Impact of passive smoking, cooking with solid fuel exposure, and MBL/MASP-2 gene polymorphism upon susceptibility to tuberculosis

International Journal of Infectious Diseases

Volumn 29, Issue , 2014, Pages 1-6

  Chen, Mengshi ^a,e   Deng, Jing ^a   Su, Congxu ^b   Li, Jun ^c   Wang, Mian ^a   Abuaku, Benjamin Kwaku ^a   Hu, ShiMin ^a   Tan, Hongzhuan ^a   Wen, Shi Wu ^a,d  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b Yueyanglou Center for Disease Control and Prevention   (China)

^c HUNAN CANCER HOSPITAL   (China)

^d UNIVERSITY OF OTTAWA   (Canada)

^e HUNAN CHILDREN'S HOSPITAL   (China)

Author keywords

Cooking with solid fuel; Gene environment interaction; MASP 2; MBL; Passive smoking; Tuberculosis

Indexed keywords

FUEL; MANNAN BINDING LECTIN ASSOCIATED SERINE PROTEINASE; MANNOSE BINDING LECTIN; MASP2 PROTEIN, HUMAN; PASSIVE SMOKING;

ADULT; AGED; ARTICLE; BCG VACCINATION; CASE CONTROL STUDY; CONTROLLED STUDY; COOKING; DNA POLYMORPHISM; DRINKING BEHAVIOR; ENVIRONMENTAL EXPOSURE; EXPOSURE; FEMALE; GENE; GENOTYPE; GENOTYPE ENVIRONMENT INTERACTION; HUMAN; INFECTION SENSITIVITY; LUNG TUBERCULOSIS; MAJOR CLINICAL STUDY; MALE; MASP 2 GENE; MBL GENE; PASSIVE SMOKING; POLYMERASE CHAIN REACTION; RISK ASSESSMENT; ROOM VENTILATION; DISEASE PREDISPOSITION; GENETIC POLYMORPHISM; GENETICS; MIDDLE AGED; TUBERCULOSIS; VERY ELDERLY; YOUNG ADULT;

ADULT; AGED; AGED, 80 AND OVER; CASE-CONTROL STUDIES; COOKING; DISEASE SUSCEPTIBILITY; ENVIRONMENTAL EXPOSURE; FEMALE; GENE-ENVIRONMENT INTERACTION; GENOTYPE; HUMANS; MALE; MANNOSE-BINDING LECTIN; MANNOSE-BINDING PROTEIN-ASSOCIATED SERINE PROTEASES; MIDDLE AGED; POLYMORPHISM, GENETIC; TOBACCO SMOKE POLLUTION; TUBERCULOSIS; YOUNG ADULT;

EID: 84922779197     PISSN: 12019712     EISSN: 18783511     Source Type: Journal    
DOI: 10.1016/j.ijid.2014.08.010     Document Type: Article

References (46)

1. Bates M.N., Khalakdina A., Pai M., Chang L., Lessa F., Smith K.R. Risk of tuberculosis from exposure to tobacco smoke: a systematic review and meta-analysis. Arch Intern Med 2007, 167:335-342.
2. Slama K., Chiang C.Y., Enarson D.A., Hassmiller K., Fanning A., Gupta P., et al. Tobacco and tuberculosis: a qualitative systematic review and meta-analysis. Int J Tuberc Lung Dis 2007, 11:1049-1061.
3. Lin H.H., Ezzati M., Murray M. Tobacco smoke, indoor air pollution and tuberculosis: a systematic review and meta-analysis. PLoS Med 2007, 4:e20.
4. Lin H.H., Chiang Y.T., Chuang J.H., Yang S.L., Chang H.Y., Ezzati M., et al. Exposure to secondhand smoke and risk of tuberculosis: prospective cohort study. PLoS One 2013, 8:e77333.
5. den Boon S., Verver S., Marais B.J., Enarson D.A., Lombard C.J., Bateman E.D., et al. Association between passive smoking and infection with Mycobacterium tuberculosis in children. Pediatrics 2007, 119:734-739.
6. Leung C.C., Lam T.H., Ho K.S., Yew W.W., Tam C.M., Chan W.M., et al. Passive smoking and tuberculosis. Arch Intern Med 2010, 170:287-292.
7. Patra S., Sharma S., Behera D. Passive smoking, indoor air pollution and childhood tuberculosis: a case control study. Indian J Tuberc 2012, 59:151-155.
8. Kan X., Chiang C.Y., Enarson D.A., Chen W., Yang J., Chen G. Indoor solid fuel use and tuberculosis in China: a matched case-control study. BMC Public Health 2011, 11:498.
9. Lakshmi P.V., Virdi N.K., Thakur J.S., Smith K.R., Bates M.N., Kumar R. Biomass fuel and risk of tuberculosis: a case-control study from northern India. J Epidemiol Community Health 2012, 66:457-461.
10. Kolappan C., Subramani R. Association between biomass fuel and pulmonary tuberculosis: a nested case-control study. Thorax 2009, 64:705-708.
11. Madsen H.O., Garred P., Thiel S., Kurtzhals J.A., Lamm L.U., Ryder L.P., et al. Interplay between promoter and structural gene variants control basal serum level of mannan-binding protein. J Immunol 1995, 155:3013-3020.
12. Boldt A.B., Petzl-Erler M.L. A new strategy for mannose-binding lectin gene haplotyping. Hum Mutat 2002, 19:296-306.
13. Heitzeneder S., Seidel M., Forster-Waldl E., Heitger A. Mannan-binding lectin deficiency-good news, bad news, doesn't matter?. Clin Immunol 2012, 143:22-38.
14. Selvaraj P., Jawahar M.S., Rajeswari D.N., Alagarasu K., Vidyarani M., Narayanan P.R. Role of mannose binding lectin gene variants on its protein levels and macrophage phagocytosis with live Mycobacterium tuberculosis in pulmonary tuberculosis. FEMS Immunol Med Microbiol 2006, 46:433-437.
15. Soborg C., Madsen H.O., Andersen A.B., Lillebaek T., Kok-Jensen A., Garred P. Mannose-binding lectin polymorphisms in clinical tuberculosis. J Infect Dis 2003, 188:777-782.
16. da Cruz H.L., da Silva R.C., Segat L., de Carvalho M.S., Brandao L.A., Guimaraes R.L., et al. MBL2 gene polymorphisms and susceptibility to tuberculosis in a northeastern Brazilian population. Infect Genet Evol 2013, 19:323-329.
17. Liu W., Zhang F., Xin Z.T., Zhao Q.M., Wu X.M., Zhang P.H., et al. Sequence variations in the MBL gene and their relationship to pulmonary tuberculosis in the Chinese Han population. Int J Tuberc Lung Dis 2006, 10:1098-1103.
18. Thiel S., Steffensen R., Christensen I.J., Ip W.K., Lau Y.L., Reason I.J., et al. Deficiency of mannan-binding lectin associated serine protease-2 due to missense polymorphisms. Genes Immun 2007, 8:154-163.
19. Thiel S., Kolev M., Degn S., Steffensen R., Hansen A.G., Ruseva M., et al. Polymorphisms in mannan-binding lectin (MBL)-associated serine protease 2 affect stability, binding to MBL, and enzymatic activity. J Immunol 2009, 182:2939-2947.
20. Boldt A.B., Luz P.R., Messias-Reason I.J. MASP2 haplotypes are associated with high risk of cardiomyopathy in chronic Chagas disease. Clin Immunol 2011, 140:63-70.
21. Sorensen R., Thiel S., Jensenius J.C. Mannan-binding-lectin-associated serine proteases, characteristics and disease associations. Springer Semin Immunopathol 2005, 27:299-319.
22. Tulio S., Faucz F.R., Werneck R.I., Olandoski M., Alexandre R.B., Boldt A.B., et al. MASP2 gene polymorphism is associated with susceptibility to hepatitis C virus infection. Hum Immunol 2011, 72:912-915.
23. Le Hir H., Nott A., Moore M.J. How introns influence and enhance eukaryotic gene expression. Trends Biochem Sci 2003, 28:215-220.
24. Niu D.K., Yang Y.F. Why eukaryotic cells use introns to enhance gene expression: splicing reduces transcription-associated mutagenesis by inhibiting topoisomerase I cutting activity. Biol Direct 2011, 6:24.
25. Ministry of Health of China. Diagnostic criteria for pulmonary tuberculosis. Ministry of Health of China; 2008.
26. Berhe G., Enquselassie F., Aseffa A. Assessment of risk factors for development of active pulmonary tuberculosis in northern part of Ethiopia: a matched case control study. Ethiop Med J 2013, 51:227-237.
27. Chen M., Kwaku A.B., Chen Y., Huang X., Tan H., Wen S.W. Gender and regional disparities of tuberculosis in Hunan, China. Int J Equity Health 2014, 13:32.
28. VanderWeele T.J., Vansteelandt S. A weighting approach to causal effects and additive interaction in case-control studies: marginal structural linear odds models. Am J Epidemiol 2011, 174:1197-1203.
29. Hoyt J.C., Robbins R.A., Habib M., Springall D.R., Buttery L.D., Polak J.M., et al. Cigarette smoke decreases inducible nitric oxide synthase in lung epithelial cells. Exp Lung Res 2003, 29:17-28.
30. Rubbo H., Radi R., Trujillo M., Telleri R., Kalyanaraman B., Barnes S., et al. Nitric oxide regulation of superoxide and peroxynitrite-dependent lipid peroxidation. Formation of novel nitrogen-containing oxidized lipid derivatives. J Biol Chem 1994, 269:26066-26075.
31. Davies P.D., Yew W.W., Ganguly D., Davidow A.L., Reichman L.B., Dheda K., et al. Smoking and tuberculosis: the epidemiological association and immunopathogenesis. Trans R Soc Trop Med Hyg 2006, 100:291-298.
32. Zhang L., Cui Y., Wang C., Jiang Y., Yang L. [Survey on status of smoking, passive smoking and quitting smoking in rural areas of the midwestern provinces in China]. Zhonghua Liu Xing Bing Xue Za Zhi 2013, 34:137-139.
33. Garcia-Sancho M.C., Garcia-Garcia L., Baez-Saldana R., Ponce-De-Leon A., Sifuentes-Osornio J., Bobadilla-Del-valle M., et al. Indoor pollution as an occupational risk factor for tuberculosis among women: a population-based, gender oriented, case-control study in southern Mexico. Rev Invest Clin 2009, 61:392-398.
34. Gninafon M., Ade G., Ait-Khaled N., Enarson D.A., Chiang C.Y. Exposure to combustion of solid fuel and tuberculosis: a matched case-control study. Eur Respir J 2011, 38:132-138.
35. Adewole O.O., Desalu O.O., Nwogu K.C., Adewole T.O., Erhabor G.E. Respiratory symptoms and lung function patterns in workers exposed to wood smoke and cooking oil fumes (mai suya) in Nigeria. Ann Med Health Sci Res 2013, 3:38-42.
36. Speaks J.T., Thomas E.C., Thompson L.M. Household air pollution from cooking fires: a challenge for nurses globally and a call to action. J Community Health Nurs 2012, 29:236-244.
37. Ward E.C., Murray M.J., Lauer L.D., House R.V., Dean J.H. Persistent suppression of humoral and cell-mediated immunity in mice following exposure to the polycyclic aromatic hydrocarbon 7,12-dimethylbenz[a]anthracene. Int J Immunopharmacol 1986, 8:13-22.
38. Miyata R., van Eeden S.F. The innate and adaptive immune response induced by alveolar macrophages exposed to ambient particulate matter. Toxicol Appl Pharmacol 2011, 257:209-226.
39. Ferecatu I., Borot M.C., Bossard C., Leroux M., Boggetto N., Marano F., et al. Polycyclic aromatic hydrocarbon components contribute to the mitochondria-antiapoptotic effect of fine particulate matter on human bronchial epithelial cells via the aryl hydrocarbon receptor. Part Fibre Toxicol 2010, 7:18.
40. Akhtar U.S., McWhinney R.D., Rastogi N., Abbatt J.P., Evans G.J., Scott J.A. Cytotoxic and proinflammatory effects of ambient and source-related particulate matter (PM) in relation to the production of reactive oxygen species (ROS) and cytokine adsorption by particles. Inhal Toxicol 2010, 22(Suppl 2):37-47.
41. Wang G., Zhao J., Jiang R., Song W. Rat lung response to ozone and fine particulate matter (PM) exposures. Environ Toxicol 2013, http://10.1002/tox.21912.
42. Vasconcelos L.R., Fonseca J.P., do Carmo R.F., de Mendonca T.F., Pereira V.R., Lucena-Silva N., et al. Mannose-binding lectin serum levels in patients with leprosy are influenced by age and MBL2 genotypes. Int J Infect Dis 2011, 15:e551-e557.
43. Wiertsema S.P., Herpers B.L., Veenhoven R.H., Salimans M.M., Ruven H.J., Sanders E.A., et al. Functional polymorphisms in the mannan-binding lectin 2 gene: effect on MBL levels and otitis media. J Allergy Clin Immunol 2006, 117:1344-1350.
44. Carmolli M., Duggal P., Haque R., Lindow J., Mondal D., Petri W.A., et al. Deficient serum mannose-binding lectin levels and MBL2 polymorphisms increase the risk of single and recurrent Cryptosporidium infections in young children. J Infect Dis 2009, 200:1540-1547.
45. Sorensen G.L., Petersen I., Thiel S., Fenger M., Christensen K., Kyvik K.O., et al. Genetic influences on mannan-binding lectin (MBL) and mannan-binding lectin associated serine protease-2 (MASP-2) activity. Genet Epidemiol 2007, 31:31-41.
46. Ying S.Y., Lin S.L. Intron-mediated RNA interference and microRNA biogenesis. Methods Mol Biol 2009, 487:387-413.