baucheron S, Cloeckaert A. ramR mutations involved in efflux-mediated multidrug resistance in Salmonella enterica serovar Typhimurium. Antimicrob Agents Chemother. 2008;52(7):2428–2434. doi: 10.1128/AAC.00084-08. PubMed DOI PMC

Kehrenberg C, Cloeckaert A, Klein G, Schwarz S. Decreased fluoroquinolone susceptibility in mutants of Salmonella serovars other than Typhimurium: detection of novel mutations involved in modulated expression of ramA and soxS. J Antimicrob Chemother. 2009;64(6):1175–1180. doi: 10.1093/jac/dkp347. PubMed DOI

Ricci V, Piddock LJ. Ciprofloxacin selects for multidrug resistance in Salmonella enterica serovar Typhimurium mediated by at least two different pathways. J Antimicrob Chemother. 2009;63(5):909–916. doi: 10.1093/jac/dkp054. PubMed DOI

Akiyama T, Presedo J, Khan AA. The tetA gene decreases tigecycline sensitivity of Salmonella enterica isolates. Int J Antimicrob Agents. 2013;42(2):133–140. doi: 10.1016/j.ijantimicag.2013.04.017. PubMed DOI

Aires JR, Köhler T, Nikaido H, Plésiat P. Involvement of an active efflux system in the natural resistance of Pseudomonas aeruginosa to aminoglycosides. Antimicrob Agents Chemother. 1999;43(11):2624–2628. doi: 10.1128/AAC.43.11.2624. PubMed DOI PMC

Ko¨ hler T, Michéa-Hamzehpour M, Henze U, Gotoh N, Kocjancic Curty L, Pechère JC (1997) Characterization of MexE–MexF–OprN, a positively regulated multidrug efflux system of Pseudomonas aeruginosa. Mol Microbiol 23 (2):345-354 PubMed

Li X-Z, Nikaido H, Poole K. Role of mexA-mexB-oprM in antibiotic efflux in Pseudomonas aeruginosa. Antimicrob Agents Chemother. 1995;39(9):1948–1953. doi: 10.1128/AAC.39.9.1948. PubMed DOI PMC

Mine T, Morita Y, Kataoka A, Mizushima T, Tsuchiya T. Expression in Escherichia coli of a new multidrug efflux pump, MexXY, from Pseudomonas aeruginosa. Antimicrob Agents Chemother. 1999;43(2):415–417. doi: 10.1128/AAC.43.2.415. PubMed DOI PMC

Poole K, Gotoh N, Tsujimoto H, Zhao Q, Wada A, Yamasaki T, Neshat S, Ji Y, Li XZ, Nishino T. Overexpression of the mexC–mexD–oprJ efflux operon in nfxB-type multidrug-resistant strains of Pseudomonas aeruginosa. Mol Microbiol. 1996;21(4):713–725. doi: 10.1046/j.1365-2958.1996.281397.x. PubMed DOI

Dean CR, Visalli MA, Projan SJ, Sum P-E, Bradford PA. Efflux-mediated resistance to tigecycline (GAR-936) in Pseudomonas aeruginosa PAO1. Antimicrob Agents Chemother. 2003;47(3):972–978. doi: 10.1128/AAC.47.3.972-978.2003. PubMed DOI PMC

Noskin GA (2005) Tigecycline: a new glycylcycline for treatment of serious infections. Clinical infectious diseases 41 (Supplement_5):S303-S314 PubMed

Pumbwe L, Piddock LJ. Two efflux systems expressed simultaneously in multidrug-resistant Pseudomonas aeruginosa. Antimicrob Agents Chemother. 2000;44(10):2861–2864. doi: 10.1128/AAC.44.10.2861-2864.2000. PubMed DOI PMC

Beinlich KL, Chuanchuen R, Schweizer HP. Contribution of multidrug efflux pumps to multiple antibiotic resistance in veterinary clinical isolates of Pseudomonas aeruginosa. FEMS Microbiol Lett. 2001;198(2):129–134. doi: 10.1111/j.1574-6968.2001.tb10631.x. PubMed DOI

McAleese F, Petersen P, Ruzin A, Dunman PM, Murphy E, Projan SJ, Bradford PA. A novel MATE family efflux pump contributes to the reduced susceptibility of laboratory-derived Staphylococcus aureus mutants to tigecycline. Antimicrob Agents Chemother. 2005;49(5):1865–1871. doi: 10.1128/AAC.49.5.1865-1871.2005. PubMed DOI PMC

Dönhöfer A, Franckenberg S, Wickles S, Berninghausen O, Beckmann R, Wilson DN. Structural basis for TetM-mediated tetracycline resistance. Proc Natl Acad Sci. 2012;109(42):16900–16905. doi: 10.1073/pnas.1208037109. PubMed DOI PMC

Fiedler S, Bender J, Klare I, Halbedel S, Grohmann E, Szewzyk U, Werner G. Tigecycline resistance in clinical isolates of Enterococcus faecium is mediated by an upregulation of plasmid-encoded tetracycline determinants tet (L) and tet (M) J Antimicrob Chemother. 2015;71(4):871–881. doi: 10.1093/jac/dkv420. PubMed DOI

Food U, Administration D (2011) FDA drug safety communication: increased risk of death with Tygacil (tigecycline) compared to other antibiotics used to treat similar infections. Drugs

Eckmann C, Heizmann WR, Leitner E, Von Eiff C, Bodmann K-F. Prospective, non-interventional, multi-centre trial of tigecycline in the treatment of severely ill patients with complicated infections–new insights into clinical results and treatment practice. Chemotherapy. 2011;57(4):275–284. doi: 10.1159/000329406. PubMed DOI

Kwon SH, Ahn HL, Han OY, La HO. Efficacy and safety profile comparison of colistin and tigecycline on the extensively drug resistant Acinetobacter baumannii. Biol Pharm Bull. 2014;37(3):340–346. doi: 10.1248/bpb.b13-00109. PubMed DOI

Chuang Y-C, Cheng C-Y, Sheng W-H, Sun H-Y, Wang J-T, Chen Y-C, Chang S-C. Effectiveness of tigecycline-based versus colistin-based therapy for treatment of pneumonia caused by multidrug-resistant Acinetobacter baumanniiin a critical setting: a matched cohort analysis. BMC Infect Dis. 2014;14(1):102. doi: 10.1186/1471-2334-14-102. PubMed DOI PMC

Food Administration D (2015) Investigational New Drug Applications (INDs)—Determining Whether Human Research Studies Can Be Conducted Without an IND.

Bai X-R, Liu J-M, Jiang D-C, Yan S-Y. Efficacy and safety of tigecycline monotherapy versus combination therapy for the treatment of hospital-acquired pneumonia (HAP): a meta-analysis of cohort studies. J Chemother. 2018;30(3):172–178. doi: 10.1080/1120009X.2018.1425279. PubMed DOI

Wang J, Pan Y, Shen J, Xu Y. The efficacy and safety of tigecycline for the treatment of bloodstream infections: a systematic review and meta-analysis. Ann Clin Microbiol Antimicrob. 2017;16(1):24. doi: 10.1186/s12941-017-0199-8. PubMed DOI PMC

Conde-Estévez D, Grau S, Horcajada JP, Luque SJIJOAA (2010) Off-label prescription of tigecycline: clinical and microbiological characteristics and outcomes. 36 (5):471-472 PubMed

Curcio D, Fernández F, Vergara J, Vazquez W, Luna CJJOC (2009) Late onset ventilator-associated pneumonia due to multidrug-resistant Acinetobacter spp.: experience with tigecycline. 21 (1):58-62 PubMed

Kuo S-C, Wang F-D, Fung C-P, Chen L-Y, Chen S-J, Chiang M-C, Hsu S-F, Liu C-YJJoM, Immunology, Infection (2011) Clinical experience with tigecycline as treatment for serious infections in elderly and critically ill patients. 44 (1):45-51 PubMed

Guner R, Hasanoglu I, Keske S, Kalem A, Tasyaran MJI. Outcomes in patients infected with carbapenem-resistant. Acinetobacter baumannii and treated with tigecycline alone or in combination therapy. 2011;39(6):515–518. PubMed

Moghnieh RA, Abdallah DI, Fawaz IA, Hamandi T, Kassem M, El-Rajab N, Jisr T, Mugharbil A, Droubi N, Al Tabah SJFIM (2017) Prescription patterns for tigecycline in severely ill patients for non-FDA approved indications in a developing country: A compromised outcome. 8:497 PubMed PMC

Ipek M. Colistin/tigecycline. Reactions. 2019;1749:143–120.

İpek MS, Gunel ME, Ozbek E. Tigecycline Use in Neonates: 5-Year Experience of a Tertiary Center. J Pediatr Infect Dis. 2019;14(03):103–107. doi: 10.1055/s-0038-1675582. DOI

Sharland M, Rodvold KA, Tucker HR, Baillon-Plot N, Tawadrous M, Hickman MA, Raber S, Korth-Bradley JM, Díaz-Ponce H, Wible MJTPIDJ (2019) Safety and efficacy of tigecycline to treat multidrug-resistant infections in pediatrics: an evidence synthesis. 38 (7):710-715 PubMed

Chen F, Shen C, Pang X, Zhang Z, Deng Y, Han L, Chen X, Zhang J, Xia Q, Qian YJTID (2020) Effectiveness of tigecycline in the treatment of infections caused by carbapenem-resistant gram-negative bacteria in pediatric liver transplant recipients: A retrospective study. 22 (1):e13199 PubMed

Emiroglu M, Alkan G, Dagi HTJP (2017) Tigecycline therapy in an infant for ventriculoperitoneal shunt meningitis. 139 (1):e20160963 PubMed

Shen F, Han Q, Xie D, Fang M, Zeng H, Deng Y. Efficacy and safety of tigecycline for the treatment of severe infectious diseases: an updated meta-analysis of RCTs. Int J Infect Dis. 2015;39:25–33. doi: 10.1016/j.ijid.2015.08.009. PubMed DOI

Insert TP (2005) Philadelphia (PA): Wyeth Pharmaceuticals Inc.(June, 2005). Organism (no tested)/% susceptible/antimicrobial agent MIC50 MIC90 Range resistant a

Bassetti M, Poulakou G, Giamarellou H (2014) Is there a future for tigecycline? Springer PubMed

Song Y, Hu L, Shu Q, Ye J, Liang J, Chen X, Tan LJIJOID (2018) Tigecycline salvage therapy for critically ill children with multidrug-resistant/extensively drug-resistant infections after surgery. 75:82-88 PubMed

Edwards BJ, Bunta AD, Lane J, Odvina C, Rao DS, Raisch DW, McKoy JM, Omar I, Belknap SM, Garg V. Bisphosphonates and nonhealing femoral fractures: analysis of the FDA Adverse Event Reporting System (FAERS) and international safety efforts: a systematic review from the Research on Adverse Drug Events And Reports (RADAR) project. J Bone Joint Surg Am. 2013;95(4):297. doi: 10.2106/JBJS.K.01181. PubMed DOI PMC

Ozturk S, Ustun C, Pehlivan S, Ucak H. Acute generalized exanthematous pustulosis associated with tigecycline. Ann Dermatol. 2014;26(2):246–249. doi: 10.5021/ad.2014.26.2.246. PubMed DOI PMC

Cai Y, Wang R, Liang B, Bai N, Liu Y. Systematic review and meta-analysis of the effectiveness and safety of tigecycline for treatment of infectious disease. Antimicrob Agents Chemother. 2011;55(3):1162–1172. doi: 10.1128/AAC.01402-10. PubMed DOI PMC

Zuckerman JM, Qamar F, Bono BR. Review of macrolides (azithromycin, clarithromycin), ketolids (telithromycin) and glycylcyclines (tigecycline) Med Clin. 2011;95(4):761–791. PubMed

Yahav D, Lador A, Paul M, Leibovici L. Efficacy and safety of tigecycline: a systematic review and meta-analysis. J Antimicrob Chemother. 2011;66(9):1963–1971. doi: 10.1093/jac/dkr242. PubMed DOI

Hasan M, Rabbani R, Bachar S, Huq S. High Dose Tigecycline-Induced Mitochondrial Dysfunction-Associated Acute Metabolic Acidosis: A Retrospective Study. J Mol Genet Med. 2019;13(407):1747–0862.1000407.

Lin J, Wang R, Chen J. Tigecycline-induced acute pancreatitis in a renal transplant patient: a case report and literature review. BMC Infect Dis. 2018;18(1):201. doi: 10.1186/s12879-018-3103-z. PubMed DOI PMC

Rose WE, Rybak MJ. Tigecycline: first of a new class of antimicrobial agents. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy. 2006;26(8):1099–1110. doi: 10.1592/phco.26.8.1099. PubMed DOI

Brink AJ, Bizos D, Boffard KD, Feldman C, Grolman D, Pretorius J, Richards GA, Senekal M, Steyn E, Welkovic N. Guideline: appropriate use of tigecycline. SAMJ: South Afr Med J. 2010;100(6):388–394. doi: 10.7196/SAMJ.4109. PubMed DOI

Dryden M (2013) Tigecycline: an antibiotic for the twenty-first century. Journal of Antimicrobial Chemotherapy 68 (suppl_2):ii3-ii4 PubMed

Anthony KB, Fishman NO, Linkin DR, Gasink LB, Edelstein PH, Lautenbach E. Clinical and microbiological outcomes of serious infections with multidrug-resistant gram-negative organisms treated with tigecycline. Clin Infect Dis. 2008;46(4):567–570. doi: 10.1086/526775. PubMed DOI

Schafer JJ, Goff DA, Stevenson KB, Mangino JE. Early experience with tigecycline for ventilator-associated pneumonia and bacteremia caused by multidrug-resistant Acinetobacter baumannii. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy. 2007;27(7):980–987. doi: 10.1592/phco.27.7.980. PubMed DOI

Reid GE, Grim SA, Aldeza CA, Janda WM, Clark NM. Rapid development of Acinetobacter baumannii resistance to tigecycline. Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy. 2007;27(8):1198–1201. doi: 10.1592/phco.27.8.1198. PubMed DOI

Vasilev K, Reshedko G, Orasan R, Sanchez M, Teras J, Babinchak T, Dukart G, Cooper A, Dartois N, Gandjini H. A Phase 3, open-label, non-comparative study of tigecycline in the treatment of patients with selected serious infections due to resistant Gram-negative organisms including Enterobacter species, Acinetobacter baumannii and Klebsiella pneumoniae. Journal of Antimicrobial Chemotherapy. 2008;62(suppl_1):i29–i40. doi: 10.1093/jac/dkn249. PubMed DOI

Muralidharan G, Getsy J, Mayer P, Paty I, Micalizzi M, Speth J, Wester B, Mojaverian P (1999) Pharmacokinetics (PK), safety and tolerability of GAR-936, a novel glycylcycline antibiotic, in healthy subjects. 39th Interscience Conference on. Antimicrobial Agents and Chemotherapy, p 303

Xu Z, Yan Y, Li Z, Qian L, Gong Z. The antibiotic drug tigecycline: a focus on its promising anticancer properties. Front Pharmacol. 2016;7:473. doi: 10.3389/fphar.2016.00473. PubMed DOI PMC

Davido B, Shourick J, Makhloufi S, Dinh A, Salomon J. True incidence of tigecycline-induced pancreatitis: how many cases are we missing? J Antimicrob Chemother. 2016;71(10):2994–2995. doi: 10.1093/jac/dkw255. PubMed DOI

Eckmann C, Heizmann W, Bodmann K-F, von Eiff C, Petrik C, Loeschmann P-A. Tigecycline in the treatment of patients with necrotizing skin and soft tissue infections due to multiresistant bacteria. Surg Infect. 2015;16(5):618–625. doi: 10.1089/sur.2014.089. PubMed DOI

Sabanis N, Paschou E, Gavriilaki E, Kalaitzoglou A, Vasileiou S. Hypofibrinogenemia induced by tigecycline: a potentially life-threatening coagulation disorder. Infect Dis. 2015;47(10):743–746. doi: 10.3109/23744235.2015.1043942. PubMed DOI

McMahan J, Moenster RP. Tigecycline-induced coagulopathy. Am J Health Syst Pharm. 2017;74(3):130–134. doi: 10.2146/ajhp150894. PubMed DOI

Leng B, Xue YC, Zhang W, tian Gao T, quan Yan G, Tang H (2019) A Retrospective Analysis of the Effect of Tigecycline on Coagulation Function. Chem Pharm Bull 67 (3):258-264 PubMed

Zimmerman JJ, Raible DG, Harper DM, Matschke K, Speth JLJPTJOHP, Therapy D (2008) Evaluation of a potential tigecycline-warfarin drug interaction. 28 (7):895-905 PubMed

Al-Qadheeb NS, Althawadi S, Alkhalaf A, Hosaini S, Alrajhi AA. Evolution of tigecycline resistance in Klebsiella pneumoniae in a single patient. Ann Saudi Med. 2010;30(5):404–407. doi: 10.4103/0256-4947.67087. PubMed DOI PMC

Taneja N, Singh G, Singh M, Sharma M. Emergence of tigecycline & colistin resistant Acinetobacter baumanii in patients with complicated urinary tract infections in north India. Indian J Med Res. 2011;133(6):681. PubMed PMC

Al-Sweih N, Al-Hubail M, Rotimi V. Emergence of tigecycline and colistin resistance in Acinetobacter species isolated from patients in Kuwait hospitals. J Chemother. 2011;23(1):13–16. doi: 10.1179/joc.2011.23.1.13. PubMed DOI

Manoharan A, Chatterjee S, Madhan S, Mathai D. Evaluation of tigecycline activity in clinical isolates among Indian medical centers. Indian J Pathol Microbiol. 2010;53(4):734. doi: 10.4103/0377-4929.72061. PubMed DOI

Hsu M-S, Liao C-H, Liu C-Y, Yang C-J, Huang Y-T, Hsueh P-R. In vitro susceptibilities of clinical isolates of ertapenem-non-susceptible Enterobacteriaceae to nemonoxacin, tigecycline, fosfomycin and other antimicrobial agents. Int J Antimicrob Agents. 2011;37(3):276–278. doi: 10.1016/j.ijantimicag.2010.12.003. PubMed DOI

Wu H, Wang J-T, Shiau Y-R, Wang H-Y, Lauderdale T-LY, Chang S-C. A multicenter surveillance of antimicrobial resistance on Stenotrophomonas maltophilia in Taiwan. J Microbiol Immunol Infect. 2012;45(2):120–126. doi: 10.1016/j.jmii.2011.09.028. PubMed DOI

Zhang R, Sun Q, Hu Y-J, Yu H, Li Y, Shen Q, Li G-X, Cao J-M, Yang W, Wang Q. Detection of the Smqnr quinolone protection gene and its prevalence in clinical isolates of Stenotrophomonas maltophilia in China. J Med Microbiol. 2012;61(4):535–539. doi: 10.1099/jmm.0.037309-0. PubMed DOI

Liao IC, Chen HM, Wu JJ, Tsai PF, Wang LR, Yan JJ. Metallo-β-lactamase-producing Enterobacteriaceae isolates at a Taiwanese hospital: lack of distinctive phenotypes for screening. Apmis. 2011;119(8):543–550. doi: 10.1111/j.1600-0463.2011.02772.x. PubMed DOI

Perry JD, Naqvi SH, Mirza IA, Alizai SA, Hussain A, Ghirardi S, Orenga S, Wilkinson K, Woodford N, Zhang J. Prevalence of faecal carriage of Enterobacteriaceae with NDM-1 carbapenemase at military hospitals in Pakistan, and evaluation of two chromogenic media. J Antimicrob Chemother. 2011;66(10):2288–2294. doi: 10.1093/jac/dkr299. PubMed DOI

Araj GF, Ibrahim GY. Tigecycline in vitro activity against commonly encountered multidrug-resistant Gram-negative pathogens in a Middle Eastern country. Diagn Microbiol Infect Dis. 2008;62(4):411–415. doi: 10.1016/j.diagmicrobio.2008.08.011. PubMed DOI

Liu J-W, Wang L-S, Cheng Y-J, Hsu G-J, Lu P-L, Liu Y-C, Chen C-M, Lee C-M, Sun W, Jang T-N. In-vitro activity of tigecycline against clinical isolates of Acinetobacter baumannii in Taiwan. Int J Antimicrob Agents. 2008;32:S188–S191. doi: 10.1016/S0924-8579(08)70026-8. PubMed DOI

Behera B, Das A, Mathur P, Kapil A, Gadepalli R, Dhawan B. Tigecycline susceptibility report from an Indian tertiary care hospital. Indian J Med Res. 2009;129(4):446. PubMed

Lee Y-T, Huang L-Y, Chiang D-H, Chen C-P, Chen T-L, Wang F-D, Fung C-P, Siu L-K, Cho W-L. Differences in phenotypic and genotypic characteristics among imipenem-non-susceptible Acinetobacter isolates belonging to different genomic species in Taiwan. Int J Antimicrob Agents. 2009;34(6):580–584. doi: 10.1016/j.ijantimicag.2009.06.027. PubMed DOI

Tribuddharat C, Thamlikitkul V. In vitro activity of tigecycline against clinical isolates of multidrug-resistant Acinetobacter baumannii in Siriraj Hospital, Thailand. J Med Assoc Thail. 2006;89(5):S102–S105. PubMed

Navon-Venezia S, Leavitt A, Carmeli Y. High tigecycline resistance in multidrug-resistant Acinetobacter baumannii. J Antimicrob Chemother. 2007;59(4):772–774. doi: 10.1093/jac/dkm018. PubMed DOI

Chang K-C, Lin M-F, Lin N-T, Wu W-J, Kuo H-Y, Lin T-Y, Yang T-L, Chen Y-C, Liou M-L. Clonal spread of multidrug-resistant Acinetobacter baumannii in eastern Taiwan. J Microbiol Immunol Infect. 2012;45(1):37–42. doi: 10.1016/j.jmii.2011.09.019. PubMed DOI

Park Y, Choi J, Song J, Ko K. In vitro activity of tigecycline against colistin-resistant Acinetobacter spp. isolates from Korea. Int J Antimicrob Agents. 2009;33(3):289–290. doi: 10.1016/j.ijantimicag.2008.09.005. PubMed DOI

Kim C-K, Lee Y, Lee H, Woo G-J, Song W, Kim M-N, Lee W-G, Jeong SH, Lee K, Chong Y. Prevalence and diversity of carbapenemases among imipenem-nonsusceptible Acinetobacter isolates in Korea: emergence of a novel OXA-182. Diagn Microbiol Infect Dis. 2010;68(4):432–438. doi: 10.1016/j.diagmicrobio.2010.07.014. PubMed DOI

Dizbay M, Altuncekic A, Sezer BE, Ozdemir K, Arman D. Colistin and tigecycline susceptibility among multidrug-resistant Acinetobacter baumannii isolated from ventilator-associated pneumonia. Int J Antimicrob Agents. 2008;32(1):29–32. doi: 10.1016/j.ijantimicag.2008.02.016. PubMed DOI

Sharma S, Bhowmik D, Bhattacharjee A. Tigecycline Resistance among Clinical Isolates of Staphylococcus aureus from North-east India. J Microbiol Infect Dis. 2017;7(04):173–177.

Liao C-H, Kung H-C, Hsu G-J, Lu P-L, Liu Y-C, Chen C-M, Lee C-M, Sun W, Jang T-N, Chiang P-C. In-vitro activity of tigecycline against clinical isolates of Acinetobacter baumannii in Taiwan determined by the broth microdilution and disk diffusion methods. Int J Antimicrob Agents. 2008;32:S192–S196. doi: 10.1016/S0924-8579(08)70027-X. PubMed DOI

Zhao J, Liu Y, Liu Y, Wang D, Ni W, Wang R, Liu Y, Zhang B. Frequency and genetic determinants of tigecycline resistance in clinically isolated stenotrophomonas maltophilia in Beijing, China. Front Microbiol. 2018;9:549. doi: 10.3389/fmicb.2018.00549. PubMed DOI PMC

Chiu S-K, Chan M-C, Huang L-Y, Lin Y-T, Lin J-C, Lu P-L, Siu LK, Chang F-Y, Yeh K-M. Tigecycline resistance among carbapenem-resistant Klebsiella pneumoniae: clinical characteristics and expression levels of efflux pump genes. PloS one. 2017;12(4):e0175140. doi: 10.1371/journal.pone.0175140. PubMed DOI PMC

Seifert H, Blondeau J, Dowzicky MJ. In vitro activity of tigecycline and comparators (2014–2016) among key WHO ‘priority pathogens’ and longitudinal assessment (2004–2016) of antimicrobial resistance: a report from the TEST study. Int J Antimicrob Agents. 2018;52(4):474–484. doi: 10.1016/j.ijantimicag.2018.07.003. PubMed DOI

Nagy E. ESCMID Study Group on Antimicrobial Resistance in Anaerobic Bacteria. Antimicrobial susceptibility of Bacteroides fragilis group isolates in Europe: 20 years of experience. Clin Microbiol Infect. 2011;17:371–379. doi: 10.1111/j.1469-0691.2010.03256.x. PubMed DOI

Insa R, Cercenado E, Goyanes M, Morente A, Bouza E. In vitro activity of tigecycline against clinical isolates of Acinetobacter baumannii and Stenotrophomonas maltophilia. J Antimicrob Chemother. 2007;59(3):583–585. doi: 10.1093/jac/dkl496. PubMed DOI

Tubau F, Liñares J, Rodríguez M-D, Cercenado E, Aldea M-J, González-Romo F, Torroba L, Berdonces P, Plazas J, Aguilar L. Susceptibility to tigecycline of isolates from samples collected in hospitalized patients with secondary peritonitis undergoing surgery. Diagn Microbiol Infect Dis. 2010;66(3):308–313. doi: 10.1016/j.diagmicrobio.2009.10.018. PubMed DOI

Grandesso S, Sapino B, Mazzucato S, Alessandrini R, Solinas M, Gion M. Study on in-vitro susceptibility of ESBL-positive Escherichia coli isolated from urine specimens. Le infezioni in medicina: rivista periodica di eziologia, epidemiologia, diagnostica, clinica e terapia delle patologie infettive. 2010;18(3):162–168. PubMed

Sekowska A, Gospodarek E. Susceptibility of Klebsiella spp. to tigecycline and other selected antibiotics. Med Sci Monit. 2010;16(6):BR193–BR196. PubMed

Naesens R, Ursi J, Van Schaeren J, Jeurissen A. In vitro activity of tigecycline against multidrug-resistant Enterobacteriaceae isolates from a Belgian hospital. Eur J Clin Microbiol Infect Dis. 2009;28(4):381–384. doi: 10.1007/s10096-008-0629-9. PubMed DOI

Gomis PF, Jean-Pierre H, Rousseau-Didelot M, Compan B, Michon A, Godreuil S. Tigecycline: CMI 50/90 towards 1766 Gram-negative bacilli (3rd generation cephalosporins resistant Enterobacteriaceae), Acinetobacter baumannii and Bacteroides fragilis group, University Hospital-Montpellier, 2008-2011. Pathol Biol (Paris) 2013;61:282–285. PubMed

Falagas ME, Maraki S, Karageorgopoulos DE, Kastoris AC, Mavromanolakis E, Samonis G. Antimicrobial susceptibility of multidrug-resistant (MDR) and extensively drug-resistant (XDR) Enterobacteriaceae isolates to fosfomycin. Int J Antimicrob Agents. 2010;35(3):240–243. doi: 10.1016/j.ijantimicag.2009.10.019. PubMed DOI

Sader HS, Castanheira M, Flamm RK, Mendes RE, Farrell DJ, Jones RN. Tigecycline activity tested against carbapenem-resistant Enterobacteriaceae from 18 European nations: results from the SENTRY surveillance program (2010–2013) Diagn Microbiol Infect Dis. 2015;83(2):183–186. doi: 10.1016/j.diagmicrobio.2015.06.011. PubMed DOI

Papaparaskevas J, Tzouvelekis LS, Tsakris A, Pittaras TE, Legakis NJ, Group HTS In vitro activity of tigecycline against 2423 clinical isolates and comparison of the available interpretation breakpoints. Diagn Microbiol Infect Dis. 2010;66(2):187–194. doi: 10.1016/j.diagmicrobio.2009.09.012. PubMed DOI

Balode A, Punda-Polić V, Dowzicky MJ. Antimicrobial susceptibility of gram-negative and gram-positive bacteria collected from countries in Eastern Europe: results from the Tigecycline Evaluation and Surveillance Trial (TEST) 2004–2010. Int J Antimicrob Agents. 2013;41(6):527–535. doi: 10.1016/j.ijantimicag.2013.02.022. PubMed DOI

Cattoir V, Dowzicky MJ. A longitudinal assessment of antimicrobial susceptibility among important pathogens collected as part of the Tigecycline Evaluation and Surveillance Trial (TEST) in France between 2004 and 2012. Antimicrob Resist Infect Control. 2014;3(1):36. doi: 10.1186/2047-2994-3-36. PubMed DOI PMC

Daurel C, Fiant A-L, Brémont S, Courvalin P, Leclercq R. Emergence of an Enterobacter hormaechei strain with reduced susceptibility to tigecycline under tigecycline therapy. Antimicrob Agents Chemother. 2009;53(11):4953–4954. doi: 10.1128/AAC.01592-08. PubMed DOI PMC

Werner G, Gfrörer S, Fleige C, Witte W, Klare I. Tigecycline-resistant Enterococcus faecalis strain isolated from a German intensive care unit patient. J Antimicrob Chemother. 2008;61(5):1182–1183. doi: 10.1093/jac/dkn065. PubMed DOI

Ahmed NH, Baba K, Clay C, Lekalakala R, Hoosen AA. In vitro activity of tigecycline against clinical isolates of carbapenem resistant Acinetobacter baumannii complex in Pretoria, South Africa. BMC Res Notes. 2012;5(1):215. doi: 10.1186/1756-0500-5-215. PubMed DOI PMC

Perovic O, Ismail H, Schalkwyk EV. Antimicrobial resistance surveillance in the South African public sector. South Afr J Infect Dis. 2018;33(4):118–129.

Perovic O, Ismail H, Van Schalkwyk E, Lowman W, Prentice E, Senekal M, Govind CN. Antimicrobial resistance surveillance in the South African private sector report for 2016. South Afr J Infect Dis. 2018;33(4):114–117.

Sherwood JE, Fraser S, Citron DM, Wexler H, Blakely G, Jobling K, Patrick S. Multi-drug resistant Bacteroides fragilis recovered from blood and severe leg wounds caused by an improvised explosive device (IED) in Afghanistan. Anaerobe. 2011;17(4):152–155. doi: 10.1016/j.anaerobe.2011.02.007. PubMed DOI

DiPersio JR, Dowzicky MJ. Regional variations in multidrug resistance among Enterobacteriaceae in the USA and comparative activity of tigecycline, a new glycylcycline antimicrobial. Int J Antimicrob Agents. 2007;29(5):518–527. doi: 10.1016/j.ijantimicag.2006.10.019. PubMed DOI

Rossi F, García P, Ronzon B, Curcio D, Dowzicky MJ. Rates of antimicrobial resistance in Latin America (2004-2007) and in vitro activity of the glycylcycline tigecycline and of other antibiotics. Braz J Infect Dis. 2008;12(5):405–415. doi: 10.1590/S1413-86702008000500012. PubMed DOI

Denys GA, Callister SM, Dowzicky MJ. Antimicrobial susceptibility among gram-negative isolates collected in the USA between 2005 and 2011 as part of the Tigecycline Evaluation and Surveillance Trial (TEST) Ann Clin Microbiol Antimicrob. 2013;12(1):24. doi: 10.1186/1476-0711-12-24. PubMed DOI PMC

Fernández-Canigia L, Dowzicky MJ. Susceptibility of important Gram-negative pathogens to tigecycline and other antibiotics in Latin America between 2004 and 2010. Ann Clin Microbiol Antimicrob. 2012;11(1):29. doi: 10.1186/1476-0711-11-29. PubMed DOI PMC

Dowzicky MJ, Park CH. Update on antimicrobial susceptibility rates among gram-negative and gram-positive organisms in the United States: results from the Tigecycline Evaluation and Surveillance Trial (TEST) 2005 to 2007. Clin Ther. 2008;30(11):2040–2050. doi: 10.1016/j.clinthera.2008.11.006. PubMed DOI

Garza-González E, Llaca-Díaz JM, Bosques-Padilla FJ, Gonzalez GM. Prevalence of multidrug-resistant bacteria at a tertiary-care teaching hospital in Mexico: special focus on Acinetobacter baumannii. Chemotherapy. 2010;56(4):275–279. doi: 10.1159/000319903. PubMed DOI

Lagacé-Wiens PR, Simner PJ, Forward KR, Tailor F, Adam HJ, DeCorby M, Karlowsky J, Hoban DJ, Zhanel GG, Alliance CAR. Analysis of 3789 in-and outpatient Escherichia coli isolates from across Canada—results of the CANWARD 2007–2009 study. Diagn Microbiol Infect Dis. 2011;69(3):314–319. doi: 10.1016/j.diagmicrobio.2010.10.027. PubMed DOI

Castanheira M, Sader HS, Jones RN. Antimicrobial susceptibility patterns of KPC-producing or CTX-M-producing Enterobacteriaceae. Microb Drug Resist. 2010;16(1):61–65. doi: 10.1089/mdr.2009.0031. PubMed DOI

Giammanco A, Calà C, Fasciana T, Dowzicky MJ. Global assessment of the activity of tigecycline against multidrug-resistant Gram-negative pathogens between 2004 and 2014 as part of the Tigecycline Evaluation and Surveillance Trial. Msphere. 2017;2(1):e00310–e00316. doi: 10.1128/mSphere.00310-16. PubMed DOI PMC

Kehl SC, Dowzicky MJ. Global assessment of antimicrobial susceptibility among Gram-negative organisms collected from pediatric patients between 2004 and 2012: results from the Tigecycline Evaluation and Surveillance Trial. J Clin Microbiol. 2015;53(4):1286–1293. doi: 10.1128/JCM.03184-14. PubMed DOI PMC

Mendes RE, Farrell DJ, Sader HS, Jones RN. Comprehensive assessment of tigecycline activity tested against a worldwide collection of Acinetobacter spp.(2005–2009) Diagn Microbiol Infect Dis. 2010;68(3):307–311. doi: 10.1016/j.diagmicrobio.2010.07.003. PubMed DOI

Garrison MW, Mutters R, Dowzicky MJ. In vitro activity of tigecycline and comparator agents against a global collection of Gram-negative and Gram-positive organisms: tigecycline Evaluation and Surveillance Trial 2004 to 2007. Diagn Microbiol Infect Dis. 2009;65(3):288–299. doi: 10.1016/j.diagmicrobio.2009.07.010. PubMed DOI

Hoban DJ, Reinert RR, Bouchillon SK, Dowzicky MJ. Global in vitro activity of tigecycline and comparator agents: Tigecycline Evaluation and Surveillance Trial 2004–2013. Ann Clin Microbiol Antimicrob. 2015;14(1):27. doi: 10.1186/s12941-015-0085-1. PubMed DOI PMC

Sader HS, Flamm RK, Jones RN. Tigecycline activity tested against antimicrobial resistant surveillance subsets of clinical bacteria collected worldwide (2011) Diagn Microbiol Infect Dis. 2013;76(2):217–221. doi: 10.1016/j.diagmicrobio.2013.02.009. PubMed DOI

Bertrand X, Dowzicky MJJCt (2012) Antimicrobial susceptibility among gram-negative isolates collected from intensive care units in North America, Europe, the Asia-Pacific Rim, Latin America, the Middle East, and Africa between 2004 and 2009 as part of the Tigecycline Evaluation and Surveillance Trial 34 (1):124-137 PubMed

Hsu M-S, Liao C-H, Liu C-Y, Yang C-J, Huang Y-T. In vitro susceptibilities of clinical isolates of ertapenem-non-susceptible Enterobacteriaceae to nemonoxacin, tigecycline, fosfomycin and other antimicrobial agents. Int J Antimicrob Agents (Print) 2011;37(3):276–278. doi: 10.1016/j.ijantimicag.2010.12.003. PubMed DOI

Veeraraghavan B, Poojary A, Shankar C, Bari AK, Kukreja S, Thukkaram B, Neethimohan RG, Bakhtavachalam YD, Kamat S. In-vitro activity of tigecycline and comparator agents against common pathogens: Indian experience. The Journal of Infection in Developing Countries. 2019;13(03):245–250. doi: 10.3855/jidc.10376. PubMed DOI

Chen Y-H, Liu C-Y, Ko W-C, Liao C-H, Lu P-L, Huang C-H, Lu C-T, Chuang Y-C, Tsao S-M, Chen Y-S. Trends in the susceptibility of methicillin-resistant Staphylococcus aureus to nine antimicrobial agents, including ceftobiprole, nemonoxacin, and tyrothricin: results from the Tigecycline In Vitro Surveillance in Taiwan (TIST) study, 2006–2010. Eur J Clin Microbiol Infect Dis. 2014;33(2):233–239. doi: 10.1007/s10096-013-1949-y. PubMed DOI

Yang Q, Xu Y-C, Kiratisin P, Dowzicky MJ. Antimicrobial activity among gram-positive and gram-negative organisms collected from the Asia-Pacific region as part of the Tigecycline Evaluation and Surveillance Trial: Comparison of 2015 results with previous years. Diagn Microbiol Infect Dis. 2017;89(4):314–323. doi: 10.1016/j.diagmicrobio.2017.08.014. PubMed DOI

Ricciardi R, Ricciardi A, Danzi G. In vitro activity of tigecycline against multidrug-resistant Acinetobacter baumannii clinical isolates. Le infezioni in medicina: rivista periodica di eziologia, epidemiologia, diagnostica, clinica e terapia delle patologie infettive. 2009;17(4):236–239. PubMed

Capone A, D’Arezzo S, Visca P, Petrosillo N. In vitro activity of tigecycline against multidrug-resistant Acinetobacter baumannii. J Antimicrob Chemother. 2008;62(2):422–423. doi: 10.1093/jac/dkn172. PubMed DOI

Kopterides P, Papageorgiou C, Antoniadou A, Papadomichelakis E, Tsangaris I, Dimopoulou I, Armaganidis A. Failure of tigecycline to treat severe Clostridium difficile infection. Anaesth Intensive Care. 2010;38(3):755–758. doi: 10.1177/0310057X1003800339. PubMed DOI

Caneiras C, Calisto F, Jorge da Silva G, Lito L, Melo-Cristino J, Duarte A. First description of colistin and tigecycline-resistant Acinetobacter baumannii producing KPC-3 carbapenemase in Portugal. Antibiotics. 2018;7(4):96. doi: 10.3390/antibiotics7040096. PubMed DOI PMC

Verkade E, Verhulst C, Huijsdens X, Kluytmans J. In vitro activity of tigecycline against methicillin-resistant Staphylococcus aureus, including livestock-associated strains. Eur J Clin Microbiol Infect Dis. 2010;29(5):503–507. doi: 10.1007/s10096-010-0886-2. PubMed DOI PMC

Nagy E, Urbán E, Nord CE, Bacteria ESGoARiA (2011) Antimicrobial susceptibility of Bacteroides fragilis group isolates in Europe: 20 years of experience. Clin Microbiol Infect 17 (3):371-379 PubMed

Gallagher JC, Rouse HM. Tigecycline for the treatment of Acinetobacter infections: a case series. Ann Pharmacother. 2008;42(9):1188–1194. doi: 10.1345/aph.1L171. PubMed DOI

Peleg AY, Potoski BA, Rea R, Adams J, Sethi J, Capitano B, Husain S, Kwak EJ, Bhat SV, Paterson DL. Acinetobacter baumannii bloodstream infection while receiving tigecycline: a cautionary report. J Antimicrob Chemother. 2006;59(1):128–131. doi: 10.1093/jac/dkl441. PubMed DOI

Hoban DJ, Bouchillon SK, Dowzicky MJ. Antimicrobial susceptibility of extended-spectrum β-lactamase producers and multidrug-resistant Acinetobacter baumannii throughout the United States and comparative in vitro activity of tigecycline, a new glycylcycline antimicrobial. Diagn Microbiol Infect Dis. 2007;57(4):423–428. doi: 10.1016/j.diagmicrobio.2006.10.013. PubMed DOI

Sekyere JO, Govinden U, Essack S. The molecular epidemiology and genetic environment of carbapenemases detected in Africa. Microb Drug Resist. 2016;22(1):59–68. doi: 10.1089/mdr.2015.0053. PubMed DOI

Osei Sekyere J. Current state of resistance to antibiotics of last-resort in South Africa: a review from a public health perspective. Front Public Health. 2016;4:209. doi: 10.3389/fpubh.2016.00209. PubMed DOI PMC

Govind C, Moodley K, Peer A, Pillay N, Maske C, Wallis C, Viana R, Chetty A, Perovic O. NDM-1 imported from India–first reported case in South Africa. S Afr Med J. 2013;103(7):476–478. doi: 10.7196/SAMJ.6593. PubMed DOI

Osei Sekyere J, Govinden U, Bester L, Essack S. Colistin and tigecycline resistance in carbapenemase-producing Gram-negative bacteria: emerging resistance mechanisms and detection methods. J Appl Microbiol. 2016;121(3):601–617. doi: 10.1111/jam.13169. PubMed DOI

Sekyerea JO, Pedersenb T, Sivertsenb A, Govindena U, Essacka SY, Moodleyc K, Samuelsenb O, Sundsfjordb A. Molecular epidemiology of carbapenem, colistin and tigecycline resistant Enterobacteriaceae in Durban. South: Africa; 2016.

Nejnovějších 20 citací...

Zobrazit více v
Medvik | PubMed

Tetracycline-modifying enzyme SmTetX from Stenotrophomonas maltophilia

. 2023 Jul 01 ; 79 (Pt 7) : 180-192. [epub] 20230705

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...