Courses

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Flyer Tuberculosis, Shezhen 2018

Flyer Tuberculosis, Shezhen 2018


IP International TB course


Epidemiology of TB

Overview of the Epidemiology of Tuberculosis

Philippe Glaziou, Howard Takiff, Institut Pasteur, France

Population Structures and Evolution of M. Tuberculosis

Iñaki Comas, Biomedicine Institute of Valencia (IBV-CSIC), Spain

TB Molecular Epidemiology

Qian Gao, Fudan University


TB in China

Risk Response to Public Health Incidents

Qiulan Yang Deputy Editor of Health News PDF in Chinese.

Informatization Facilitates the Prevention and Control of TB

Liang Chen, Guagdong TB Control Center. PDF in Chinese

A handheld App for DOTS Therapy

Shengyuan Liu, Nanshan CCDC. PDF in Chinese.


Clinical aspects, NTM

Clinical Aspects in Tuberculosis

Steffen Stenger, Ulm University, Germany

Pediatric TB

Christophe Delacourt, Necker Children’s Hospital , France

TB HIV/Diabetes

Véronique Joly, Hospital Bichat–Claude Bernard, France

NTM Detection and Speciation; When to Treat

Jean-Louis Herrmann, Hospital Raymond Poincaré , France


Diagnosis

Phenotypic and Molecular Tests for Diagnosis

Catherine Pierre-Audigier, Hospital Bichat–Claude Bernard; Institut Pasteur, France

IGRA and Biomarkers

Elisabeth Bouvet, Hospital Bichat–Claude Bernard, France

Current and Future Technical Options for MDR Diagnosis

Francis Drobniewski, Imperial College, London

Clinical Usefulness of WGS

Howard Takiff Institut Pasteur, France

Evaluation of New Diagnostic Techniques

Howard Takiff, Institut Pasteur, France


Fight and treatment

The Fight Against Tuberculosis-General Aspects

Steffen Stenger, Ulm University, Germany

Treatment of Tuberculosis

Wenhong Zhang, Hua Shan Hospital

Short-Term Treatment of MDR-TB

Arnaud Trébucq, Union Against Tuberculosis and Lung Disease, France

Treatment of MDR-TB and XDR-TB

Nicolas Veziris, Hospital Pitié Salpétrière, France

Drug Discovery

Vincent Delorme, Institut Pasteur, Korea

New Drugs, New Regimens, Drug Trials

Ray Chen, NIAID, NIH, USA

Drug resitance mechanisms in M. tuberculosis

Ying Zhang, Johns Hopkings University, Baltimore, USA


Practical session

Practical session


-Practical session

-Practical session


Students

Students


Flyer Tuberculosis course , Paris 2017

Flyer Tuberculosis course , Paris 2017


Introduction

One third of the world population is infected with Tuberculosis and at risk to develop the disease. The WHO estimates that there are more than nine million new TB cases and 1,5 million deaths from TB each year. Multi-drug resistant (MDR) strains are a growing problem, with 500 000 new cases every year, 10% of these being extremely drug resistant (XDR). Many laboratories and international consortia are searching for effective new drugs and vaccines, and clinical trials are testing new therapeutic regimens to shorten standardized treatment. However, despite considerable efforts for the discovery of new drugs, only ten new antibiotic candidates or repurposed drugs have been subjected to preclinical trials.


Perhaps the greatest progress has been in the introduction of rapid diagnostic tools based on molecular biology. The incorporation of new technologies has revolutionized the detection of microbial pathogens and antibiotic resistance. The growing availability of high capacity sequencing has opened new doors for understanding host-pathogen interactions and immunological responses by identifying critical determinants in both the bacterial and the human genomes.


The training course will review all techniques currently used for the rapid diagnosis of tuberculosis and detection of antibiotic resistance, and provide a background on the genetic basis of the tests.


Genomics markers are used to study tuberculosis transmission and also the phylogeny and evolution of M. tuberculosis complex bacteria. The first techniques were based on the detection of polymorphisms in repeated DNA sequences, but newer, more precise tools are based on single nucleotide polymorphisms. These tools are useful for molecular epidemiology but need to be practiced and evaluated to determine if they are appropriate for local and regional mycobacterial laboratories.


The course will include lectures by international experts to provide up-to-date information on all of these new developments in the study and control of Tuberculosis. Lectures will cover general aspects of Tuberculosis including the immune response, diagnosis, drug susceptibility testing, treatment of MDR-TB, evolution of the M. tuberculosis complex bacteria and molecular epidemiology. In the practical sessions the participants will work with the latest PCR-based diagnostic and drug susceptibility tests commercially available. They will also identify resistance using DNA sequencing of antibiotic resistance determinants and learn how genomic analysis can be used for complete drug sensitivity determination. All of the topics discussed are posted on the WEB site www.moleculartb.org.


The tuberculosis course at the Institut Pasteur in Paris promotes laboratory up-grading, intercontinental exchanges and the discussion of future projects amongst the participants. It is an exceptional opportunity for the participants to acquire new knowledge and to exchange experiences and critically analyze the utility of the techniques in the context of their own countries. The course will stress the importance of implementing the right tools in the right settings for optimal efficacy.





Protocols

Staining and Microscopy

Microscopic examination is a fast and cheap method to detect acid-fast bacilli (AFB) in stained clinical specimens smears. Both living and dead (viable and non-viable) bacilli will stain and be counted. A positive direct smear is suggestive of contagious Tuberculosis.

Amplification test set-up

How to organize amplification methods to prevent false positive result.

Agarose Gel Electrophoresis

Gel electrophoresis is a method for separation and analysis of amplified DNA fragments, based on their size and charge. The protocol describes how to prepare agarose gel, load samples and migrate by applying an electric field.

Antibiotic Resistance Sequencing

Sequencing of specific genes allows to detection of mutations known to be associated to antibiotic resistance and the prediction of their resistance level Target genes – or part of them – are here amplified and sequenced. Results are compared to wild type sequence of each target gene. Mutations are compared to mutations known to be associated with antibiotic resistance.

Mycobacteria sputum culture with Kudoh method

Description of the simple and inexpensive Ogawa-Kudoh method that doesn’t require a centrifugation step for the culture of clinical samples.

Spoligotyping

Spoligotyping is a molecular fingerprinting method based on the "Direct Repeat" (DR) region, which is uniquely present in Mycobacterium tuberculosis com¬plex bacteria. The DR region in M. bovis BCG consists of directly repeated sequences of 36 base pairs, which are interspersed by non-repetitive DNA spacers. By spoligotyping one can detect the presence or absence of spacers of known sequence to compare M. tuberculosis com¬plex strains.

MIRU/VNTR

Multilocus Variable Number Tandem Repeat Genotyping of Mycobacterium tuberculosis. Here is presented the discriminatory subset of 15 loci with the highest evolutionary rates proposed as the MIRU standard for routine epidemiological discrimination of M. tuberculosis isolates, using simpler electrophoresis with agarose gels.

HAIN GenoType®

GenoType® is a Line Probe Assay for identification of the M. tuberculosis complex from pulmonary clinical specimens or cultivated samples and its resistance to Rifampicin and/or Isoniazid (GenoType® MTBDRplus kit) and Fluoroquinolones and Aminoglycosides/Cyclic Peptides (GenoType® MTBDRsl ver 2.0 kit). The whole procedure includes DNA extraction from clinical or cultivated samples, a multiplex amplification with biotinilated primers and reverse hybridization.

CEPHEID Xpert® MTB/RIF

The Xpert MTB/RIF test for use with the Cepheid GeneXpert® System is a semi-quantitative nested real-time PCR in vitro diagnostic test for detection of M. tuberculosis complex DNA and detection of rifampin- resistance associated mutations of the rpoB gene from clinical samples.


Programme

Program 2017 TB course