To investigate the aetiology of the 2015 A(H1N1)pdm09 influenza outbreak in India, 1,083 nasopharyngeal swabs from suspect patients were screened for influenza A(H1N1)pdm09 in the state of Madhya Pradesh. Of 412 positive specimens, six were further characterised by phylogenetic analysis of haemagglutinin (HA) sequences revealing that they belonged to genogroup 6B. A new mutation (E164G) was observed in HA2 of two sequences. Neuraminidase genes in two of 12 isolates from fatal cases on prior oseltamivir treatment harboured the H275Y mutation.An epidemic of influenza A(H1N1)pdm09, affecting over 39,000 persons and causing more than 2,500 deaths occurred in India in 2015 [1]. We show that genotype 6B strains forming two sub-lineages circulated during the outbreak. Comparison of the sequences of six outbreak strains recovered in this work, to other published genotype 6B sequences, also reveals a unique combination of previously-reported mutations in the haemagglutinin (HA) gene. Two of the six sequences additionally display a E164G mutation in HA2, which has not been reported to date, moreover a N129D mutation in HA1 is observed for two sequences derived from patients with severe disease. Among strains analysed from 12 fatal cases on prior oseltamivir treatment, two harbour the H275Y mutation in the neuraminidase (NA) gene, which confers resistance to this antiviral.
A method of creating nanoclusters
(NCs) from soluble peptide molecules
is described utilizing an approach based on a tyrosine-tyrosine cross-linking
reaction. A reactive tag comprising histidine and tyrosine residues
was introduced at the termini of the peptide molecules. The cross-linking
reaction led to the creation of dityrosine bonds within the tag, which
allowed for the generation of peptide NCs. We show that it is essential
for the reactive tag to be present at both the “N” and
“C” termini of the peptide for cluster formation to
occur. Additionally, the cross-linking reaction was systematically
characterized to show the importance of reaction conditions on final
cluster diameter, allowing us to generate NCs of various sizes. To
demonstrate the immunogenic potential of the peptide clusters, we
chose to study the conserved influenza peptide, M2e, as the antigen.
M2e NCs were formulated using the cross-linking reaction. We show
the ability of the clusters to generate protective immunity in a dose,
size, and frequency dependent manner against a lethal influenza A
challenge in BALB/c mice. Taken together, the data presented suggest
this new cluster formation technique can generate highly immunogenic
peptide NCs in a simple and controllable manner.
Customized one-component dental implants have been fabricated using Electron Beam Melting(®) (EBM(®)), which is a rapid prototyping and manufacturing technique. The goal of our study was to determine the effect of electron beam orientation on the fatigue resistance of EBM Ti-6Al-4V ELI alloy. EBM technique was used to fabricate Ti-6Al-4V ELI alloy blocks, which were cut into rectangular beam specimens with dimensions of 25 × 4 × 3 mm, such that electron beam orientation was either parallel (group A) or perpendicular (group B) to the long axis of the specimens. The specimens were subjected to cyclic fatigue (R = 0.1) in four-point flexure under ambient conditions using various stress amplitudes below the yield stress. The fatigue lifetime data were fit to an inverse power law-Weibull model to predict the peak stress corresponding to failure probabilities of 5 and 63% at 2M cycles (σ(max, 5%) and σ(max, 63%)). Groups A and B did not have significantly different Weibull modulus, m (p > 0.05). The specimens with parallel orientation showed significantly higher σ(max, 63%) (p ≤ 0.05), but there was no significant difference in the σ(max, 5%) (p > 0.05). Thus, it can be concluded that the fatigue resistance of the material was greatest when the electron beam orientation was perpendicular to the direction of crack propagation.
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