scholarly journals Capsular K-antigen-PLGA nanoparticles vaccine against Klebsiella pneumoniae K2O1 infection

2022 ◽  
Vol 30 (1) ◽  
pp. 1-2
Author(s):  
Kobra Rostamizadeh ◽  
Parivash Ghaderinia ◽  
Reza Shapoury ◽  
Alireza Khodavandi ◽  
Mehdi Mahdavi ◽  
...  
2020 ◽  
Vol 21 (18) ◽  
pp. 6572
Author(s):  
Daria Artyszuk ◽  
Radosław Izdebski ◽  
Anna Maciejewska ◽  
Marta Kaszowska ◽  
Aleksandra Herud ◽  
...  

Klebsiella pneumoniae is a nosocomial pathogen, pointed out by the World Helth Organisation (WHO) as “critical” regarding the highly limited options of treatment. Lipopolysaccharide (LPS, O-antigen) and capsular polysaccharide (K-antigen) are its virulence factors and surface antigens, determining O- and K-serotypes and encoded by O- or K-loci. They are promising targets for antibody-based therapies (vaccines and passive immunization) as an alternative to antibiotics. To make such immunotherapy effective, knowledge about O/K-antigen structures, drift, and distribution among clinical isolates is needed. At present, the structural analysis of O-antigens is efficiently supported by bioinformatics. O- and K-loci-based genotyping by polymerase chain reaction (PCR) or whole genome sequencing WGS has been proposed as a diagnostic tool, including the Kaptive tool available in the public domain. We analyzed discrepancies for O2 serotyping between Kaptive-based predictions (O2 variant 2 serotype) and the actual phenotype (O2 variant 1) for two K. pneumoniae clinical isolates. Identified length discrepancies from the reference O-locus resulted from insertion sequences (ISs) within rfb regions of the O-loci. In silico analysis of 8130 O1 and O2 genomes available in public databases indicated a broader distribution of ISs in rfbs that may influence the actual O-antigen structure. Our results show that current high-throughput genotyping algorithms need to be further refined to consider the effects of ISs on the LPS O-serotype.


1994 ◽  
Vol 71 (06) ◽  
pp. 768-772 ◽  
Author(s):  
Gerhard Dickneite ◽  
Jörg Czech

SummaryRats which were infected with the gramnegative pathogen Klebsiella pneumoniae develop disseminated intravascular coagulation (DIC), multi-organ failure (MOF) and finally die in a septic shock. We investigated the therapeutic effect of antibiotic (tobramycin) treatment combined with the infusion of the highly specific thrombin inhibitor rec. hirudin. Although administration of 2 mg/kg tobramycin alone leads to a decrease of the bacterial burden, DIC could not be prevented. Infusion of rec. hirudin (0.25 mg/kg x h) for 4 h (start of treatment 1 h post infection), in addition to a bolus administration of tobramycin, led to an amelioration of DIC parameters as fibrinogen, thrombin-antithrombin complex (TAT) and platelets. Serum transaminase levels (GOT, GPT) as a marker of MOF were significantly improved by rec. hirudin, the T50 value increased from 17 h in the tobramycin group to 42 h in the tobramycin + rec. hirudin giuup, muilality rates were 90% or 60%, respectively. Combination of heparin (10011/kg x h) and tobramycin was not effective on survival.


2004 ◽  
Vol 221 (S 5) ◽  
Author(s):  
A Scharipow ◽  
M Blum ◽  
K Ende ◽  
B Knau

2016 ◽  
Vol 4 (2) ◽  
pp. 47-53
Author(s):  
Anna Chrapusta ◽  
Roman Wach ◽  
Beata Śpiewak ◽  
Małgorzata Makowska ◽  
Paweł Palacz

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