Volume-1 ~ Issue-2
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Abstract: Background : Lactate dehydrogenase (LDH) activity was assayed in the sera of 40 adult male and 40 adult female patients within the age group of 16-50 years presenting with acute, Plasmodium falciparum malaria infection and a control group of 40 healthy adults within the same age group.
Study objective: Study was design to determine diagnostic value of serum LDH activity in patient with acute P.falciparum Infection.
Methods: Patient selection and pre-qualification were done by simple random sampling of individuals presenting at the MBS Hospital Outpatient Department with a history of fever and malaise within a period of one to eight days, and who were confirmed to be infected with the P. falciparum malaria parasite by microscopically examination of Giemsa-stained thin blood slides.
Results: The mean serum LDH activity in male patients was found to be 564 ±236.0 IU. This activity is significantly higher than the control LDH activity of 237.10±19.0 IU (p-value is less than 0.05). The mean serum LDH activity among female patients was 468 ±177.0 IU, which is a relatively higher activity compared to the control LDH activity of 237.10 ±19.0 IU (p-value is less than 0.05).
Conclusion: The combination of acute hepatocellular injury and red cell haemolysis induced by the invading merozoites may account for the increase in serum LDH activity during this infection. Therefore serum LDH activity is a potentially valuable enzymatic marker of falciparum malaria infection.
Study objective: Study was design to determine diagnostic value of serum LDH activity in patient with acute P.falciparum Infection.
Methods: Patient selection and pre-qualification were done by simple random sampling of individuals presenting at the MBS Hospital Outpatient Department with a history of fever and malaise within a period of one to eight days, and who were confirmed to be infected with the P. falciparum malaria parasite by microscopically examination of Giemsa-stained thin blood slides.
Results: The mean serum LDH activity in male patients was found to be 564 ±236.0 IU. This activity is significantly higher than the control LDH activity of 237.10±19.0 IU (p-value is less than 0.05). The mean serum LDH activity among female patients was 468 ±177.0 IU, which is a relatively higher activity compared to the control LDH activity of 237.10 ±19.0 IU (p-value is less than 0.05).
Conclusion: The combination of acute hepatocellular injury and red cell haemolysis induced by the invading merozoites may account for the increase in serum LDH activity during this infection. Therefore serum LDH activity is a potentially valuable enzymatic marker of falciparum malaria infection.
[1] Stryer L. Biochemistry. 2nd ed. New York: WH Freeman, 1982.
[2] Sullivan JM, Alpers JP. In vitro regulation of rat heart5'-nucleotidase by adenine nucleotides and magnesium. J Bio Chem 1971; 246:3057-63.
[3] Podlasek SJ, McPherson RA. Streptokinase binds lactatedehydrogenase subunit-M, which shares an epitope with plasminogen.Clin Chem 1989; 35:69-73.
[4] Calbreath DF. Clinical Chemistry. Philadelphia: WB Saunders, 1992.
[5] Wills MR. The Biochemical Consequences of Chronic Renal Failure.New York: Harvey, Miller and Medcalf, 1971.
[6] Timmis AD, Nathan AW. Essentials of Cardiology. Oxford: Blackwell Scientific, 1993.
[7] Castaldo G, Oriani G, Cimino L, et al. Total discrimination of peritoneal malignant ascites from cirrhosis- and hepatocarcinoma-associated ascites by assays of ascitic cholesterol and lactatedehydrogenase. Clin Chem 1994; 40:478-83.
[8] Kanowski D, Clague A. Increased lactate dehydrogenase isoenzyme-1in a case of glucagonoma. Clin Chem 1994; 40:158-9.
[9] Sugaya N, Kanno J, Nirasawa M, et al. Increased activities of cytosolaminopeptidase and lactate dehydrogenase in serum originate from lymphocytes in necrotizing lymphadenitis. Clin Chem 1990; 36:304-6.
[10] Pressley RH, Muntz HG, Falkenberry S, et al. Serum lactic dehydrogenaseas a tumour marker in dysgerminoma. Gynecol Oncol 1992; 4:281-3.
[2] Sullivan JM, Alpers JP. In vitro regulation of rat heart5'-nucleotidase by adenine nucleotides and magnesium. J Bio Chem 1971; 246:3057-63.
[3] Podlasek SJ, McPherson RA. Streptokinase binds lactatedehydrogenase subunit-M, which shares an epitope with plasminogen.Clin Chem 1989; 35:69-73.
[4] Calbreath DF. Clinical Chemistry. Philadelphia: WB Saunders, 1992.
[5] Wills MR. The Biochemical Consequences of Chronic Renal Failure.New York: Harvey, Miller and Medcalf, 1971.
[6] Timmis AD, Nathan AW. Essentials of Cardiology. Oxford: Blackwell Scientific, 1993.
[7] Castaldo G, Oriani G, Cimino L, et al. Total discrimination of peritoneal malignant ascites from cirrhosis- and hepatocarcinoma-associated ascites by assays of ascitic cholesterol and lactatedehydrogenase. Clin Chem 1994; 40:478-83.
[8] Kanowski D, Clague A. Increased lactate dehydrogenase isoenzyme-1in a case of glucagonoma. Clin Chem 1994; 40:158-9.
[9] Sugaya N, Kanno J, Nirasawa M, et al. Increased activities of cytosolaminopeptidase and lactate dehydrogenase in serum originate from lymphocytes in necrotizing lymphadenitis. Clin Chem 1990; 36:304-6.
[10] Pressley RH, Muntz HG, Falkenberry S, et al. Serum lactic dehydrogenaseas a tumour marker in dysgerminoma. Gynecol Oncol 1992; 4:281-3.
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- Abstract
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Abstract- Introduction: Gram-negative pathogens are an important cause of hospital acquired infections throughout the world. Klebsiella pneumoniae has become one of the more common causes of nosocomial infections.
Materials and methods: A total number of 1264 urine, 544 pus and 784 sputum samples from January 2008 to October 2010 were included in the study. Isolates of klebsiella pneumoniae were identified by their morphological and biochemical characteristics. All the isolates of klebsiella pneumoniae identified were subjected to antibiotic sensitivity testing by modified Kirby-bauer disc diffusion method.
Results: The number of klebsiella pneumoniae isolates were 254 from 1264 urine samples, 135 from 544 pus samples and 191 from 784 sputum samples. Majority of the strains isolated were sensitive to Amikacin.
Conclusion: The present study from 2008 to 2010 reveals the incidence of infections due to klebsiella pneumoniae strains in the hospitalized patients and their tendency towards antibiotic resistance.
Key words: Kebsiella pneumoniae, nosocomial infections, pneumonia, urinary tract infections, beta-lactamase, ESBL's, Gram-negative, non-motile, urease.
Materials and methods: A total number of 1264 urine, 544 pus and 784 sputum samples from January 2008 to October 2010 were included in the study. Isolates of klebsiella pneumoniae were identified by their morphological and biochemical characteristics. All the isolates of klebsiella pneumoniae identified were subjected to antibiotic sensitivity testing by modified Kirby-bauer disc diffusion method.
Results: The number of klebsiella pneumoniae isolates were 254 from 1264 urine samples, 135 from 544 pus samples and 191 from 784 sputum samples. Majority of the strains isolated were sensitive to Amikacin.
Conclusion: The present study from 2008 to 2010 reveals the incidence of infections due to klebsiella pneumoniae strains in the hospitalized patients and their tendency towards antibiotic resistance.
Key words: Kebsiella pneumoniae, nosocomial infections, pneumonia, urinary tract infections, beta-lactamase, ESBL's, Gram-negative, non-motile, urease.
[1] 1.Hadi Mehrgan, Mohammad Rahbar, Zohreh Arab-Halvaii, "High prevalence of extended spectrum beta lactamase producing Klebsiella pneumoniae in a tertiary care hospital in Tehran, Iran", The Journal of infection in developing countries,Vol.4,No.3,2009.
[2] 2.M.Shahid, A.Malik, M.Akram, L.M.Agarwal, A.U.Khan, M.Agarwal, "Prevalent phenotypes and antibiotic resistance in Escherichia coli and klebsiella pneumonia at an Indian tertiary care hospital: plasmid-mediated cefoxitin resistance", International journal of infectious diseases, Vol.2, issue 3, May 2008, Pg:256-264.
[3] 3.Aminzadeh.Z, Sadat kashi.M, Shabani.M, "Bacteriuria by extended spectrum beta lactamase producing Escherichia coli and klebsiella pneumonia isolates in a government hospital in south of Tehran, Iran, Iranian journal of kidney diseases, 2008 Oct;2(4):197-200.
[4] 4.Ami Y Varaiya, Jyotsana D Dogra, Manasi H Kulkarni, Pallavi N Bhalekar, "Extended spectrum beta lactamase producing Escherichia coli and klebsiella pneumonia in diabetic foot infections", Indian journal of medical microbiology, Vol.51, issue 3, 2008, Pg:370-372.
[5] 5. Anguzyjr.R, Olila.D, "Drug sensitivity patterns of bacterial isolates from septic post-operative wounds in a regional referral hospital in Uganda", Journal of African health sciences, 2007 Sep:7(3):Pg:148-54.
[6] 6.Yengkokpam.C, Inqudam.D, Yengkokpam.I.S., Jha.BK, "Antibiotic susceptibility pattern of urinary isolates in Imphal(Manipur), India", Nepal medical college journal, 2007Sep;9(3):170-2.
[7] 7.Shobha KL, Gowrish rao.S, Sugandhi rao, Sreeja C.K., "Prevalence of extended spectrum beta lactamases in urinary isolates of Escherichia coli, Klebsiella and Citrobacter species and their antimicrobial susceptibility pattern in a tertiary care hospital," Indian journal for the Practising Doctor, Vol.3,No.6(2007-01-2007-02).
[8] 8.Krista loivukene,Epp Sepp, Vivika Adamson, Piret Mitt, Ulle Kallandi, Karin Otter, Paul Naaber, "Prevalence and antibiotic susceptibility of Acinetobacter baumanni, Pseudomonas aeruginosa and Klebsiella pneumonia in Estonian intensive care units in comparison with European Data", Scandinavian journal of infectious diseases, 2006, Vol.38,No.11-12,Pg:1001-1008.
[9] 9.Das RN, Chandrasekhar TS, Joshi HS, Gurung M, Shrestha N, Shivananda PG, "Frequency and susceptibility profile of pathogens causing urinary tract infections at a tertiary care hospital in Western Nepal," Singapore medical journal, 2006;47(4):281.
[10] 10.Arya M, Arya PK, Biswas D, Prasad R, "Antimicrobial susceptibility pattern of bacterial isolates from post-operative wound infections", Indian journal of Pathology and Microbiology, 2005 Apr 48(2):266-9.
[2] 2.M.Shahid, A.Malik, M.Akram, L.M.Agarwal, A.U.Khan, M.Agarwal, "Prevalent phenotypes and antibiotic resistance in Escherichia coli and klebsiella pneumonia at an Indian tertiary care hospital: plasmid-mediated cefoxitin resistance", International journal of infectious diseases, Vol.2, issue 3, May 2008, Pg:256-264.
[3] 3.Aminzadeh.Z, Sadat kashi.M, Shabani.M, "Bacteriuria by extended spectrum beta lactamase producing Escherichia coli and klebsiella pneumonia isolates in a government hospital in south of Tehran, Iran, Iranian journal of kidney diseases, 2008 Oct;2(4):197-200.
[4] 4.Ami Y Varaiya, Jyotsana D Dogra, Manasi H Kulkarni, Pallavi N Bhalekar, "Extended spectrum beta lactamase producing Escherichia coli and klebsiella pneumonia in diabetic foot infections", Indian journal of medical microbiology, Vol.51, issue 3, 2008, Pg:370-372.
[5] 5. Anguzyjr.R, Olila.D, "Drug sensitivity patterns of bacterial isolates from septic post-operative wounds in a regional referral hospital in Uganda", Journal of African health sciences, 2007 Sep:7(3):Pg:148-54.
[6] 6.Yengkokpam.C, Inqudam.D, Yengkokpam.I.S., Jha.BK, "Antibiotic susceptibility pattern of urinary isolates in Imphal(Manipur), India", Nepal medical college journal, 2007Sep;9(3):170-2.
[7] 7.Shobha KL, Gowrish rao.S, Sugandhi rao, Sreeja C.K., "Prevalence of extended spectrum beta lactamases in urinary isolates of Escherichia coli, Klebsiella and Citrobacter species and their antimicrobial susceptibility pattern in a tertiary care hospital," Indian journal for the Practising Doctor, Vol.3,No.6(2007-01-2007-02).
[8] 8.Krista loivukene,Epp Sepp, Vivika Adamson, Piret Mitt, Ulle Kallandi, Karin Otter, Paul Naaber, "Prevalence and antibiotic susceptibility of Acinetobacter baumanni, Pseudomonas aeruginosa and Klebsiella pneumonia in Estonian intensive care units in comparison with European Data", Scandinavian journal of infectious diseases, 2006, Vol.38,No.11-12,Pg:1001-1008.
[9] 9.Das RN, Chandrasekhar TS, Joshi HS, Gurung M, Shrestha N, Shivananda PG, "Frequency and susceptibility profile of pathogens causing urinary tract infections at a tertiary care hospital in Western Nepal," Singapore medical journal, 2006;47(4):281.
[10] 10.Arya M, Arya PK, Biswas D, Prasad R, "Antimicrobial susceptibility pattern of bacterial isolates from post-operative wound infections", Indian journal of Pathology and Microbiology, 2005 Apr 48(2):266-9.
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ABSTRACTS: Xanthomonas campestris pv. mangiferaeindicae (Xcm) caused bacterial black spot of mango in Karnataka. The extent to which bactericides control this disease effectively is low. In this study the bactericidal effect of different products was assessed in vitro on mango plants under greenhouse conditions. Six commercial formulate and combinations were tested. In vitro analysis showed that minimal inhibitory concentration (MIC) of copper sulphate with a MIC value of 100 μl/ml and bavistin which was not active at 500 μl/ml. MIC values of commercial formulate bactrinashak ranged between 5 and 30 μg/ml, and combinations of copper oxychloride + copper sulphate; streptocycline + bactrinashak; mancozeb + copper oxychloride, mancozeb + bavistin and bavistin + bactrinashak, showed a great effect at sub-inhibitory concentrations. Treatments including copper sulphate and copper oxychloride significantly shows inhibition zone, whereas bavistin alone was less effective, these combinations of different antibacterial substances results were better than copper sulphate alone. We conclude that the combination of copper sulphate with streptocycline, bactrinashak may be useful in controlling symptoms of this disease in greenhouses.
Key Words: Commercial formulates, in vitro, Mango, Black spot disease.
Key Words: Commercial formulates, in vitro, Mango, Black spot disease.
[1] Andersen, G.L., Menkissoglou, O., Lindow, S.E., 1991. Occurrence and properties of copper-tolerant strains of Pseudomonas syringae isolated from fruit trees in California. Phytopath. 81, 648–656.
[2] Anonymous. 2009. Horticultural crop statistics of Karnataka state at a glance, Lalbagh, Bangalore.1-32.
[3] Carlton, W.M., Braun, E.J., Gleason, M.L., 1998. Ingress of Clavibacter michiganensis subsp. michiganensis into tomato leaves through hydathodes. Phytopath. 88, 525– 529.
[4] Carlton, W.M., Gleason, M.L., Braun, E.J., 1994. Effect of pruning on tomato plants supporting epiphytic populations of Clavibacter michiganensis subsp. michiganensis. Plant Dis. 78, 742–745.
[5] Cazorla M.F., Tores A.J., Olalla L., Garcia P.A., Farre M.J. and Vicente A.D. 1998. Bacterial apical necrosis of southern Spain: A disease caused by Pseudomonas syringae pv. syringae. Phytopath, 88: 614-620.
[6] Dayakar B.V and Gnanamanickam S.S. 1996. Biochemical and pathogenic variation in strains of Xanthomonas campestris pv. mangiferaeindicaae from Southern India. Ind phytopath. 49: 227-233.
[7] Gleason, M.L., Gitaitis, R.D., Ricker, M.D., 1993. Recent progress in understanding and controlling bacterial canker of tomato in eastern North America. Plant Dis. 77, 1069– 1076.
[8] Govender, V., Korsten, L., 2006. Evaluation of different formulations of Bacillus licheniformis in mango pack house trials. Biol Control. 37,237-242.
[9] Hausbeck, M.K., Bell, J., Medina-Mora, C.M., Podolsky, R., Fulbright, D.W., 2000. Effect of bactericides on population sizes and spread of Clavibacter michiganensis subsp. michiganensis on tomatoes in the greenhouse and on disease development and crop yield in the field. Phytopath 90, 38–44.
[10] Ji, P., Campbell, H.L., Kloepper, J. W., Jones, J.B., Suslow, T.V., Wilson, M. 2006. Integrated biological control of bacterial speck and spot of tomato under field conditions using foliar biological control agents and plant growth promoting rhizobacteria. Biol Control. 36, 358-367.
[2] Anonymous. 2009. Horticultural crop statistics of Karnataka state at a glance, Lalbagh, Bangalore.1-32.
[3] Carlton, W.M., Braun, E.J., Gleason, M.L., 1998. Ingress of Clavibacter michiganensis subsp. michiganensis into tomato leaves through hydathodes. Phytopath. 88, 525– 529.
[4] Carlton, W.M., Gleason, M.L., Braun, E.J., 1994. Effect of pruning on tomato plants supporting epiphytic populations of Clavibacter michiganensis subsp. michiganensis. Plant Dis. 78, 742–745.
[5] Cazorla M.F., Tores A.J., Olalla L., Garcia P.A., Farre M.J. and Vicente A.D. 1998. Bacterial apical necrosis of southern Spain: A disease caused by Pseudomonas syringae pv. syringae. Phytopath, 88: 614-620.
[6] Dayakar B.V and Gnanamanickam S.S. 1996. Biochemical and pathogenic variation in strains of Xanthomonas campestris pv. mangiferaeindicaae from Southern India. Ind phytopath. 49: 227-233.
[7] Gleason, M.L., Gitaitis, R.D., Ricker, M.D., 1993. Recent progress in understanding and controlling bacterial canker of tomato in eastern North America. Plant Dis. 77, 1069– 1076.
[8] Govender, V., Korsten, L., 2006. Evaluation of different formulations of Bacillus licheniformis in mango pack house trials. Biol Control. 37,237-242.
[9] Hausbeck, M.K., Bell, J., Medina-Mora, C.M., Podolsky, R., Fulbright, D.W., 2000. Effect of bactericides on population sizes and spread of Clavibacter michiganensis subsp. michiganensis on tomatoes in the greenhouse and on disease development and crop yield in the field. Phytopath 90, 38–44.
[10] Ji, P., Campbell, H.L., Kloepper, J. W., Jones, J.B., Suslow, T.V., Wilson, M. 2006. Integrated biological control of bacterial speck and spot of tomato under field conditions using foliar biological control agents and plant growth promoting rhizobacteria. Biol Control. 36, 358-367.
