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1.
Indian J Med Microbiol ; 2015 Jan-Mar ; 33 (1): 21-24
Article in English | IMSEAR | ID: sea-156984

ABSTRACT

Purpose: Linezolid is an effective drug against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE). We describe the emergence of linezolid resistance in MRSA and VRE from India. Material and Methods: One MRSA and two VRE strains were isolated from a patient on linezolid therapy of one week duration. All three isolates were resistant to linezolid with minimal inhibitory concentrations (MIC) ≥4 mg/L. The 746-bp region fl anking the possible G2576U mutation on the corresponding DNA from the 23S rRNA was amplifi ed by polymerase chain reaction (PCR) and amplicons were sequenced for all the three isolates. Conjugation experiments using the linezolid resistant MRSA (LRMRSA) and linezolid resistant VRE (LRVRE) isolates as donors and wild strains of corresponding genera as recipients were performed. Results: The MRSA isolate had the classical G2576U mutation. High quality value scores in the sequencing software validated the mutation. Conjugation studies did not indicate presence of transferable resistance for linezolid. Sequencing did not indicate presence of any mutation in the two LRVRE isolates. Conclusions: This is the fi rst report from India citing resistance in Staphylococcus and Enterococcus against Linezolid.

2.
Indian J Med Sci ; 2008 Mar; 62(3): 105-12
Article in English | IMSEAR | ID: sea-68698

ABSTRACT

Background : The present investigation is aimed at examining the Apolipoprotein E (APOE) genotypic influence on coronary heart disease (CHD) risk in northwest India (Punjab), where this disease is emerging as a major threat to public-health care system. Materials and Methods: The present study comprised of angiographically diagnosed coronary heart disease patients (n = 193) and controls (n = 150) of Punjab. Genetic polymorphism of APOE gene was investigated by polymerase chain reaction (PCR), and its association with lipid levels was evaluated. Results : The allele frequencies of epsilon2, epsilon3, and epsilon4 were 0.054, 0.795, 0.151; and 0.077, 0.856, 0.067 in patients and controls respectively. The bearers of E3/E4 genotype had threefold higher propensity of developing CHD in this population (OR, 3.04; CI, 1.55-6.25; P P P Conclusions : A significant association (P = 0.016) of epsilon4 allele, especially E3/E4 genotype, with CHD was observed, along with HDL-C and LDL-C concentrations, in the population of northwest India.

3.
Article in English | IMSEAR | ID: sea-51578

ABSTRACT

Hemifacial microsomia (HFM) is a variable asymmetric craniofacial malformation resulting in hypoplasia of the components of the first and second branchial arches. Because of the extremely variable expressively of the HFM, treatment measures also vary considerably from the use of activator to total reconstruction of TM joint and management of secondary deformities of maxilla, nose, orbit and zygomatic bone. We present a case of HFM type I of mild deformity treated with onlay bone grafting.


Subject(s)
Adolescent , Bone Transplantation/methods , Esthetics, Dental , Facial Asymmetry/classification , Female , Humans , Mandible/abnormalities , Mandibular Condyle/abnormalities , Masseter Muscle/abnormalities , Maxilla/abnormalities , Zygoma/abnormalities
4.
Article in English | IMSEAR | ID: sea-20732

ABSTRACT

Vibrio cholerae produce a variety of extracellular products that have deleterious effects on eukaryotic cells. The massive diarrhoea produced by V. cholerae is caused by cholera toxin (CT). CT is composed of 1A and 5B units. CT causes a significant amount of fluid secretion and haemorrhage in the ligated rabbit ileal loops. Its action involves the role of various biochemical pathways. CT acts by activation of adenylate cyclase-cAMP system located at the basolateral membrane of intestinal epithelial cells. The increase in cyclic AMP levels is mainly responsible for the altered transport of Na+ and Cl-. Besides activating cAMP, CT is also known to act through release of prostaglandins and involvement of intramural nerves. Besides CT, other bacterial toxins like Escherichia coli LT, Salmonella toxin, Shigella toxin and Campylobacter toxin also possess A-B structure. The structure and function of E. coli LT resembles closely that of CT. Most of the bacterial toxins exert their effect through involvement of ADP-ribosylating proteins whereas other toxins involve guanylate cyclase system, calcium and protein kinases for their ultimate action.


Subject(s)
Adenylyl Cyclases/metabolism , Animals , Bacterial Toxins/toxicity , Cholera Toxin/chemistry , Enterotoxins/toxicity , Escherichia coli Proteins , Humans , Prostaglandins/physiology , Rabbits , Shiga Toxins
5.
Indian J Chest Dis Allied Sci ; 1994 Apr-Jun; 36(2): 77-81
Article in English | IMSEAR | ID: sea-30287
6.
Indian J Pediatr ; 1989 May-Jun; 56(3): 343-7
Article in English | IMSEAR | ID: sea-78641

ABSTRACT

Lameness survey was conducted in a rural community development block of Haryana in 1985. Enumerators contacted school teachers, anganwadi workers and several key informants in the community to identify lame children in 1-11 years age-group. Physician verified 219 lame cases to be due to poliomyelitis. Prevalence of poliomyelitis lameness was 7.3/1000 children born in 1974-76, 7.7/1000 children born in 1977-1980 and 2.3/1000 children born in 1981-1984 (expected to increase to 3.1/1000 when all children born in 1981-84 cross 5th year of life). Immunisation coverage with 3 doses of oral polio vaccine (OPV) was less than 10% during 1974-80 when immunisation was a clinic based activity. Coverage increased from 50 to 80% during 1981-85 when OPV was given in annual immunisation campaign. The results indicate that prevalence of paralytic poliomyelitis dropped at least by 60% after giving OPV in annual immunisation campaigns.


Subject(s)
Child , Child, Preschool , Humans , Immunization Schedule , India/epidemiology , Infant , Paralysis/epidemiology , Poliomyelitis/epidemiology , Poliovirus Vaccine, Oral/administration & dosage , Rural Population
8.
J Indian Med Assoc ; 1980 May; 74(9): 165-8
Article in English | IMSEAR | ID: sea-105426
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