Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add more filters










Database
Language
Publication year range
1.
Rev Sci Instrum ; 90(6): 063902, 2019 Jun.
Article in English | MEDLINE | ID: mdl-31255007

ABSTRACT

A specially developed experimental platform to measure the wettability of molten metals on solid substrates under high magnetic fields in combination with the sessile drop method is presented in this work. The desired magnetic field was generated by a superconducting magnet containing a channel with a diameter of 300 mm, in which the main body of the experimental apparatus was installed. The developed setup was used to observe the in situ wetting behavior of a molten metal on a solid substrate and simultaneously record sample images in real time under a high magnetic field during the wetting process. Contact angles were determined by analyzing the recorded images with the help of analytical software. Experiments using a typical molten metal and a solid substrate were conducted. The results revealed that the wettability of the molten metal on the solid substrate was obviously improved under a high external magnetic field.

2.
Sci Rep ; 6: 28827, 2016 07 01.
Article in English | MEDLINE | ID: mdl-27363681

ABSTRACT

Anthrax is a disease caused by Bacillus anthracis. Specifically, the anthrax toxins and capsules encoded by the pXO1 and pXO2 plasmids, respectively, are the major virulence factors. We previously reported that the pXO1 plasmid was retained in the attenuated strain of B. anthracis vaccine strains even after subculturing at high temperatures. In the present study, we reinvestigate the attenuation mechanism of Pasteur II. Sequencing of pXO1 and pXO2 from Pasteur II strain revealed mutations in these plasmids as compared to the reference sequences. Two deletions on these plasmids, one each on pXO1 and pXO2, were confirmed to be unique to the Pasteur II strain as compared to the wild-type strains. Gene replacement with homologous recombination revealed that the mutation in the promoter region of the pagR gene on pXO2, but not the mutation on pXO1, contributes to lethal levels of toxin production. This result was further confirmed by RT-PCR, western blot, and animal toxicity assays. Taken together, our results signify that the attenuation of the Pasteur II vaccine strain is caused by a mutation in the pagR gene on its pXO2 plasmid. Moreover, these data suggest that pXO2 plasmid encoded proteins are involved in the virulence of B. anthracis.


Subject(s)
Bacillus anthracis/genetics , Bacterial Proteins/genetics , Plasmids/genetics , Repressor Proteins/genetics , Animals , Anthrax/virology , Antigens, Bacterial/genetics , Antigens, Bacterial/metabolism , Bacillus anthracis/metabolism , Bacillus anthracis/pathogenicity , Bacterial Proteins/classification , Bacterial Proteins/metabolism , Bacterial Toxins/genetics , Bacterial Toxins/metabolism , Base Sequence , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Male , Mice, Inbred BALB C , Mutation , Plasmids/metabolism , Promoter Regions, Genetic/genetics , Repressor Proteins/classification , Repressor Proteins/metabolism , Sequence Analysis, DNA , Survival Analysis , Virulence/genetics
3.
Virulence ; 7(5): 578-86, 2016 07 03.
Article in English | MEDLINE | ID: mdl-27029580

ABSTRACT

Anthrax toxins and capsule are the major virulence factors of Bacillus anthracis. They are encoded by genes located on the plasmids pXO1 and pXO2, respectively. The vaccine strain Pasteur II was produced from high temperature subcultures of B. anthracis, which resulted in virulence attenuation through the loss of the plasmid pXO1. However, it is unclear whether the high temperature culture completely abolishes the plasmid DNA or affects the replication of the plasmid pXO1. In this study, we tested 3 B. anthracis vaccine strains, including Pasteur II from France, Qiankefusiji II from Russia, and Rentian II from Japan, which were all generated from subcultures at high temperatures. Surprisingly, we detected the presence of pXO1 plasmid DNA using overlap PCR in all these vaccine strains. DNA sequencing analysis of overlap PCR products further confirmed the presence of pXO1. Moreover, the expression of the protective antigen (PA) encoded on pXO1 was determined by using SDS-PAGE and western blotting. In addition, we mimicked Pasteur's method and exposed the A16R vaccine strain, which lacks the pXO2 plasmid, to high temperature, and identified the pXO1 plasmid in the subcultures at high temperatures. This indicated that the high temperature treatment at 42.5°C was unable to eliminate pXO1 plasmid DNA from B. anthracis. Our results suggest that the attenuation of the Pasteur II vaccine strain is likely due to the impact of high temperature stress on plasmid replication, which in turn limits the copy number of pXO1. Our data provide new insights into the mechanisms of the remaining immunogenicity and toxicity of the vaccine strains.


Subject(s)
Anthrax Vaccines/genetics , Bacillus anthracis/genetics , Plasmids , Vaccines, Attenuated/genetics , Anthrax Vaccines/immunology , Antigens, Bacterial/genetics , Bacillus anthracis/immunology , Bacillus anthracis/pathogenicity , Bacterial Toxins/genetics , DNA, Bacterial/analysis , Hot Temperature , Immunogenicity, Vaccine , Plasmids/genetics , Plasmids/isolation & purification , Polymerase Chain Reaction , Vaccines, Attenuated/immunology , Virulence , Virulence Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...