2,158 research outputs found
Cell differentiation assisting in evaluating mastitis treatment prognosis
Bovine mastitis is commonly treated with antibiotics, which does notalways succeed and therefore, sometimes is unnecessary. Bacteriologicalcure is the goal of antibiotic therapy and depends on the causingmicroorganism, the applied therapy, and on animal-related factors.Determining the animal-related part of the probability of bacteriologicalcure before applying antibiotics might help to reduce unnecessaryusage. By now, this is only possible by considering individual cowdata including animal-related factors such as age, mastitis history andsomatic cell count. Former studies revealed that chronic mastitis lowersthe probability of cure and leads to specific characteristics foundin the differential cell count. The aim of this study was to develop aflow cytometric cell differentiation tool to determine animal-relatedfactors correlating with a score-based probability of bacteriologicalcure. Therefore, the proportions of different cell types and their vitalityin 874 Dairy Herd Improvement milk samples of 239 cows weredetermined by flow cytometry. The results were tested for a correlationbetween data of flow cytometry and the calculated animal-relatedprobability of bacteriological cure of each individual cow by binomiallogistic regression analysis. A statistically significant association to thecalculated and animal-related probability of bacteriological cure couldbe shown for highly granulated cells, non-vital cells and macrophages.With this model, 84.4 % of all animals could be allocated to theirestimated animal-related probability of bacteriological cure correctly.These findings suggest that flow cytometric cell differentiation mightbecome an innovative tool to estimate animal-related prognosis forbacteriological cure
Longitudinal study of the effects of teat condition on the risk of new intramammary infections in dairy cows
Machine milking–induced alterations of teat tissue may impair local defense
mechanisms and increase the risk of new intramammary infections. The objective
of the current study was to assess the influence of short-term and long-term
alterations of teat tissue and infectious status of the udder quarter on the
risk of naturally occurring new intramammary infections, inflammatory
responses, and mastitis. Short-term and long-term changes in teat condition of
right udder quarters of 135 cows of a commercial dairy farm in Saxony-Anhalt,
Germany, were recorded monthly for 10 mo using simple classification schemes.
Quarter milk samples were collected from all examined quarters at each farm
visit. Bacteriological culture results and somatic cell counts of quarter milk
samples were used to determine new inflammatory responses (increase from
≤100,000 cells/mL to >100,000 cells/mL between 2 samples), new infections
(detection of a pathogen from a quarter that was free of the same pathogen at
the preceding sampling), and new mastitis (combination of new inflammatory
response and new infection). Separate Poisson mixed models for new
inflammatory responses, new infections, and new mastitis caused by specific
pathogens or groups of pathogens (contagious, environmental, major, minor, or
any) were used to estimate risk ratios and 95% confidence intervals. Data
preparation and parameter estimation were performed using the open source
statistical analysis software R. We observed no effect of any variable
describing teat condition on the risk of new intramammary infections,
inflammatory responses, or mastitis. Intramammary infections of the same udder
quarter in the preceding month did not affect risk either
On the Lack of Correlation Between [OIII]/[OII] and Lyman-Continuum Escape Fraction
We present the first results of our pilot study of 8 photometrically selected
Lyman continuum (LyC) emitting galaxy candidates from the COSMOS field and
focus on their optical emission line ratios. Observations were performed in the
H and K bands using the Multi-Object Spectrometer for Infra-Red Exploration
(MOSFIRE) instrument at the Keck Observatory, targeting the [OII], H,
and [OIII] emission lines. We find that photometrically selected LyC emitting
galaxy candidates have high ionization parameters, based on their high
[OIII]/[OII] ratios (O32), with an average ratio for our sample of 2.50.2.
Preliminary results of our companion Low Resolution Imaging Spectrometer (LRIS)
observations, targeting LyC and Ly, show that those galaxies with the
largest O32 are typically found to also be Ly emitters. High O32
galaxies are also found to have tentative non-zero LyC escape fractions
() based on band photometric detections. These results are
consistent with samples of highly ionized galaxies, including confirmed LyC
emitting galaxies from the literature. We also perform a detailed comparison
between the observed emission line ratios and simulated line ratios from
density bounded H regions modeled using the photoionization
code MAPPINGS V. Estimates of for our sample fall in the range
from 0.0-0.23 and suggest possible tension with published correlations between
O32 and , adding weight to dichotomy of arguments in the
literature. We highlight the possible effects of clumpy geometry and mergers
that may account for such tension.Comment: 21 pages, 11 figures, 3 tables, accepted for publication in MNRA
Usefulness of event-related potentials in the assessment of mild cognitive impairment
<p>Abstract</p> <p>Background</p> <p>The aim of this study was to determine if changes in latencies and amplitudes of the major waves of Auditory Event-Related Potentials (AERP), correlate with memory status of patients with mild cognitive impairment (MCI) and conversion to Alzheimer's disease (AD).</p> <p>91 patients with MCI (mean ± SD age = 66.6 ± 5.4, MMSE score = 27.7) and 30 age-matched healthy control (AMHC) subjects (mean ± SD age = 68.9 ± 9.9) were studied. 54 patients were re-examined after an average period of 14(± 5.2) months. During this time period 5 patients converted to AD. Between-group differences in latency and amplitude of the major AERP waves (N200, P300 and Slow Wave) were determined. Within each group, correlation coefficients (CC) between these characteristics of the different AERP waves were calculated. Finally, for patients, CCs were determined among each AERP wave and their age and MMSE scores. Confirmatory factor analysis (CFA) was used to examine the underlying structure of waveforms both in the control and the patient groups.</p> <p>Results</p> <p>Latencies of all major AERP components were prolonged in patients compared to controls. Patients presented with significantly higher N200 amplitudes, but no significant differences were observed in P300 amplitudes. Significant differences between follow-up and baseline measurements were found for P300 latency (p = 0.009), N200 amplitude (p < 0.001) and P300 amplitude (p = 0.05). MMSE scores of patients did not correlate with latency or amplitude of the AERP components. Moreover, the establishment of a N200 latency cut-off value of 287 ms resulted in a sensitivity of 100% and a specificity of 91% in the prediction of MCI patients that converted to AD.</p> <p>Conclusion</p> <p>Although we were not able to establish significant correlations between latencies and amplitudes of N200, P300 and SW and the patients' performance in MMSE, which is a psychometric test for classifying patients suffering from MCI, our results point out that the disorganization of the AERP waveform in MCI patients is a potential basis upon which a neurophysiologic methodology for identifying and "staging" MCI can be sought. We also found that delayed N200 latency not only identifies memory changes better than the MMSE, but also may be a potential predictor of the MCI patients who convert to AD.</p
Study of B -> \rho \pi decays at Belle
This paper describes a study of B meson decays to the pseudoscalar-vector
final state \rho\pi using 31.9\times 10^6 B\bar{B} events collected with the
Belle detector at KEKB. The branching fractions B(B^+ \to \rho^0\pi^+) =
(8.0^{+2.3+0.7}_{-2.0-0.7}) \times 10^{-6} and B(B^0 -> \rho^{+-} \pi^{-+}) =
(20.8^{+6.0+2.8}_{-6.3-3.1}) \times 10^{-6} are obtained. In addition, a 90%
confidence level upper limit of B(B^0 \to \rho^0\pi^0) < 5.3 \times 10^{-6}is
reported.Comment: 14 pages, 3 figures, to be submitted to Phys. Lett.
The long non-coding {RNA} {H19} suppresses carcinogenesis and chemoresistance in hepatocellular carcinoma
The long non-coding RNA (lncRNA) H19 represents a maternally expressed and epigenetically regulated imprinted gene product and is discussed to have either tumor-promoting or tumor-suppressive actions. Recently, H19 was shown to be regulated under inflammatory conditions. Therefore, aim of this study was to determine the function of H19 in hepatocellular carcinoma (HCC), an inflammation-associated type of tumor. In four different human HCC patient cohorts H19 was distinctly downregulated in tumor tissue compared to normal or non-tumorous adjacent tissue. We therefore determined the action of H19 in three different human hepatoma cell lines (HepG2, Plc/Prf5, and Huh7). Clonogenicity and proliferation assays showed that H19 overexpression could suppress tumor cell survival and proliferation after treatment with either sorafenib or doxorubicin, suggesting chemosensitizing actions of H19. Since HCC displays a highly chemoresistant tumor entity, cell lines resistant to doxorubicin or sorafenib were established. In all six chemoresistant cell lines H19 expression was significantly downregulated. The promoter methylation of the H19 gene was significantly different in chemoresistant cell lines compared to their sensitive counterparts. Chemoresistant cells were sensitized after H19 overexpression by either increasing the cytotoxic action of doxorubicin or decreasing cell proliferation upon sorafenib treatment. An H19 knockout mouse model (H19Δ3) showed increased tumor development and tumor cell proliferation after treatment with the carcinogen diethylnitrosamine (DEN) independent of the reciprocally imprinted insulin-like growth factor 2 (IGF2). In conclusion, H19 suppresses hepatocarcinogenesis, hepatoma cell growth, and HCC chemoresistance. Thus, mimicking H19 action might be a potential target to overcome chemoresistance in future HCC therapy
Study of the Baryon-Antibaryon Low-Mass Enhancements in Charmless Three-body Baryonic B Decays
The angular distributions of the baryon-antibaryon low-mass enhancements seen
in the charmless three-body baryonic B decays B+ -> p pbar K+, B0 -> p pbar Ks,
and B0 -> p Lambdabar pi- are reported. A quark fragmentation interpretation is
supported, while the gluonic resonance picture is disfavored. Searches for the
Theta+ and Theta++ pentaquarks in the relevant decay modes and possible
glueball states G with 2.2 GeV/c2 < M-ppbar < 2.4 GeV/c2 in the ppbar systems
give null results. We set upper limits on the products of branching fractions,
B(B0 -> Theta+ p)\times B(Theta+ -> p Ks) Theta++
pbar) \times B(Theta++ -> p K+) G K+) \times
B(G -> p pbar) < 4.1 \times 10^{-7} at the 90% confidence level. The analysis
is based on a 140 fb^{-1} data sample recorded on the Upsilon(4S) resonance
with the Belle detector at the KEKB asymmetric-energy e+e- collider.Comment: 14 pages, 13 figure files, update of hep-ex/0409010 for journal
submisssio
Evidence for B- -> Ds+ K- l- nubar and search for B- -> Ds*+ K- l- nubar
We report measurements of the decays B- -> Ds(*)+ K- l- nubar in a data
sample containing 657x10^6 BBbar pairs collected with the Belle detector at the
KEKB asymmetric-energy e+e- collider. We observe a signal with a significance
of 6 sigma for the combined Ds and Ds* modes and find the first evidence of the
B- -> Ds+ K- l- nubar decay with a significance of 3.4 sigma. We measure the
following branching fractions: BF(B- -> Ds+ K- l nubar) = (0.30 +/- 0.09(stat)
+0.11 -0.08(syst)) x 10^-3 and BF(B- -> Ds*+ K- l- nubar) = (0.59 +/-
0.12(stat) +/- 0.15(syst)) x 10^-3 and set an upper limit BF(B- -> Ds*+ K- l-
nubar) < 0.56 x 10^-3 at the 90% confidence level. We also present the first
measurement of the Ds+K- invariant mass distribution in these decays, which is
dominated by a prominent peak around 2.6 GeV/c^2.Comment: Submitted to Phys. Rev.
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