60 research outputs found
The use of biolistic inoculation of cassava mosaic begomoviruses in screening cassava cultivars from Ghana for resistance/susceptibility to cassava mosaic disease
The resistance/susceptibility of 5 cassava cultivars from Ghana to infectious clones of two cassava mosaic viruses (ACMV-[CM] and EACMV/ACMV-[CM]) was investigated in this study. Plantlets ofcassava cultivars were obtained using nodal cuttings initiated from tissue culture. These cassava cultivars were challenged with both DNA A and B components of the infectious clones named above using particle gun bombardment. The cassava cultivars showed varying degrees of susceptibility/resistance to the two infectious clones used. All symptoms of Cassava Mosaic Disease (CMD) observed were systemic in nature. Generally, all cassava cultivars used in this study exhibited varying degrees of recovery from virus infection. This report demonstrates the ability of using biolistic technology to screen cassava cultivars for tolerance/resistance and that it may be used to recommend resistant cultivars to the farming community
Comprehensive annotation and evolutionary insights into the canine (Canis lupus familiaris) antigen receptor loci
Dogs are an excellent model for human disease. For example, the treatment of canine lymphoma has been predictive of the human response to that treatment. However, an incomplete picture of canine (Canis lupus familiaris) immunoglobulin (IG) and T cell receptor (TR) - or antigen receptor (AR) - gene loci has restricted their utility. This work advances the annotation of the canine AR loci and looks into breed-specific features of the loci. Bioinformatic analysis of unbiased RNA sequence data was used to complete the annotation of the canine AR genes. This annotation was used to query 107 whole genome sequences from 19 breeds and identified over 5,500 alleles across the 550 genes of the seven AR loci: the IG heavy, kappa, and lambda loci; and the TR alpha, beta, gamma, and delta loci. Of note was the discovery that half of the IGK variable (V) genes were located downstream of, and inverted with respect to, the rest of the locus. Analysis of the germline sequences of all the AR V genes identified greater conservation between dog and human than mouse with either. This work brings our understanding of the genetic diversity and expression of AR in dogs to the same completeness as that of mice and men, making it the third species to have all AR loci comprehensively and accurately annotated. The large number of germline sequences serves as a reference for future studies, and has allowed statistically powerful conclusions to be drawn on the pressures that have shaped these loci.This work was supported by funding from the BBSRC and the Wellcome Trust
Characterizing Collision and Second-Preimage Resistance in Linicrypt
Linicrypt (Carmer & Rosulek, Crypto 2016) refers to the class of algorithms that make calls to a random oracle and otherwise manipulate values via fixed linear operations. We give a characterization of collision-resistance and second-preimage resistance for a significant class of Linicrypt programs (specifically, those that achieve domain separation on their random oracle queries via nonces). Our characterization implies that collision-resistance and second-preimage resistance are equivalent, in an asymptotic sense, for this class. Furthermore, there is a polynomial-time procedure for determining whether such a Linicrypt program is collision/second-preimage resistant
Can a genetic signature for metastatic head and neck squamous cell carcinoma be characterised by comparative genomic hybridisation?
Catalyst preparation for CMOS-compatible silicon nanowire synthesis
Metallic contamination was key to the discovery of semiconductor nanowires,
but today it stands in the way of their adoption by the semiconductor industry.
This is because many of the metallic catalysts required for nanowire growth are
not compatible with standard CMOS (complementary metal oxide semiconductor)
fabrication processes. Nanowire synthesis with those metals which are CMOS
compatible, such as aluminium and copper, necessitate temperatures higher than
450 C, which is the maximum temperature allowed in CMOS processing. Here, we
demonstrate that the synthesis temperature of silicon nanowires using copper
based catalysts is limited by catalyst preparation. We show that the
appropriate catalyst can be produced by chemical means at temperatures as low
as 400 C. This is achieved by oxidizing the catalyst precursor, contradicting
the accepted wisdom that oxygen prevents metal-catalyzed nanowire growth. By
simultaneously solving material compatibility and temperature issues, this
catalyst synthesis could represent an important step towards real-world
applications of semiconductor nanowires.Comment: Supplementary video can be downloaded on Nature Nanotechnology
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Assessment of MMP-9, TIMP-1, and COX-2 in normal tissue and in advanced symptomatic and asymptomatic carotid plaques
<p>Abstract</p> <p>Background</p> <p>Mature carotid plaques are complex structures, and their histological classification is challenging. The carotid plaques of asymptomatic and symptomatic patients could exhibit identical histological components.</p> <p>Objectives</p> <p>To investigate whether matrix metalloproteinase 9 (MMP-9), tissue inhibitor of MMP (TIMP), and cyclooxygenase-2 (COX-2) have different expression levels in advanced symptomatic carotid plaques, asymptomatic carotid plaques, and normal tissue.</p> <p>Methods</p> <p>Thirty patients admitted for carotid endarterectomy were selected. Each patient was assigned preoperatively to one of two groups: group I consisted of symptomatic patients (n = 16, 12 males, mean age 66.7 ± 6.8 years), and group II consisted of asymptomatic patients (n = 14, 8 males, mean age 67.6 ± 6.81 years). Nine normal carotid arteries were used as control. Tissue specimens were analyzed for fibromuscular, lipid and calcium contents. The expressions of MMP-9, TIMP-1 and COX-2 in each plaque were quantified.</p> <p>Results</p> <p>Fifty-eight percent of all carotid plaques were classified as Type VI according to the American Heart Association Committee on Vascular Lesions. The control carotid arteries all were classified as Type III. The median percentage of fibromuscular tissue was significantly greater in group II compared to group I (<it>p </it>< 0.05). The median percentage of lipid tissue had a tendency to be greater in group I than in group II (<it>p </it>= 0.057). The percentages of calcification were similar among the two groups. MMP-9 protein expression levels were significantly higher in group II and in the control group when compared with group I (p < 0.001). TIMP-1 expression levels were significantly higher in the control group and in group II when compared to group I, with statistical difference between control group and group I (p = 0.010). COX-2 expression levels did not differ among groups. There was no statistical correlation between MMP-9, COX-2, and TIMP-1 levels and fibrous tissue.</p> <p>Conclusions</p> <p>MMP-9 and TIMP-1 are present in all stages of atherosclerotic plaque progression, from normal tissue to advanced lesions. When sections of a plaque are analyzed without preselection, MMP-9 concentration is higher in normal tissues and asymptomatic surgical specimens than in symptomatic specimens, and TIMP-1 concentration is higher in normal tissue than in symptomatic specimens.</p
Chromosomal analysis of non-small-cell lung cancer by multicolour fluorescent in situ hybridisation
Acute immune signatures and their legacies in severe acute respiratory syndrome coronavirus-2 infected cancer patients
Given the immune system’s importance for cancer surveillance and treatment, we have investigated how it
may be affected by SARS-CoV-2 infection of cancer patients. Across some heterogeneity in tumor type,
stage, and treatment, virus-exposed solid cancer patients display a dominant impact of SARS-CoV-2,
apparent from the resemblance of their immune signatures to those for COVID-19+ non-cancer patients.
This is not the case for hematological malignancies, with virus-exposed patients collectively displaying heterogeneous humoral responses, an exhausted T cell phenotype and a high prevalence of prolonged virus
shedding. Furthermore, while recovered solid cancer patients’ immunophenotypes resemble those of nonvirus-exposed cancer patients, recovered hematological cancer patients display distinct, lingering immunological legacies. Thus, while solid cancer patients, including those with advanced disease, seem no more at
risk of SARS-CoV-2-associated immune dysregulation than the general population, hematological cancer
patients show complex immunological consequences of SARS-CoV-2 exposure that might usefully inform
their care
Fast Authentication from Aggregate Signatures with Improved Security
An attempt to derive signer-efficient digital signatures from aggregate signatures was made in a signature scheme referred to as Structure-free Compact Rapid Authentication (SCRA) (IEEE TIFS 2017). In this paper, we first mount a practical universal forgery attack against the NTRU instantiation of SCRA by observing only 8161 signatures. Second, we propose a new signature scheme (FAAS), which transforms any single-signer aggregate signature scheme into a signer-efficient scheme. We show two efficient instantiations of FAAS, namely, FAAS-NTRU and FAAS-RSA, both of which achieve high computational efficiency. Our experiments confirmed that FAAS schemes achieve up to 100x faster signature generation compared to their underlying schemes. Moreover, FAAS schemes eliminate some of the costly operations such as Gaussian sampling, rejection sampling, and exponentiation at the signature generation that are shown to be susceptible to side-channel attacks. This enables FAAS schemes to enhance the security and efficiency of their underlying schemes. Finally, we prove that FAAS schemes are secure (in random oracle model), and open-source both our attack and FAAS implementations for public testing purposes
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