Use of microvirin in the identification of mycobacterium tuberculosis mannose-capped lipoarabinomannan
US-2024085416-A1 · Mar 14, 2024 · US
US12007392B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12007392-B2 |
| Application number | US-201916585391-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 27, 2019 |
| Priority date | Sep 27, 2018 |
| Publication date | Jun 11, 2024 |
| Grant date | Jun 11, 2024 |
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The present invention provides a semi-quantitative phage-based assay for Mycobacterial infection, in which the phage assay plaque count correlates to the number of viable Mycobacterial organisms in the subject sample, and methods of use thereof for diagnosing, treating or monitoring Mycobacterial infection.
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We claim: 1. A method of treating Crohn's Disease in a subject in need thereof comprising the steps of: a) obtaining a human blood or peripheral blood mononuclear cell (PBMC) sample from a subject diagnosed with Crohn's Disease; b) lysing cells of the sample to release any viable target mycobacterial cell; c) admixing a broad host range mycobacteriophage with the sample under conditions suitable to allow the bacteriophage to infect any viable target mycobacterial cell present in the sample; d) removing any bacteriophage not infecting a viable target mycobacterial cell; e) admixing at least a portion of the admixture of step c) following the removal of step d) with bacteria capable of supporting replication of the bacteriophage; f) plating at least a portion of the admixture of step e) on a substrate to support growth of the bacteria; g) quantifying the number of bacteriophage plaques that form; h) discriminating between infected and asymptomatic subjects, comprising identifying the subject as infected when the number of bacteriophage plaques is statistically significantly greater than a reference number of bacteriophage plaques, or as asymptomatic when the number of bacteriophage plaques is not statistically significantly greater than a reference number of bacteriophage plaques, wherein the reference number of bacteriophage plaques is a reference number of plaques in asymptomatic human hosts; and i) administering a pharmaceutical composition for inhibiting or disrupting microorganism growth or treating a microbial infection to a subject identified as infected. 2. The method of claim 1 , wherein the cells are lysed by osmotic shock. 3. The method of claim 1 , wherein the sample is from a human suspected of being infected with the target mycobacterial cell. 4. The method of claim 3 , wherein the target mycobacterial cell is selected from the group consisting of Mycobacterium avium subspecies paratuberculosis (MAP), Mycobacterium avium complex (MAC), Mycobacterium avium hominissuis (MAH), Mycobacterium tuberculosis (MTB), Mycobacterium leprae, Mycobacterium vaccae, Mycobacterium celatum, Mycobacterium kansasii, Mycobacterium gordonae, Mycobacterium porcinum, Mycobacterium cheloni, Mycobacterium flavescens, Mycobacterium bovis, Mycobacterium sylvaticum and Mycobacterium bovis Bacillus Calmette Guerin (BCG). 5. The method of claim 1 wherein the bacteriophage is D29 or TM4. 6. The method of claim 1 further comprising the step of analyzing DNA from a lysed target mycobacterial cell obtained from a bacteriophage plaque to identify a signature DNA sequence that occurs in the target mycobacterial cell. 7. The method of claim 6 wherein the DNA is analyzed by a method selected from the group consisting of whole genome sequencing (WGS) and a PCR based DNA amplification system. 8. The method of claim 6 wherein the DNA is analyzed by PCR using primers that anneal specifically to a signature DNA sequence that occurs in the target mycobacterial cell. 9. The method of claim 8 , wherein the signature DNA sequence is selected from the group consisting of IS900, IS1245, f57 and IS6110. 10. The method of claim 1 , further comprising a step of identifying latent paratuberculosis in asymptomatic humans.
Bowel diseases, e.g. Crohn, ulcerative colitis, IBS · CPC title
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