509 research outputs found
Cabibbo-suppressed non-leptonic B- and D-decays involving tensor mesons
The Cabibbo-suppressed non-leptonic decays of B (and D) mesons to final
states involving tensor mesons are computed using the non-relativistic quark
model of Isgur-Scora-Grinstein-Wise with the factorization hypothesis. We find
that some of these B decay modes, as B --> (K^*, D^*)D^*_2, can have branching
ratios as large as 6 x 10^{-5} which seems to be at the reach of future B
factories.Comment: Latex, 11 pages, to appear in Phys. Rev.
Diagnostic value of in situ polymerase chain reaction in childhood leprosy
Objective: Our aim was to assess the diagnostic value of in situ polymerase chain reaction (PCR) in leprosy, particularly for enhancing histopathological diagnosis. Methods: We prospectively studied 20 children (aged <16 years) with leprosy. Clinical examination of each case was performed, and skin smear for acid-fast bacillus was prepared. A biopsy of the lesion site was performed for histopathological examination and in situ PCR testing. Results: Histopathological examination confirmed the clinical diagnosis in only 45% of the cases; nonspecific histopathology was reported for the remaining 55% of the cases. In situ PCR showed a positivity of 57.1% in the early/localized form of leprosy (indeterminate/borderline tuberculoid) and 61.5% in the borderline borderline/borderline lepromatous group. When compared with the histopathological examination, a significant enhancement of 15% in diagnosis was seen. With in situ PCR, the diagnosis could be confirmed in 4 (36.3%) of 11 cases with nonspecific histopathological features (which is common in early disease) in addition to confirmation of 8 (88.8%) of 9 histopathologically confirmed tissue sections. Histopathology and in situ PCR combined together confirmed the diagnosis in 13 (65%) of the 20 cases. Conclusions: In situ PCR is an important diagnostic tool, especially in early and doubtful cases of leprosy
Evidence for genetic divergence in ribosomal RNA genes in mycobacteria
DNA was isolated from Mycobacterium phlei and from M. smegmatis. Each DNA sample was restricted with endonucleases, the fragments were separated by agarose gel electrophoresis and transferred to nitrocellulose film. Fragments of DNA containing rRNA sequences were identified by means of 125I-labelled rRNA of M. phlei or of M. smegmatis. The distributions of restriction endonuclease sites within the rRNA gene(s) and flanking sequences were found to be characteristic for each of the two species. Hybridizations with heterologous probes indicate that although M. phlei rRNA and M. smegmatis rRNA share regions of sequence homology, they are probably not identical in primary structure. The results suggest that the rRNA genes might prove to be useful taxonomic markers for mycobacteria
In Vitro Evaluation of Ethanolic Extracts of Ageratum conyzoides
In vitro efficacy of ethanolic extracts obtained from the aerial parts of Ageratum conyzoides and Artemisia absinthium was assessed on Rhipicephalus microplus using adult immersion test (AIT). Five concentrations of the extract (1.25%, 2.5%, 5%, 10%, and 20%) with three replications for each concentration were used in the bioassay. In AIT, the maximum mortality was recorded as 40% and 66.7% at 20% concentration for A. conyzoides and A. absinthium, respectively. Acaricidal activity was found to be higher in the extract of A. absinthium with LC50 and LC95 values of 11.2% and 61.7%, respectively. Egg mass weight of the live ticks treated with different concentrations of the extracts was significantly (P<0.05) lower than that of control ticks; consequently, the reproductive index and oviposition values of the treated ticks were reduced significantly (P<0.05). The A. conyzoides inhibited 90% hatching of eggs at the 20% concentration, whereas A. absinthium showed 100% inhibition at 5%, 10%, and 20% concentrations. The results show that A. absinthium has better acaricidal properties than A. conyzoides and could be useful in controlling R. microplus
Mutations in RpoB Gene and Their Association with Rifampicin-resistance Levels in Clinical Isolates of Mycobacterium Tuberculosis
Present study was aimed to identify most frequent mutations in rpoB gene region and to evaluate the association between mutations in rpoB gene and resistance levels to Rifampicin in clinical isolates of Mycobacterium tuberculosis of different geographical regions of India. A total of 100 clinical isolates of Mycobacterium tuberculosis were included in this study. Drug susceptibility testing against first line anti-tuberculosis drugs was performed on LJ medium by conventional minimal inhibitory concentration (MIC) method and the mutation(s) in rpoB gene of M. tuberculosis isolates were analyzed by sequencing method. Of the 100 M. tuberculosis isolates, 31 (31.0%) and 18 (18.0%) were found resistant and susceptible for all four first-line anti-tuberculosis drugs. The genetic mutations were observed in 96% (72/75) rifampicin-resistant M. tuberculosis isolates, while 4% (3/75) of rifampicin-resistant isolates did not have any mutation in rpoB gene. The mutation TCG531TTG (Ser531Leu) was found as most common and frequent mutation in 69.3% (52/75) of rifampicin-resistant isolates of M. tuberculosis with MIC level (≥ 512mg/l). The mutation at codon 511 was associated with low degree (128mg/l) of rifampicin-resistance, deletions at codons 514-516 or substitution at codon 516 were found to be associated with moderate degree (256mg/l) of rifampicin-resistance and mutations at codon 526, 531 were associated with the high degree (512mg/l) of rifampicin-resistance in M. tuberculosis isolates of Indian origin. The findings of this study will be useful for the development of raid and more specific indigenous molecular tools for the early diagnosis of multidrug-resistant tuberculosis in the country
Non-leptonic B decays involving tensor mesons
Two-body non-leptonic decays of B mesons into PT and VT modes are calculated
using the non-relativistic quark model of Isgur et al.. The predictions
obtained for are a factor of below
present experimental upper limits. Interesting patterns are obtained for ratios
of B decays involving mesons with different spin excitations and their
relevance for additional tests of forms factor models are briefly discussed.Comment: 11 pages, Latex, to appear in Phys. Rev.
Characterization of catalase by micro-immunoprecipitation in tissue-derived cells of Mycobacterium lepraemurium TMC 1701
Cell-free extracts of tissue-derived cells of Mycobacterium lepraemurium TMC 1701 have been found to have mycobacterial catalase which is of the T type. Immunological distance measurements of this catalase against three reference mycobacterial systems, as determined by a micro-immunoprecipitation technique, showed that catalase from M. lepraemurium TMC 1701 is most closely related to that of Mycobacterium avium but is still distinct from it. In this respect, this strain is uniquely positioned between Mycobacterium tuberculosis and M. avium
Hadronic Charmed Meson Decays Involving Tensor Mesons
Charmed meson decays into a pseudoscalar meson P and a tensor meson T are
studied. The charm to tensor meson transition form factors are evaluated in the
Isgur-Scora-Grinstein-Wise (ISGW) quark model. It is shown that the
Cabibbo-allowed decay is dominated by the
W-annihilation contribution and has the largest branching ratio in
decays. We argue that the Cabibbo-suppressed mode
should be suppressed by one order of magnitude relative to . When the finite width effect of the tensor resonances is taken
into account, the decay rate of is generally enhanced by a factor of
. Except for , the predicted branching ratios
of decays are in general too small by one to two orders of magnitude
compared to experiment. However, it is very unlikely that the
transition form factors can be enhanced by a factor of within the
ISGW quark model to account for the discrepancy between theory and experiment.
As many of the current data are still preliminary and lack sufficient statistic
significance, more accurate measurements are needed to pin down the issue.Comment: 11 page
Hadronic B Decays Involving Even Parity Charmed Mesons
Hadronic B decays containing an parity-even charmed meson in the final state
are studied. Specifically we focus on the Cabibbo-allowed decays and , where denotes generically a p-wave charmed meson.
The transition form factors are studied in the improved version
of the Isgur-Scora-Grinstein-Wise quark model. We apply heavy quark effective
theory and chiral symmetry to study the strong decays of p-wave charmed mesons
and determine the magnitude of the mixing angle. Except
the decay to the predictions for agree
with experiment. The sign of mixing angle is found to be
positive in order to avoid a severe suppression on the production of
. The interference between color-allowed and color-suppressed
tree amplitudes is expected to be destructive in the decay . Hence, an observation of the ratio
can be used to test the relative signs of
various form factors as implied by heavy quark symmetry. Although the predicted
at the level of exceeds the
present upper limit, it leads to the ratio
as expected from the factorization
approach and from the ratio . Therefore, it is
crucial to have a measurement of this mode to test the factorization
hypothesis. For decays, it is expected that \bar
D_{s0}^*D\gsim \bar D_{s1}D as the decay constants of the multiplet
become the same in the heavy quark limit.Comment: 27 pages, Belle's new data on DD_s^{**} productions in B decays and
on the radiative decay D_{s1}-> D_s\gamma are updated and discussed. Add two
reference
Identification of a repetitive sequence belonging to a PPE gene of Mycobacterium tuberculosis and its use in diagnosis of tuberculosis
A repetitive sequence specific to Mycobacterium tuberculosis was isolated from a gt11 library of M. tuberculosis by DNA-DNA hybridization using genomic DNA of M. tuberculosis as probe followed by subtractive hybridization with a cocktail of other mycobacterial DNA. This led to identification of CD192, a 1291 bp fragment of M. tuberculosis containing repetitive sequences, which produced positive hybridization signals with M. tuberculosis DNA within 30 min. Nucleotide sequencing revealed the presence of several direct and inverted repeats within the 1291 bp fragment that belonged to a PPE family gene (Rv0355) of M. tuberculosis. The use of CD192 as a DNA probe for the identification of M. tuberculosis in culture and clinical samples was investigated. The 1291 bp sequence was present in M. tuberculosis, Mycobacterium bovis and M. bovis BCG, but was not present in many of the other mycobacterial strains tested, including M. tuberculosis H37Ra. More than 300 clinical isolates of M. tuberculosis were probed with CD192, and the presence of the 1291 bp sequence was observed in all the clinical strains, including those lacking IS6110. The sequence displayed RFLP among the clinical isolates. A PCR assay was developed which detected M. tuberculosis with 100 % specificity from specimens of sputum, cerebrospinal fluid and pleural effusion from clinically diagnosed cases of tuberculosis
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