Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review

被引:106
作者
Hatherell, Hollie-Ann [1 ,2 ]
Colijn, Caroline [3 ]
Stagg, Helen R. [2 ]
Jackson, Charlotte [2 ]
Winter, Joanne R. [2 ]
Abubakar, Ibrahim [2 ,4 ]
机构
[1] UCL, CoMPLEX, Mortimer St, London WC1E 6BT, England
[2] UCL, Ctr Infect Dis Epidemiol Infect & Populat Hlt, London WC1E 6JB, England
[3] Univ London Imperial Coll Sci Technol & Med, Dept Math, Huxley Bldg, London SW7 2AZ, England
[4] MRC, Clin Trials Unit, 125 Kingsway, London WC2B 6NH, England
基金
英国工程与自然科学研究理事会; 英国医学研究理事会; 美国国家卫生研究院;
关键词
Whole genome sequencing; Tuberculosis; Transmission; Systematic review; RESISTANT MYCOBACTERIUM-TUBERCULOSIS; DRUG-RESISTANCE; OUTBREAK; MICROEVOLUTION; RELAPSE; STRAIN; HETEROGENEITY; POLYMORPHISM; REINFECTION; RECURRENCE;
D O I
10.1186/s12916-016-0566-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Whole genome sequencing (WGS) is becoming an important part of epidemiological investigations of infectious diseases due to greater resolution and cost reductions compared to traditional typing approaches. Many public health and clinical teams will increasingly use WGS to investigate clusters of potential pathogen transmission, making it crucial to understand the benefits and assumptions of the analytical methods for investigating the data. We aimed to understand how different approaches affect inferences of transmission dynamics and outline limitations of the methods. Methods: We comprehensively searched electronic databases for studies that presented methods used to interpret WGS data for investigating tuberculosis (TB) transmission. Two authors independently selected studies for inclusion and extracted data. Due to considerable methodological heterogeneity between studies, we present summary data with accompanying narrative synthesis rather than pooled analyses. Results: Twenty-five studies met our inclusion criteria. Despite the range of interpretation tools, the usefulness of WGS data in understanding TB transmission often depends on the amount of genetic diversity in the setting. Where diversity is small, distinguishing re-infections from relapses may be impossible; interpretation may be aided by the use of epidemiological data, examining minor variants and deep sequencing. Conversely, when within-host diversity is large, due to genetic hitchhiking or co-infection of two dissimilar strains, it is critical to understand how it arose. Greater understanding of microevolution and mixed infection will enhance interpretation of WGS data. Conclusions: As sequencing studies have sampled more intensely and integrated multiple sources of information, the understanding of TB transmission and diversity has grown, but there is still much to be learnt about the origins of diversity that will affect inferences from these data. Public health teams and researchers should combine epidemiological, clinical and WGS data to strengthen investigations of transmission.
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页数:13
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共 75 条
[1]   Microevolution of Mycobacterium tuberculosis in a Tuberculosis Patient [J].
Al-Hajoj, Sahal A. M. ;
Akkerman, Onno ;
Parwati, Ida ;
Al-Gamdi, Saad ;
Rahim, Zeaur ;
van Soolingen, Dick ;
van Ingen, Jakko ;
Supply, Philip ;
van der Zanden, Adri G. M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2010, 48 (10) :3813-3816
[2]   Genetic hitchhiking [J].
Barton, NH .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2000, 355 (1403) :1553-1562
[3]   Whole genome sequencing reveals genomic heterogeneity and antibiotic purification in Mycobacterium tuberculosis isolates [J].
Black, P. A. ;
de Vos, M. ;
Louw, G. E. ;
van der Merwe, R. G. ;
Dippenaar, A. ;
Streicher, E. M. ;
Abdallah, A. M. ;
Sampson, S. L. ;
Victor, T. C. ;
Dolby, T. ;
Simpson, J. A. ;
van Helden, P. D. ;
Warren, R. M. ;
Pain, A. .
BMC GENOMICS, 2015, 16
[4]   Whole-genome sequencing to establish relapse or re-infection with Mycobacterium tuberculosis: a retrospective observational study [J].
Bryant, Josephine M. ;
Harris, Simon R. ;
Parkhill, Julian ;
Dawson, Rodney ;
Diacon, Andreas H. ;
van Helden, Paul ;
Pym, Alex ;
Mahayiddin, Aziah A. ;
Chuchottaworn, Charoen ;
Sanne, Ian M. ;
Louw, Cheryl ;
Boeree, Martin J. ;
Hoelscher, Michael ;
McHugh, Timothy D. ;
Bateson, Anna L. C. ;
Hunt, Robert D. ;
Mwaigwisya, Solomon ;
Wright, Laura ;
Gillespie, Stephen H. ;
Bentley, Stephen D. .
LANCET RESPIRATORY MEDICINE, 2013, 1 (10) :786-792
[5]   Inferring patient to patient transmission of Mycobacterium tuberculosis from whole genome sequencing data [J].
Bryant, Josephine M. ;
Schurch, Anita C. ;
van Deutekom, Henk ;
Harris, Simon R. ;
de Beer, Jessica L. ;
de Jager, Victor ;
Kremer, Kristin ;
van Hijum, Sacha A. F. T. ;
Siezen, Roland J. ;
Borgdorff, Martien ;
Bentley, Stephen D. ;
Parkhill, Julian ;
van Soolingen, Dick .
BMC INFECTIOUS DISEASES, 2013, 13
[6]   Sequential Bottlenecks Drive Viral Evolution in Early Acute Hepatitis C Virus Infection [J].
Bull, Rowena A. ;
Luciani, Fabio ;
McElroy, Kerensa ;
Gaudieri, Silvana ;
Pham, Son T. ;
Chopra, Abha ;
Cameron, Barbara ;
Maher, Lisa ;
Dore, Gregory J. ;
White, Peter A. ;
Lloyd, Andrew R. .
PLOS PATHOGENS, 2011, 7 (09)
[7]   Evolution and transmission of drug-resistant tuberculosis in a Russian population [J].
Casali, Nicola ;
Nikolayevskyy, Vladyslav ;
Balabanova, Yanina ;
Harris, Simon R. ;
Ignatyeva, Olga ;
Kontsevaya, Irina ;
Corander, Jukka ;
Bryant, Josephine ;
Parkhill, Julian ;
Nejentsev, Sergey ;
Horstmann, Rolf D. ;
Brown, Timothy ;
Drobniewski, Francis .
NATURE GENETICS, 2014, 46 (03) :279-+
[8]   Elucidating Emergence and Transmission of Multidrug-Resistant Tuberculosis in Treatment Experienced Patients by Whole Genome Sequencing [J].
Clark, Taane G. ;
Mallard, Kim ;
Coll, Francesc ;
Preston, Mark ;
Assefa, Samuel ;
Harris, David ;
Ogwang, Sam ;
Mumbowa, Francis ;
Kirenga, Bruce ;
O'Sullivan, Denise M. ;
Okwera, Alphonse ;
Eisenach, Kathleen D. ;
Joloba, Moses ;
Bentley, Stephen D. ;
Ellner, Jerrold J. ;
Parkhill, Julian ;
Jones-Lopez, Edward C. ;
McNerney, Ruth .
PLOS ONE, 2013, 8 (12)
[9]   Mixed-Strain Mycobacterium tuberculosis Infections and the Implications for Tuberculosis Treatment and Control [J].
Cohen, Ted ;
van Helden, Paul D. ;
Wilson, Douglas ;
Colijn, Caroline ;
McLaughlin, Megan M. ;
Abubakar, Ibrahim ;
Warren, Robin M. .
CLINICAL MICROBIOLOGY REVIEWS, 2012, 25 (04) :708-+
[10]   Whole Genome Sequencing of Mycobacterium tuberculosis Reveals Slow Growth and Low Mutation Rates during Latent Infections in Humans [J].
Colangeli, Roberto ;
Arcus, Vic L. ;
Cursons, Ray T. ;
Ruthe, Ali ;
Karalus, Noel ;
Coley, Kathy ;
Manning, Shannon D. ;
Kim, Soyeon ;
Marchiano, Emily ;
Alland, David .
PLOS ONE, 2014, 9 (03)