Bacteriology

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Overview


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Head of the Department:

Dr. Sivakumar, S, M.Sc., Ph.D., Scientist 'E'


Email id :

shanmugam[dot]sk[at]icmr[dot]gov[dot]in

Sr. No. Name of the Staff Designation
1 Dr. Sivakumar S Scientist E
2 Dr. Azger Dusthackeer V.N Scientist D
3 Dr. Priya R Scientist D
4 Dr. Ramakrishnan K Sr. Technical Officer(2)
5 Ms. Angayarkanni B Technical Officer-C
6 Ms. Devika K Technical Officer-C
7 Mrs. Mahizhaveni B Technical Officer-C
8 Mr. Michel Prem Kumar M Technical Officer-C
9 Mr. Radhakrishnan A Technical Officer-C
10 Mr. Rajaraman K Technical Officer-C
11 Mr. Ravikumar D Technical Officer-C
12 Ms. Saraswathi D Technical Officer-C
13 Mr. Thiyagarajan V Technical Officer-C
14 Mrs. Vadivu G Technical Officer-C
15 Mr. Baskaran M Technical Officer-B
16 Mr. Govindaraj S Technical Officer-B
17 Mr. Govindarajan S Technical Officer-B
18 Ms. Radhika G Technical Officer-B
19 Mr. Ramesh Kumar K Technical Officer-B
20 Ms. Sumathi K Technical Officer-B
21 Ms. Devi Sangamithrai Technical Officer-A
22 Ms. Jeyasree K Technical Officer-A
23 Mr. Aaron M Technical Assistant
24 Ms. Aarthi M Technical Assistant
25 Mr. Aashish Ahshan A S Technical Assistant
26 Mr. Adil Rana Technical Assistant
27 Mr. Arun Vasista Muktinutalapati Technical Assistant
28 Ms. Arushi Kabra Technical Assistant
29 Mr. Bablu Kumar Das (PwBD) Technical Assistant
30 Ms. Gowsalya Saminathan Technical Assistant
31 Ms. Jeevarahini R Technical Assistant
32 Mr. Manish Kumar Technical Assistant
33 Mr. Munishwar Technical Assistant
34 Mr. Prabhat Ranjan Technical Assistant
35 Ms. Sandra Jacob Technical Assistant
36 Mr. Sathishkumar G Technical Assistant
37 Ms. Shrijona Hazarika Technical Assistant
38 Mr. Siva Kishore S Technical Assistant
39 Mr. Vasudevan Manoharan Technical Assistant
40 Ms. Veena R Technical Assistant
41 Ms. Nithya R Senior Technician (1)
42 Mr. Rajkumar R Senior Technician (1)
43 Mr. Sivaraman P Senior Technician (1)
44 Mr. Pandidurai M Technician (2)
45 Mrs. Sathya R Technician (2)
46 Mr. Senthilvelan P Lab Assistant-1
47 Ms. Pavithra M Lab Attendant -1
48 Mr. Saravanan M Lab Attendant -1
49 Mr. Kuttappan K Lab Assistant
50 Mr. Rajavarman A Lab Assistant
51 Mr. Sundararajan V Lab Assistant
52 Mr. Venkatesan S Lab Assistant
53 Ms. Silambu Chelvi K Sr. Technical Officer

  • Isolation and Characterisation of the first temperate phage capable of lysogenising M. tuberculosis

    In an effort to develop luciferase reporter phage (LRP) constructs with high sensitivity of detection, attempts were made successfully for isolating a temperate mycobacteriophage capable of infecting and lysogenising M. tuberculosis.

    Well stained acid fast bacilli (AFB) were demonstrated in smears prepared from pot stained sputum and smear results were comparable with conventional ZN method.

    The efficiency of the construct was found to be higher than the existing LRPs with cultures as anticipated. The attempt marked the beginning of diverse attempts to improve the LRP diagnostic assay.

  • LRPs for the rapid detection of dormant tubercle bacilli

    The luciferase reporter phages (LRP) show great promise for diagnostic mycobacteriology.

    Since the tuberculosis (TB) cases among HIV infected population result from the reactivation of latent bacilli, development of LRPs capable of detecting dormant bacteria would be useful.

    In a milestone study, 3 LRP constructs were developed using promoters of genes functioning during dormancy. These LRP constructs exhibited detectable luciferase activity in dormant as well as in actively growing M. tuberculosis .

  • Phagebiotics cocktail as substitute for antibiotic supplements in liquid culture of M. tuberculosis

    Organisms of the normal flora that survive the action of the decontaminating agent during sputum processing can cause heavy contamination of the culture, especially liquid culture.

    Antibiotic supplements are used in liquid cultures to control such growth despite reports that these agents have deleterious effect on the tubercle bacilli.

    This study demonstrated a novel hypothesis that a cocktail of phages that infect and lyse these organisms could be used in liquid cultures instead of the antibiotic supplements with better decontaminating efficiency and M. tuberculosis retrieving capacity.

    Further study established the feasibility of using phage lysin supplement to phagebiotics in decontaminating processed sputum samples in liquid culture of M. tuberculosis . The study opened up new possibility of developing a novel biofriendly method of sputum processing.

  • Phagebiotics cocktail as substitute for antibiotic supplements in liquid culture of M. tuberculosis

    Organisms of the normal flora that survive the action of the decontaminating agent during sputum processing can cause heavy contamination of the culture, especially liquid culture.

    Antibiotic supplements are used in liquid cultures to control such growth despite reports that these agents have deleterious effect on the tubercle bacilli.

    This study demonstrated a novel hypothesis that a cocktail of phages that infect and lyse these organisms could be used in liquid cultures instead of the antibiotic supplements with better decontaminating efficiency and M. tuberculosis retrieving capacity.

    Further study established the feasibility of using phage lysin supplement to phagebiotics in decontaminating processed sputum samples in liquid culture of M. tuberculosis . The study opened up new possibility of developing a novel biofriendly method of sputum processing.

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