ABSTRACT
Multi-drug resistant tuberculosis (MDR-TB) remains a major challenge for
the control of tuberculosis worldwide. Susceptibility testing of Mycobacterium tuberculosis isolates to
first line drugs is therefore necessary to ascertain the diagnosis of MDR-TB. A
total of 437 re-treatment patients’ samples were screened for Acid Fast Bacilli
(AFB), 72 were smear positive giving a prevalence of 16.47%. Out of 72 smears
positive, 62 were culture positive, 6 were culture negative and 4 were
contaminant using Lowenstein Jensen medium. Out of 62 cultures positive, 57
were found to be Mycobacterium tuberculosis complex (MTBC) using
immunochromatographic test while 5 were negative which were considered to be
NTM (Non-Tuberculosis Mycobacteria). In this study the susceptibility of 57
MTBC isolates to isoniazid (INH), rifampicin (RIF), streptomycin (STR) and
Ethambutol (EMB) was determined by Lowenstein Jensen proportion method (LJPM)
and Nitrate Reductase Assay (NRA). LJ PM detected 41(71.93%) MDR-TB while NRA
detected 44(77.19%) MDR-TB isolates. The occurrence of poly resistance to
anti-TB drugs using NRA and LJ PM was 12% and 14% while pan susceptible were of
11% and 14% by LJ PM and NRA respectively. The sensitivities and specificities
of NRA compared to those of LJPM were observed to be 98% and 98%, 64% and 68%,
89% and 92%, 80% and 77% for RIF, INH, STR, and EMB respectively. Positive
predictive values were 91%, 93%, 87% and 83% for RIF, INH, STR and EMB
respectively. Negative values were 80%, 92%, 67% and 90% for RIF, INH, STR and
EMB respectively. Good agreement was found in all the tests with κ values of
0.63, 0.61, 0.59, and 0.61for RIF, INH, STR, and EMB respectively. The HIV/TB
co-infections and HIV/MDR-TB co-infections were reported to be 9.7% and 7%
respectively. Highest MDR-TB among age groups of 21-30 and 31-40 years were
detected by NRA and LJPM and higher MDR-TB and TB were observed in male. The
NRA has the potential to be a useful tool for rapid detection of MDR-TB in
resource-limited settings because of its higher sensitivity and specificity.
vi
TABLE OF
CONTENTS
COVER PAGE................................................................................................................................ i
FLY LEAF..................................................................................................................................... ii
TITLE
PAGE........................................................................................................... Error! Bookmark not defined.
CERTIFICATION........................................................................................................................ iv
ACKNOWLEDGEMENTS........................................................................................................... v
TABLE OF CONTENTS............................................................................................................. vii
CHAPTER ONE............................................................................................................................. 1
1.0 INTRODUCTION.................................................................................................................... 1
1.1 Background of the Study.......................................................................................................... 1
1.2 Statements of Problems............................................................................................................. 5
1.3 Justification............................................................................................................................... 6
1.4 Aim and Objectives................................................................................................................... 7
1.4.1 Aim......................................................................................................................................... 7
1.4.2 Objectives.......................................................................................................................... 7
CHAPTER TWO............................................................................................................................ 8
2.0 LITERATURE REVIEW...................................................................................................... 8
2.1 Mycobacteria............................................................................................................................ 8
2.1.1 Classification of the Genus Mycobacterium........................................................................ 8
2.1.3 Growth and Metabolic Characteristics of Mycobacteria...................................................... 10
2.1.4 Mycobacterial Antigens........................................................................................................ 11
2.1.5 The M. tuberculosis
Genome................................................................................................ 11
2.1.6 The Origins and evolution of Mycobacterium
tuberculosis.................................................. 12
2.1.7 Epidemiology of tuberculosis............................................................................................... 13
2.1.8. Pathogenesis and Virulence of Tuberculosis....................................................................... 15
2.1.9 Primary infection.................................................................................................................. 15
2.1.11 Pulmonary tuberculosis....................................................................................................... 17
2.1.13 Diagnosis of tuberculosis.................................................................................................... 18
2.1.13.1 Mantoux test..................................................................................................................... 18
2.1.13.2 Chest X-ray...................................................................................................................... 19
2.2 TB Drug Susceptibility Testing............................................................................................... 22
vii
ACP
AFB
AIDS
ATCC
BCG
Bp
BSL
C
CC
CFU
CR
DMSO
DNA
DR
DST
EMB
G
HIV
ICT
IJTLD
INH
InhA
Acyl carrier protein
Acid-fast bacilli
Acquired
Immunodeficiency Syndrome
American
Type Culture Collection
Baccile Calmette Guerin
Base pair
Biosafety
level
Cytosine
Critical Concentration
Colony
Forming Unit
Compliment
Receptors
Dimethyl
sulphoxide
Deoxyribonucleic
acid
Drug
resistant
Drug
Susceptibility Testing
Ethambutol
guanine
Human
immunodeficiency virus
Immunochromatographic
Test
International
Journal of Tuberculosis and Lung Disease
Isoniazid
Enoyl-acyl
carrier protein reductase
IPM
IUATLD
KasA
KatG
KNO3
LJ
LJPM
LPA
MDR-TB
MGIT
MIC
MODS
MTB
MTBC
MTT
NADH
NALC
NAOH
NRA
NTBLCP
NTM
NTRL
OADC
Indirect Proportion Method
International
Union against Tuberculosis and Lung Disease
β-ketoacyl-ACP
synthase
Catalase-peroxidase
enzyme
Potassium
nitrate
Lowenstein-Jensen
Lowenstein-Jensen
proportion method
Line
probe assay
Multidrug
resistant tuberculosis
Mycobacterium
Growth Indicator Tube
Minimum
inhibitory concentration
Microscopic
observation drug susceptibility
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