No abstract

The NPR1 or NPR1-like genes play a pivotal role in systemic acquired resistance in plants. Here, we isolated and identified a novel tobacco (Nicotiana glutinosa) NPR1-like gene (designated as NgNPR3). The full-length cDNA is 2049 bp in length with a 1767 bp open reading frame which encodes a 588 amino acids protein with an estimated molecular mass of 66 kDa and a calculated pI of 7.14. Homology analysis suggested that the NgNPR3 protein shares significant similarity to AtNPR3 of Arabidopsis. Transient expression assay of NgNPR3-GFP fusion gene in onion epidermal cells revealed that the NgNPR3 protein was localized to the cytoplasm and moved into the nucleus after redox change. RT-PCR results indicated that NgNPR3 was up-regulated after treatment with SA, INA, H(2)O(2,) and MeJA, which play important roles in various resistance responses in tobacco. Transcriptional level of NgNPR3 was also up-regulated after inoculation with Rhizoctonia solani, Phytophthora parasitica, Alternaria alternata, Pseudomonas solanacearum, and potato virus Y (PVY), respectively. When NgNPR3 was overexpressed in N. tabacum cv. Samsun plants, the transgenic plants showed enhanced resistance to the pathogens A. alternate, P. solanacearum and PVY. Furthermore, NgNPR3-mediated disease resistance is dosage-dependent. Our results suggest that NgNPR3 could be a putative NPR1-like gene, and might play an important role in resistance to a broad range of pathogens in tobacco.

As one of the top pork producers in China, Shandong Province suffered frequent outbreaks of porcine epidemic diarrhoea virus (PEDV) on pig farms from January 2012 to July 2015, resulting in significant economic losses. To better understand the prevalence situation, we conducted molecular epidemiological analyses of 38 PEDV strains isolated from 13 cities in Shandong Province. The detection rate of PEDV was 71.2% (146/205) by reverse transcription polymerase chain reaction (RT-PCR). The S genes of the 38 isolated samples were 4146 to 4161 nt in length and shared high levels of sequence identity (93.3-99.6% nt, 92.1-99.4% aa) with those of the 41 reference strains. Among the 38 strains, 31 strains that occupied 12 cities were classed into G3 genotype, while the other seven that only existed in four cities were classed into G2 genotype. In addition, the strains CH-SDLY-2-2014 and CH-SDLY-3-2014 isolated from Linyi were classed into the Gd subgenotype. Notably, there were multiple insertions or deletions in the S genes and several mutations in the neutralizing epitopes of the PEDV S protein. Overall, the results revealed that G2 and G3 are the predominant PEDV genotypes circulating in Shandong Province during 2012-2015, and Gd subgenotype in G3 group had already spread towards northern China in 2014.