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1.
Front Cell Infect Microbiol ; 14: 1435123, 2024.
Artículo en Inglés | MEDLINE | ID: mdl-39139766

RESUMEN

Background: Aminoglycoside-modifying enzymes (AMEs) play an essential role in bacterial resistance to aminoglycoside antimicrobials. With the development of sequencing techniques, more bacterial genomes have been sequenced, which has aided in the discovery of an increasing number of novel resistance mechanisms. Methods: The bacterial species was identified by 16S rRNA gene homology and average nucleotide identity (ANI) analyses. The minimum inhibitory concentration (MIC) of each antimicrobial was determined by the agar dilution method. The protein was expressed with the pCold I vector in E. coli BL21, and enzyme kinetic parameters were examined. The whole-genome sequence of the bacterium was obtained via the Illumina and PacBio sequencing platforms. Reconstruction of the phylogenetic tree, identification of conserved functional residues, and gene context analysis were performed using the corresponding bioinformatic techniques. Results: A novel aminoglycoside resistance gene, designated aph(3')-Ie, which confers resistance to ribostamycin, kanamycin, sisomicin and paromomycin, was identified in the chromosome of the animal bacterium Citrobacter gillenii DW61, which exhibited a multidrug resistance phenotype. APH(3')-Ie showed the highest amino acid identity of 74.90% with the functionally characterized enzyme APH(3')-Ia. Enzyme kinetics analysis demonstrated that it had phosphorylation activity toward four aminoglycoside substrates, exhibiting the highest affinity (K m, 4.22 ± 0.88 µM) and the highest catalytic efficiency [k cat/K m, (32.27 ± 8.14) × 104] for ribomycin. Similar to the other APH(3') proteins, APH(3')-Ie contained all the conserved functional sites of the APH family. The aph(3')-Ie homologous genes were present in C. gillenii isolates from different sources, including some of clinical significance. Conclusion: In this work, a novel chromosomal aminoglycoside resistance gene, designated aph(3')-Ie, conferring resistance to aminoglycoside antimicrobials, was identified in a rabbit isolate C. gillenii DW61. The elucidation of the novel resistance mechanism will aid in the effective treatment of infections caused by pathogens carrying such resistance genes.


Asunto(s)
Aminoglicósidos , Antibacterianos , Citrobacter , Pruebas de Sensibilidad Microbiana , Filogenia , ARN Ribosómico 16S , Animales , Antibacterianos/farmacología , Antibacterianos/metabolismo , Citrobacter/enzimología , Citrobacter/genética , Citrobacter/metabolismo , Citrobacter/clasificación , Aminoglicósidos/farmacología , Aminoglicósidos/metabolismo , ARN Ribosómico 16S/genética , Conejos , Farmacorresistencia Bacteriana Múltiple/genética , Genoma Bacteriano , Secuenciación Completa del Genoma , Sisomicina/farmacología , Sisomicina/análogos & derivados , Sisomicina/metabolismo , Kanamicina Quinasa/genética , Kanamicina Quinasa/metabolismo , Ribostamicina/metabolismo , Farmacorresistencia Bacteriana/genética , Kanamicina/farmacología , Escherichia coli/genética , Escherichia coli/metabolismo , Infecciones por Enterobacteriaceae/microbiología
2.
Sci Rep ; 11(1): 11614, 2021 06 02.
Artículo en Inglés | MEDLINE | ID: mdl-34078922

RESUMEN

Plazomicin is currently the only next-generation aminoglycoside approved for clinical use that has the potential of evading the effects of widespread enzymatic resistance factors. However, plazomicin is still susceptible to the action of the resistance enzyme AAC(2')-Ia from Providencia stuartii. As the clinical use of plazomicin begins to increase, the spread of resistance factors will undoubtedly accelerate, rendering this aminoglycoside increasingly obsolete. Understanding resistance to plazomicin is an important step to ensure this aminoglycoside remains a viable treatment option for the foreseeable future. Here, we present three crystal structures of AAC(2')-Ia from P. stuartii, two in complex with acetylated aminoglycosides tobramycin and netilmicin, and one in complex with a non-substrate aminoglycoside, amikacin. Together, with our previously reported AAC(2')-Ia-acetylated plazomicin complex, these structures outline AAC(2')-Ia's specificity for a wide range of aminoglycosides. Additionally, our survey of AAC(2')-I homologues highlights the conservation of residues predicted to be involved in aminoglycoside binding, and identifies the presence of plasmid-encoded enzymes in environmental strains that confer resistance to the latest next-generation aminoglycoside. These results forecast the likely spread of plazomicin resistance and highlight the urgency for advancements in next-generation aminoglycoside design.


Asunto(s)
Acetiltransferasas/química , Antibacterianos/química , Proteínas Bacterianas/química , Farmacorresistencia Bacteriana/genética , Providencia/enzimología , Sisomicina/análogos & derivados , Acetiltransferasas/genética , Acetiltransferasas/metabolismo , Amicacina/química , Amicacina/metabolismo , Amicacina/farmacología , Antibacterianos/metabolismo , Antibacterianos/farmacología , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Sitios de Unión , Clonación Molecular , Cristalografía por Rayos X , Escherichia coli/genética , Escherichia coli/metabolismo , Expresión Génica , Vectores Genéticos/química , Vectores Genéticos/metabolismo , Humanos , Cinética , Modelos Moleculares , Netilmicina/química , Netilmicina/metabolismo , Netilmicina/farmacología , Unión Proteica , Conformación Proteica en Hélice alfa , Conformación Proteica en Lámina beta , Dominios y Motivos de Interacción de Proteínas , Providencia/química , Providencia/efectos de los fármacos , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Sisomicina/química , Sisomicina/metabolismo , Sisomicina/farmacología , Especificidad por Sustrato , Tobramicina/química , Tobramicina/metabolismo , Tobramicina/farmacología
3.
Commun Biol ; 4(1): 729, 2021 06 11.
Artículo en Inglés | MEDLINE | ID: mdl-34117352

RESUMEN

The approval of plazomicin broadened the clinical library of aminoglycosides available for use against emerging bacterial pathogens. Contrarily to other aminoglycosides, resistance to plazomicin is limited; still, instances of resistance have been reported in clinical settings. Here, we present structural insights into the mechanism of plazomicin action and the mechanisms of clinical resistance. The structural data reveal that plazomicin exclusively binds to the 16S ribosomal A site, where it likely interferes with the fidelity of mRNA translation. The unique extensions to the core aminoglycoside scaffold incorporated into the structure of plazomicin do not interfere with ribosome binding, which is analogously seen in the binding of this antibiotic to the AAC(2')-Ia resistance enzyme. The data provides a structural rationale for resistance conferred by drug acetylation and ribosome methylation, i.e., the two mechanisms of resistance observed clinically. Finally, the crystal structures of plazomicin in complex with both its target and the clinically relevant resistance factor provide a roadmap for next-generation drug development that aims to ameliorate the impact of antibiotic resistance.


Asunto(s)
Antibacterianos/farmacología , Sisomicina/análogos & derivados , Antibacterianos/química , Antibacterianos/metabolismo , Sitios de Unión , Cristalografía por Rayos X , Farmacorresistencia Bacteriana , Metilación , Providencia/efectos de los fármacos , Providencia/metabolismo , ARN Ribosómico 16S/metabolismo , ARN de Transferencia/metabolismo , Ribosomas/metabolismo , Sisomicina/química , Sisomicina/metabolismo , Sisomicina/farmacología , Relación Estructura-Actividad
4.
Diagn Microbiol Infect Dis ; 97(4): 115092, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32569921

RESUMEN

Comparative in vitro activity of plazomicin and 4 older aminoglycosides was evaluated with broth microdilution in 714 blood isolates from 14 hospitals in Turkey. Isolates included Escherichia coli (n=320), Klebsiella spp. (n=294), Enterobacter spp. (n=69), Serratia marcescens (n=20), and Citrobacter spp. (n=11). Isolates resistant to older aminoglycosides (n=240) were screened for aminoglycoside modifying enzyme genes: aac(6')-Ib, aac(3)-Ia, aac(3)-IIa, ant(2″)-Ia. Isolates with high MICs for plazomicin (n=41) were screened for 16S rRNA methyltransferase genes (armA, rmtA, rmtB, rmtC, rmtD, rmtE, rmtF, rmtG, rmtH, npmA) and 2 carbapenemase genes (blaOXA-48, blaNDM-1). Overall, resistance to plazomicin, amikacin, netilmicin, gentamicin, and tobramycin was 7.7%, 7.4%, 31.5%, 32.9%, and 34.7%, respectively. aac(6')-Ib and aac(3)-IIa were the most common AME genes. Co-occurrence of blaNDM-1 with armA and rmtC and blaOXA-48 with armA was striking. Enterobacter cloacae carrying rmtC+blaNDM-1, S. marcescens with armA+blaOXA-48, and rmtF+ blaOXA-48 in K. pneumoniae were reported for the first time.


Asunto(s)
Aminoglicósidos/farmacología , Infecciones por Enterobacteriaceae/microbiología , Enterobacteriaceae/efectos de los fármacos , Enterobacteriaceae/enzimología , Acetiltransferasas/genética , Aminoglicósidos/metabolismo , Proteínas Bacterianas/genética , Farmacorresistencia Bacteriana/efectos de los fármacos , Farmacorresistencia Bacteriana/genética , Enterobacteriaceae/genética , Enterobacteriaceae/aislamiento & purificación , Infecciones por Enterobacteriaceae/epidemiología , Humanos , Metiltransferasas/genética , Pruebas de Sensibilidad Microbiana , Prevalencia , ARN Ribosómico 16S/metabolismo , Sisomicina/análogos & derivados , Sisomicina/metabolismo , Sisomicina/farmacología , Turquía/epidemiología , beta-Lactamasas/genética
5.
ACS Synth Biol ; 8(9): 1991-1997, 2019 09 20.
Artículo en Inglés | MEDLINE | ID: mdl-31487454

RESUMEN

Direct cloning of natural product pathways for efficient refactoring and heterologous expression has become an important strategy for microbial natural product research and discovery, especially for those kept silent or poorly expressed in the original strains. Accordingly, the development of convenient and efficient cloning approaches is becoming increasingly necessary. Here we presented an in vitro packaging mediated cloning approach that combines CRISPR/Cas9 system with in vitro λ packaging system, for targeted cloning of natural product pathways. In such a scheme, pathways of Tü3010 (27.4 kb) and sisomicin (40.7 kb) were respectively cloned, and stuR was further depicted to positively regulate Tü3010 production. In vitro packaging mediated approach not only enables to activate cryptic pathways, but also facilitates refactoring or interrogating the pathways in conjunction with various gene editing systems. This approach features an expedited, convenient, and generic manner, and it is conceivable that it may be widely adopted for targeted cloning of the natural product pathways.


Asunto(s)
Productos Biológicos/metabolismo , Sistemas CRISPR-Cas/genética , Proteínas Bacterianas/genética , Productos Biológicos/química , Clonación Molecular , Edición Génica , Familia de Multigenes , Plásmidos/genética , Plásmidos/metabolismo , Proteínas Represoras/genética , Sisomicina/química , Sisomicina/metabolismo , Streptomyces/genética , Transactivadores/genética
6.
Int J Antimicrob Agents ; 50(2): 191-196, 2017 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-28577932

RESUMEN

This study investigated the in-vitro activity of clinically relevant aminoglycosides and new antimicrobial agents-plazomicin, ceftobiprole and dalbavancin-against 55 methicillin-resistant Staphylococcus aureus (MRSA) isolates producing aminoglycoside-modifying enzymes (AMEs). The checkerboard method was used to assess synergism between plazomicin and four antibiotics (fosfomycin, ceftobiprole, cefoxitin and meropenem), and time-kill assays were performed for the most active combinations. Among the aminoglycosides tested, plazomicin was the most active agent against MRSA, with >90% of isolates being inhibited at a minimum inhibitory concentration (MIC) of ≤1 mg/L. MIC50 and MIC90 values for ceftobiprole and dalbavancin were 2 and 4 mg/L, and 0.125 and 0.125 mg/L, respectively. The most prevalent AME gene was aac(6')Ie-aph(2″)Ia (87.3%), followed by ant(4')Ia (52.7%) and aph(3')IIIa (52.7%). Plazomicin activity was not affected by the type or number of enzymes detected. In checkerboard and time-kill assays, indifference was the most common result achieved for the antibiotic combinations. Notably, no antagonism was observed with any combination tested. Overall, plazomicin in combination with meropenem had the highest synergistic effect, demonstrating synergy against seven isolates in the checkerboard assay and three isolates in time-kill curves. In conclusion, plazomicin showed potent activity against aminoglycoside-resistant MRSA isolates, regardless of the number and type of AMEs present. These findings indicate the potential utility of plazomicin in combination with meropenem for the treatment of MRSA infections.


Asunto(s)
Antiinfecciosos/farmacología , Sinergismo Farmacológico , Staphylococcus aureus Resistente a Meticilina/efectos de los fármacos , Staphylococcus aureus Resistente a Meticilina/enzimología , Sisomicina/análogos & derivados , Aminoglicósidos/metabolismo , Antiinfecciosos/metabolismo , Humanos , Inactivación Metabólica , Pruebas de Sensibilidad Microbiana , Viabilidad Microbiana/efectos de los fármacos , Sisomicina/metabolismo , Sisomicina/farmacología
7.
Proteins ; 85(7): 1258-1265, 2017 07.
Artículo en Inglés | MEDLINE | ID: mdl-28316100

RESUMEN

Kinetic, thermodynamic, and structural properties of the aminoglycoside N3-acetyltransferase-VIa (AAC-VIa) are determined. Among the aminoglycoside N3-acetyltransferases, AAC-VIa has one of the most limited substrate profiles. Kinetic studies showed that only five aminoglycosides are substrates for this enzyme with a range of fourfold difference in kcat values. Larger differences in KM (∼40-fold) resulted in ∼30-fold variation in kcat /KM . Binding of aminoglycosides to AAC-VIa was enthalpically favored and entropically disfavored with a net result of favorable Gibbs energy (ΔG < 0). A net deprotonation of the enzyme, ligand, or both accompanied the formation of binary and ternary complexes. This is opposite of what was observed with several other aminoglycoside N3-acetyltransferases, where ligand binding causes more protonation. The change in heat capacity (ΔCp) was different in H2 O and D2 O for the binary enzyme-sisomicin complex but remained the same in both solvents for the ternary enzyme-CoASH-sisomicin complex. Unlike, most other aminoglycoside-modifying enzymes, the values of ΔCp were within the expected range of protein-carbohydrate interactions. Solution behavior of AAC-VIa was also different from the more promiscuous aminoglycoside N3-acetyltransferases and showed a monomer-dimer equilibrium as detected by analytical ultracentrifugation (AUC). Binding of ligands shifted the enzyme to monomeric state. Data also showed that polar interactions were the most dominant factor in dimer formation. Overall, thermodynamics of ligand-protein interactions and differences in protein behavior in solution provide few clues on the limited substrate profile of this enzyme despite its >55% sequence similarity to the highly promiscuous aminoglycoside N3-acetyltransferase. Proteins 2017; 85:1258-1265. © 2017 Wiley Periodicals, Inc.


Asunto(s)
Acetiltransferasas/química , Antibacterianos/química , Proteínas Bacterianas/química , Enterobacter cloacae/química , Protones , Sisomicina/química , Acetiltransferasas/genética , Acetiltransferasas/metabolismo , Secuencias de Aminoácidos , Antibacterianos/metabolismo , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Sitios de Unión , Clonación Molecular , Óxido de Deuterio/química , Enterobacter cloacae/enzimología , Escherichia coli/genética , Escherichia coli/metabolismo , Expresión Génica , Gentamicinas/química , Gentamicinas/metabolismo , Kanamicina/química , Kanamicina/metabolismo , Cinética , Ligandos , Modelos Moleculares , Unión Proteica , Dominios y Motivos de Interacción de Proteínas , Proteínas Recombinantes/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Sisomicina/metabolismo , Homología Estructural de Proteína , Especificidad por Sustrato , Termodinámica , Tobramicina/química , Tobramicina/metabolismo , Agua/química
8.
Antimicrob Agents Chemother ; 60(9): 5208-14, 2016 09.
Artículo en Inglés | MEDLINE | ID: mdl-27297487

RESUMEN

We compared the in vitro activities of gentamicin (GEN), tobramycin (TOB), amikacin (AMK), and plazomicin (PLZ) against 13 Enterobacter isolates possessing both Klebsiella pneumoniae carbapenemase and extended-spectrum ß-lactamase (KPC+/ESBL+) with activity against 8 KPC+/ESBL-, 6 KPC-/ESBL+, and 38 KPC-/ESBL- isolates. The rates of resistance to GEN and TOB were higher for KPC+/ESBL+ (100% for both) than for KPC+/ESBL- (25% and 38%, respectively), KPC-/ESBL+ (50% and 17%, respectively), and KPC-/ESBL- (0% and 3%, respectively) isolates. KPC+/ESBL+ isolates were more likely than others to possess an aminoglycoside-modifying enzyme (AME) (100% versus 38%, 67%, and 5%; P = 0.007, 0.06, and <0.0001, respectively) or multiple AMEs (100% versus 13%, 33%, and 0%, respectively; P < 0.01 for all). KPC+/ESBL+ isolates also had a greater number of AMEs (mean of 4.6 versus 1.5, 0.9, and 0.05, respectively; P < 0.01 for all). GEN and TOB MICs were higher against isolates with >1 AME than with ≤1 AME. The presence of at least 2/3 of KPC, SHV, and TEM predicted the presence of AMEs. PLZ MICs against all isolates were ≤4 µg/ml, regardless of KPC/ESBL pattern or the presence of AMEs. In conclusion, GEN and TOB are limited as treatment options against KPC+ and ESBL+ Enterobacter PLZ may represent a valuable addition to the antimicrobial armamentarium. A full understanding of AMEs and other aminoglycoside resistance mechanisms will allow clinicians to incorporate PLZ rationally into treatment regimens. The development of molecular assays that accurately and rapidly predict antimicrobial responses among KPC- and ESBL-producing Enterobacter spp. should be a top research priority.


Asunto(s)
Antibacterianos/farmacología , Proteínas Bacterianas/genética , Farmacorresistencia Bacteriana Múltiple/genética , Enterobacter/efectos de los fármacos , Sisomicina/análogos & derivados , beta-Lactamasas/genética , Amicacina/metabolismo , Amicacina/farmacología , Antibacterianos/metabolismo , Proteínas Bacterianas/metabolismo , Biotransformación , Enterobacter/enzimología , Enterobacter/genética , Enterobacter/crecimiento & desarrollo , Escherichia coli/química , Escherichia coli/enzimología , Expresión Génica , Gentamicinas/metabolismo , Gentamicinas/farmacología , Klebsiella pneumoniae/química , Klebsiella pneumoniae/enzimología , Pruebas de Sensibilidad Microbiana , Sisomicina/metabolismo , Sisomicina/farmacología , Tobramicina/metabolismo , Tobramicina/farmacología , beta-Lactamasas/metabolismo
9.
Antimicrob Agents Chemother ; 58(8): 4443-51, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-24867988

RESUMEN

We measured in vitro activity of plazomicin, a next-generation aminoglycoside, and other aminoglycosides against 50 carbapenem-resistant Klebsiella pneumoniae strains from two centers and correlated the results with the presence of various aminoglycoside-modifying enzymes (AMEs). Ninety-four percent of strains were sequence type 258 (ST258) clones, which exhibited 5 ompK36 genotypes; 80% and 10% of strains produced Klebsiella pneumoniae carbapenemase 2 (KPC-2) and KPC-3, respectively. Ninety-eight percent of strains possessed AMEs, including AAC(6')-Ib (98%), APH(3')-Ia (56%), AAC(3)-IV (38%), and ANT(2")-Ia (2%). Gentamicin, tobramycin, and amikacin nonsusceptibility rates were 40, 98, and 16%, respectively. Plazomicin MICs ranged from 0.25 to 1 µg/ml. Tobramycin and plazomicin MICs correlated with gentamicin MICs (r = 0.75 and 0.57, respectively). Plazomicin exerted bactericidal activity against 17% (1× MIC) and 94% (4× MIC) of strains. All strains with AAC(6')-Ib were tobramycin-resistant; 16% were nonsusceptible to amikacin. AAC(6')-Ib combined with another AME was associated with higher gentamicin, tobramycin, and plazomicin MICs than AAC(6')-Ib alone (P = 0.01, 0.0008, and 0.046, respectively). The presence of AAC(3)-IV in a strain was also associated with higher gentamicin, tobramycin, and plazomicin MICs (P = 0.0006, P < 0.0001, and P = 0.01, respectively). The combination of AAC(6')-Ib and another AME, the presence of AAC(3)-IV, and the presence of APH(3')-Ia were each associated with gentamicin resistance (P = 0.0002, 0.003, and 0.01, respectively). In conclusion, carbapenem-resistant K. pneumoniae strains (including ST258 clones) exhibit highly diverse antimicrobial resistance genotypes and phenotypes. Plazomicin may offer a treatment option against strains resistant to other aminoglycosides. The development of molecular assays that predict antimicrobial responses among carbapenem-resistant K. pneumoniae strains should be a research priority.


Asunto(s)
Antibacterianos/metabolismo , Farmacorresistencia Bacteriana Múltiple/genética , Klebsiella pneumoniae/enzimología , Sisomicina/análogos & derivados , Amicacina/metabolismo , Amicacina/farmacología , Aminoglicósidos/metabolismo , Aminoglicósidos/farmacología , Antibacterianos/farmacología , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Combinación de Medicamentos , Pruebas de Enzimas , Expresión Génica , Gentamicinas/metabolismo , Gentamicinas/farmacología , Isoenzimas/genética , Isoenzimas/metabolismo , Klebsiella pneumoniae/efectos de los fármacos , Klebsiella pneumoniae/genética , Klebsiella pneumoniae/crecimiento & desarrollo , Pruebas de Sensibilidad Microbiana , Sisomicina/metabolismo , Sisomicina/farmacología , Resistencia betalactámica/genética , beta-Lactamasas/genética , beta-Lactamasas/metabolismo , beta-Lactamas/farmacología
10.
FEMS Microbiol Lett ; 166(1): 9-13, 1998 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-9741079

RESUMEN

Sisomicin binding sites are located in the cell wall. They are the carboxyl groups of peptidoglycans, which are major components of the cell wall. The carboxyl groups have negative charges which can bind the positively charged amino groups of sisomicin. When the negative charges of the carboxyl groups of the peptidoglycans are changed to neutral or positive charges, sisomicin does not bind to the cell wall. Magnesium ions bind to the cell wall in competition with sisomicin, and have a weak affinity for the cell wall binding sites compared with sisomicin. The binding molar ratio of sisomicin to magnesium ions was approximately 1 to 10.


Asunto(s)
Antibacterianos/metabolismo , Micromonospora/metabolismo , Sisomicina/metabolismo , Antibacterianos/química , Sitios de Unión , Unión Competitiva , Pared Celular/química , Pared Celular/metabolismo , Electroquímica , Concentración de Iones de Hidrógeno , Magnesio/metabolismo , Sisomicina/química
11.
Se Pu ; 16(5): 445-7, 1998 Sep.
Artículo en Chino | MEDLINE | ID: mdl-11498926

RESUMEN

A high performance liquid chromatography-indirect photometric detection (HPLC-IPD) method for determination of sisomicin sulfate in body fluid (serum, urine, saliva, cerebrospinal fluid and fluid oozed out from wound) was established. The conditions in this method were a mobile phase solution of methyl alcohol-acetonitrile-water (20:10:70) containing nicotinamide 0.5 mmol/L, sodium 1-heptanesulfonate 5 mmol/L and phosphoric acid 0.05 mol/L, a Spherisorb C18 column (4.6 mm x 250 mm) and an UV detector with sensitivity of 0.05 Aufs (0.1 Aufs for urine). The detection wavelength was fixed at 268 nm. The average recovery for sisomicin in serum was 96.92% +/- 4.63% and the coefficients of variation were 4.75% and 5.65% for within-day and day-to-day tests respectively. The detectable limit was 0.1 ng. The concentration of sisomicin in body fluid of 4 patients was determined.


Asunto(s)
Antibacterianos/metabolismo , Líquidos Corporales/química , Cromatografía Líquida de Alta Presión/métodos , Sisomicina/metabolismo , Humanos , Fotometría/métodos
13.
J Antimicrob Chemother ; 19(2): 233-8, 1987 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-3571044

RESUMEN

5-epi-sisomicin was given as a single intramuscular injection of 1 mg/kg to six healthy male adults. Serum peak concentrations averaged 3.07 mg/l, the mean elimination half life was 179 min and the mean 24 h urinary recovery was 85.3%. Local and systemic tolerance was good.


Asunto(s)
Sisomicina/análogos & derivados , Adulto , Semivida , Humanos , Inyecciones Intramusculares , Cinética , Masculino , Sisomicina/administración & dosificación , Sisomicina/metabolismo
14.
Antibiot Med Biotekhnol ; 32(2): 122-9, 1987 Feb.
Artículo en Ruso | MEDLINE | ID: mdl-3105433

RESUMEN

Alternative variants of the available methods for estimating the antimicrobial effect kinetics in the in vitro dynamic systems were analyzed. For defining and analyzing the concentration-effect relations in the in vitro dynamic systems it was recommended that two integral parameters characterizing the antimicrobial effect duration (TE) and intensity (IE) irrespective of the recording means be used. TE is defined by the time from the moment of antibiotic administration into the dynamic system till the moment when the count of the microorganisms reaches again its initial level. IE is defined by the area between the curves of the microbial growth kinetics in the presence and absence of an antibiotic. The possible application of TE and IE is exemplified by relation between the sisomicin antimicrobial effect on P. aeruginosa 58, E. coli 93 and K. pneumoniae 5056 and the antibiotic concentration under conditions of sisomicin pharmacokinetic profiles reproduction after intramuscular administration within the levels of the therapeutic doses with an account of individual variability of the aminoglycoside concentration in the blood of humans.


Asunto(s)
Antibacterianos/farmacología , Modelos Biológicos , Antibacterianos/metabolismo , Calorimetría , Relación Dosis-Respuesta a Droga , Escherichia coli/efectos de los fármacos , Escherichia coli/crecimiento & desarrollo , Humanos , Cinética , Klebsiella pneumoniae/efectos de los fármacos , Klebsiella pneumoniae/crecimiento & desarrollo , Matemática , Pseudomonas aeruginosa/efectos de los fármacos , Pseudomonas aeruginosa/crecimiento & desarrollo , Sisomicina/metabolismo , Sisomicina/farmacología , Factores de Tiempo
15.
Antibiot Med Biotekhnol ; 31(10): 785-90, 1986 Oct.
Artículo en Ruso | MEDLINE | ID: mdl-3789689

RESUMEN

The action of cefazolin on the pharmacokinetics and nephrotoxic effect of sisomicin was studied on Wistar rats. Sisomicin in doses of 12.5 and 25 mg/kg alone or in combination with cefazolin in doses of 90 and 360 mg/kg was administered intramuscularly to the animals daily for 16 days. It was shown that in both the doses cefazolin had no noticeable action on the level of the functional and morphological changes in the kidneys. Consequently, there were no significant changes in the levels of sisomicin in serum and the site of the nephrotoxic effect (cortical layer of the kidneys) and in the half-life of the aminoglycoside in the kidney cortical layer under the action of cefazolin. At the same time there was observed a marked individual variability of the levels of urea nitrogen and sisomicin in serum of the rats treated with the aminoglycoside alone or in combination with cefazolin. Analysis of the dependence of the nephrotoxic effect on concentration of sisomicin in serum after its use alone or in combination with cefazolin revealed that the changes in the individual intensity of the effect in all the cases were mainly induced by the changes in the sisomicin blood levels. Therefore, control of the blood levels of the aminoglycoside should provide prevention of the development of its nephrotoxic effect not only in monotherapy but also in the use of aminoglycosides in combination with cefazolin.


Asunto(s)
Cefazolina/farmacología , Riñón/efectos de los fármacos , Sisomicina/metabolismo , Animales , Relación Dosis-Respuesta a Droga , Interacciones Farmacológicas , Femenino , Riñón/metabolismo , Cinética , Masculino , Ratas , Ratas Endogámicas , Sisomicina/toxicidad , Factores de Tiempo
16.
Jpn J Antibiot ; 38(11): 3097-104, 1985 Nov.
Artículo en Japonés | MEDLINE | ID: mdl-4094049

RESUMEN

The pharmacokinetics of sisomicin (SISO) were determined in 3 patients including a case with mild renal dysfunction after intravenous infusion over 1 hour of a single dose of 50 mg. The peak serum concentration was ranged from 3.3 to 3.9 micrograms/ml with about 2 hours of half-life in patients with normal renal function and 4.5 hours in a patient with renal impaired function. This result suggested that dosage regimen should be adjusted in patients with renal impaired function. Clinical response was evaluated in treatment of 16 cases with chronic complicated UTI. SISO was administered intravenously over 1 or 1.5 hours at a daily dose of 100 or 150 mg. An overall excellent or moderate effect was seen in 68.8% of treatment cases with the evaluation by the UTI committee's criteria. As for clinical laboratory abnormal values, a slight but reversible increase of BUN was observed in 1 case. In conclusion, intravenous administration of SISO appeared to be effective and useful method for treatment of complicated UTI.


Asunto(s)
Sisomicina/administración & dosificación , Infecciones Urinarias/tratamiento farmacológico , Adolescente , Adulto , Anciano , Enfermedad Crónica , Evaluación de Medicamentos , Femenino , Humanos , Infusiones Parenterales , Cinética , Masculino , Persona de Mediana Edad , Sisomicina/metabolismo , Infecciones Urinarias/microbiología
17.
Antibiot Med Biotekhnol ; 30(10): 765-70, 1985 Oct.
Artículo en Ruso | MEDLINE | ID: mdl-4091513

RESUMEN

To elucidate the possibility of predicting the level of aminoglycoside antibiotic penetration into the fluids of the internal ear by the antibiotic blood levels, the pharmacokinetics of sisomicin in the perilymph and blood serum was studied on guinea pigs. The antibiotic was administered to the animals subcutaneously in doses of 50, 100 and 200 mg/kg. On the basis of the comparison of the sisomicin concentrations in the perilymph normalized against the dose it was concluded that the pharmacokinetics of sisomicin in the perilymph and blood serum of the animals was linear. Comparison of the areas under the curves of the antibiotic concentration versus time in the perilymph (AUCp) and blood serum (AUCs) showed that the tissue availability of the antibiotic in this study characterized by its penetration into the perilymph and defined by the ratio of the AUCp to AUCs amounted to 55 per cent. In a two-compartment model it was not possible to predict the antibiotic levels in the perilymph by concentrations in the blood. However, by the antibiotic blood levels it was possible to characterize in a complex the pharmacokinetic behaviour of the antibiotic in the perilymph by predicting the areas under the respective curves of the antibiotic concentration versus time. The proportional relation between the values of the AUCp and AUCs suggested that the level of the antibiotic penetration into the internal ear and consequently the intensity of the potential ototoxic effect could be more reliably predicted not by separate values of the antibiotic concentration but by the areas under curves of aminoglycoside concentrations versus time.


Asunto(s)
Oído/efectos de los fármacos , Líquidos Laberínticos/metabolismo , Perilinfa/metabolismo , Sisomicina/metabolismo , Animales , Relación Dosis-Respuesta a Droga , Cobayas , Cinética , Modelos Biológicos , Pronóstico , Sisomicina/toxicidad , Factores de Tiempo
18.
Antibiot Med Biotekhnol ; 30(5): 352-5, 1985 May.
Artículo en Ruso | MEDLINE | ID: mdl-4026255

RESUMEN

The effect of hemosorption and hemodialysis on the pharmacokinetics of sisomicin was studied in 17 patients with acute and chronic renal insufficiency. The value of the antibiotic extraction coefficient in hemosorption was almost 2 times higher than that in hemodialysis. In patients on hemosorption, extracorporeal elimination of the antibiotic was of the saturation nature. It was characterized by systematic diminishing of the extraction coefficient, while in patients on hemodialysis, it did not depend on the time (the value of the extraction coefficient was constant). In this connection it is recommended that the rate of diminishing of the extraction coefficient in hemosorption be estimated. Since sisomicin is rapidly absorbed by the column it is not advisable to administer sisomicin to patients before hemosorption.


Asunto(s)
Lesión Renal Aguda/terapia , Hemoperfusión , Fallo Renal Crónico/terapia , Diálisis Renal , Sisomicina/metabolismo , Lesión Renal Aguda/metabolismo , Humanos , Fallo Renal Crónico/metabolismo , Factores de Tiempo
19.
J Antimicrob Chemother ; 15(5): 607-11, 1985 May.
Artículo en Inglés | MEDLINE | ID: mdl-3839236

RESUMEN

5-epi-sisomicin was given as a single 1 mg/kg intramuscular injection to six adult male volunteers. No adverse effects were observed and the pharmacology was very similar to that of sisomicin. The extended spectrum of 5-epi-sisomicin and its enhanced antipseudomonal activity prompt further clinical evaluation of this agent.


Asunto(s)
Sisomicina/metabolismo , Adulto , Femenino , Humanos , Isomerismo , Cinética , Tasa de Depuración Metabólica , Sisomicina/sangre , Sisomicina/orina
20.
Antibiot Med Biotekhnol ; 30(3): 190-6, 1985 Mar.
Artículo en Ruso | MEDLINE | ID: mdl-4015061

RESUMEN

The effect of cephalothin on the nephrotoxicity and pharmacokinetics of sisomicin was studied on Wistar rats. Sisomicin was injected intramuscularly in doses of 12.5 and 25 mg/kg alone or in combination with cephalothin in a dose of 360 mg/kg once a day for 16 days. It was shown that the combined use of sisomicin and cephalothin resulted in less pronounced functional and morphological changes in the kidneys as compared to the use of sisomicin alone. The decrease in the nephrotoxic effect was accompanied by a decrease in the sisomicin concentration in the blood serum and the site of the nephrotoxic effect (the kidney cortical layer) and the period of the aminoglycoside half-life in the kidney cortical layer under the action of cephalothin. The analysis of the relation between the nephrotoxic effect and the concentration of sisomicin in the kidney cortical layer and blood serum demonstrates that the nephrotoxicity of the sisomicin combination with cephalothin is mainly due to a decrease in the aminoglycoside concentration in the zone of the nephrotoxic effect.


Asunto(s)
Cefalotina/farmacología , Necrosis de la Corteza Renal/inducido químicamente , Riñón/efectos de los fármacos , Sisomicina/toxicidad , Animales , Femenino , Semivida , Riñón/metabolismo , Corteza Renal/efectos de los fármacos , Corteza Renal/patología , Necrosis de la Corteza Renal/patología , Cinética , Masculino , Ratas , Ratas Endogámicas , Sisomicina/antagonistas & inhibidores , Sisomicina/metabolismo
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