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1.
J Immunother ; 35(7): 544-54, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22892451

ABSTRACT

This study investigates the effect of Listeria administration on differentiation of macrophages from precursor bone marrow cells and functional status of tumor-associated macrophages (TAM). Listeria administration not only resulted in an augmented infiltration of tumor by F4/80 macrophages but also repolarized the functional status of TAM displaying features of some M1 macrophage subtype with upregulated phagocytosis and tumoricidal activity accompanied by altered expression of monocarboxylate transporter-1, toll-like receptor-2, surface markers: CD11c, interleukin-2 receptor, CD62L, and secreted molecules: nitric oxide, interleukin (IL)-1, IL-6, tumor necrosis factor-α, and vascular endothelial growth factor. Declined tumor cell survival and modulated repertoire of cytokines: interferon-γ, IL-6, IL-10, and transforming growth factor-ß in tumor microenvironment indicated their role in polarization of TAM towards proinflammatory state. Bone marrow cell of Listeria-administered tumor-bearing mice showed augmented survival, declined expression of p53 upregulated modulator of apoptosis with an upregulated differentiation into activation responsive bone marrow-derived macrophages along with altered expression of macrophage-colony stimulating factor, macrophage-colony stimulating factor receptor, and granulocyte macrophage-colony stimulating factor receptor. These findings indicate that Listeria infection is associated with an augmented differentiation of macrophages accompanied by tumoricidal activation of TAM.


Subject(s)
Listeria/immunology , Listeriosis/immunology , Lymphoma, T-Cell/immunology , Macrophages/immunology , Animals , Antigens, CD/metabolism , Antigens, Differentiation/metabolism , Cell Differentiation , Cytokines/metabolism , Cytotoxicity, Immunologic , Humans , Inflammation Mediators/metabolism , Listeriosis/complications , Lymphoma, T-Cell/complications , Macrophages/microbiology , Male , Mice , Mice, Inbred BALB C , Monocarboxylic Acid Transporters/metabolism , Nitric Oxide/metabolism , Phagocytosis , Symporters/metabolism
2.
J Antibiot (Tokyo) ; 64(6): 401-12, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21468079

ABSTRACT

The c group of Gram-negative gliding bacteria, has a long history of cosmopolitan occurrence. It has great biodiversity despite the absence of sexual reproduction. This wide biodiversity may be reflected in the wide spectrum of its secondary metabolites. These cyanobacterial secondary metabolites are biosynthesized by a variety of routes, notably by non-ribosomal peptide synthetase or polyketide synthetase systems, and show a wide range of biological activities including anticancer, antibacterial, antiviral and protease inhibition activities. This high degree of chemical diversity in cyanobacterial secondary metabolites may thus constitute a prolific source of new entities leading to the development of new pharmaceuticals.


Subject(s)
Biological Products/pharmacology , Cyanobacteria/metabolism , Drug Discovery/methods , Animals , Biological Products/isolation & purification , Drug Design , Humans
3.
J Health Popul Nutr ; 28(3): 281-5, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20635639

ABSTRACT

The latex agglutination test (KAtex), direct agglutination test (DAT), and the rK39 immuno-chromatographic strip test (dipstick test) were evaluated for their role in the diagnosis and prognosis of visceral leishmaniasis (kala-azar) in India. Sera and urine samples from 455 subjects--150 confirmed visceral leishmaniasis cases, 160 endemic controls, 100 non-endemic controls, and 45 other febrile diseases--were included in the study. The sensitivity of the KAtex, DAT, and rK39 strip test was 87% [95% confidence interval (CI) 80-96], 93.3% (95% CI 88-100), and 98% (95% CI 93-100) respectively. The specificity of these tests was 98% (95% CI 93-100), 93% (95% CI 87-100), and 89% (95% CI 82-97) for the KAtex, DAT, and rK39 strip test respectively. Fifty cases were followed up and subjected to the KAtex, DAT, and rK39 strip test after 30 days of successful treatment. The DAT and rK39 strip test showed positive results in all the 50 cases whereas the KAtex showed no positive reaction in any case. Based on the results, it is concluded that the sensitivity and specificity of the DAT and rK39 strip test are comparable but the greater convenience of use of the strip test makes it a better tool for the diagnosis of visceral leishmaniasis in the peripheral areas of endemic regions whereas the sensitivity of the KAtex needs to be improved to promote its use as a first-line diagnostic test in the field-setting. It may be used for the prognosis of the disease as antigen becomes undetectable in urine after 30 days of the completion of the treatment. Alternatively, it can be used as an adjunct with rK39 for sero-epidemiological surveys.


Subject(s)
Endemic Diseases , Leishmania donovani/isolation & purification , Leishmaniasis, Visceral/diagnosis , Serologic Tests/methods , Diagnosis, Differential , Humans , India , Leishmania donovani/immunology , Leishmaniasis, Visceral/blood , Leishmaniasis, Visceral/epidemiology , Leishmaniasis, Visceral/urine , Prognosis , Sensitivity and Specificity
4.
BMC Microbiol ; 10: 11, 2010 Jan 15.
Article in English | MEDLINE | ID: mdl-20078872

ABSTRACT

BACKGROUND: Enteric protozoa and sporozoa have emerged as important opportunistic parasites and can cause fatal infections in AIDS patients. The line of treatment being different for them necessitates an accurate and prompt identification of these to avoid empirical treatment. In this study which is the first of its kind from India we did a comprehensive evaluation of different techniques, comparing them on the basis of the attributes like yield, cost, time taken, expertise and infrastructure. For the first time combination of Calcoflour White and DAPI, a nuclear stain, were used to identify Microsporidia spp. Thus, a diagnostic protocol was devised for rapid, sensitive and cost effective identification of the opportunistic enteric protozoa. RESULTS: The organisms isolated from the stool samples of the cases (450 HIV patients) were predominantly Cryptosporidium spp., Microsporidia spp. and Cyclospora spp. Interestingly, the control group (200 relatives of the patients who were HIV negative) showed a high incidence (21%) of Cryptosporidium spp. We found a significant increase in the sensitivity of microscopy in detecting Cryptosporidium spp. and Cyclospora spp. after formol ether concentration. Kinyoun's staining was better compared to Modified safranin staining for Cryptosporidium spp. identification. Although ELISA had a sensitivity of 93.25% and specificity of 97% for Cryptosporidium spp. detection, we ranked Kinyoun's staining better than ELISA because it is not affordable to most of our patients. For detecting Cyclospora cayetanensis, autoflourescence was the easiest and most cost effective method followed by Safranin technique. Combination of Calcoflour White stain and DAPI gave good results for the identification of Microsporidia spp. We assessed the above techniques and graded the attributes in the following descending order: cost effectiveness, sensitivity, ease of use and interpretation, time taken for the procedure and batch testing. CONCLUSION: Thus, we conclude that a combination of minimum three procedures should be carried out for the screening of stool specimens of HIV positive patients. Kinyoun's staining should be made mandatory for every diarrheal stool sample from HIV patients. Also every laboratory should assign its own value to the attributes and apply Multiattribute utility theory or the Analytical hierarchy process to decide the most appropriate methodology.


Subject(s)
AIDS-Related Opportunistic Infections/parasitology , Acquired Immunodeficiency Syndrome/parasitology , Diarrhea/etiology , Protozoan Infections/diagnosis , AIDS-Related Opportunistic Infections/complications , Acquired Immunodeficiency Syndrome/complications , Case-Control Studies , Cryptosporidium/isolation & purification , Cyclospora/isolation & purification , Diarrhea/parasitology , Enzyme-Linked Immunosorbent Assay , Feces/parasitology , Humans , India , Microscopy, Fluorescence , Microsporidia/isolation & purification , Protozoan Infections/complications , Protozoan Infections/parasitology , Sensitivity and Specificity
6.
BMC Res Notes ; 2: 187, 2009 Sep 22.
Article in English | MEDLINE | ID: mdl-19772616

ABSTRACT

BACKGROUND: The rK39 strip test is reported to be simple, sensitive, specific, non-invasive and economical test. Since this method is supposed to be patient friendly, it may easily be accepted for sero-epidemiological surveys. An attempt was made to evaluate the role of rK39 strip test in pre and post treatment phases of Kala azar, as a diagnostic and prognostic marker, in addition to other laboratory investigations, in order to evaluate its role in sero-epidemiological surveys. FINDINGS: A total of 210 cases were selected for the study. One hundred clinically and parasitologically confirmed cases were corroborated with other hematological profiles. The formol-gel test was included along with well matched control group comprising of normal endemic controls (50), non-endemic normals (20) and other febrile cases (40). All groups were tested by rK39 strip test. Fifty Kala azar cases were followed up after completion of successful treatment. They were subjected to rK39 strip test after 0, 90 and 180 days of completion of successful treatment.The rK39 showed sensitivity, specificity, PPV, NPV, and diagnostic accuracy of 98% (95% CI 91.7-100), 100%, 100%, 90% (95% CI 66-100) and 98% (95% CI 92.6-100) respectively. All the 50 cured followed up cases showed positive result by rK39 strip test even after 180 days of completion of successful treatment. CONCLUSION: The test seems an ideal qualitative test for the diagnosis of kala-azar. But for sero-epidemiological studies the test may be used with other parameters. Alternatively a quantitative ELISA using rK39 antigen may be used.

7.
J Infect Dev Ctries ; 3(7): 554-60, 2009 Aug 30.
Article in English | MEDLINE | ID: mdl-19762974

ABSTRACT

BACKGROUND: Apart from being a major cause of mortality, nosocomial infections due to Staphylococcus aureus have been imposing a burden on patients, hospitals and health care systems. The present study was designed to determine the prevalence of methicillin resistant S. aureus (MRSA) among nosocomial isolates along with their phenotypic characterization. METHODOLOGY: MRSA and methicillin sensitive S. aureus (MSSA) were determined by performing four different tests viz: disc diffusion, oxacillin screen agar test, MRSA latex agglutination test, and MIC of oxacillin by E test. RESULTS: Of the 149 S. aureus nosocomial isolates, 44.9% were MRSA, which included 82.1% of homogeneous MRSA and 17.9% of heterogeneous MRSA. Association of MRSA infection was found to be significantly higher in skin and lower respiratory tract infections. Of the MRSA isolates, 65 were multiresistant oxacillin resistant Staphylococcus aureus (MORSA) and 2 were nonmultiresistant oxacillin resistant Staphylococcus aureus (NORSA). D tests performed on 136 isolates showed that Inducible macrolide-lincosamide-streptogramin B (MLSB) and constitutive MLSB resistance were found to be associated with MRSA. On the contrary, susceptibility to both erythromycin and clindamycin was found to be associated with MSSA. However, MSB (macrolide-streptogramin B) resistance was not found associated either with MRSA or MSSA. Furthermore, both inducible and constitutive MLSB were found to be associated with only homogenous MRSA. CONCLUSION: D tests may be made mandatory in all S. aureus isolates as inducible MLSB resistance cannot be detected in routine susceptibility test unless erythromycin and clindamycin are placed 15-26 mm apart.


Subject(s)
Cross Infection/microbiology , Methicillin-Resistant Staphylococcus aureus/isolation & purification , Methicillin-Resistant Staphylococcus aureus/physiology , Staphylococcal Infections/microbiology , Anti-Bacterial Agents/pharmacology , Drug Resistance, Multiple, Bacterial , Humans , Macrolides/pharmacology , Microbial Sensitivity Tests/methods , Oxacillin/pharmacology
10.
BMC Gastroenterol ; 8: 36, 2008 Aug 20.
Article in English | MEDLINE | ID: mdl-18713475

ABSTRACT

BACKGROUND: Protozoan infections are the most serious among all the superimposed infections in HIV patients and claim a number of lives every year. The line of treatment being different for diverse parasites necessitates a definitive diagnosis of the etiological agents to avoid empirical treatment. Thus, the present study has been aimed to elucidate the associations between diarrhoea and CD4 counts and to study the effect of HAART along with management of diarrhoea in HIV positive patients. This study is the first of its kind in this area where an attempt was made to correlate seasonal variation and intestinal protozoan infestations. METHODS: The study period was from January 2006 to October 2007 wherein stool samples were collected from 366 HIV positive patients with diarrhea attending the ART centre, inpatient department and ICTC of S.S. hospital, I.M.S., B.H.U., Varanasi. Simultaneously, CD4 counts were recorded to assess the status of HIV infection vis-à-vis parasitic infection. The identification of pathogens was done on the basis of direct microscopy and different staining techniques. RESULTS: Of the 366 patients, 112 had acute and 254 had chronic diarrhea. The percentages of intestinal protozoa detected were 78.5% in acute and 50.7% in chronic cases respectively. Immune restoration was observed in 36.6% patients after treatment on the basis of clinical observation and CD4 counts. In 39.8% of HIV positive cases Cryptosporidium spp. was detected followed by Microsporidia spp. (26.7%). The highest incidence of intestinal infection was in the rainy season. However, infection with Cyclospora spp. was at its peak in the summer. Patients with chronic diarrhea had lower CD4 cell counts. The maximum parasitic isolation was in the patients whose CD4 cell counts were below 200 cells/microl. CONCLUSION: There was an inverse relation between the CD4 counts and duration of diarrhea. Cryptosporidium spp. was isolated maximum among all the parasites in the HIV patients. The highest incidence of infection was seen in the rainy season.


Subject(s)
CD4 Antigens/blood , Diarrhea/immunology , HIV Infections/immunology , Protozoan Infections/immunology , Seasons , Adult , Antiretroviral Therapy, Highly Active , Case-Control Studies , Cryptosporidiosis/complications , Cryptosporidiosis/epidemiology , Cryptosporidiosis/immunology , Cyclosporiasis/complications , Cyclosporiasis/epidemiology , Cyclosporiasis/immunology , Diarrhea/etiology , Feces/parasitology , Female , HIV Infections/drug therapy , HIV Infections/epidemiology , HIV Infections/parasitology , Humans , India , Male , Microsporidiosis/complications , Microsporidiosis/epidemiology , Microsporidiosis/immunology , Prevalence , Protozoan Infections/complications , Protozoan Infections/epidemiology
11.
Int J Antimicrob Agents ; 29(4): 446-50, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17270402

ABSTRACT

Eighty-six strains of Acinetobacter baumannii from India and Nepal were investigated for the presence of integrons in relation to multiple drug resistance by integrase gene polymerase chain reaction (PCR). Integrons were found to be present at a rate of 43.02% (37/86). Integrons were significantly correlated with multidrug resistance to several antibiotics. Class 1 integrons were detected in 81.1% of integron-positive strains, whilst 18.9% were found to be positive for class 2 integrons. The majority of class 2 integrons (71%) were encountered in strains isolated from post-operative wards of both countries. The highest integron carriage in isolates of A. baumannii (63.6%) was observed in 2005. Hence, it is likely that integrons play an important role in antibiotic resistance and possibly indicate epidemic behaviour of A. baumannii. Integrase gene PCR may be used as routine screening and identification for the surveillance of clinical isolates of A. baumannii with epidemic potential.


Subject(s)
Acinetobacter Infections/epidemiology , Acinetobacter baumannii/genetics , Drug Resistance, Multiple, Bacterial/genetics , Integrases/genetics , Polymerase Chain Reaction/methods , Acinetobacter Infections/microbiology , Acinetobacter baumannii/isolation & purification , Acinetobacter baumannii/pathogenicity , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Cross Infection/epidemiology , Cross Infection/microbiology , Humans , India/epidemiology , Integrons , Intensive Care Units , Nepal/epidemiology
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