scholarly journals Two-Component Direct Fluorescent-Antibody Assay for Rapid Identification ofBacillus anthracis

2002 ◽  
Vol 8 (10) ◽  
pp. 1060-1065 ◽  
Author(s):  
Barun K. De ◽  
Sandra L. Bragg ◽  
Gary N. Sanden ◽  
Kathy E. Wilson ◽  
Lois A. Diem ◽  
...  
1996 ◽  
Vol 70 (3) ◽  
pp. 224-231 ◽  
Author(s):  
Naoyuki MIYASHITA ◽  
Akira MATSUMOTO ◽  
Rinzo SOEJIMA ◽  
Yoshifumi KUBOTA ◽  
Toshio KISHIMOTO ◽  
...  

2009 ◽  
Vol 46 (3) ◽  
pp. 279-281 ◽  
Author(s):  
Luciano Kapelusznik ◽  
Rupa Patel ◽  
Jennifer Jao ◽  
Gopi Patel ◽  
Simon Daefler ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Ernest V. Boiko ◽  
Alexei L. Pozniak ◽  
Dmitrii S. Maltsev ◽  
Alexei A. Suetov ◽  
Irina V. Nuralova

Aim. To determine the frequency of detection of conjunctivalC. trachomatis(CT),M. hominis(MH), andU. urealyticum(UU) infections in young adults with dry eye disease (DED), since these infections may potentially produce the chronic subclinical inflammation characteristic of DED.Materials and Methods. The study included subjects of 25–45 years of age, divided into the DED (n=114) and nondry eye control (n=98) groups, with the diagnosis based on self-reported complaints, biomicroscopy, the Schirmer I test, and break-up time. All patients had conjunctival scrapings taken to detect CT, MH, and UU with direct fluorescent-antibody assay kits.Results. At least one of the three microorganisms was found in 87.7% of the DED patients versus 8.2% of the controls. Of all the DED patients, 63.2%, 50.8%, and 42.1% were found to be infected with CT, MH, and UU, respectively. Multiple pathogens were identified in 65% of the DED patients found to be infected. CT infection was detected in 6.1% of the controls.Conclusion.C. trachomatis,M. hominis, andU. urealyticumwere detected with high frequency in the conjunctiva of young adults with DED and may be an important risk factor for DED in them.


1995 ◽  
Vol 7 (3) ◽  
pp. 301-304 ◽  
Author(s):  
Rafique A. Tahir ◽  
Kern A. Pomeroy ◽  
Sagar M. Goyal

The effect of blind passage and centrifugation on the isolation of bovine coronavirus in human rectal tumor cells cultured in shell vials was investigated. A total of 68 fecal samples known to be positive for bovine coronavirus by transmission electron microscopic (TEM) examination were used. The samples were centrifuged onto human rectal tumor cell monolayers and incubated in the presence of trypsin. The growth of bovine coronavirus in infected cells was demonstrated by fluorescent antibody staining, and the extracellular virus was detected and confirmed by hemagglutination and hemagglutination-inhibition tests, respectively. Of the 68 TEM-positive samples, 51 (75%), 58 (85%), and 61 (90%) grew in shell vial cell cultures at first, second, and third passages, respectively. Of the 51 cultures positive on first passage, 19 were examined by TEM; 18 of these were positive for bovine coronavirus. The shell vial technique was also compared with direct detection of bovine coronavirus by staining cryostat sections of infected tissues in a direct fluorescent antibody assay. The results of direct fluorescent antibody assay were available for 54 of the 68 samples, of which 53 (98%) and 43 (80%) were positive by shell vial technique and direct fluorescent antibody assay, respectively. For identification of bovine coronavirus, shell vials using human rectal tumor cells in the presence of trypsin is more sensitive than direct fluorescent antibody assay but is relatively less sensitive than transmission electron microscopy.


Clinics ◽  
2011 ◽  
Vol 66 (12) ◽  
pp. 2013-2018 ◽  
Author(s):  
Maria Cristina Nishiwaki-Dantas ◽  
Mariza Toledo de Abreu ◽  
Cynthia Mendonça de Melo ◽  
Ivana Lopes Romero ◽  
Rubens Belfort Matos Neto ◽  
...  

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