Correlates between Models of Virulence for Mycobacterium tuberculosis among Isolates of the Central Asian Lineage: a Case for Lysozyme Resistance Testing?

被引:1
作者
Pardieu, Claire [1 ]
Casali, Nicola [1 ,2 ]
Clark, Simon O. [3 ]
Hooper, Richard [4 ]
Williams, Ann [3 ]
Velji, Preya [1 ]
Gonzalo, Ximena [1 ,2 ]
Drobniewski, Francis [1 ,2 ,5 ]
机构
[1] Queen Mary Univ London, Ctr Immunol & Infect Dis, Clin TB & HIV Grp, London, England
[2] Univ London Imperial Coll Sci Technol & Med, Hammersmith Hosp, Dept Infect Dis & Immun, London, England
[3] Publ Hlth England, Porton Down, Salisbury, Wilts, England
[4] Queen Mary Univ London, Ctr Primary Care & Publ Hlth, London, England
[5] Publ Hlth England, Natl Mycobacterium Reference Lab, London, England
基金
英国惠康基金;
关键词
BEIJING GENOTYPE; NUCLEOTIDE POLYMORPHISMS; BOVIS STRAINS; GUINEA-PIG; DISEASE; COMPLEX; POPULATION; DIVERSITY; INFECTION; VARIANTS;
D O I
10.1128/IAI.03080-14
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Virulence factors (VFs) contribute to the emergence of new human Mycobacterium tuberculosis strains, are lineage dependent, and are relevant to the development of Mycobacterium tuberculosis drugs/vaccines. VFs were sought within Mycobacterium tuberculosis lineage 3, which has the Central Asian (CAS) spoligotype. Three isolates were selected from clusters previously identified as dominant in London, United Kingdom. Strain-associated virulence was studied in guinea pig, monocyte-derived macrophage, and lysozyme resistance assays. Whole-genome sequencing, single nucleotide polymorphism (SNP) analysis, and a literature review contributed to the identification of SNPs of interest. The animal model revealed borderline differences in strain-associated pathogenicity. Ex vivo, isolate C72 exhibited statistically significant differences in intracellular growth relative to C6 and C14. SNP candidates inducing lower fitness levels included 123 unique nonsynonymous SNPs, including three located in genes (lysX, caeA, and ponA2) previously identified as VFs in the laboratory-adapted reference strain H37Rv and shown to confer lysozyme resistance. C72 growth was most affected by lysozyme in vitro. A BLAST search revealed that all three SNPs of interest (C35F, P76Q, and P780R) also occurred in Tiruvallur, India, and in Uganda. Unlike C72, however, no single isolate identified through BLAST carried all three SNPs simultaneously. CAS isolates representative of three medium-sized human clusters demonstrated differential outcomes in models commonly used to estimate strain-associated virulence, supporting the idea that virulence varies within, not just across, Mycobacterium tuberculosis lineages. Three VF SNPs of interest were identified in two additional locations worldwide, which suggested independent selection and supported a role for these SNPs in virulence. The relevance of lysozyme resistance to strain virulence remains to be established.
引用
收藏
页码:2213 / 2223
页数:11
相关论文
共 74 条
  • [21] Joint Effects of Host Genetic Background and Mycobacterial Pathogen on Susceptibility to Infection
    Di Pietrantonio, Tania
    Correa, Jose A.
    Orlova, Marianna
    Behr, Marcel A.
    Schurr, Erwin
    [J]. INFECTION AND IMMUNITY, 2011, 79 (06) : 2372 - 2378
  • [22] A MOBILE FORM OF HENDERSON APPARATUS
    DRUETT, HA
    [J]. JOURNAL OF HYGIENE-CAMBRIDGE, 1969, 67 (03): : 437 - +
  • [23] Faksri K, 2014, ASIAN PAC J ALLERGY, V32, P124, DOI 10.12932/AP0361.32.2.2013
  • [24] Virulence factors of the Mycobacterium tuberculosis complex
    Forrellad, Marina A.
    Klepp, Laura I.
    Gioffre, Andrea
    Sabio y Garcia, Julia
    Morbidoni, Hector R.
    de la Paz Santangelo, Mara
    Cataldi, Angel A.
    Bigi, Fabiana
    [J]. VIRULENCE, 2013, 4 (01) : 3 - 66
  • [25] Variable host-pathogen compatibility in Mycobacterium tuberculosis
    Gagneux, S
    DeRiemer, K
    Van, T
    Kato-Maeda, M
    de Jong, BC
    Narayanan, S
    Nicol, M
    Niemann, S
    Kremer, K
    Gutierrez, MC
    Hilty, M
    Hopewell, PC
    Small, PM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (08) : 2869 - 2873
  • [26] Global phylogeography of Mycobacterium tuberculosis and implications for tuberculosis product development
    Gagneux, Sebastien
    Small, Peter M.
    [J]. LANCET INFECTIOUS DISEASES, 2007, 7 (05) : 328 - 337
  • [27] Antimicrobial polypeptides in host defense of the respiratory tract
    Ganz, T
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (06) : 693 - 697
  • [28] Unexpected Role for IL-17 in Protective Immunity against Hypervirulent Mycobacterium tuberculosis HN878 Infection
    Gopal, Radha
    Monin, Leticia
    Slight, Samantha
    Uche, Uzodinma
    Blanchard, Emmeline
    Junecko, Beth A. Fallert
    Ramos-Payan, Rosalio
    Stallings, Christina L.
    Reinhart, Todd A.
    Kolls, Jay K.
    Kaushal, Deepak
    Nagarajan, Uma
    Rangel-Moreno, Javier
    Khader, Shabaana A.
    [J]. PLOS PATHOGENS, 2014, 10 (05)
  • [29] Evidence that the spread of Mycobacterium tuberculosis strains with the Beijing genotype is human population dependent
    Hanekom, M.
    van der Spuy, G. D.
    Gey van Pittius, N. C.
    McEvoy, C. R. E.
    Ndabambi, S. L.
    Victor, T. C.
    Hoal, E. G.
    van Helden, P. D.
    Warren, R. M.
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2007, 45 (07) : 2263 - 2266
  • [30] A recently evolved sublineage of the Mycobacterium tuberculosis Beijing strain family is associated with an increased ability to spread and cause disease
    Hanekom, M.
    van der Spuy, G. D.
    Streicher, E.
    Ndabambi, S. L.
    McEvoy, C. R. E.
    Kidd, M.
    Beyers, N.
    Victor, T. C.
    van Helden, P. D.
    Warren, R. M.
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2007, 45 (05) : 1483 - 1490