Rapid drug resistance and transmission profiling of tuberculosis using portable genome sequencing technology
Lead Research Organisation:
London School of Hygiene and Tropical Medicine
Department Name: Infectious and Tropical Diseases
Abstract
Tuberculosis, caused by Mycobacterium tuberculosis (Mtb), remains a serious global health
problem, with increasing drug resistance (DR-TB) complicating disease control. Less than 1/3
of DR-TB cases are detected, contributing to the ongoing transmission and spread of resistant
strains [1]. Current methods for Mtb detection and DR-TB diagnosis are non-timely or use
only limited molecular markers [2]. Rapid tools to detect DR-TB, their transmission, and
understand the genetic diversity of loci interacting with the human host, are urgently
needed. Transmission events can be identified by finding (near-)identical Mtb genomes [3],
and we are applying whole genome sequencing (WGS), bioinformatic and phylogenetic
analysis techniques to understand DR-TB transmissibility globally (including in South Africa
and Thailand). The proposed project will generate both portable Oxford Nanopore MinION
"real-time" and high-throughput Illumina sequencing data with global partnering clinics and
laboratories. We will assess the performance of MinION technology to:
(1) Characterise DR-TB in clinical samples, using both WGS and targeted amplicon candidate
loci assays;
(2) Understand transmission patterns of DR-TB using phylogenetic-based analyses;
(3) Assess genetic diversity in highly variable genes (e.g. pe/ppe families), which can interact
with the human host and are potential vaccine candidates.
A large inhouse WGS dataset of ~37k global Mtb samples (with phenotypic DR-TB data) [2-5]
is immediately available for "mining" using big-data methods, including to understand
genetic diversity in DR-TB loci. The MinION platform, molecular amplicon design tools, and
bioinformatic pipelines are established in our laboratory [2]. The project will be supervised by
Taane Clark (genomic epidemiology, PI on studies generating data), Susana Campino
(microbiology, WGS), and Jody Phelan ((bio)informatics). This project uses cutting-edge
sequencing technologies and "big data" bioinformatics methods, and it is expected to
facilitate the deployment of a MinION platform from bench to near-patient settings. The
project will lead to scientific papers in journals of high standing that provide insights into
transmission and DR-TB genetics.
problem, with increasing drug resistance (DR-TB) complicating disease control. Less than 1/3
of DR-TB cases are detected, contributing to the ongoing transmission and spread of resistant
strains [1]. Current methods for Mtb detection and DR-TB diagnosis are non-timely or use
only limited molecular markers [2]. Rapid tools to detect DR-TB, their transmission, and
understand the genetic diversity of loci interacting with the human host, are urgently
needed. Transmission events can be identified by finding (near-)identical Mtb genomes [3],
and we are applying whole genome sequencing (WGS), bioinformatic and phylogenetic
analysis techniques to understand DR-TB transmissibility globally (including in South Africa
and Thailand). The proposed project will generate both portable Oxford Nanopore MinION
"real-time" and high-throughput Illumina sequencing data with global partnering clinics and
laboratories. We will assess the performance of MinION technology to:
(1) Characterise DR-TB in clinical samples, using both WGS and targeted amplicon candidate
loci assays;
(2) Understand transmission patterns of DR-TB using phylogenetic-based analyses;
(3) Assess genetic diversity in highly variable genes (e.g. pe/ppe families), which can interact
with the human host and are potential vaccine candidates.
A large inhouse WGS dataset of ~37k global Mtb samples (with phenotypic DR-TB data) [2-5]
is immediately available for "mining" using big-data methods, including to understand
genetic diversity in DR-TB loci. The MinION platform, molecular amplicon design tools, and
bioinformatic pipelines are established in our laboratory [2]. The project will be supervised by
Taane Clark (genomic epidemiology, PI on studies generating data), Susana Campino
(microbiology, WGS), and Jody Phelan ((bio)informatics). This project uses cutting-edge
sequencing technologies and "big data" bioinformatics methods, and it is expected to
facilitate the deployment of a MinION platform from bench to near-patient settings. The
project will lead to scientific papers in journals of high standing that provide insights into
transmission and DR-TB genetics.
People |
ORCID iD |
Studentship Projects
| Project Reference | Relationship | Related To | Start | End | Student Name |
|---|---|---|---|---|---|
| BB/T008709/1 | 30/09/2020 | 29/09/2028 | |||
| 2578099 | Studentship | BB/T008709/1 | 30/09/2021 | 29/09/2025 |