Evaluation of a Novel Immunochromatographic Assay for Detection of Human Adenoviruses from Throat Swab Samples Compared with Real-time PCR

2018 ◽  
Vol 64 (10/2018) ◽  
Author(s):  
Nobuhisa Ishiguro ◽  
Miki Kaiho ◽  
Hideaki Kikuta ◽  
Takehiro Togashi ◽  
Daisuke Sato ◽  
...  
2014 ◽  
Vol 20 (5) ◽  
pp. 303-306 ◽  
Author(s):  
Miyuki Morozumi ◽  
Hideaki Shimizu ◽  
Yuki Matsushima ◽  
Keiko Mitamura ◽  
Takeshi Tajima ◽  
...  

2021 ◽  
Vol 45 (3) ◽  
pp. 189-192
Author(s):  
Nobuhisa Ishiguro ◽  
Hideaki Kikuta ◽  
Mutsuko Konno ◽  
Rikako Sato ◽  
Atsushi Manabe

Abstract Objectives Mycoplasma pneumoniae is one of the common causative pathogens of community-acquired respiratory tract infections mainly in children and young adults. Rapid and accurate diagnostic techniques for identifying the causative pathogen would be useful for initiating treatment with an appropriate antibiotic. The purpose of the present study was to evaluate the sensitivity and specificity of a novel immunochromatographic assay using silver amplification technology using FUJI DRI-CHEM IMMUNO AG2 and FUJI DRI-CHEM IMMUNO AG cartridge Myco (FUJIFILM Co., Tokyo, Japan) for detection of M. pneumoniae. Methods Throat swab samples were collected from 170 pediatric patients who were diagnosed with bronchitis or pneumonia. The silver amplification immunochromatographic (SAI) assay was performed using these samples and the results were compared with those of real-time PCR. The time required for the SAI assay is approximately 20 min (5 min for sample preparation and 15 min for waiting time after starting the assay). Results The sensitivity and specificity of the SAI assay for detection of M. pneumoniae were 85.2 and 99.1%, respectively, and the assay showed positive and negative predictive values of 98.1 and 92.3%, respectively, compared with the results of real-time PCR. The diagnostic accuracy was 94.1%. Conclusions FUJI DRI-CHEM IMMUNO AG2 and FUJI DRI-CHEM IMMUNO AG cartridge Myco are appropriate for clinical use. The optimal timing of this assay is five days or more after the onset of M. pneumoniae infection. However, PCR or other molecular methods are superior, especially with regard to sensitivity and negative predictive value.


2007 ◽  
Vol 191 (1-4) ◽  
pp. 83-93 ◽  
Author(s):  
M. Muscillo ◽  
M. Pourshaban ◽  
M. Iaconelli ◽  
S. Fontana ◽  
A. Di Grazia ◽  
...  

2008 ◽  
Vol 80 (5) ◽  
pp. 856-865 ◽  
Author(s):  
Sallene Wong ◽  
Kanti Pabbaraju ◽  
Xiaoli L. Pang ◽  
Bonita E. Lee ◽  
Julie D. Fox

2006 ◽  
Vol 54 (3) ◽  
pp. 225-230 ◽  
Author(s):  
E. Haramoto ◽  
H. Katayama ◽  
K. Oguma ◽  
Y. Koibuchi ◽  
H. Furumai ◽  
...  

A two-month survey was conducted in order to evaluate the effects of rainfall on the fate of microorganisms in seawater in the Tokyo Bay, Japan. The seawater sample (1,000 mL) was applied to a method to concentrate virus, followed by a quantification of human adenoviruses using the real-time PCR. Total coliforms and E. coli, which were determined by the colony forming method, were detected in all 47 seawater samples, while human adenoviruses were detected in 38 (81%) of the samples. The concentration of tested microorganisms showed 1–2 log units increase after rainfall events, followed by the gradual decrease to the level before the rainfall within a few days.


2014 ◽  
Vol 53 (1) ◽  
pp. 273-277 ◽  
Author(s):  
Koji Toriyama ◽  
Takashi Suzuki ◽  
Tomoyuki Inoue ◽  
Hiroshi Eguchi ◽  
Saichi Hoshi ◽  
...  

We developed an immunochromatographic assay kit that uses fluorescent silica nanoparticles bound to anti-Acanthamoebaantibodies (fluorescent immunochromatographic assay [FICGA]) and evaluated its efficacy for the detection ofAcanthamoebaand diagnosis ofAcanthamoebakeratitis (AK). The sensitivity of the FICGA kit was evaluated using samples ofAcanthamoebatrophozoites and cysts diluted to various concentrations. A conventional immunochromatographic assay kit with latex labels (LICGA) was also evaluated to determine its sensitivity in detectingAcanthamoebatrophozoites. To check for cross-reactivity, the FICGA was performed by using samples of other common causative pathogens of infectious keratitis, such asPseudomonas aeruginosa,Staphylococcus aureus,Staphylococcus epidermidis, andCandida albicans. Corneal scrapings from patients with suspected AK were tested with the FICGA kit to detect the presence ofAcanthamoeba, and the results were compared with those of real-time PCR. The FICGA kit detected organisms at concentrations as low as 5 trophozoites or 40 cysts per sample. There were no cross-reactivities with other pathogens. The FICGA was approximately 20 times more sensitive than the LICGA for the detection ofAcanthamoebatrophozoites. The FICGA kit yielded positive results for all 10 patients, which corresponded well with the real-time PCR results. The FICGA kit demonstrated high sensitivity for the detection ofAcanthamoebaand may be useful for the diagnosis of AK.


2014 ◽  
Vol 20 (12) ◽  
pp. O1010-O1016 ◽  
Author(s):  
S. Bonot ◽  
L. Ogorzaly ◽  
B. El Moualij ◽  
W. Zorzi ◽  
H.-M. Cauchie

2007 ◽  
Vol 73 (24) ◽  
pp. 7874-7881 ◽  
Author(s):  
Irene Xagoraraki ◽  
David H.-W. Kuo ◽  
Kelvin Wong ◽  
Mark Wong ◽  
Joan B. Rose

ABSTRACT Human adenoviruses (HAdVs) have been related to several waterborne diseases such as acute gastroenteritis, conjunctivitis, and respiratory illness, and it has been shown that an important human exposure pathway is through recreational waters. However, HAdV occurrence at recreational freshwater beaches has not been previously investigated. In this study, a total of 58 water samples were collected from two recreational beaches on Lake Michigan (i.e., Silver Beach and Washington Park Beach) during the summer of 2004. Occurrences of HAdVs in these lake samples were determined using two hexon-based real-time PCR assays (one for monitoring all 51 serotypes of HAdVs and another for specifically detecting F species HAdVs, i.e., serotypes 40 and 41) and compared to an integrated cell culture (ICC) PCR method. The real-time PCR results showed that 8 of 30 Silver Beach samples and 6 of 28 Washington Park Beach samples contained HAdVs, and F species HAdVs were detected in three of these positive samples. The concentrations of HAdVs ranged from (1.7 ± 0.7) × 101 to (3.4 ± 0.8) × 102 and from (7 ± 2) × 100 to (3.8 ± 0.3) × 103 virus particles/liter for Silver Beach and Washington Park Beach, respectively. F species HAdVs were detected at levels ranging from (4.8 ± 0.8) × 101 to (4.6 ± 1.5) × 102 virus particles/liter. Approximately 60% of the ICC-PCR analyses agreed with the real-time PCR results. This study revealed the occurrence of HAdVs at Lake Michigan recreational beaches. Given the potential health risks, further assessment regarding sources, virus transport, and survival is needed to improve the safety of the region.


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