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1.
Virol J ; 16(1): 75, 2019 06 03.
Article in English | MEDLINE | ID: mdl-31159841

ABSTRACT

Porcine parvovirus (PPV) is a DNA virus that causes reproductive failure in gilts and sows, resulting in embryonic and fetal losses worldwide. Epitope mapping of PPV is important for developing new vaccines. In this study, we used spot synthesis analysis for epitope mapping of the capsid proteins of PPV (NADL-2 strain) and correlated the findings with predictive data from immunoinformatics. The virus was exposed to three conditions prior to inoculation in pigs: native (untreated), high hydrostatic pressure (350 MPa for 1 h) at room temperature and high hydrostatic pressure (350 MPa for 1 h) at - 18 °C, and was compared with a commercial vaccine produced using inactivated PPV. The screening of serum samples detected 44 positive spots corresponding to 20 antigenic sites. Each type of inoculated antigen elicited a distinct epitope set. In silico prediction located linear and discontinuous epitopes in B cells that coincided with several epitopes detected in spot synthesis of sera from pigs that received different preparations of inoculum. The conditions tested elicited antibodies against the VP1/VP2 antigen that differed in relation to the response time and the profile of structurally available regions that were recognized.


Subject(s)
Antibodies, Viral/blood , Antigens, Viral/immunology , Capsid Proteins/immunology , Epitopes/immunology , Parvovirus, Porcine/immunology , Animals , Antigens, Viral/chemistry , Epitope Mapping , Epitopes/chemistry , Male , Neutralization Tests , Peptides/genetics , Peptides/immunology , Swine
2.
Appl Microbiol Biotechnol ; 97(16): 7417-25, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23836348

ABSTRACT

Mycobacterium abscessus is an important hospital-acquired pathogen involved in infections associated with medical, surgical, and biopharmaceutical materials. In this work, we investigated the pressure-induced inactivation of two strains [2544 and American Type Culture Collection (ATCC) 19977] of M. abscessus in combination with different temperatures and pH conditions. For strain 2544, exposure to 250 MPa for 90 min did not significantly inactivate the bacteria at 20 °C, whereas at -15 °C, there was complete inactivation. Exposure to 250 MPa at ≥60 °C caused rapid inactivation, with no viable bacteria after 45 min. With 45 min of exposure, there were no viable bacteria at any temperature when a higher pressure (350 MPa) was used. Extremes of pH (4 or 9) also markedly enhanced the pressure-induced inactivation of bacteria at 250 MPa, with complete inactivation after 45 min. In comparison, exposure of this strain to the disinfecting agent glutaraldehyde (0.5 %) resulted in total inactivation within 5 min. Strain 19977 was more sensitive to high pressure but less sensitive to glutaraldehyde than strain 2544. These results indicate that high hydrostatic pressure in combination with other physical parameters may be useful in reducing the mycobacterial contamination of medical materials and pharmaceuticals that are sensitive to autoclaving.


Subject(s)
Disinfection/methods , Hydrostatic Pressure , Mycobacterium/physiology , Glutaral/toxicity , Hydrogen-Ion Concentration , Microbial Viability/drug effects , Microbial Viability/radiation effects , Mycobacterium/drug effects , Mycobacterium/radiation effects , Temperature , Time Factors
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