Evaluation of Rv0220, Rv2958c, Rv2994 and Rv3347c of M ycobacterium tuberculosis for serodiagnosis of tuberculosis
Tuberculosis ( TB ), the leading cause of death among infectious diseases worldwide, is caused by Mycobacterium tuberculosis ( M. tuberculosis ). Early accurate diagnosis means earlier prevention, treatment and control of TB . To confirm efficient diagnostic antigens for M. tuberculosis , the serodi...
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Veröffentlicht in: | Microbial biotechnology 2017-05, Vol.10 (3), p.604-611 |
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Zusammenfassung: | Tuberculosis (
TB
), the leading cause of death among infectious diseases worldwide, is caused by
Mycobacterium tuberculosis
(
M. tuberculosis
). Early accurate diagnosis means earlier prevention, treatment and control of
TB
. To confirm efficient diagnostic antigens for
M. tuberculosis
, the serodiagnosis value of four recombinant proteins including Rv0220, Rv2958c, Rv2994 and Rv3347c was evaluated in this study. The specificities and sensitivities of four recombinant proteins were determined based on enzyme‐linked immunosorbent assay (
ELISA
) by screening sera from smear‐positive pulmonary
TB
patients (
n
= 92), uninfected individuals (
n
= 60) and patients with
Mycoplasma pneumoniae
(
n
= 32) that potentially cross‐react with
M. tuberculosis
. The
ELISA
s showed that Rv0220, Rv2958c, Rv2994 and Rv3347c exhibited high specificities and sensitivities in detecting immunoglobulin G (IgG) antibody, with 98.3/91.3%, 91.7/85.9%, 93.3/89.1% and 93.3/80.4% respectively. According to the receiver‐operating characteristic (
ROC
) analysis, the area under the
ROC
of the target proteins was 0.988, 0.969, 0.929 and 0.945 respectively. Western blot was established to evaluate the immunoreactivities of target proteins to mice and human sera. Results demonstrated that Rv0220, Rv2958c, Rv2994 and Rv3347c could specifically recognize
TB
‐positive sera and the sera of mice immunized with the corresponding protein. Thus, Rv0220, Rv2958c, Rv2994 and Rv3347c were valuable potential diagnostic antigens for
M. tuberculosis
. |
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ISSN: | 1751-7915 1751-7915 |
DOI: | 10.1111/1751-7915.12697 |