Maher Obeidat

Ecology, toxicity, and hydrolytic activities of Bacillus thuringiensis in forests

* Correspondence: obeidatgh@yahoo.com

Identifying Selection Signatures Related to Domestication Process in Barley ( Hordeum Vulgare L. ) Landraces of Jordan Using Microsatellite Markers

Domestication process and the subsequent breeding may result in a genetic mutation and selection pressures that possibly contributed to the emergence of two phenotypes of barley spikelets, namely six-row and two-row barley. The present study used microsatellite genetic markers to investigate the population genetics of a selected set of accessions of domesticated barley representing different populations of Jordan, to identify a signature of selection resulted from domestication process. Genomic and statistical approaches, such as the analysis of molecular variance (AMOVA) and the so-called hierarchical “outlier” tests, were utilized to identify signatures of selection. Generally, there was a high level of polymorphisms in all the studied populations, which ranged from 19.23 for Ramtha to 69.23 (%) for Zarga, with an average of 53.61 (%). The average number of allele per locus for the entire sample set was of 9.346 and it ranged 2 occurring at [(Bmag0136), (EBmac0970_a), (EBmac0970_c) loci], to 27 at (Bmac0040) locus. The results of AMOVA showed that the main portion (~72%) of total diversity was attributed to differentiations within populations. Other portions of diversity (11.040%) were explained by the diversity among populations. As revealed by the hierarchical outlier tests and AMOVA results, 9 microsatellites were identified to be under possible selection pressures, possibly indicates that these loci were important in the past improvement of barley by early cultivators. In conclusion, the present study shows that barley landraces of Jordan possess high levels of genetic diversity and allelic richness that could be utilized in barley improvement and breeding program.

Detection of Sac Brood and Black Queen Cell Viruses from Honeybee Colonies of Jordan Using RT- PCR Technique

The Reverse Transcription-polymerase Chain Reaction (RT-PCR) is an excellent technique for the detection of honeybee viruses. In this study, the presence of Sac Brood Virus (SBV) and Black Queen Cell Virus (BQCV) was demonstrated in 100 samples, collected from Jordanian honeybee colonies by employing RT-PCR. The collected samples represented infected (depopulation, paralysis, or dark coloring), dead, and apparently healthy honeybees of different developmental stages (adult and larvae). SBV was detected in 37% of the samples, whereas BQCV was detected in 5%. Nucleotide sequences of the PCR products from each virus was determined and found to be 433 and 309 nucleotides in SBV and BQCV, respectively. The identities to the Gene Bank were 95% for SBV and 91% for BQCV. This is the first record of BQCV in Jordan.