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1.
Microbiol Resour Announc ; 12(11): e0049023, 2023 Nov 16.
Article in English | MEDLINE | ID: mdl-37811945

ABSTRACT

Escherichia coli MRE162 was originally isolated from a toilet pan in 1949 and since been utilized in numerous studies. Here, we sequence, assemble, and annotate clones held at three laboratories providing reference-level assemblies. We show the uniqueness of MRE162 to strains in open databases and make the UK clone publically available.

2.
Sci Rep ; 13(1): 2634, 2023 02 14.
Article in English | MEDLINE | ID: mdl-36788326

ABSTRACT

Vibrational spectroscopies offer great potential for standoff detection of chemical and biological warfare agents, avoiding contamination to the operator and equipment. Among them, particularly promising is Coherent anti-Stokes Raman scattering (CARS) spectroscopy, using synchronized pump/Stokes laser pulses to set up a vibrational coherence of target molecules at a laser focus, which is read by further interaction with a probe pulse, resulting in the emission of a coherent beam detectable at a distance. CARS has previously demonstrated the capability to detect bacterial spores based on the Raman spectrum of the characteristic molecule calcium dipicolinate (CaDPA); however, a complex and bulky laser technology, which is only suitable for a laboratory environment, was employed. Here we develop a broadband CARS setup based on a compact, industrial grade ytterbium laser system. We demonstrate high signal-to-noise ratio detection of Bacillus atrophaeus spores at a concentration of 105 cfu/mm2, at a standoff distance of 1 m, and an acquisition time of 1 s. Our system, which combines chemical specificity and sensitivity along with improved ruggedness and portability, paves the way to a new generation of instruments for real-world standoff detection of chemical and biological threats.


Subject(s)
Spectrum Analysis, Raman , Spores, Bacterial , Spectrum Analysis, Raman/methods , Lasers , Vibration
3.
J Immunol Res ; 2014: 392170, 2014.
Article in English | MEDLINE | ID: mdl-24892035

ABSTRACT

Melioidosis is a severe infectious disease caused by Burkholderia pseudomallei. It is refractory to antibiotic treatment and there is currently no licensed vaccine. In this report we detail the construction and protective efficacy of a polysaccharide-protein conjugate composed of B. pseudomallei lipopolysaccharide and the Hc fragment of tetanus toxin. Immunisation of mice with the lipopolysaccharide-conjugate led to significantly reduced bacterial burdens in the spleen 48 hours after challenge and afforded significant protection against a lethal challenge with B. pseudomallei. The conjugate generated significantly higher levels of antigen-specific IgG1 and IgG2a than in lipopolysaccharide-immunised mice. Immunisation with the conjugate also demonstrated a bias towards Th1 type responses, evidenced by high levels of IgG2a. In contrast, immunisation with unconjugated lipopolysaccharide evoked almost no IgG2a demonstrating a bias towards Th2 type responses. This study demonstrates the effectiveness of this approach in the development of an efficacious and protective vaccine against melioidosis.


Subject(s)
Antibodies, Bacterial/biosynthesis , Bacterial Vaccines/immunology , Burkholderia pseudomallei/immunology , Immunoconjugates/administration & dosage , Lipopolysaccharides/immunology , Melioidosis/prevention & control , Peptide Fragments/immunology , Tetanus Toxin/immunology , Animals , Bacterial Vaccines/administration & dosage , Bacterial Vaccines/chemistry , Female , Immunity, Humoral/drug effects , Immunization , Immunoconjugates/chemistry , Immunoconjugates/immunology , Immunoglobulin G/biosynthesis , Lipopolysaccharides/chemistry , Melioidosis/immunology , Melioidosis/microbiology , Melioidosis/mortality , Mice , Mice, Inbred BALB C , Peptide Fragments/chemistry , Recombinant Proteins/chemistry , Recombinant Proteins/immunology , Survival Analysis , Tetanus Toxin/chemistry , Th1-Th2 Balance , Vaccines, Conjugate
4.
PLoS One ; 8(5): e62726, 2013.
Article in English | MEDLINE | ID: mdl-23671629

ABSTRACT

A colorimetric sensor array is a high-dimensional chemical sensor that is cheap, compact, disposable, robust, and easy to operate, making it a good candidate technology to detect pathogenic bacteria, especially potential bioterrorism agents like Yersinia pestis and Bacillus anthracis which feature on the Center for Disease Control and Prevention's list of potential biothreats. Here, a colorimetric sensor array was used to continuously monitor the volatile metabolites released by bacteria in solid media culture in an Advisory Committee on Dangerous Pathogen Containment Level 3 laboratory. At inoculum concentrations as low as 8 colony-forming units per plate, 4 different bacterial species were identified with 100% accuracy using logistic regression to classify the kinetic profile of sensor responses to culture headspace gas. The sensor array was able to further discriminate between different strains of the same species, including 5 strains of Yersinia pestis and Bacillus anthracis. These preliminary results suggest that disposable colorimetric sensor arrays can be an effective, low-cost tool to identify pathogenic bacteria.


Subject(s)
Bacteria/metabolism , Biosensing Techniques/methods , Colorimetry/methods , Gases/analysis , Bacillus anthracis/growth & development , Bacillus anthracis/metabolism , Bacteria/classification , Bacteria/growth & development , Bacterial Typing Techniques/methods , Bioterrorism/prevention & control , Culture Media/metabolism , Gases/chemistry , Gases/metabolism , Logistic Models , Reproducibility of Results , Species Specificity , Yersinia pestis/growth & development , Yersinia pestis/metabolism
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