cDNA-AFLP analysis of cold-acclimated wheat plants reveals unique transcript profiles in crown tissues

Non-Peer ReviewedLow temperature (LT) adversely affects the productivity of plants. Hence, improving the cold hardiness of crop plants is an important goal in agriculture. However, further understanding of LT tolerance mechanisms in plants is required to achieve this objective. In wheat, survival of crown tissues after exposure to below freezing temperatures during the winter determines successful crop stand establishment at the onset of spring season. Therefore, identification of differentially expressed genes in crown tissues of cold acclimated wheat plants is important as it can allow dissection of molecular mechanisms and biochemical pathways within these tissues. In this study, cDNA-AFLP global transcriptomic profiles of crown tissues cold acclimated at 6oC for 0, 2, 14, 21, 35, 42, 56 and 70 days were compared among a cold hardy winter (vrn-A1) cv. Norstar, a tender spring habit (Vrn-A1) cv. Manitou and two reciprocal near-isogenic lines derived from these two parents differing at the vernalization locus. A total of 2061 differentially expressed transcript-derived fragments (TDFs) were identified using 37 pairs of standard AFLP primer combinations, 30 of which were considered unique due to their genotypic and temporal presence or absence. The remaining TDFs showed differential expression patterns in the four genotypes. Cluster analysis of the unique TDFs revealed influence of the genetic background on expression of these TDFs. BLAST searches of 240 sequenced TDFs showed that 87% of the TDFs had similarity to genes coding for products involved in known functions such as signal transduction, RNA processing and translation, transcription, flowering, cell wall synthesis, metabolism, and protein folding. Thirty-two TDFs did not show similarity to any known genes. Quantitative real-time PCR (QPCR) analyses of these unknown TDFs validated their differential expression patterns. Characterization of their biological function will contribute to an understanding of the role of these novel genes in LT tolerance in wheat. These results suggest that crown tissues undergo a complex adaptive process by changing the expression levels of several genes that determine the level of LT tolerance

Peritoneal Fluid Analysis in Canine Disease Diagnosis

Abdominal effusion is a relatively common problem in small animal practice. Proper collection and evaluation of peritoneal effusion can provide valuable information about the disease which is responsible for the fluid accumulation in the body cavity. The classification of effusions based on their underlying etio-pathology is clinically useful for the clinician to ensure proper diagnosis and treatment. Present article reports briefly regarding pathophysiology of effusion, sample collection, physical, microscopic, biochemical changes, and their clinical significance in various disease conditions

Expression analysis of low temperature-induced genes in wheat

Non-Peer ReviewedWheat (Triticum aestivum L.) is a widely adapted, economically important crop exhibiting winter, spring and intermediate growth habits. Winter wheat is seeded in the fall, over-winters, resumes growth in spring and is harvested in early summer. It also requires a period of low temperature (LT) exposure, experienced during the fall, to switch from the vegetative to reproductive phase in spring, a process known as vernalization. Low temperature also allows the wheat plant to cold-acclimate to withstand freezing winter temperatures. There has always been an interest to grow winter wheat because of its yield advantage over spring wheat. However, LT tolerance needs to be improved to prevent winter kill and maximize its yield potential. To achieve this more detailed understanding of molecular mechanisms underlying LT tolerance is required. Thus, objectives of this study were to determine the expression of a LT-induced gene and cDNA-AFLP profile in leaf and crown tissues of LT-exposed wheat plants. Survival of crown tissues after exposure to sub-zero temperatures is an indication of the level of LT tolerance of a cultivar. Thus, pattern and levels of expression of LT-induced genes and identification of LT-induced transcripts in this tissue will add to understanding of LT tolerance. Genotypes used in this study included a winter hardy cultivar, Norstar, a tender spring cultivar, Manitou and two-near-isogenic lines with the Vrn-A1 (spring Norstar) and vrn-A1 (winter Manitou) alleles of Manitou and Norstar, respectively. The dominant Vrn-A1 locus confers spring habit and therefore no requirement for vernalization. Quantitative real-time polymerase chain reaction (QPCR) for the cold-regulated gene, Wcor410, indicated that in leaf tissue the Vrn-A1 locus determined level of expression, being higher in the lines having the recessive vrn-A1 allele compared to the dominant Vrn-A1 allele lines. In the crown tissue, the Norstar genetic background led to the higher level of expression than in the Manitou background. cDNA-AFLP analysis also exhibited variable profiles between the two tissues

Pumping current of a Luttinger liquid with finite length

We study transport properties in a Tomonaga-Luttinger liquid in the presence of two time-dependent point like weak impurities, taking into account finite-length effects. By employing analytical methods and performing a perturbation theory, we compute the backscattering pumping current (I_bs) in different regimes which can be established in relation to the oscillatory frequency of the impurities and to the frequency related to the length and the renormalized velocity (by the electron-electron interactions) of the charge density modes. We investigate the role played by the spatial position of the impurity potentials. We also show how the previous infinite length results for I_bs are modified by the finite size of the system.Comment: 9 pages, 7 figure

Single seed-based high-throughput genotyping and rapid generation advancement for accelerated groundnut genetics and breeding research

The groundnut breeding program at International Crops Research Institute for the Semi-Arid Tropics routinely performs marker-based early generation selection (MEGS) in thousands of segregating populations. The existing MEGS includes planting of segregating populations in fields or glasshouses, label tagging, and sample collection using leaf-punch from 20–25 day old plants followed by genotyping with 10 single nucleotide polymorphisms based early generation selection marker panels in a high throughput genotyping (HTPG) platform. The entire process is laborious, time consuming, and costly. Therefore, in order to save the time of the breeder and to reduce the cost during MEGS, we optimized a single seed chipping (SSC) process based MEGS protocol and deployed on large scale by genotyping >3000 samples from ongoing groundnut breeding program. In SSC-based MEGS, we used a small portion of cotyledon by slicing-off the posterior end of the single seed and transferred to the 96-deep well plate for DNA isolation and genotyping at HTPG platform. The chipped seeds were placed in 96-well seed-box in the same order of 96-well DNA sampling plate to enable tracking back to the selected individual seed. A high germination rate of 95–99% from the chipped seeds indicated that slicing of seeds from posterior end does not significantly affect germination percentage. In addition, we could successfully advance 3.5 generations in a year using a low-cost rapid generation turnover glass-house facility as compared to routine practice of two generations in field conditions. The integration of SSC based genotyping and rapid generation advancement (RGA) could significantly reduce the operational requirement of person-hours and expenses, and save a period of 6–8 months in groundnut genetics and breeding research

T-Cell Immune Dysregulation and Mortality in Women with Human Immunodeficiency Virus

Summary: In women with HIV, higher activation and exhaustion of CD4+ T cells were associated with risk of non-HIV-related mortality during a median of 13.3 years of follow-up, independent of baseline demographic, behavioral, HIV-related, and cardiometabolic factors and longitudinal HIV disease progression. Background: Dysregulation of adaptive immunity is a hallmark of human immunodeficiency virus (HIV) infection that persists on antiretroviral therapy (ART). Few long-term prospective studies have related adaptive immunity impairments to mortality in HIV, particularly in women. Methods: Among 606 women with HIV in the Women's Interagency HIV Study, peripheral blood mononuclear cells collected from 2002 to 2005 underwent multiparameter flow cytometry. Underlying cause of death was ascertained from the National Death Index up to 2018. We examined associations of CD4+ and CD8+ T-cell activation (%CD38+HLA-DR+), senescence (%CD57+CD28-), exhaustion (%PD-1+), and nonactivation/normal function (%CD57-CD28+) with natural-cause, HIV-related, and non-HIV-related mortality. Results: At baseline, median participant age was 41, and 67% were on ART. Among 100 deaths during a median of 13.3 years follow-up, 90 were natural-cause (53 non-HIV-related, 37 HIV-related). Higher activation and exhaustion of CD4+ T cells were associated with risk of natural-cause and non-HIV-related mortality, adjusting for age, demographic, behavioral, HIV-related, and cardiometabolic factors at baseline. Additional adjustment for time-varying viral load and CD4+ T-cell count did not attenuate these associations. CD8+ T-cell markers were not associated with any outcomes adjusting for baseline factors. Conclusions: Persistent CD4+ T-cell activation and exhaustion may contribute to excess long-term mortality risk in women with HIV, independent of HIV disease progression

Study of the B^0 Semileptonic Decay Spectrum at the Upsilon(4S) Resonance

We have made a first measurement of the lepton momentum spectrum in a sample of events enriched in neutral B's through a partial reconstruction of B0 --> D*- l+ nu. This spectrum, measured with 2.38 fb**-1 of data collected at the Upsilon(4S) resonance by the CLEO II detector, is compared directly to the inclusive lepton spectrum from all Upsilon(4S) events in the same data set. These two spectra are consistent with having the same shape above 1.5 GeV/c. From the two spectra and two other CLEO measurements, we obtain the B0 and B+ semileptonic branching fractions, b0 and b+, their ratio, and the production ratio f+-/f00 of B+ and B0 pairs at the Upsilon(4S). We report b+/b0=0.950 (+0.117-0.080) +- 0.091, b0 = (10.78 +- 0.60 +- 0.69)%, and b+ = (10.25 +- 0.57 +- 0.65)%. b+/b0 is equivalent to the ratio of charged to neutral B lifetimes, tau+/tau0.Comment: 14 page, postscript file also available at http://w4.lns.cornell.edu/public/CLN

Radiative Decay Modes of the D0D^{0} Meson

Using data recorded by the CLEO-II detector at CESR we have searched for four radiative decay modes of the $D^0$ meson: $D^0\to\phi\gamma$, $D^0\to\omega\gamma$, $D^0\to\bar{K}^{*}\gamma$, and $D^0\to\rho^0\gamma$. We obtain 90% CL upper limits on the branching ratios of these modes of $1.9\times 10^{-4}$, $2.4\times 10^{-4}$, $7.6\times 10^{-4}$ and $2.4\times 10^{-4}$ respectively.Comment: 15 page postscript file, postscript file also available through http://w4.lns.cornell.edu/public/CLN

Measurement of the Mass Splittings between the bbˉχb,J(1P)b\bar{b}\chi_{b,J}(1P) States

We present new measurements of photon energies and branching fractions for the radiative transitions: Upsilon(2S)->gamma+chi_b(J=0,1,2). The masses of the chi_b states are determined from the measured radiative photon energies. The ratio of mass splittings between the chi_b substates, r==(M[J=2]-M[J=1])/(M[J=1]-M[J=0]) with M the chi_b mass, provides information on the nature of the bbbar confining potential. We find r(1P)=0.54+/-0.02+/-0.02. This value is in conflict with the previous world average, but more consistent with the theoretical expectation that r(1P)<r(2P); i.e., that this mass splittings ratio is smaller for the chi_b(1P) triplet than for the chi_b(2P) triplet.Comment: 11 page postscript file, postscript file also available through http://w4.lns.cornell.edu/public/CLN