Identification and Characterization of a Novel Meningococcal Autotransporter Protein: A New Virulence Factor?

2001 ◽  
Vol 101 (s45) ◽  
pp. 18P-19P
Author(s):  
DPJ Turner ◽  
KG Wooldridge ◽  
Daa Ala'aldeen
Genetics ◽  
1999 ◽  
Vol 153 (1) ◽  
pp. 391-400 ◽  
Author(s):  
Go Suzuki ◽  
Naoko Kai ◽  
Tamaki Hirose ◽  
Kiichi Fukui ◽  
Takeshi Nishio ◽  
...  

Abstract In Brassica, two self-incompatibility genes, encoding SLG (S locus glycoprotein) and SRK (S-receptor kinase), are located at the S locus and expressed in the stigma. Recent molecular analysis has revealed that the S locus is highly polymorphic and contains several genes, i.e., SLG, SRK, the as-yet-unidentified pollen S gene(s), and other linked genes. In the present study, we searched for expressed sequences in a 76-kb SLG/SRK region of the S9 haplotype of Brassica campestris (syn. rapa) and identified 10 genes in addition to the four previously identified (SLG9, SRK9, SAE1, and SLL2) in this haplotype. This gene density (1 gene/5.4 kb) suggests that the S locus is embedded in a gene-rich region of the genome. The average G + C content in this region is 32.6%. An En/Spm-type transposon-like element was found downstream of SLG9. Among the genes we identified that had not previously been found to be linked to the S locus were genes encoding a small cysteine-rich protein, a J-domain protein, and an antisilencing protein (ASF1) homologue. The small cysteine-rich protein was similar to a pollen coat protein, named PCP-A1, which had previously been shown to bind SLG.


2014 ◽  
Vol 8 (3) ◽  
pp. 103-111
Author(s):  
FATIMAH FATIMAH ◽  
◽  
APON ZAENAL MUSTOPA ◽  
IQBAL KUSNANDARSYAH

Author(s):  
Sejal S. Chaudhary ◽  
Harshad C. Chauhan ◽  
Kishan Kumar Sharma ◽  
Sandip S. Patel ◽  
Sushil Kumar Mohapatra ◽  
...  

Background: The present study was done to ascertain prevalence of Staphylococcus aureus from various canine affections in Banaskantha district of Gujarat, India. Along with this, use of classical and molecular techniques were compared in identification and virulence characterization of this pathogen.Methods: A total of 165 samples were collected and bacterial identification was carried out with bacteriological (phenotypic) techniques and confirmed by genus specific 16S rDNA and Staphylococcus aureus specific sa442 gene based PCR. Isolates were characterized for coagulase production, haemolysis activity and presence of spa gene. Result: Samples yielded, 88 (53.33%) Staphylococcus spp. via bacteriological and PCR methods. Clinically, 19 (21.59%), 28 (31.82%), 12 (13.64%), 15 (17.04%) and 14 (15.91%) isolates were from abscess/wound, pyoderma, respiratory problems, eye infections and Otitis, respectively. A total of 46/88 (52.27%) isolates were confirmed as Staphylococcus aureus in PCR. In tube coagulase test, 51/88 (57.95%) isolates were found positive. A tota of 42 isolates revealed presence of coa gene, including two tube coagulase negative isolates. Haemolytic activity revealed beta (51.14%) gamma (31.82%), alpha (13.64%) and alpha-beta (3.41%) haemolysis, respectively. X-region of Protein A (spa gene) was detected in 26 /46 (56.52%) isolates in PCR.


2012 ◽  
Vol 111 (3) ◽  
pp. 1143-1150 ◽  
Author(s):  
Yan Huang ◽  
Wenfang Li ◽  
Lisi Huang ◽  
Yue Hu ◽  
Wenjun Chen ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (3) ◽  
pp. e0149891 ◽  
Author(s):  
Jennifer M. Kress-Bennett ◽  
N. Luisa Hiller ◽  
Rory A. Eutsey ◽  
Evan Powell ◽  
Mark J. Longwell ◽  
...  

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