A Study on Bacterial Pathogens causing Secondary Infections in Patients Suffering from Tuberculosis and their Pattern of Antibiotic Sensitivity

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Int.J.Curr.Microbiol.App.ci (2016) 5(8): 197-203 International Journal of Current Microbiology and Applied ciences IN: 2319-7706 Volume 5 Number 8 (2016) pp. 197-203 Journal homepage: http://www.ijcmas.com Original esearch Article http://dx.doi.org/10.20546/ijcmas.2016.508.021 A tudy on Bacterial Pathogens causing econdary Infections in Patients uffering from Tuberculosis and their Pattern of Antibiotic ensitivity Amaryllis Langbang 1, Nabajit Deka 2 *, Hafizur ahman 1 and Devjyoti Kalita 3 1 egional Drug Testing Laboratory, Guwahati, 781037, Assam, India 2 Department of Microbiology, Gauhati Medical College Hospital, Guwahati, 781032, Assam, India 3 Department of Pharmaceutical ciences, Dibrugarh University, Dibrugarh, 786004, Assam, India *Corresponding author A B T A C T K e y w o r d s Antibiotics, Disc diffusion Method, ugar Fermentation, econdary Infection. Article Info Accepted: 12 July 2016 Available Online: 10 August 2016 Tuberculosis (TB) is a potentially serious infectious disease infections began increasing in 1985, partly because of the emergence of HIV. India is the highest TB burden country with World Health Organisation (WHO) statistics for 2011 giving an estimated incidence figure of 2.2 million cases of TB for India out of a global incidence of 8.0 million cases. econdary bacterial infection is one of the most important complications in patients with pulmonary tuberculosis. o it become important to study about secondary infection associated with tuberculosis. In our study we tried to isolate Bacterial pathogens causing secondary Bacterial infection in patients suffering from tuberculosis. In duration of 3 months, w.e.f February to April 2015 the total number of 50 positive sputum samples examined for secondary infection where taphylococcus aureus is the most common pathogen isolated which constitute around 32% while Klebsiella pneumonia constitute the least with just $%.After isolation we have studied about drug sensitivity of these pathogens by disc diffusion method and found all 8 isolates of Moraxella catarahallis are resistant against ciprofloxacin. 3 isolate among the 16 isolates of taphylococcus aureusis resistant against erythromycin and oxacillin..most of isolated gram negative bacilli was resistant against Amikacine, Ampicillin,Ciprofloxacin.All the isolates of Pseudomonas aeruginosa was resistant against Amikacine, Ciprofloxacin. Introduction Tuberculosis (TB) is a potentially serious infectious disease that mainly affects our lungs. Once rare in developed countries, tuberculosis infections began increasing in 1985, partly because of the emergence of HIV. India has approximately two to three million people infected with Tuberculosis. India is the highest TB burden country with World Health Organisation (WHO) statistics for 2011 giving an estimated incidence 197

Int.J.Curr.Microbiol.App.ci (2016) 5(8): 197-203 figure of 2.2 million cases of TB for India out of a global incidence of 8.0 million cases (outhwick et al., 2007). Tuberculosis is the biggest health issue that lies around India, but what makes is worse is the newly and recently discovered global phenomenon of TD-TB-Totally Drug-esistant TB started off with MD-TB, and moved on to XD- TB. Along with drug resistance, econdary bacterial infection also become the most important complications in patients with pulmonary tuberculosis. The major reason is the inhibition of human defence forces during the course of active tuberculosis. It has been confirmed by studies who worked on immune response of lung cell during experimental tuberculosis in mice. In another study, T lymphocyte deficiency in patients with infiltrative pulmonary tuberculosis was observed. Another reason for lowering of immune system of tuberculosis patients might be the hormonal changes such as inhibited pituitary function, higher adrenal activity, elevated cortisol level, altered thyroid function and increased pancrease functional activity during the initial period of tuberculosis. It has also been observed that the alveolar lining material of patient with active Pulmonary tuberculosis has less bactericidal activity against bacterial infection. Materials and Methods Place and Duration of study The study was conducted at the Department of Microbiology, Assam Down Town University from February 2015 to April 2015. election of isolates Patients admitted in TB Hospital, Guwahati and TB Chest Hospital, hillong for their tuberculosis treatment are the subject of the study. On the basis of the clinical finding and physician s recommendation patients having some complication like nonsubsiding fever, cough, tomach pain, muscle pain, Chest pain in spite of taking antituberculosis drugs were selected as subject of the study. Processing of samples Isolates were identified by standard microbiological procedures (Gram staining, colonial morphology, slide and tube coagulase test, motility, biochemical tests). eference strain of gram positive cocci taphylococcus aureus ATCC 35556, gram negative bacilli Pseudomonas aeruginosa ATCC were used as control. After proper identification we have studied about the drug pattern of the identified microorganisms by disc diffusion method based on Clinical Laboratory tandards Institute (CLI, formerly National Committee for Clinical Laboratory tandards (NCCL), 2004. Mueller-Hinton agar (hi-media) was inoculated with a suspension prepared from identified micro-organisms. The antifungal disc (hi-media) was then placed on the medium and the plate was incubated at 37 0 C. The zone size was measured after 24 hours and interpreted as per approved CLI guideline. esult and Discussion Total 50 numbers of sputum sample from T.B. patient with secondary infection were collected. The organisms isolated from the sputum sample and identified where taphylococcus aureus (32%) is major pathogen followed by Pseudomonas aeruginosa (16%), Moraxella catarahallis (14%), taphylococcus epidermidis (12%), Escherichia coli and treptococcus pyogenes (8%), Hemophilus influenza (6%). Here we found Klebsiella pneumonia as 198

Int.J.Curr.Microbiol.App.ci (2016) 5(8): 197-203 least found micro-organsim which is 4%.When we studied their drug pattern, found that all 8 isolates of Moraxella catarahallis are resistant against ciprofloxacin. 3 isolate among the 16 isolates of taphylococcus aureus is resistant against erythromycin and oxacillin. Most of isolated gram negative bacilli was resistant against Amikacine, Ampicillin, Ciprofloxacin. All the isolates of Pseudomonas aeruginosa was resistant against Amikacine, Ciprofloxacin, ceflazidine. M. Nagatak et al., (2014), had studied that the causative microorganism of the secondary infections in patients with tuberculosis sequele were essentially similar in those with other lower respiratory tract infection.i.e. Chronic bronchitis, bronchiectasis, diffuse panbonchiolitis, chronic pulmonary emphysema, etc. According to their clinical observation they clearly demonstrated that there were differences between the causative microorganism in patients hospitalalized during 1988 to1989 and those in patients without admission. Gram-negative bacilli, including P.aeruginosa, GNF-GNB and GF- GNB, and taphylococcus aureus were predominant in hospitalized patients. On the contrary, treptococcus pneumonia, H.influenza, and Branhamella catarrhalis were major pathogenic bacteria in patients without hospitalization (hishido et al., 2014). Here in our study also we have found taphylococcus aureus as most predominant micro-organism followed by P.aeruginosa. Zakaria et al., 2013 in a studied on the current tatus of secondary Infection of Pulmonary T.B. among 450 TB suspected patients during eptember to December 2012 periods in Bangladesh. Among those, 100 samples were cultured for isolating secondary bacterial infection of newly detected pulmonary TB (PTB) patients whose are already treated by TB drugs. From these cultured samples, 22 were isolated as Klebsiella spp and 10 were isolated as taphylococus (Joynal et al., 2013). Here in our study we have found taphylococcus as mostly found isolates nearly 44%including coagulase negative staphylococcus but Klebsiella is found least numbers nearly 4% outhwick et al., (2007) had studied that Isolation of secondary bacterial infection from the pulmonary tuberculosis patients from the new cases and failure of tuberculosis treatment. The antimicrobial susceptibility to the isolated secondary bacterial infection in pulmonary tuberculosis in the new and failed treated cases. Table.1 List of Isolated Micro-organisms from putum amples Name of Isolated organism No of Isolate from sputum sample taphylococcus aureus 32% Pseudomonas aeruginosa 16% Moraxella catarahallis 14% taphylococcus epidermidis 12% Escherichia coli 8% treptococcus pyogenes 8% Hemophilus influenza 6% Klebsiella pneumoniae 4% 199

Int.J.Curr.Microbiol.App.ci (2016) 5(8): 197-203 Table.2 Antibiotic usceptibility profile of isolates Isolated Micro-organism Antibiotic used usceptible esistance taphylococcus aureus Cefoxitine Cefuroxime Cephaloxin Co-trimoxazole Erythromycin (3 isolates) Oxacillin (3 isolates) Penicillin Chloramphenicol Linezolid Ofloxacin Vancomycin Pseudomonas aeruginosa Amikacin Ceflazidine Tazobactum Ciprofloxacin Gentamycin Ofloxacin Cefeprime Imipenem Tobramycin Amikacin Ampicillin Ceftriaxone Moraxella catarahallis Cefuroxime Escherichia coli Cephalothin Klebsiella pneumonia Ciprofloxacin Gentamycineulbactum Cefepime Ceftazidine Clavulonic acid Imipenem Ofloxacin Hemophilus influenza Ampicillin Cefuroxime Chrolamphenicol C0-trimoxazole Tetracycline Ampicillin Ciprofloxacin Erythromycin Penicillin 200

Int.J.Curr.Microbiol.App.ci (2016) 5(8): 197-203 Vancomycin treptococcus pyogenes Cephalothin Clindomycin Co-trimoxazole Erythromycin Penicillin Fig.1 ugar fermentation test for pecies identification Fig.2 Antibiotic usceptibility Testing by disc Diffusion Method 201

Int.J.Curr.Microbiol.App.ci (2016) 5(8): 197-203 Fig.3 From the 50 collected sputum specimens, the results show the percentage of positive secondary bacterial infection is 72%(n. 36), and negative is 28% (n.14), also the study showed that 27 from the 36 cases had a positive secondary bacterial infection were from new cases 75%, while only 9 of 36 cases had a positive secondary bacterial infection were from failure of tuberculosis treatment 25%.The secondary bacterial infection in pulmonary tuberculosis were found in 21 male patients(58.3%) and 15 in female patients (40.7%). In this study there was an isolation four types of secondary bacterial infection in those 36 patients such as: 20 patients with treptococcus pneumoniae (55.6%), 8 with treptococcus pyogens (22.2%), 4 with taphylococcus auras (11.1%) and 4 with Klebsiela pneumoniae (11.1%). In this most of organisms were resistance against respected antibiotics (outhwick et al., 2007). Here in our study except treptococcus pneumoniae, we have found all other micro-organisms and their drug pattern shows that they were resistant against some important drugs like Amikacine, Ampicillin, Ciprofloxacin, Erythromycin, Oxacillin. Jasmer et al., (2002) in a study titled Clinical practice. Latent tuberculosis infection found that Pseudomonas aeruginosa, was the major pathogenic bacteria responsible for the chronic respiratory failure and/or fatal outcome in the post tuberculosis patients. Patients with complication, including aspergilosis, atypical mycobacteriosis, bronchial asthma, and so forth, showed no specific causative microorganism for the secondary infection except frequent isolation of Haemophilus influenza (Jasmer et al., 2002). In our study we have found staphylococcus aureus (32%) as a major pathogen followed by Pseudomonas aeruginosa (16%). eferences Bergeys manual of determinative Bacteriology(9 th Edition) Connie,. Mohan, George Manuselis : Textbook of Diagnostic Microbiology. haddock, E., N. Bosman, T. Nana, C. riruttan, C. Feldman. 2014. outh Afr. J. Infect. Dis., 29(1): 23-26. Jasmer,.M., Nahid, P., Hopewell, P.C. 2002. Clinical practice. Latent 202

Int.J.Curr.Microbiol.App.ci (2016) 5(8): 197-203 tuberculosis infection. N. Engl. J. Med., 347(23): 1860-6. Kenneth, J., yan, C., George yan. herris Medical Microbiology(an introduction to infectious disease). Cristina, M., Peter, M., mall, et al. 2006. Variable host-pathogen in Mycobacterium tuberculosis. Nature Int. Interdisciplinary J. sci..vol.103:,2869-2873 Joynal Abedin Khan, Md., Zakaria Ahmed. Department of Microbiology, Primeasia University, etrived on May 2,2013,tudy on the Current tatus of econdary Infection of Pulmonary tuberculosis, www.academia.edu, 3223351: 11-16. Patrick,., Murry, Ellen Jo Baron, James, H., Jorgensens, Marie Lewis Landy, Michael, A., P. Pallem. Manual of clinical microbiology. Patric,., Murry, Ken,., osenthal, Michael A., Pfakeer. Medical Microbiology. NTCP Guidelines on PMDT in India. Central TB Division, Directorate General of Health ervices, Ministry of Health & Family Welfare, Nirman Bhavan, New Delhi-110011. owland, K. 2012. Totally drug-resistant TB emerged in India: Nature News & Comment. Nature Publishing Group: cience journals,job and information. etrieved April 3, 2013 hishido, H., Nagai, H., Kurashima, A., Yoneda, M., Nagatake, T., Matsumoto, K. et al. 2014. International Journal of Tuberculosis and Lung Disease, Tuberculosis sequelae: secondary bacterial infections, 873-880. outhwick, Frederick. 2007. Chapter 4: pulmonary infection. Infectious Diseases: A Clinical short course, 2 nd ed. McGraw-Hill Medical Publishing Division.P.104IBN 0071477225. unita Bansod and Mahendra ai. 2008. Emerging Mycotic Infection in Patient infected with T.B., World J. medical sci.,3(2): 74-80. hailaja, V.V., L.A. Pai, D.. Mathur, V. Lakshmi. et al. 2004. Prevalence of bacterial and fungal agents causing lower respiratory tract infection in patients with HIV infection, Indian J. Med. Microbiol., 22: 28-33. How to cite this article: Amaryllis Langbang, Nabajit Deka, Hafizur ahman and Devjyoti Kalita. 2016. A tudy on Bacterial Pathogens causing econdary Infections in Patients uffering from Tuberculosis and their Pattern of Antibiotic ensitivity. Int.J.Curr.Microbiol.App.ci. 5(8): 197-203. doi: http://dx.doi.org/10.20546/ijcmas.2016.508.021 203