scholarly journals MOLECULAR IDENTIFICATION OF Salmonella Enterica FROM PATIENTS WITH DIARRHEA IN DUHOK GOVERNORATE KURDISTAN REGION / IRAQ

2019 ◽  
Vol 22 (1) ◽  
pp. 148-154
Author(s):  
DOAA SALIH ◽  
◽  
JASSIM ABDO ◽  
ABDULRAHMAN SAADI ◽  
◽  
...  
2019 ◽  
Vol 11 (1) ◽  
pp. 5-15
Author(s):  
Sulaiman Naif Ami ◽  
Ibrahim Esa Taher ◽  
Fenik Sherzad Hussen ◽  
Ayoub Ibrahim Ahmed

Abstract This study was conducted to identify races of wheat seed gall nematode Anguina tritici by using molecular identification for this nematode species parasitized on durum and bread wheat cultivars. Wheat seed galls of both cultivars were collected from two cities, Erbil and Duhok, from the Kurdistan Region and Iraq respectively. DNA was extracted from both nematode isolates (populations), and then PCR reactions were performed with Internal Transcribed Spacer (ITS) region using primers TW81/AB28 with 2 µl of template DNA of A. tritici for both nematode isolates on both wheat cultivars. The bands of both amplification products of PCR reactions were visualized in position about 800 bp on agarose gel, which indicates that both isolates of A. tritici belong to the same race. On the other hand, no nucleotide differences were observed between the two nematode isolations, as revealed by the sequence alignment of DNA of the internal transcribed spacer (ITS) region and phylogenetic tree, which emphasizes at the same time that both nematode isolates are of the same genetic structure or have the same identity and confirms their belonging to the same nematode race.


2016 ◽  
Vol 28 (4) ◽  
pp. 419-422 ◽  
Author(s):  
Diego Felipe Alves Batista ◽  
Oliveiro Caetano de Freitas Neto ◽  
Adriana Maria de Almeida ◽  
Paul Andrew Barrow ◽  
Fernanda de Oliveira Barbosa ◽  
...  

Author(s):  
S. E. Miller

The techniques for detecting viruses are many and varied including FAT, ELISA, SPIRA, RPHA, SRH, TIA, ID, IEOP, GC (1); CF, CIE (2); Tzanck (3); EM, IEM (4); and molecular identification (5). This paper will deal with viral diagnosis by electron microscopy and will be organized from the point of view of the electron microscopist who is asked to look for an unknown agent--a consideration of the specimen and possible agents rather than from a virologist's view of comparing all the different viruses. The first step is to ascertain the specimen source and select the method of preparation, e. g. negative stain or embedment, and whether the sample should be precleared by centrifugation, concentrated, or inoculated into tissue culture. Also, knowing the type of specimen and patient symptoms will lend suggestions of possible agents and eliminate some viruses, e. g. Rotavirus will not be seen in brain, nor Rabies in stool, but preconceived notions should not prejudice the observer into missing an unlikely pathogen.


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