scholarly journals Cloning and characterization of the SERK1 gene in triploid Pingyi Tiancha [Malus hupehensis (Pamp.) Rehd. var. pingyiensis Jiang] and a tetraploid hybrid strain

2015 ◽  
Vol 14 (4) ◽  
pp. 14576-14586
Author(s):  
L.J. Zhang ◽  
W.X. Dong ◽  
S.M. Guo ◽  
Y.X. Wang ◽  
A.D. Wang ◽  
...  
2018 ◽  
Vol 7 (10) ◽  
pp. 2365-2378 ◽  
Author(s):  
Alice Checcucci ◽  
George C. diCenzo ◽  
Veronica Ghini ◽  
Marco Bazzicalupo ◽  
Anke Becker ◽  
...  

2018 ◽  
Vol 8 (4) ◽  
pp. 351 ◽  
Author(s):  
Nasr-Eldin M. Aref ◽  
Abdel-Raheem A. Abdel-Raheem ◽  
Hanaa F. Kamaly ◽  
Soher Z. Hussien

2008 ◽  
Vol 27 (1) ◽  
pp. 69-78 ◽  
Author(s):  
Kaixuan Duan ◽  
Hongqiang Yang ◽  
Kun Ran ◽  
Shuzhen You ◽  
Haizhou Zhao ◽  
...  

2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
C. H. Mallawarachchi ◽  
T. G. A. N. Chandrasena ◽  
G. P. Withanage ◽  
R. Premarathna ◽  
S. M. N. S. M. Mallawarachchi ◽  
...  

Sri Lanka achieved elimination status for lymphatic filariasis in 2016; still, the disease remains a potential public health issue. The present study is aimed at identifying a subperiodic Brugia sp. parasite which has reemerged in Sri Lanka after four decades via molecular-based analysis. Polymerase chain reaction performed with pan-filarial primers specific for the internal transcribed spacer region-2 (ITS-2) of the rDNA of Brugia filarial parasites isolated from human, canine, and feline blood samples yielded a 615 bp band establishing the species identity as Brugia malayi. Comparison of the ITS2 sequences of the reemerged B. malayi isolates with GenBank sequences revealed a higher sequence homology with B. pahangi than B. malayi with similar phylogenetic evidence. However, the mean interspecies Kimura-2-parameter pairwise divergence between the generated Brugia sequences with B. malayi and B. pahangi was less than 3%. During the analysis of parsimony sites of the new ITS2 sequences, substitutions at A36T, A296G, T373A, and G482A made the sequences different from both B. pahangi and B. malayi suggesting the possibility of a new genetic variant or a hybrid strain of B. malayi and B. pahangi. Mosquito dissections and xenomonitoring identified M. uniformis and M. annulifera as vectors of this novel strain of B. malayi circulating among cats, dogs, and humans in Sri Lanka.


2011 ◽  
Vol 30 (3) ◽  
pp. 760-767 ◽  
Author(s):  
Ji-Yu Zhang ◽  
Zhong-Ren Guo ◽  
Shen-Chun Qu ◽  
Zhen Zhang

2008 ◽  
pp. 41-48
Author(s):  
Guangli Sha ◽  
Xianghui Gong ◽  
Yanjing Shi ◽  
Yongchun Shao ◽  
Tao Yin ◽  
...  

2016 ◽  
Vol 82 (14) ◽  
pp. 4309-4319 ◽  
Author(s):  
Susan R. Leonard ◽  
Mark K. Mammel ◽  
David A. Rasko ◽  
David W. Lacher

ABSTRACTHybrid isolates of Shiga toxin-producingEscherichia coli(STEC) and enterotoxigenicE. coli(ETEC) encoding heat-stable enterotoxin (ST) are being reported with increasing frequency from a variety of sources. However, information regarding the plasmids that these strains harbor is scarce. In this study, we sequence and characterize a plasmid, p7v, from the STEC/ETEC hybrid strain 7v. Whole-genome phylogenetic analyses of STEC/ETEC hybrid strains and prototypeE. coliisolates of other pathotypes placed 7v in theEscherichiasp. cryptic lineage 1 (CL1) clade. The complete plasmid, p7v, was determined to be 229,275 bp and encodes putative virulence factors that are typically carried on STEC plasmids as well as those often carried on ETEC plasmids, indicating that the hybrid nature of the strain extends beyond merely encoding the two toxins. Plasmid p7v carries two copies ofstawith identical sequences, which were discovered to be divergent from thestasequences found in the prototype human ETEC strains. Using a nomenclature scheme based on a phylogeny constructed fromstaandstbsequences, thestaencoded on p7v is designated STa4.In silicoanalysis determined that p7v also encodes the K88 fimbria, a colonization factor usually associated with porcine ETEC plasmids. The p7v sequence and the presence of plasmid-encoded virulence factors are compared to those of other STEC/ETEC CL1 hybrid genomes and reveal gene acquisition/loss at the strain level. In addition, the interrogation of 24 STEC/ETEC hybrid genomes for identification of plasmid replicons, colonization factors, Stx and ST subtypes, and other plasmid-encoded virulence genes highlights the diversity of these hybrid strains.IMPORTANCEHybrid Shiga toxin-producingEscherichia coli/enterotoxigenicEscherichia coli(STEC/ETEC) strains, which have been isolated from environmental, animal, and human clinical samples, may represent an emerging threat as food-borne pathogens. Characterization of these strains is important for assessing virulence potential, aiding in the development of pathogen detection methods, and understanding how the hybrid strains evolve to potentially have a greater impact on public health. This study represents, to our knowledge, both the first characterization of a closed plasmid sequence from a STEC/ETEC hybrid strain and the most comprehensive phylogenetic analysis of available STEC/ETEC hybrid genomes to date. The results demonstrate how the mobility of plasmid-associated virulence genes has resulted in the creation of a diverse plasmid repertoire within the STEC/ETEC hybrid strains.


HortScience ◽  
1999 ◽  
Vol 34 (3) ◽  
pp. 450D-450
Author(s):  
Laura L. Benson ◽  
Warren F. Lamboy ◽  
Richard H. Zimmerman

Simple sequence repeats (SSRs) are highly polymorphic regions of DNA that can be used for the molecular characterization of apple (Malus) germplasm. SSR markers are sufficiently variable to distinguish between individual plants in wild Malus species. In this study, accessions of Malus hupehensis were screened for fragment length variation in PCR amplified simple sequence repeat regions of DNA. The fragment length phenotype produced by five SSR primer pairs showed no variation between two lineages of M. hupehensis collected in the Changjiang (Yangtse) River valley. One lineage was collected by E.H. Wilson in 1908 near the city of Ichang, Hubei Province. The second lineage was collected by cooperators at China's Southwest Agricultural University (SWAU) in 1997 near the city of Chongqing (Chungking). M. hupehensis Plant Introduction No. 588760 from the National Plant Germplasm System lacks provenance, but displays a fragment length phenotype identical to both the Wilson and SWAU lineages. The spread of a clone may be aided by asexual reproduction through seed, which is not uncommon in polyploid apples. Two seedlings each of 15 maternal trees from the SWAU lineage were assayed for ploidy level by flow cytometry. The DNA content per nucleus for all SWAU progeny fell within the range for triploids, 2.19 to 2.68 pg DNA/nucleus. It appears that plant explorers in China separated by almost 90 years have succeeded in sampling a single clonal lineage of M. hupehensis.


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