To Understand the Role of Heme Molecules in the Survival and
Pathogenesis of Mycobacterium tuberculosis
Swati Meena and Laxman S Meena
*
CSIR-Institute of Genomics and Integrative Biology, Council of Scientific and Industrial Research, Mall Road, Delhi, India
*
Corresponding author: Laxman S Meena, CSIR-Institute of Genomics and Integrative Biology, Mall Road, Delhi-110007, India, Tel: 011-27666156; Fax:
011-27667471; E-mail: Laxmansm72@yahoo.com
Received date: January 31, 2017; Accepted date: February 17, 2017; Published date: February 24, 2017
Copyright: © 2017 Meena LS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted
use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Mycobacterium tuberculosis is an aerobic gram positive pathogen which causes deadly disease called
tuberculosis (TB) which is still a major threat to life. Mycobacterium tuberculosis Pathogen enters in host by
inhalation of air because these pathogens are present in air droplets released by other TB infected persons. It
ultimately reaches to lung alveoli and gives rise to primary TB. In macrophages Mycobacterium replicates itself and
increases its number in host cell. Artemisinin is a drug obtained from the plant Artemisia which target the heme
molecule in mycobacterium and stop its replication.
Keywords: Mycobacterium tuberculosis; H37Rv; Rv0203; Heme
molecule; Artemisia afra
Abbreviation
Mtb: Mycobacterium tuberculosis; M Fold cells: Micro Fold Cells;
His: Histidine; CNS: Central Nervous System; E. coli: Escherichia coli;
S. aureus: Staphylococcus aureus; WHO: World Health Organisation;
Tyr: Tyrosine
Introduction
Mycobacterium is gram positive and aerobic bacteria.
Mycobacterium strains are present in air and enter in host through
nasal inhalation as these pathogens are present in air droplets which
are released by sneezing or coughing of Mycobacterium tuberculosis
infected person and ultimately reach to the lungs which infect lungs in
primary infection and lymphoid organs in secondary infection in
lymphoid organs. In body circulation pathogen enters by respiratory
tract through air droplets and attack on macrophages for its
replication.
Mycobacterium tuberculosis H37Rv is a highly successful pathogen
and it successfully attacks on host [1]. Besides respiration, this
pathogen also enters in host circulation by Micro fold cells. Microfold
cell can directly mediate primary infection by Mycobacterium and
facilitate distribution beyond the mucosa [2] as shown in Figure 1.
According to WHO report of 2016, In 2015, 6.1 million new T.B.
cases were notiied to national authorities and reported to WHO and
an increment was observed in T.B. from 2013-2015 [3].
Iron is the molecule which is required for the survival of this
pathogen because it is a co-factor for at least 40 enzymes in
mycobacterium and it also maintains the iron homeostasis [4]. he
virulence of Mycobacterium depends on its ability to assimilate iron; it
synthesizes and utilizes siderophores (low-molecular-weight iron
chelators) to sequester iron [5]. he uptake of oxygen is possible only
when the heme is in ferrous (Fe
2+
) in host circulation. Reduction is
deined as a loss of O
2
(CO
2
+ C→2CO), an increase in hydrogen (C +
2H
2
→CH
4
) or a gain of electrons (O
2
+e
–
→O
2
•–
). On phagocytosis of
Mycobacterium, lung macrophages and neutrophils produce large
quantities of reactive oxygen species (ROS) and reactive nitrogen
species (RNS). NADPH oxidase catalyses one-electron reduction of O
2
using NADPH as electron donor, generating O2
•–
2O
2
+ NADPH →
O2
•−
+ NADP
+
+ H
+
[6].
Figure 1: Mycobacterium infection in host.
Mycobacterium has developed so many mechanisms to uptake iron,
one of them is it uses siderophore molecules to scavenge iron from
host body and another way of iron uptake is through heme molecule as
shown in Figure 2.
As we have discussed in above lines that heme is the molecule which
accepts only nascent oxygen to generate aerobic environment for
survival of pathogen. Heme is a protein molecule which might be
translated by a gene Rv0203 in pathogen. Rv0203 has a unique fold and
it is highly atypical in heme transfer proteins. It has alpha-helical
structure contains dimer of dimmers where each monomer consists 5
Journal of Tuberculosis and
Therapeutics
Meena and Meena, J Tuberc Ther 2017, 2:1
Short Communication OMICS International
J Tuberc her, an open access journal Volume 2 • Issue 1 • 1000104