https://microbewiki.kenyon.edu/index.

php/Mycobacterium_tuberculosis#Cell_structure_and_metaboli
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Description and significance

Mycobacterium tuberculosis is a acid fast bacteria, which can form acid-stable complexes when certain
arylmethane dyes are added. (4) All species of mycobacteria have ropelike structures of peptidoglycan that are
arranged in such a way to give them properties of an acid fast bacteria. (4) Mycobacteria are abundant in soil
and water, but Mycobacterium tuberculosis is mainly identified as a pathogen that lives in the host. Some
species in its Mycobacterium tuberculosis complex have adapted their genetic structure specifically to infect
human populations.
M. tuberculosis can be isolated in labs and stored at –80 degrees to be studied extensively, and the most
commonly used strain of M. tuberculosis is the H37Rv strain. One way to study M. tuberculosis in culture is to
collect samples of mononuclear cells in peripheral blood samples from a healthy human donor and challenge
macrophages with the MTC. M. tuberculosis has very simple growth requirements and is able to grow slowly in
harsh conditions. Their acid-fast property is the strongest when there is glycerol around. However, when
glucose is the main source of nutrient, the utilization of glycerol by M. tuberculosis is inhibited. Therefore, it’s
been shown that glutatmate, and not glucose, is actually the main source of nutrient for initiating growth. (4)
Since as many as 32% of the human population is affected by Tuberculosis (TB), an airborne disease caused
by infection of M. tuberculosis in one way or another, and about 10% of them becomes ill per year (6), it is not
hard to imagine the significance in understanding the genome of the pathogen to develop and improve
strategies for treatment by developing specific drugs that target the gene products of M. tuberculosis.

Genome structure
Mycobacterium tuberculosis has circular chromosomes of about 4,200,000 nucleotides long. The G+C content
is about 65%. (13)
The genome of M. tuberculosis was studied generally using the strain M. tuberculosis H37Rv. The genome
contains about 4000 genes. Genes that code for lipid metabolism are a very important part of the bacterial
genome, and 8% of the genome is involved in this activity. (7)
The different species of the Mycobacterium tuberculosis complex show a 95-100% DNA relatedness based on
studies of DNA homology, and the sequence of the 16S rRNA gene are exactly the same for all the species. So
some scientists suggest that they should be grouped as a single species while others argue that they should be
grouped as varieties or subspecies of M. tuberculosis. (2)
Plasmids in M. tuberculosis are important in transferring virulence because genes on the plasmids are more
easily transferred than genes located on the chromosome. One such 18kb plasmid in the M. tuberculosis
H37Rv strain was proven to conduct gene transfers.

Cell structure and metabolism

M. tuberculosis has a tough cell wall that prevents passage of nutrients into and excreted from the cell,
therefore giving it the characteristic of slow growth rate. The cell wall of the pathogen looks like a Gram-positive
cell wall. The cell envelope contains a polypeptide layer, a peptidoglycan layer, and free lipids. In addition,
there is also a complex structure of fatty acids such as mycolic acids that appear glossy. (8) The M.
tuberculosis cell wall contains three classes of mycolic acids: alpha-, keto- and methoxymycolates. The cell
wall also contains lipid complexes including acyl glcolipids and other complex such as free lipids and
sulfolipids. There are porins in the membrane to facilitate transport. Beneath the cell wall, there are layers of
arabinogalactan and peptidoglycan that lie just above the plasma membrane. (14)
The M. tuberculosis genome encodes about 190 transcriptional regulators, including 13 sigma factors, 11 two-
component system and more than 140 transcription regulators. Several regulators have been found to respond
to environmental distress, such as extreme cold or heat, iron starvation, and oxidative stress. (11) To survive in
these harsh conditions for a prolonged period in the host, M. tuberculosis had learned to adapt to the
environment by allowing or inhibiting transcription according to its surroundings.(3)
Cholesterol Catabolism

A figure of cholesterol with rings labeled. From http://chemistry.gravitywaves.com/CHE450/02_MolecLifeWater.htm

(note: references for this section are included at the bottom of this section)
Cholesterol metabolism has been studied extensively because of its possible therapeutic applications
in Tuberculosis(TB) infections. It has been shown numerous times that TB requires cholesterol for virulence in
vivo, because Mycobacterium tuberculosis (Mtb), the causative agent, utilizes cholesterol as a source of
carbon, energy, and steroid-derived metabolites throughout the course of infection (1-3,13,18). As a result,
therapies targeting this catabolic dependency may be developed to treat TB once it’s better understood.

Regulation

Example of TetR proteins at work. It is theorized that KstR and KstR2 work in a similar fashion. Picture
from http://en.wikipedia.org/wiki/Tetracycline-controlled_transcriptional_activation

The cholesterol catabolic pathway in Mycobacteria is regulated by KstR and KstR2, which regulate gene
expression in a similar fashion to Tetracycline resistance regulators (TetR-like proteins) (4, 5). These TetR-like
proteins function by binding to the operator and repressing transcription of its regulon, which represses
cholesterol catabolism genes, in the absence of cholesterol (4, 5). In the presence of cholestenone – a
cholesterol metabolite – KstR and KstR2 are released from the operator to allow transcription of cholesterol
catabolism genes; furthermore, they also repress transcription of their own gene, resulting in less overall KstR
and KstR2 being made (6).
Of these two proteins, KstR is better understood. KstR regulates a large regulon of proteins involved in lipid
and cholesterol catabolism, while KstR2 is known to be involved in regulating a smaller and independent
regulon within the KstR regulon that is hypothesized to be involved in the cholesterol catabolism pathway (4, 5).
These two proteins also work independently from each other, suggesting perhaps the transcription of these
regulons happen during different stages of infection (4).

Uptake
The uptake of cholesterol uses the Mce4 transport system on the M. tuberculosis cell wall, and is regulated by
KstR (3,7-9). The exact mechanism of this transporter is not known, but it is known that Mce4 is an ATP-
binding cassette transport system consisting of more than 8 proteins (7). Additionally, this transporter is able to
transport other steroids that are similar in structure to cholesterol, including 4-androstene-3,17-dione (AD),
which is a metabolite of cholesterol catabolism (7).

Catabolic Pathway

The overall pathway of cholesterol catabolism to our current understanding. Adapted from figure 3 of Ouellet et. al (2011)

First, cholesterol is first oxidized into cholest-4-en-3-one (cholestenone) by a dehydrogenase protein in MTB
called ChoD (1,10). This dehydrogenase oxidizes cholesterol into cholestenone, using the reduction of NAD + to
NADH as the oxidizing agent (11). The catabolism of cholesterol is then split into two parts: 1) the alkyl side
chain degradation which eventually feeds into the TCA cycle (1) and 2) the ring cleavage of the steroid body
(12). There is strong evidence that the alkyl side chain degradation occurs first (10).
The alkyl side chain degradation pathway is similar to normal alkane degradation systems. The pathway
involves many oxygenases leading up to three beta-oxidation cycles (8,12). This process yields one molecule
of acetyl-CoA and 2 molecules of propanyl-CoA, which can then generate energy via the TCA cycle or be used
for anabolism. The enzymes that are involved in this oxidation process are homologous to the enzymes
involved in classical fatty acid beta oxidation, however, they have evolved a unique structure in order to
accommodate large, bulky steroid substrates (19).
The pathway for the degradation of the steroid rings is much less understood compared to the alkyl side chain.
After the alkyl side chain is degraded, the remaining AD molecule is converted into 1,4-androstenedione (ADD)
(8). This is followed by many ring-opening steps catalyzed by various oxygenases (15). After the opening of the
A and B rings, the alkene that is produced is degraded into propionyl-CoA and pyruvate, which can be used for
energy or anabolism. It is not known how the C and D rings are degraded (8).

Role of Cholesterol in Tuberculosis Infections

The big picture of cholesterol catabolism: highlighting important intermediates and associated enzymes that are promising
therapeutic targets.

Tuberculosis infections have unique virulence factors compared to most pathogens. They infect host cell
[ http://en.wikipedia.org/wiki/Macrophage macrophages] and persist inside phagosomes where there are limited
nutrients (3). Tuberculosis’ unique ability to utilize cholesterol, which is a common component of human cell
membranes, plays a role in its persistence (3). Furthermore, because the cholesterol catabolism pathway
requires a large number of oxygenases, it is no surprise that TB infects the lungs where oxygen concentrations
are highest (8).

Therapeutic applications
Because TB requires cholesterol to persist during an infection, inhibiting the Mce4 transporter can be a novel
therapeutic option. Understanding the mechanism of the Mce4 transport system can provide insight into
possible anti-mycobacterial targets.
Targeting the KstR regulation system may also be a possible treatment. If the KstR proteins are prohibited from
unbinding its operator and de-repressing its regulon, TB’s cholesterol catabolism genes would not be
expressed. As a result, the ability for TB to persist inside macrophages would be lost and thus would be faster
to treat.
Within the cholesterol catabolism pathway, there are many metabolites that may be toxic. Cholestenone, the
first product of the cholesterol pathway, has shown to be toxic and can kill the cell (13). Cholestenone is used
up by CYP125, and knocking out CYP125 causes an accumulation of toxic cholestenone which kills the cell.16
Furthermore, a previous study revealed that knocking out HsaC resulted in catechol formation15, which can
harm the cell due to formation of free radicals that can cause irreparable DNA damage (17). Inhibiting CYP125
and HsaC may also be possible therapeutic options in which the cell poisons itself to death (16).

References
1. Brzostek, A., Dziadek, B., Rumijowska-Galewicz, A., Pawelczyk, J. & Dziadek, J. Cholesterol oxidase is
required for virulence of Mycobacterium tuberculosis. FEMS Microbiol. Lett. 275, 106 (2007).
2. Brzostek, A., Pawelczyk, J., Rumijowska-Galewicz, A., Dziadek, B. & Dziadek, J. Mycobacterium
tuberculosis Is Able To Accumulate and Utilize Cholesterol. The Journal of Bacteriology 191, 6584-6591
(2009).
3. Pandey, A. K. & Sassetti, C. M. Mycobacterial Persistence Requires the Utilization of Host Cholesterol. Proc.
Natl. Acad. Sci. U. S. A. 105, 4376-4380 (2008).
4. Uhía, I., Galán, B., Medrano, F. J. & García, J. L. Characterization of the KstR-dependent promoter of the
gene for the first step of the cholesterol degradative pathway in Mycobacterium smegmatis. Microbiology 157,
2670 (2011).
5. Kendall, S. L. et al. A highly conserved transcriptional repressor controls a large regulon involved in lipid
degradation in Mycobacterium smegmatis and Mycobacterium tuberculosis. Mol. Microbiol. 65, 684-699 (2007).
6. Ramos, J. L. et al. The TetR family of transcriptional repressors. Microbiology and molecular biology
reviews : MMBR 69, 326-356 (2005).
7. William W. Mohn et al. The Actinobacterial mce4 Locus Encodes a Steroid Transporter. J. Biol. Chem. 283,
35368-35374 (2008).
8. Van der Geize, R. et al. A Gene Cluster Encoding Cholesterol Catabolism in a Soil Actinomycete Provides
Insight into Mycobacterium tuberculosis Survival in Macrophages. Proc. Natl. Acad. Sci. U. S. A. 104, 1947-
1952 (2007).
9. Chang, J. C. et al. igr Genes and Mycobacterium tuberculosis cholesterol metabolism. J. Bacteriol. 191,
5232-5239 (2009).
10. Chiang, Y. R. et al. Cholest-4-en-3-one-delta 1-dehydrogenase, a flavoprotein catalyzing the second step in
anoxic cholesterol metabolism. Appl. Environ. Microbiol. 74, 107-113 (2008).
11. Yang, X., Dubnau, E., Smith, I. & Sampson, N. S. Rv1106c from Mycobacterium tuberculosis is a 3beta-
hydroxysteroid dehydrogenase. Biochemistry (N. Y. ) 46, 9058 (2007).
12. Griffin, J. E. et al. High-resolution phenotypic profiling defines genes essential for mycobacterial growth and
cholesterol catabolism. PLoS pathogens 7, e1002251 (2011).
13. Ouellet, H. et al. Mycobacterium tuberculosis CYP125A1, a steroid C27 monooxygenase that detoxifies
intracellularly generated cholest-4-en-3-one. Mol. Microbiol. 77, 730 (2010).
14. Thomas, S. T., VanderVen, B. C., Sherman, D. R., Russell, D. G. & Sampson, N. S. Pathway profiling in
Mycobacterium tuberculosis: elucidation of cholesterol-derived catabolite and enzymes that catalyze its
metabolism. The Journal of biological chemistry 286, 43668-43678 (2011).
15. Yam, K. C. et al. Studies of a ring-cleaving dioxygenase illuminate the role of cholesterol metabolism in the
pathogenesis of Mycobacterium tuberculosis. PLoS pathogens 5, e1000344 (2009).
16. Ouellet, H., Johnston, J. B. & de Montellano, P. R. O. Cholesterol catabolism as a therapeutic target in
Mycobacterium tuberculosis. Trends Microbiol. 19, 530 (2011).
17. Schweigert, N., Zehnder, A. J. & Eggen, R. I. Chemical properties of catechols and their molecular modes
of toxic action in cells, from microorganisms to mammals. Environ. Microbiol. 3, 81 (2001).
18. Wipperman, Matthew, F., Sampson, Nicole, S., Thomas, Suzanne, T. Pathogen Roid Rage: Cholesterol
utilization by Mycobacterium tuberculosis. Crit Rev Biochem Mol Biol. 49(4):269-93. (2014) doi:
10.3109/10409238.2014.895700.
19. Wipperman, M.F., Yang, M., Thomas, S.T., Sampson, N.S. Shrinking the FadE proteome of Mycobacterium
tuberculosis: Insights into cholesterol metabolism through identification of an α2β2 heterotetrameric acyl
coenzyme A dehydrogenase family. J Bacteriol. 195(19):4331-41. (2013) doi: 10.1128/JB.00502-13.

Ecology
The Mycobacterium tuberculosis forms a complex with other higher related bacteria called the M.
tuberculosis complex that consists of 6 members: Mycobacterium tuberculosis and Mycobacterium
africanmum, which infect humans; Mycobacterium microti, which infects vole; Mycobacterium bovis, which
infects other mammalian species as well as humans; M. bovis BCG, a variant of Mycobacterium
bovis and Mycobacterium canettii, a pathogen that infects humans. (7) M. tuberculosis first infected humans
10,000-15,000 years ago. (10) It has been found in early hominids originating in East-Africa. Therefore,
studying the population structure of the species might provide insights about Homo sapiens' migratory and
demographic history.
Once inside the human host cell, Mycobacterium tuberculosis inflicts a contagious-infectious disease called
tuberculosis (TB), although the disease could either be latent or active depending on the ability of the person’s
immune system to defend against the pathogen. In 1993, the World Health Organization declared TB a global
public health emergency. It is estimated that one third of the world population is infected by Mycobacterium
tuberculosis, which leads to 8 to 10 million new cases, and 3 million deaths each year. (10) The disease
especially affects those in developing countries, those of the aging population and those who have HIV/AIDs
because of their weak immune system. (10)
Because TB is an infectious disease for humans, it is important to sequence the genome of the Mycobacterium
tuberculosis in order to find drugs fight against the bacteria by developing potential drug targets. Especially
since Mycobacterium tuberculosis is multi-drug resistance and could cause latent infection, it is especially hard
to treat and prompts scientists to research for new drug targets by looking through the Mycobacterium
tuberculosis genome and gene products.

Tuberculosis
The Disease
Tuberculosis (TB) is a disease caused by infection from the bacteria M. tuberculosis. If not treated properly, TB
can be fatal (1). Currently, the World Health Organization estimates that over 13 million people have TB and
about 1.5 million die each year from the disease. Tuberculosis most commonly affects the lungs (pulmonary
TB). Patients with active pulmonary TB usually have a cough, an abnormal chest x-ray, and are infectious. TB
can also occur outside of the lungs (extrapulmonary), most commonly in the central nervous, lymphatic, or
genitourinary systems, or in the bones and joints (1). Tuberculosis which occurs scattered throughout the body
is referred to as miliary TB. Extrapulmonary TB is more common in immunosuppressed persons and in young
children (2).

When a person with active pulmonary TB coughs, sneezes, or talks, the bacteria that cause TB may spread
throughout the air. If another person breathes in these bacteria, there is a chance that they will become
infected with tuberculosis. Repeated contact is usually required for infection (1). However, not everyone
infected with TB bacteria becomes sick. Roughly 5% of people infected with M. tuberculosisactually develop
TB. People who are infected but not sick have latent TB infection. Those who have a latent infection are
asymptomatic, do not feel sick, and are not contagious.

Symptoms
Early symptoms of active pulmonary TB can include weight loss,fever, night sweats, and loss of appetite (1).
Due to the vague initial symptoms of TB, an infected person may not feel that there is anything wrong. The
infection can either go into remission or become more serious with the onset of chest pain and coughing up
bloody sputum (3). The exact symptoms of extrapulmonary TB vary according to the site of infection in the
body.

Transmission
TB is spread through the air from one person to another. Microscopic droplets that contain the bacteria may be
expelled when a person who has infectious TB coughs or sneezes. They can remain suspended in the air for
several hours, depending on the environment. When a person breathes in M. tuberculosis, the bacteria can
settle in the lungs and begin to grow. From there, they can move through the blood to other parts of the body.
TB in the lungs can be infectious because the bacteria are easily spread to other people. TB in other parts of
the body, such as the kidney or spine, is usually not infectious (1). If a person has confirmed TB or is suspected
of having TB, the best way to stop transmission is through immediate isolation. Therapy should begin
immediately. Contagiousness declines rapidly after a standard treatment regimen has begun, provided the
patient adheres to the course of therapy.

Risk Groups
Anyone can get TB. However, some groups are at higher risk to get active TB disease. People at high risk
include those (2):
1. with HIV infection
2. in close contact with those known to be infectious with TB
3. with medical conditions that make the body less able to protect itself from disease (for example: diabetes, or
people undergoing treatment with drugs that can suppress the immune system, such as long-term use of
corticosteroids)
4. from countries with high TB rates
5. who work in or are residents of long-term care facilities (nursing homes, prisons, some hospitals)
6. who are malnourished
7. who are alcoholics or IV drug users

Infection
Infection can develop when a person breathes in tubercle bacilli from expelled droplets from an infected
individual. The droplets reach the alveoli of the lungs where the bacilli can be deposited (4). Alveolar
macrophages ingest the tubercle bacilli and destroy most of them. Some can multiply within the macrophage
and be released when the macrophage dies. From there, the bacilli can spread to other regions of the body
through the bloodstream. The areas in which TB is most likely to develop are: the apex of the lung, the kidneys,
the brain, bones and lymph nodes. This process of dissemination prepares the immune system for a reaction
(2).

In most infected individuals, the response from the immune system kills most of the bacilli. At this stage, a
latent TB infection has been created, which may be detected by using the Mantoux tuberculin skin test (see
below). Within weeks after infection, the immune system is usually able to halt the multiplication of the tubercle
bacilli, preventing further progression. Most people recover completely from an initial infection, and the bacteria
eventually die off (3,4). In some people, the tubercle bacilli overcome the defenses of the immune system and
begin to multiply, resulting in the advancement to active TB disease. This process may occur shortly after
infection or several years later (5).

Diagnosis
The Mantoux tuberculin skin test, also known as the PPD (purified protein derivative) test, is used to detect TB
infection. It is performed by injecting a small amount of tuberculin, a complex of purified M.
tuberculosis proteins, into the skin of the arm. The reaction formed on the arm determines the result of the test.
A positive reaction for TB infection only reports that a person has been infected with TB bacteria. It does not tell
whether or not the person has active disease. Other tests, inclluding a chest x-ray and a sample of sputum, are
needed to determine whether the person has active disease(6). In pulmonary TB, lesions on x-rays are often
seen in the apical segments of the upper lobe or in the upper segments of the lower lobe. However, lesions
may appear anywhere in the lungs, especially in HIV-positive and other immunosuppressed persons (1).

An abnormal chest x-ray may indicate TB infection which is then confirmed or not by additional tests. Chest x-
rays may be used to rule out the possibility of pulmonary TB in a person who has a positive reaction to the
tuberculin skin test and no symptoms of disease. Persons suspected of having pulmonary TB generally will
have sputum specimens examined by acid-fast bacilli smear and culture. Detection of acid-fast bacilli in stained
smears examined microscopically may provide the first clear evidence of the presence of M. tuberculosis.
Positive cultures for M. tuberculosis are used to confirm the diagnosis of TB (6).

Stained slides of sputum smears ready for microscopy.

World Lung Foundation 2006

Treatment of Tuberculosis
M. tuberculosis is a very slow-growing, intracellular organism. Consequently, treatment requires the use of
multiple drugs for several months (5). With appropriate antibiotic treatment, TB can be cured in most people.
Treatment usually combines several different antibiotic drugs that are given for at least 6 months, sometimes
for as long as 12 months. However, many M. tuberculosis strains are resistant to one or more of the standard
TB drugs, which complicates treatment greatly (3)

Currently, there are 10 drugs approved by the U.S. Food and Drug Administration for the treatment of TB. Of
the approved drugs, isoniazid (INH), rifampin (RIF), ethambutol (EMB), and pyrazinamide (PZA) are considered
first-line antituberculosis agents. These four drugs form the foundation of initial courses of therapy
Drug-resistant TB is major problem for the treatment of the disease. Multidrug-resistant TB (MDR-TB), is
defined as disease caused by TB bacilli resistant to at least isoniazid and rifampicin, the two most powerful
anti-TB drugs (7). MDR-TB is intrinsically resistant to drugs but its resistance can be exacerbated by
inconsistent or partial treatment. When patients do not take all their medicines regularly for the required period
because they start to feel better, drug-resistant bacteria can arise. While drug-resistant TB is generally
treatable, it requires extensive chemotherapy (up to two years of treatment) with second-line anti-TB drugs.
These second line drugs produce more severe adverse drug reactions more frequently than the preferred first
line drugs. There are six classes of second-line drugs used for the treatment of TB

1. aminoglycosides
2. fluoroquinolones
3. polypeptides
4. thioamides
5. cycloserine
6. p-aminosalicylic acid

Within the last few years a new form of TB has emerged, extensively drug-resistant TB (XDR-TB). Whereas
regular TB and even MDR TB progress relatively slowly, XDR TB progresses much more rapidly and can be
fatal within months or even a few weeks. XDR-TB is defined as TB that has developed resistance to at least
rifampin and isoniazid, as well as to any member of the fluoroquinolone family and at least one of the
aminoglycosides or polypeptides. The emergence of XDR-TB, particularly in settings where many TB patients
are also infected with HIV, poses a serious threat to TB control (7).

Currently, short course Direct Observation Therapy (DOTS) is a key component of the World Health
Organization's campaign to stop TB. DOTS involves patient case management by trained health professionals
who ensure that the patient is taking his/her TB drugs (7,8). Because TB has such a long course of treatment,
many patients stop their medications prematurely. DOTS sends health professionals to the patient to ensure
s/he is taking the medication and may also supply the medicine to the patient. In some areas, patients come to
the DOT clinic instead of the health worker traveling to them (7,8). Often, DOTS provides enablers or incentives
to ensure patients continue their treatment, such as transportation or free meals. DOTS also tries to support TB
patients (7,8). DOTS has been extremely successful at decreasing the default rates, with cure rates above 80%
and default rates less than 10% (8).

Supervision of drug administration

in the TB hospital in Benin, Africa
(www.WorldLungFoundation.org)

Prevention
TB is largely a preventable disease. Isolation of patients and adequate ventilation are the most important
measures to prevent its transmission in the community. In the United States, healthcare providers try to identify
people infected with M. tuberculosis as early as possible, before they have developed active TB.

In those parts of the world where the disease is more common, the World Health Organization recommends
that infants and children receive a vaccine called BCG (Bacille Calmette Guerin). BCG is made from live
weakened Mycobacterium bovis, a bacterium related to M. tuberculosis. BCG vaccine prevents M.
tuberculosis from spreading within the body, thus preventing TB from developing.
BCG has drawbacks. It is reasonably effective in preventing development of active disease in children.
However, it does not protect against TB in adults. In addition, BCG may interfere with the TB (PPD) skin test,
showing a positive skin test reaction in people who have received the vaccine. BCG is used for children in
countries where TB is endemic. Consequently, much of the population would have a positive TB test regardless
of the vaccine. However, many countries where BCG vaccine is used have a limited infrastructure and public
health system Consequently, the problem is not as important as it would be in countries without endemic TB
(3).

References
1. Centers for Disease Control and Prevention (2009) "Division of Tuberculosis Elimination (DTBE)", <HTTP:
default.htm tb www.cdc.gov>
2. American Lung Association (2009) "Tuberculosis (TB)" <HTTP:
content3.aspx?c="dvLUK9O0E&b=2060731&content_id={50031760-2D7C-4FFF-AD75-
4C49BDD1CD7D}&notoc=1" nlnet apps site www.lungusa.org>
3. National Institute of Allergy and Infectious Diseases (2009), "Tuberculosis
(TB)" http://www3.niaid.nih.gov/topics/tuberculosis/
4. Harries A.D. and C. Dye (2006) "Tuberculosis," Ann Trop Med Parasitology 100:415-431.
5. Goodman A, and M. Lipman (2008) "Tuberculosis," Clinical Med. 8:531-534.
6. Nahid P., M. Pai and P.C. Hopewell (2006) "Advances in the diagnosis and treatment of tuberculosis," Proc
Amer Thoracic Soc 3:103-110.
7. World Health Organization (2009) Tuberculosis (TB) http://www.who.int/tb/en/
8. Frieden, T.R. and J.A. Sbarbaro (2007) "Promoting adherence to treatment of tuberculosis: The importance
of direct observation," Bull World Health Org. 85 2007, 325-420.http://www.who.int/bulletin/volumes/85/5/06-
038927/en/index.html

The Sanatorium Movement for Treatment of Tuberculosis

Until the discovery of tubercle bacillus, tuberculosis was primarily treated in the home. There was no effective
treatment. Doctors prescribed a variety of treatments including snake oil and wearing a beard (1). However, in
the mid-1800s, physicians began recommending moving to temperate climates with clear air and a new
treatment regimen was born. The sanatorium made its first appearance in the 1850s in Germany. The idea was
developed by Herman Brehmer after he was apparently cured by living in the Himalayan climate (2).
Contributing to the development of sanitoria was a developing fear of the spread of the disease, due in part to
the ability to detect the bacterium. Particularly in American, the success of institutionalized treatments in
Germany led to construction of sanatoria across the United States. Sanatoria treatment was generally however
reserved for the middle and upper class due to the costs associated with providing the 24-hour care, surgeries,
and resort-type activities found at these institutions.

The Prince Albert Sanatorium was the largest

and most modern sanatorium in Saskatchewan;
it opened in 1930 at Prince Albert, Saskatchewan
(Valley Echo 34:30 (1953).

Part of the idea behind sanatoria was to assuage the societal pressure for the isolation of those infected
ensuring public health while providing the afflicted with therapeutic regimens, including patient education.
Educational programs taught the infected what was known about the disease, new health habits, and how to
live with and protect others (3). After treatment was completed, sanatoria offered rehabilitation to assist patients
in achieving a satisfactory economic status. Rehabilitation involved slowly introducing occupational therapy into
the treatment regimen in order to identify a job that was interesting for the patient while remaining appropriate
for recovery.
Patients at sanatoria were categorized into treatment groups based on the seriousness of their infection. These
treatment groups ranged from 'absolute'-meaning complete bed rest to 'graded'-allowed work and exercise.
Preliminary treatment for tuberculosis involved following two rules (4):

1. Absolute and utter rest of mind and body-no bath, no movement except to toilet once a day, no sitting up
except propped by pillows and semi-reclining, no deep breaths.
2. Eat nourishing food and have plenty of fresh air

A tuberculous mother, on strict bed rest,

leaves her room at the sanatorium
for a Sunday walk with her family.
But she does not leave her bed
(Valley Echo 11:17 (1930).

The majority of sanatoria were built in the country because it was believed that the country air aided in
recovery. Patients were encouraged to leave the pestilential cities and take in the fresh air and sunshine (1). A
woman sent to a sanatorium in England in 1945 described it as a "really nice atmosphere" with great meals and
a friendly staff (5). The Essex Sanatorium complex in New Jersey included a state of the art hospital, cottages
for patients, an auditorium and chapel. Many facilities also included farmland that was used to provide
tuberculosis patients with fresh food and milk. A typical day in the life of a tuberculosis patient in a sanatorium
was (6):

1. Breakfast
2. Sitting or laying on a screened porch for fresh air
3. Lunch
4. Sitting or laying on the porch-visiting hours
5. Dinner
6. Bedtime
Bethesda Sanatorium c1920. Interior view of balcony wing,
Bethesda Sanatorium, Denver, Colorado
( Photo by Louis Charles McClure, 1867-1957
www.hellodenver.com/Photos_People.Cfm)

This schedule varied for patients in recovery and would be modified to include 1-4 hours of exercise, activity, or
work. The social structure of sanatoria could resemble a prison, boarding school, or resort depending on the
location, staff, and the personal feelings of the patients. Some patients felt like prisoners in the sanatorium due
to all of the restrictions on their activity while others enjoyed the relaxation and outdoors. The healthier patients
oftentimes would form clubs or 'gangs' that can be compared University Greek organizations. These groups
provided distractions for the patients and a close network of friends during the isolation at the sanatorium (2).
The clubs were often very elitist and wary of outsiders; most required membership dues and a demonstration of
loyalty before a person would be admitted. Groups such as these were extremely prevalent in European
sanatoria but were less evident in the later American establishments.
A sanatorium patient receives pneumothorax treatment
from Dr. GH Hames in Saskatchewan during the 1940s
(Valley Echo 40:21 (1959))

Recovery in the sanatoria setting depended largely on the stage of disease at admission; early diagnosis was
essential for the treatments of the times (3). Stays at the sanatorium could last from months to years depending
on the success of treatment and the willingness of the patient to follow the regimen rules. Discharge only
became a possibility after three negative sputum smears and a negative culture (7).

The decline of sanatoria began with the scientific strides in the treatment of tuberculosis, particularly after the
discovery of antibiotics (2). The responsibility for recovery shifted from patients to doctors with the introduction
of antibiotic treatment. Patients were no longer required to adjust their lifestyle, personal habits, or mentality for
recovery (1). The advent of streptomycin after 1950 caused the number of patients requiring treatment declined
so drastically that sanatoria around the nation were abandoned. Many of these facilities were converted to
mental asylums or geriatric centers; others were demolished.
References
1. Tulloch, M., "Tuberculosis." Blue Ridge Sanatorium, http://www.faculty.virginia.edu/blueridgesanatorium
2. Condrau, F. (2001) 'Who Is the Captain of All These Men of Death': The Social Structure of a Tuberculosis
Sanatorium in Postwar Germany," J Interdisc Hist 32: 243-263.
3. Bobrowitz, I.D. (1940) "Sanatorium Treatment of Tuberculosis." Chest 6: 278-280.
4. Hurt, R. (2004) "Tuberculosis sanatorium regimen in the 1940s: a patient's personal diary," J Royal Soc
Med 97:350-353.
5. "History of the Essex Mountain Sanatorium http://www.mountainsanatorium.net
6. Bayne, R. (1998) "Ascending the Magic Mountain," Can Med Assoc J 159:517-8.
7. Riehl, E.D., G. Bereznicki, G. Rogers, R. Reza and J. Eagan (1977) "An Integrated Approach to
Tuberculosis Care in the Commonwealth of Pennsylvania," Amer J Publ Health 67:162-164.

Exploring the relationship between tuberculosis and nutrition

The relationship between tuberculosis and nutrition is complex and bi-directional (1). It is clear that individuals
who are malnourished are more susceptible to TB infection or to a latent infection becoming active. TB infection
also decreases the nutritional status of the patient. However, because TB decreases the nutritional status of a
patient, it is difficult to accurately determine what the patient's nutritional status was before TB infection and to
conclude whether malnutrition or infection came first. Regardless of cause and effect, 34% of TB cases are
associated with malnutrition, making malnutrition the second highest risk factor for active TB after HIV (2). In a
malnourished individual, TB may present atypically, causing difficulty in diagnosis and longer periods before
treatment (4). Similarly, protein energy malnutrition has been found to decrease the effectiveness of the
tuberculin skin test because of decreased immune response (3).

Redrawn from (1): Bidirectional interaction of tuberculosis

and malnutrition and some putative mechanisms
How does nutrition affect the risk of getting TB?
Malnutrition has been linked with decreased immune function in multiple studies in diseases unrelated to TB
(1). Cell mediated immunity is the body's way of keeping TB latent, but if a patient is malnourished, his or her
immune status is lower; consequently, the risk of progression to active TB increases (3). Some argue that
malnutrition is not actually a risk factor for active TB, but that the same risk factors for malnutrition are risk
factors for TB, most commonly, poverty (3). In many countries, even HIV negative patients without TB are
underweight so it is difficult to say if malnutrition is a risk factor for TB or just a fact of life in those countries that
are commonly affected by TB.

A severely malnourished individual

(World Lung Foundation, 2006)
How does TB change the patient's nutritional status?
During active TB infection even well-fed patients have altered protein metabolism (1). A patient with active TB
uses less protein to build up muscle, leading to increased oxidation of amino acids and increased oxidative
stress that the body has to fight. Reduced antioxidant intake (vitamins A, C, and E) causes a decrease in the
body's immune response and also means that oxidant and free radical induced damage and inflammation
increases (5). The combination of poor amino acid utilization and low antioxidant intake may lead to the
exacerbation of active TB or make the patient more susceptible to develop active TB from a latent infection. It is
difficult to say which is cause and effect. Anemia is common in TB patients, but iron overload causes oxidative
stress may exacerbate the disease (5). The risk of increasing a patient's oxidative stress levels makes treating
TB related malnutrition more difficult.

Active TB increases a patient's resting energy expenditure, which leads to wasting if extra calories are not
provided in the diet (1). Interestingly, in the wasting of TB, women seem to lose fat while men lose lean
(muscle) tissue (6). In a study in Malawi, 69% of active TB patients had a BMI (body mass index, metric
weight/metric height2) less than 19 (4). A BMI less than 19 is considered underweight, while a BMI under 17 is
considered severely underweight (see below). The Malawi study also found that a lower BMI was correlated
with a more advanced TB infection. HIV negative adults with extremely advanced TB infection had a mean BMI
of 17 (4). In another study, a BMI of 17 or less meant the individual had twice the risk of early death associated
with TB (5). Individuals who were 10% below their ideal body weight were three times more likely to become
infected with TB than those who were 10% above their ideal body weight (3). )

Body Mass Index

Classification

Classification BMI

Underweight <19

Normal Weight 19-25

Overweight 25-30

Obese >30

From http://www.nhlbi.nih.gov/guidelines/obesity/BMI/bmicalc.htm

Unfortunately, TB patients often want to eat less than healthy people, making it even more difficult to prevent
wasting or to rebuild body stores (5). HIV co-infection particularly causes a decrease in patients' appetites, and
also brings nutritional indicators down even more. Thus, nutrition and supplementation in co-infected
individuals must be closely monitored and constructed (5). It can take at least 12 months for patients to build up
their body stores after TB infection (1). Often, this is difficult if they return home because they are likely to
return to work (expending more energy), and their diet may be poorer and less balanced than at a care facility
(1).

One nutritionally related aspect of immunity is the finding that vitamin D deficiency may increase the risk of
infection and/or progression to the active form of the disease. This is because vitamin D is critical for
macrophage activity (4). Another specific nutrition related concern is vitamin A deficiency, which has been
linked to chronic infections and infection with HIV (7). In a study of TB patients and controls who were HIV
positive and negative, the lowest vitamin A levels were found in patients with HIV and TB co-infections. After
two months of TB treatment, HIV negative patients had increased vitamin A levels while those with the HIV co-
infection had decreased vitamin A levels (7). This may be related to the changes in protein metabolism noted
above since vitamin A loss is associated clinically with protein losses, while protein rich diets increase levels of
Vitamin A (7).
How does nutritional therapy help cure active TB or reduce the risk of TB infection?
When protein energy malnourishment is reversed, treatment of TB is more effective (3). However, when TB is
treated and patients begin gaining weight, it is usually fat mass that increases, not lean mass (5). Thus, specific
nutrition therapy strategies need to be developed to increase patients' lean mass. Protein supplementation may
increase the patient's restoration of lean mass, although this can take more than 12 months (5).

Vitamin rich cod liver oil was a common early treatment for TB (5), and vitamin A supplementation during
treatment may speed the patient's initial recovery and decrease their infectiousness more quickly (5). Vitamin
supplementation for family members of active TB patients may decrease their risk of acquiring active TB (3).
Policy and Treatment Implications for Malnutrition in TB
Because nutrition can help with the prevention of active TB infection, it is important that policies of
governmental or other agencies targets the problem underlying malnutrition: poverty (2). All malnourished
individuals are considered at risk for TB. Food security is a major goal for such people, not just the severely
malnourished ones. Malnutrition often continues after treatment, and low weight correlates with TB relapse (5),
so policy must be put in place to increase food security and nutrition for those who have been cured of active
TB.

Because TB is so infectious, treatment is a community problem. Providing adequate nutrition to malnourished

individuals helps the entire community. Unfortunately, in nations with endemic TB, food comes from small
community farms, TB can also create a cyclical problem because it eliminates workers from crucial activities
like farming, creating increased hunger and increased susceptibility to active TB in a community (5).

Providing food can encourage people to come for treatment, so it can be an effective part of DOTS (5).
However, programs that have tried distributing food to patients encounter many questions about who should
get the food: should rations be provided only for patients, or should food be provided for their families as well?
It costs <$1 per day in many developing countries to support an AIDS patient and their family with food, and
estimates put an equal price on supporting a TB patient and their family (5). Providing food for the family as
well as the patient may be important because patients receiving food for themselves are likely to share the food
with family members, thus decreasing the amount the patient eats. Families have positive perceptions of food
aid, and believe it helps their relative recover.

File:TB-Picture5.png
Food aid for patients with TB
(www.WorldLungFoundation.org)
References
1. Macallan, D.C. (1999) "Malnutrition in Tuberculosis," Diag Microbiol Infect Dis 34:153-157.
2. Lonnroth, K., and M. Raviglione (2008) "Global Epidemiology of Tuberculosis: Prospects for Control," Sem
Resp Crit Care Med 29:481-491.
3. Cegielski, J.P., and D.N.McMurray (2004) "The relationship between malnutrition and tuberculosis: evidence
from studies in humans and experimental animals," Int J Tuberculosis Lung Dis 8:286-298.
4. Lettow, M.V., J.J. Kumwenda, A.D. Harries, C.C. Whalen, T.E. Taha, N. Kumwenda, C. Kang'ombe and R.D.
Semba (2004) "Malnutrition and the severity of lung disease in adults with pulmonary tuberculosis in
Malawi," Int J Tuberc Lung Dis 8:211-217.
5. Papathakis, P. and E. Piwoz (2008) "Nutrition and Tuberculosis: A review of the literature and considerations
for TB control programs," USAID: Africa's Health in 2010
project, http://www.aidsportal.org/Article_Details.aspx?ID=7931
6. Swaminathan, S., C. Padmapriyadarsini, B. Sukumar, S. Iliayas, S.R. Kumar, C. Triveni, P. Gomathy, B.
Thomas, M. Matthew and P.R. Narayanan (2008) "Nutritional Status of Persons with HIV Infection, Persons
with HIV Infection and Tuberculosis, and HIV-Negative Individuals from Southern India," Clin Infect Dis 46:946-
9.
7. Mugusi, F.M., O. Rusizoka, N. Habib and W. Fawzi (2003) "Vitamin A status of patients presenting with
pulmonary tuberculosis and asymptomatic HIV-infected individuals, Dar es Salaam, Tanzania," Int J Tuberc
Lung Dis 7:804-807.

HIV and TB
Introduction
It is estimated that a third of the 36 million people on the planet with HIV/AIDS are infected with M.
tuberculosis (1). This co-infection has been dubbed the "cursed duet," draining approximately 30% of the
annual income of an infected household in both direct and indirect costs, becoming a social and economic
disaster for families (2).

The countries with the highest TB/HIV co-infection rates continue to be in Sub-saharan Africa, where HIV is
ravaging the population. One example is Zambia. It's TB rates were stable in the 1960's and 1970's, but the
number of TB cases quadrupled as HIV spread across the country (3). Worldwide, the largest increase in co-
infection with TB and HIV has occurred in the 25-44 year old population range (4). Since this age group is
generally so active in the workforce, the consequent economic impact is huge.

A TB patient who is infected with HIV has lost

over half his body weight
(www.WorldLungFoundation.org)
Co-Infection
Why is co-infection so common? HIV infection is commonly listed as the highest risk-factor for becoming
infected with TB, as well as greatly increasing a person's risk for developing active tuberculosis. Because
HIV/AIDS depletes the immune system, opportunistic infections become serious problems. (An opportunistic
infection is an infection that is kept under control in an immuno-competent person, but becomes too much for
the immune system when infected with HIV.) People with healthy immune systems can become infected with
TB but only about 5% develop active disease. In the population with latent TB, the infection may lie dormant for
years, becoming active disease only when the body's immune system is weakened, as occurs with HIV
infection (2).

Once latent TB resurfaces in an HIV-positive patient, it can move from the lungs to other organs more rapidly
than in patients without HIV infection. This is known as extrapulmonary TB. As it moves into other organs and
tissues, it causes irreversible damage. With time, more systems become involved with the extrapulmonary TB,
weakening them in turn and allowing the body to become devastated with increasing speed. These weakened
systems allow the HIV to progress more rapidly, greatly expediting both disease processes and greatly
decreasing life expectancy (2).

Treatment and Related Issues

Medical treatment of TB and HIV/AIDS is extremely complicated due to several severe medication interactions,
often malnutrition and conflicting disease processes. Treatment for TB always takes precedence over
HIV/AIDS treatment due to TB's infectious nature through the air. However, with antiretroviral therapy taking a
backseat to TB, the HIV infection may progress more quickly, weakening the immune system even more
rapidly. This makes it easier for opportunistic infections to take over, putting more stress on the patient's body,
lowering life-expectancy (5).
The anti-TB drug thiacetazone can cause serious,
sometimes fatal, side effects in many HIV-positive patients (www.WorldLungFoundation.org)

A major issue affecting treatment of HIV/TB Co-infection is the potential cost of treatment. The preferred
treatment for HIV is highly active combination anti-retroviral therapy. While these drugs are very effective at
slowing the progression of HIV to AIDS, they are expensive, especially for people in developing countries.
Adding the cost of the common antibiotics used to treat TB moves the price of medication out of reach for even
more people (6). Further complicating the problem is that the co-infection and weakened immune system
makes the patients more susceptible to adverse drug reactions from potentially quite toxic drugs.

The stigma associated with both diseases is another major issue surrounding diagnosis and treatment of both
HIV and TB. The stigma of the separate and combined diseases is intertwined with disease perception. Many
consider the TB of co-infection with HIV to be a new disease, since "the TB of today should be given another
name because it doesn't cure" (7). In many developed countries, the TB of the past was viewed as a curable,
relatively simple infection that was acquired in more mundane ways like "men smoking tobacco or marijuana,"
or "drinking home brewed liquor." In contrast, new TB is acquired though "hanging out in bars" and "sexual
transgressions" (7). When someone is diagnosed with TB, their past behavior is often viewed as improper,
immoral, with a consequent judgment passed about how the person contracted HIV/TB. These judgments can
be reinforced by moral judgments from religious leaders, since "Satan is these two diseases" (7).

This problem with TB is compounded by the presence of HIV, which has been highly stigmatized since it
exploded in the 1980's. The most common ways to transmit HIV are through intimate sexual contact and blood-
to-blood contact from transfusions or sharing needles, which is common among injection drug users. Thus, HIV
infection is commonly associated with unprotected sex and drug use.
In many parts of the world, TB and HIV are both so common and occur together so often that the distinctions
between the two diseases are obscured, creating the need to create a new label for the joint stigmatization
faced by patients. Further compound the TB-HIV stigma is the misinformation surrounding treatment of both
diseases. People with active cases of TB are considered most contagious for the first 2-3 weeks of treatment.
Close contact should be avoided during those weeks; however, misinformation often leads to exaggerated
fears about contracting the disease, causing prolonged physical and social isolation (7).

One positive aspect is that concurrent testing for HIV and TB is becoming an increasingly common intervention
at HIV treatment centers worldwide. Previously, neither HIV nor TB clinics commonly tested for the other
disease. While the disapprobation surrounding both diseases can make dual testing difficult, it is an important
step in reducing the number of co-infections. Early detection of TB/HIV infection and early treatment can help to
reduce the severe effects of co-infection on the body's immune system, increasing life expectancy. The sooner
a person begins treatment for TB, the less chance they have of infecting others, and the sooner they are aware
of their HIV positive status, the more they are able to limit their high-risk behavior, providing less chances to
infect others with HIV (6).

References
1. Colebunders, R. and M.L. Lambert 2002) "Management of co-infection with HIV and TB: Improving
tuberculosis control programmes and access to highly active antiretroviral treatment is crucial" Brit Med
J324:802-803.
2. Sharma, S.K., A. Mohan, and T. Kadhiravan (2005) "HIV-TB co-infection: Epidemiology, diagnosis and
management," Ind. J Med Res 212:550-567.
3. Godfrey-Faussett, P. and H. Ayles (2003) "Can we control tuberculosis in high HIV prevalence
settings?," Tuberculosis 83:68-76.
4. World Health Organization (2006) "Tuberculosis and HIV/AIDS - Some Questions and
Answers" http://www.searo.who.int/en/Section10/Section18/Section356/section421_1624.htm
5. Corbett, E.L., C.J. Watt, N. Walker, D. Maher, B.G. Williams, M.C. Raviglione and C. Dye (2003). "The
Growing Burden of Tuberculosis: Global Trends and Interactions with the HIV Epidemic," Arch Intern
Med 163:1009-1021.
6. Manosuthi, W., S. Chottanapand, S. Thongyen, A. Chaovavanich, and S. Sungkanuparph (2006) "Survival
Rate and Risk Factors of Mortality Among HIV/Tuberculosis Coinfected Patients With and Without Antiretroviral
Therapy," J Acq Immun Def Syndrome 431:42-46.
7. Bond, V. and L. Nyblade (2006) "Importance of Addressing the Unfolding TB-HIV Stigma in High HIV
Prevalence Settings," J Comm Appl Soc Psych 16:452-461.

Application to Biotechnology
Gene for histone-like protein (hupB [Rv2986c]) of Mycobacterium tuberculosis had been used to distinguishing
members of the MTB complex from other mycobacterium species and differentiating between members within
the complex.
In addition, in vivo complementation in Mycobacterium tuberculosisstrain H37Ra can be used to identify
genomic fragments associated with virulence. By studying the genes encoding for virulent gene products, a
combination of drugs and vaccines could be developed to target the MDR and XDR characteristic of the
pathogen.

Current Research
Since the pathogen-host interaction of Mycobacterium tuberculosis is still unknown, much of the current
research is geared towards the understanding of the mechanism of virulence. For example, one such research
showed that prokaryotic- and eukaryotic-like isoforms of the glyozxylate cycle enzyme isocitrate lyase (ICL) are
jointly required for fatty acid catabolism and virulence in Mycobacterium tuberculosis. This discovery provides
insight such as drugs that are glycoxylate cycle inhibitors could be used to treat tuberculosis. (12).
Another group of scientists found that a newly identified protein with carboxyesterase activity is required for the
virulence of Mycobacterium tuberculosis. They found that the gene MT2282 encodes a protein that is
associated with carboxyesterase. It hydrolyzes ester bonds of the substrate. When a strain containing a mutant
of this gene was used to infect mice, the mice’s life was prolonged as compared with those that were infected
with the wild type strain. (5)
In addition, as mentioned earlier, very little is known regarding host-microbe interaction that happens before M.
tuberculosis gets into the macrophages and how M. tuberculosis adheres to the host is still being researched.
One research suggested M. tuberculosis produces tiny pili that enable them to colonize the host by adhering to
the host and invading the macrophages and epithelial cells of the host. (1) The pili produced are called MTP.
The study is important because MTP could be used as vaccine because MTP-mediated events are critical for
TB infection. (1)

References
1. Alteri, C.J., Xicohtencatl-Cortes, J., Hess, S. Caballero-Olin, G., Giron, J.A., and Friedman, R.L.
“Mycobacterium tuberculosis produces pili during human infection.” Microbiology 2007; 104(12): 5145-5150.
2. Aranaz A, Liébana E, Gomez-Mampaso E, et al. “M. Tuberculosis subsp. caprae subsp. nov.: a taxonomic
study of a new member of the Mycobacterium tuberculosis complex isolated from goats in Spain. Int J Syst
Bacteriol 1999; 49:1263 73.
3. Banaiee, N., Jacobs Jr, W.R., and Ernst, J.D. “Regulation of Mycobacterium tuberculosis whiB3 in the
mouse lung and macrophages.” Infection and Immunity 2006; 74: 6449-6457.
4. Barksdale, L. and Kim, K. “Mycobacterium.” Bacteriological Reviews 1977; 41: 217-372.
5. Bishai, W.R., Lun, S. “Characterization of a novel cell wall-anchored protein with carboyesterase activity
required for virulence in Mycobacterium tuberculosis.” The Journal of Biological Chemistry 2007; 1-22.
6. Chen, M., Gan, H., and Rernold, H.G. “A mechanism of virulence: virulent M. Tuberculosis strain H37Rv, but
not attenuated H37Ra, causes significant mitochondrial inner membrane disruption in macrophages leading to
necrosis.” The Journal of Immunology 2006; 176: 3707-3716.
7. Cole, S.T. “Comparative and functional genomics of the Mycobacterium tuberculosis complex.” Microbiology
(2002); 148: 2919-2928.
8. Cole, S. T. , Brosch, R. , Parkhill, J. , Garnier, T. , Churcher, C. , Harris, D. , Gordon, S. V. , Eiglmeier, K. ,
Gas, S. , Barry, C. E. “Deciphering the biology of Mycobacterium tuberculosis from the complete genome
sequence.” Nature 1998; 393(6685): 537-44.
9. Cosma, C. L., K. Klein, R. Kim, D. Beery, and L. Ramakrishnan. “Mycobacterium marinum Erp is a virulence
determinant required for cell wall integrity and intracellular survival.” Infect. Immun. 2006; 74:3125-3133.
10. Ducati, R.G., Ruffino-Netto, A., Basso, L.A., Santos, D.S. “The resumption of consumption – A review on
tuberculosis.” Rio de Janeiro 2006; 101: 697-714.
11. Manganelli, R., Voskuil, M.I., Schoolnik, G.K., and Smith, I. “The Mycobacterium tuberculosis ECF sigma
factor sigmaE: role in global gene expression and survival in macrophages.” Mol Microbiol 2006; 41: 423– 437.
12. Munoz-Elias, E.J., McKinney, J.D. “Mycobacterium tuberculosis isocitrate lyases 1 and 2 are jointly required
for in vivo growth and virulence.” Nat Med. 2005; 11: 638-644.
13. NCBI. 24 May 2007. Welcome Trust Sanger Insitute. 2 June 2007
<http://www.ncbi.nlm.nih.gov/sites/entrez?db=genomeprj&cmd=Retrieve&dopt=Overview&list_uids=224>.
14. Riley, L.W. “Of mice, men and elephants: Mycobacterium tuberculosis cell envelope lipids and
pathogenesis.” American Society for Clinical Investigation 2006; 116:1475-1478.
Edited by Ying Liu of Rachel Larsen and Kit Pogliano

Comas, Iñaki, et al. (2013) Out-of-Africa migration and Neolithic coexpansion of Mycobacterium
tuberculosis with modern humans. Nature Genetics 45, 1176-1182.
Todar K., Todar’s Online Textbook of Bacteriology.

Siklus Hidup Organisme

Siklus hidup Mycobacterium tuberculosis terdiri
dari lima tahap.

Tahap satu adalah ketika bakteri TBC dihirup

melalui udara. Ini disebut onset. Dalam beberapa
kasus, selama onset, bakteri dapat mereproduksi
dan memulai infeksi. Tuberkulosis dimulai ketika
mikobakteri dihirup, dan mencapai makrofag
alveolar.

Tahap kedua adalah simbiosis yang dapat

berlangsung selama tujuh hingga 21 hari. Selama
tahap dua, bakteri akan bereproduksi jika tidak
terbunuh.

Tahap ketiga adalah nekrosis caseous awal,

dan berlangsung selama 14 hingga 21
hari. Ini adalah tahap di mana TBC mulai
berkembang. Hal ini disebabkan oleh
penurunan laju pembelahan biner.Kemudian,
bakteri akan membunuh makrofag yang tidak
teraktivasi di sekitarnya, dan kehabisan
sel untuk membelah diri. Bakteri ini
kemudian menghasilkan kondisi anoksik dan
kadar pH menurun.

Tahap empat adalah saling mempengaruhi

respon imun yang merusak jaringan dan
makrofag. Tahap ini dimulai setelah 21
hari. Mycobacterium tuberculosis
menggunakan makrofag tidak aktif, yang
mengelilingi tuberkulum, untuk bereproduksi
yang menyebabkan tuberkel tumbuh. Tuberkel
kemudian menyebar ke paru-paru. Jika
menyebar ke aliran darah, pasien dapat
menderita TBC di luar paru-paru.

Tahap lima adalah pencairan dan pembentukan

rongga. Sejumlah kecil orang berhasil
mencapai tahap ini. Selama periode ini,
tuberkel akan mencair di beberapa
titik. Ini menyebabkan penyakit menyebar
lebih cepat.
https://sites.google.com/site/mycobacteriumtbstudy/home/life-cycle-of-
organism
Siklus hidup Mycobacterium tuberculosis terdiri dari lima tahap.

Tahap satu adalah ketika bakteri TBC dihirup melalui udara. Ini disebut onset. Dalam beberapa
kasus, selama onset, bakteri dapat mereproduksi dan memulai infeksi. Tuberkulosis dimulai
ketika mikobakteri dihirup, dan mencapai makrofag alveolar.
Tahap kedua adalah simbiosis yang dapat berlangsung selama tujuh hingga 21 hari. Selama
tahap dua, bakteri akan bereproduksi jika tidak terbunuh.
Tahap ketiga adalah nekrosis caseous awal, dan berlangsung selama 14 hingga 21 hari. Ini
adalah tahap di mana TBC mulai berkembang. Hal ini disebabkan oleh penurunan laju
pembelahan biner.Kemudian, bakteri akan membunuh makrofag yang tidak teraktivasi di
sekitarnya, dan kehabisan sel untuk membelah diri. Bakteri ini kemudian menghasilkan kondisi
anoksik dan kadar pH menurun.
Tahap empat adalah saling mempengaruhi respon imun yang merusak jaringan dan
makrofag. Tahap ini dimulai setelah 21 hari. Mycobacterium tuberculosis menggunakan
makrofag tidak aktif, yang mengelilingi tuberkulum, untuk bereproduksi yang menyebabkan
tuberkel tumbuh. Tuberkel kemudian menyebar ke paru-paru. Jika menyebar ke aliran darah,
pasien dapat menderita TBC di luar paru-paru.
Tahap lima adalah pencairan dan pembentukan rongga. Sejumlah kecil orang berhasil mencapai
tahap ini. Selama periode ini, tuberkel akan mencair di beberapa titik. Ini menyebabkan penyakit
menyebar lebih cepat.

Struktur genom
Mycobacterium tuberculosis memiliki kromosom bundar sekitar 4.200.000 nukleotida. Konten G + C adalah sekitar
65%. (13)
Genom M. tuberculosis dipelajari secara umum menggunakan strain M. tuberculosis H37Rv. Genom mengandung
sekitar 4000 gen. Gen yang mengkode metabolisme lipid adalah bagian yang sangat penting dari genom bakteri, dan
8% genom terlibat dalam aktivitas ini. (7)
Spesies berbeda dari kompleks Mycobacterium tuberculosis menunjukkan keterkaitan DNA 95-100% berdasarkan
studi homologi DNA, dan urutan gen 16S rRNA persis sama untuk semua spesies. Jadi beberapa ilmuwan
menyarankan bahwa mereka harus dikelompokkan sebagai spesies tunggal sementara yang lain berpendapat bahwa
mereka harus dikelompokkan sebagai varietas atau subspesies dari M. tuberculosis. (2)
Plasmid dalam M. tuberculosis penting dalam mentransfer virulensi karena gen pada plasmid lebih mudah ditransfer
daripada gen yang terletak pada kromosom. Salah satu plasmid 18kb dalam strain M. tuberculosis H37Rv terbukti
melakukan transfer gen.