Association of mannose-binding lectin gene polymorphisms with the development of pulmonary tuberculosis in China
© The Author(s). 2017
Received: 5 August 2016
Accepted: 8 March 2017
Published: 15 March 2017
Mannose-binding lectin (MBL) is an important protein in the lectin pathway of the immune system. This study explores the association between MBL polymorphism and the susceptibility to tuberculosis (TB). The association between the MBL2 polymorphisms and serum MBL levels is also analyzed in the present study.
A total of 112 inpatients with pulmonary TB and 120 healthy controls were recruited to participate in this case–control study. Polymerase Chain Reaction-Restriction Fragment Length Polymorphism(PCR-RFLP) technology was used to genotype MBL gene (variants in −221Y/X and exon l codons 54 A/B). Serum MBL level was assayed by human MBL ELISA kit. Demographic data and exposure information were also obtained from the study participants.
Genotypes YA/YA of MBL gene were more prevalent in the healthy control group than in the TB patient (P =0.038, OR, 0.57; 95% CI, 0.34-0.97) and genotypes XA/XA were less frequent in the healthy control group (P =0.007, OR, 6.42; 95% CI, 1.39-29.67). The resistant diplotype was more frequently found in the younger patients and retreatment cases with TB in MBL gene sites −221Y/X or codon 54 A/B. X/Y and A/B polymorphisms were strong determinants of serum MBL levels.
The polymorphisms of MBL gene may be associated with susceptibility to TB and the recurrence of TB. The YA/YA may be a protected diplotype against TB.
KeywordsMannose-binding lectin (MBL) Polymorphism Susceptibility Tuberculosis
Tuberculosis (TB), an infectious disease caused by Mycobacterium tuberculosis (M. tuberculosis), is responsible for the mortality of approximately two million patients annually. TB is exacerbated by the emergence of multidrug-resistant and extensively drug-resistant (MDR and XDR) bacterial strains . Complex interactions of M. tuberculosis with environmental and host genetic factors play a critical role in TB development. Host genetic factors explain, at least in part, why some people are more or less susceptible to infection . Mannose-binding lectin (MBL) is an acute-phase serum protein in the collection family that recognizes a pathogen by its carbohydrate recognition domain. It is a key molecule of the innate immune system [3, 4]. MBL is encoded by MBL2, located on chromosome 10, and six MBL2 single nucleotide polymorphisms (SNPs) are associated with serum levels and/or functions of MBL. Three nonsynonymous nucleotide substitutions in exon 1 change the wild A allele to the three variant alleles (A/B, A/C, and A/D), which disrupt the collagenous structure and the formation of functional oligomers. The other alleles, H/L, X/Y, and P/Q, are distinguished by the SNPs in the promoter and 5’-untranslated regions, and the X allele shows the lowest transcriptional activity among them .
The impact of MBL gene polymorphism and the susceptibility to TB have been reported before, though the findings are inconsistent between studies. Polymerase chain reaction with sequence-specific primer (PCR-SSP) was often used in these studies. Some studies have found that low levels of serum MBL could reduce tubercle bacilli infections [6, 7], while another study has suggested the opposite [8, 9]. The results of association studies and the risk of TB are also inconsistent among studies.
We explored whether MBL2 polymorphisms or MBL levels are associated with the development of pulmonary TB (PTB) in China, a country with high TB prevalence. In this study, MBL2 -221X/Y and exon l codon 54 A/B gene polymorphism and the susceptibility to TB were evaluated by PCR-RFLP technology. At the same time, MBL levels were also detected.
From January 2010 to December 2011, a total of 112 inpatients (aged 19 to 91 years) diagnosed with PTB consisting of 78 (69.6%) men and 34 (30.4%) women were enrolled in this study. Additionally, 120 healthy donors who had undergone a physical examination in the hospital and were designated healthy were enrolled in this study. The cases and the controls were selected by simple random sampling technique according to random number table method. The inclusion criteria for the pulmonary TB cases was as follows: (1) the diagnosis of TB was based on clinical and radiological findings together with the positive identification of acid-fast bacilli (AFB) or culture; (2) the patient was registered from January 2010 to December 2011; (3) the patient was willing to participate in the study; and (4) complete medical records were available; The exclusion criterion for the cases and controls was as follows: people with comorbidities such as lung carcinoma, asthma, diabetes mellitus and other immunosuppressive conditions or people without providing correct information.
Clinical features of pulmonary TB including hemoptysis, fever, a history of treatment with anti-TB drugs and cavitary lesion as well as age, gender were reviewed.
Estimation of sample size
Sample size estimation was based on an estimated XA frequency of 12%, OR = 2.7, α = 0.05 (paired) and β = 0.20. Based on the above assumptions, 112 patients and 120 healthy controls were enrolled.
Sample collection and DNA extraction
Peripheral blood, 4 ml, was obtained from each patient and control. Samples were centrifuged for 10 min at 3000 g to separate serum. Ethylene diamine tetraacetic acid (EDTA) anticoagulant tubes were used to collect another 2 ml venous blood samples from each participant. A blood DNA isolation kit was used to extract the peripheral white blood cell genome (MBI, USA). The subsequent DNA extraction procedures were performed according to the manufacturer instructions and DNA were stored in a refrigerator at -20 °C.
MBL2 -221X/Y and exon l codon 54 A/B genotyping
We identified the X/Y and A/B gene by PCR-RFLP using the primer 5'-ACCTGGGTTTCCACTC ATTCTCAT-3' and 5'-CCCCAGGCAGTTTCCTCTGGAAGG-3'. The procedure for PCR was 4 min at 95 °C, followed by 35 cycles (95 °C for 30 s, 63 °C for 60 s, 72 °C for 30 s) and 72 °C extension for 5 min. The enzyme digestion reaction system had a volume of 20 μL, including 5 μL purified PCR product, 2 μL 10X buffer, 12 μL ddH2O,1.0 μL of the corresponding restriction endonuclease, Btg I (NEB, USA) to genotype X/Y and BshN I (MBI, USA) to genotype A/B. The digestion reaction system was kept at 37 °C overnight. Five μL of enzyme-digested product was applied to 2% agarose gel. Gel imaging processing system was used to observe the electrophoresis results of the digested PCR products to determine the genotype.
Serum MBL level assay
Serum MBL levels in samples from 112 patients and 120 healthy controls were assayed by human MBL ELISA kit (R&D Systems, USA). Procedures were performed according to manufacturer’s instructions and serum MBL levels between different diplotype groups were compared.
SPSS for Windows, Version 17.0 (Statistical Package for Social Sciences, Chicago, IL, USA) was used for statistical analyses. The chi-square test was used to analyze the data of the genotype frequencies among the different groups. The risk of disease associated with MBL2 genotype was estimated using the calculation of odds ratios with 95% of confidence interval(CI). Serum MBL levels in the TB/healthy control group were analyzed by t test. One-way analysis of variance (ANOVA) was used to compare the MBL levels among the MBL2 diplotype-based groups. The association between the MBL2 polymorphisms and serum MBL levels was analyzed using a multiple regression model. A P value of < 0.05 was considered statistically significant.
Distribution of MBL2 -221X/Y and exon l codon 54 A/B haplotypes in the Chinese population
Haplotypes and their frequencies in the healthy control (n = 120) and TB patients (n = 112)
MBL2 gene polymorphisms in TB patients with different demographic characteristic (n = 112)
exon 1 (codons 54)
A/B + B/B
MBL2 diplotypes in controls and patients with PTB
Patients (n = 112)
Controls (n = 120)
MBL levels in TB patients and control
Serum MBL levels were range from 162.4 to 4963.1 ng/mL. The average of serum MBL levels were significantly higher in patients with TB compared to control subjects (P < 0.01), 2309.1 and 1721.1 ng/mL, respectively.
In this study we used ≤500 ng/mL as the cut-off for low or partial MBL deficiency. The prevalence of MBL deficiency in TB patients and healthy control was 8%, 27.5%, respectively.
Association of MBL2 haplotypes with serum MBL levels in the population
Because of strong linkage disequilibrium, seven haplotypes are commonly observed, and often classified into three groups of higher-producing (HYPA, LYPA, and LYQA), lower-producing (LXPA), and non-functional (LYPB, LYQC, and HYPD) haplotypes . In this study, MBL gene polymorphisms were evaluated (variants in -221Y/X and exon l codons 54 A/B). The YA, XA and YB haplotypes were observed in the Chinese population. Genotypes YA/YA of MBL gene were more prevalent in the healthy control group than in the TB patients (P <0.05), while genotypes XA/XA was six times more frequent in patients with TB than in the healthy control group (P <0.01). The YA/YA may be a protected diplotype against TB compared to XA/XA which may be a susceptible diplotype to TB. This is consistent with the findings of Minako Hijikata and Rosanna Capparelli study [10, 11]. But another study has suggested that X,Y alleles were not associated with PTB from a population in China . In view of the evolutionary history of M. tuberculosis-human interactions, many of the genetic variants occur at relatively high frequencies, but negative consequences to the host could limit selective sweeps. Some researchers highlight cases where evidence of selection pressure is established as a sign that the genetic variant indeed has a strong phenotypic influence on TB . According to different demographic characteristics in TB patients, our study revealed that the promoter -221(Y/X) and exon l codons 54 (A/B) mutation of the MBL gene were significantly different between different ages, and initial or retreatment TB cases. Meanwhile, there was no significant difference among different gender, the presence of fever, cavity, or hemoptysis. The resistant diplotype was more frequently found in the younger patients and retreatment cases with TB in MBL gene sites -221Y/X or codons 54 A/B. Our study revealed that the polymorphisms of MBL gene may be associated with recurrence of TB, and increases the chances of TB infection in the younger age group. This result is a little different from another study conducted in China . All these findings suggest that the occurrence of TB infection is a complicated process.
MBL is a calcium-dependent lectin which is secreted by the liver and binds to several sugars (mannose and N-acetyl-D-glucosamine, in particular) expressed on a wide range of pathogens. MBL has been shown to play an important role in host defense against pathogens including bacteria, fungi, parasites and viruses [14–17]. A study showed that the reduction in serum MBL could increase the chances of TB infection . But it has been proposed in another study that high MBL serum levels may lead to increased TB infections by promoting M. tuberculosis opsonization. By binding to M. tuberculosis, MBL acts as an opsonin, enhances both complement dependent and independent phagocytosis, and promotes inflammation resulting in the release of cytokines. This has been strengthened by studies demonstrating that MBL enhances phagocytic activity against other mycobacteria and demonstration of a protective effect of MBL deficiency against at least some forms of Mycobacterium leprae infection . MBL genotype may be associated with the serum MBL level in the population. Promoter-221(Y/X) mutation can lower the serum MBL level and subsequently increase susceptibility to TB. In this study, Serum MBL levels were significantly lower in control than in patients with TB. MBL deficiency appeared to protect against tuberculosis. We used ≤500 ng/mL as the cut-off for low or partial MBL deficiency. XA/XA or B- carrying diplotypes were considered low or deficient genotypes. Our classification almost matched with the definition by Albert RK .
A literature review and meta-analysis  of 17 clinical trials considering the effect of MBL2 genotype and/or MBL levels and TB infection, reported no significant association between MBL2 genotype and PTB infection. Serum MBL levels were shown to be consistently elevated in the setting of TB infection. This may indicate that high MBL levels may be associated significantly with susceptibility to PTB infection. A recent study showed that passive smoking, cooking with solid fuel, and polymorphisms of MBL gene were associated with susceptibility to TB in non-smokers . The outcome of TB infection and disease depends on interactions between host and pathogen genotypes. Further studies are needed to explore details of the mechanisms of association.
There are six known polymorphism within MBL2 such as Y/X, H/L, P/Q, B, C, D. The B allele is common in Asian population . No or less mutation was found in C, D allele according to our preliminary experiment. At present, only Y/X and A/B polymorphisms were included in this study. We did not analyze the impact of other gene. There may be gene-gene interactions among them associated with TB susceptibility. More gene polymorphism sites and expanded sample size will be analyzed in the future. Although there are some shortages to this study, the possible impacts of non-genetic factors such as age, educational background, alcohol consumption or smoking were adjusted. So the results shown in this study should be reliable.
Our study revealed that the promoter -221 (Y/X) and exon l codons 54 (A/B) mutation of the MBL gene was associated with susceptibility and recurrence of TB. We found that YA/YA, associated with high plasma MBL levels, protected against the development of new cases of PTB. Although many factors are involved in the occurrence and spread of TB such as environment, heredity, and environment within the host, further in-depth understanding of the generation mechanism of TB may provide better ideas to control TB.
Reaction–restriction fragment length polymorphism
Single nucleotide polymorphisms
We appreciated that this manuscript has been edited by native English-speaking experts from BioMed Proofreading LLC.
This work was supported by Beijing health system high-level technical talent (2015-3-097). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
All the data supporting our findings are contained within this manuscript.
Y-LG and YL carried out the design of the study, data analysis,the molecular genetic studies and drafted the manuscript. W-JB and QS participated in specimen collection and carried out the molecular genetic studies. G-LS participated in the design of the study and performed the statistical analysis. All authors read and approved the final manuscript.
The authors declare that they have no competing interests and approve that the manuscript could be uploaded through online submission system.
Consent for publication
Ethics approval and consent to participate
All work was approved by the Institutional Review Boards of the Beijing Tuberculosis and Thoracic Tumor Research Institute. Informed consent was signed by every participant in the study. After each subject had signed a written informed consent form, an in-house questionnaire was used to collect data.
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