Development of two rapid lateral flow test strips for detection of foot-and-mouth disease virus SAT 1 and SAT 3

2020 ◽  
pp. 113967
Author(s):  
Ming Yang ◽  
Boitumelo Mudabuka ◽  
Codey Dueck ◽  
Wanhong Xu ◽  
Kabo Masisi ◽  
...  
PLoS ONE ◽  
2015 ◽  
Vol 10 (8) ◽  
pp. e0134931 ◽  
Author(s):  
Kazuki Morioka ◽  
Katsuhiko Fukai ◽  
Kazuo Yoshida ◽  
Rie Kitano ◽  
Reiko Yamazoe ◽  
...  

2016 ◽  
Vol 12 (1) ◽  
Author(s):  
Moses Tefula Dhikusooka ◽  
Chrisostom Ayebazibwe ◽  
Alice Namatovu ◽  
Graham J. Belsham ◽  
Hans Redlef Siegismund ◽  
...  

2009 ◽  
Vol 16 (11) ◽  
pp. 1660-1664 ◽  
Author(s):  
Jae Ku Oem ◽  
Nigel P. Ferris ◽  
Kwang-Nyeong Lee ◽  
Yi-Seok Joo ◽  
Bang-Hun Hyun ◽  
...  

ABSTRACT A simple lateral-flow assay (LFA) based on a monoclonal antibody (MAb 70-17) was developed for the detection of foot-and-mouth disease virus (FMDV) under nonlaboratory conditions. The LFA was evaluated with epithelial suspensions (n = 704) prepared from current and historical field samples which had been submitted to the Pirbright Laboratory (United Kingdom) and from negative samples (n = 100) collected from naïve animals in Korea. Four FMDV serotypes (type O, A, Asia 1, and C) were detected in the LFA, but not the remaining three FMDV serotypes (SAT 1, SAT 2, and SAT 3). The diagnostic sensitivity of the LFA for FMDV types O, A, C, and Asia 1 was similar, at approximately 87.3%, to that of 87.7% obtained with antigen enzyme-linked immunosorbent assay (Ag-ELISA). The diagnostic specificity of the LFA was 98.8%, compared to 100% for the Ag-ELISA. These results demonstrate that the LFA using the FMDV MAb 70-17 to detect FMDV is a supportive method for taking rapid measurements at the site of a suspected foot-and-mouth disease outbreak in Asia before diagnosing the disease in the laboratory, thereby offering the possibility of implementing control procedures more rapidly.


1965 ◽  
Vol 63 (3) ◽  
pp. 357-368 ◽  
Author(s):  
N. St G. Hyslop ◽  
R. H. Fagg

Foot-and-mouth disease virus of Type SAT 1 (strain Turkey 323/62) was passaged serially 34 times in cattle previously vaccinated with increasing doses of formol-treated vaccine of the homologous strain. Primary vesicles developed in all the partly immunized animals and secondary lesions occurred in the majority. Virus from the 34th passage was capable of reinfecting a steer only 76 days after primary infection early in the passage series. Virus isolated from the second infection of this animal differed from that isolated from the primary infection in complement-fixing properties and in sensitivity to antiserum, and these differences were of a degree indicative of subtype variation.The variant strain was transmissible by contact, and virus titres in tongue and foot lesions of partly immunized animals were of the same order as those encountered in susceptible cattle.These observations suggest one way in which variant strains may arise in the field.


2010 ◽  
Vol 58 (2) ◽  
pp. 173-178 ◽  
Author(s):  
W. Vosloo ◽  
S. P. Swanepoel ◽  
M. Bauman ◽  
B. Botha ◽  
J. J. Esterhuysen ◽  
...  

Biomolecules ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 841
Author(s):  
Yun-Jung Hwang ◽  
Kyung-Kwan Lee ◽  
Jong-Won Kim ◽  
Kwang-Hyo Chung ◽  
Sang-Jick Kim ◽  
...  

Foot-and-mouth disease virus (FMDV) is a highly contagious disease that affects cloven-hoofed animals. The traditional diagnostic methods for FMDV have several drawbacks such as cross-reactivity, low sensitivity, and low selectivity. To overcome these drawbacks, we present an optical and electrochemical dual-modal approach for the specific detection of FMDV serotypes O and A by utilizing a magnetic nanoparticle labeling technique with resorufin β-d-glucopyranoside (res-β-glc) and β-glucosidase (β-glc), without the use of typical lateral flow assay or polymerase chain reaction. FMDV serotypes O and A were reacted with pan-FMDV antibodies that recognize all seven FMDV serotypes (O, A, C, Asia 1, SAT 1, SAT 2, and SAT 3). The antigen–antibody complex was then immobilized on magnetic nanoparticles and reacted with β-glc-conjugated FMDV type O or type A antibodies. Subsequently, the addition of res-β-glc resulted in the release of fluorescent resorufin and glucose owing to catalytic hydrolysis by β-glc. The detection limit of fluorescent signals using a fluorescence spectrophotometer was estimated to be log(6.7) and log(5.9) copies/mL for FMDV type O and A, respectively, while that of electrochemical signals using a glucometer was estimated to be log(6.9) and log(6.1) copies/mL for FMDV type O and A, respectively. Compared with a commercially available lateral flow assay diagnostic kit for immunochromatographic detection of FMDV type O and A, this dual-modal detection platform offers approximately four-fold greater sensitivity. This highly sensitive and accurate dual-modal detection method can be used for effective disease diagnosis and treatment, and will find application in the early-stage diagnosis of viral diseases and next-generation diagnostic platforms.


Author(s):  
Christopher J. Kasanga ◽  
Raphael Sallu ◽  
Fredrick Kivaria ◽  
Mathias Mkama ◽  
Joseph Masambu ◽  
...  

This study was conducted to investigate the presence of foot-and-mouth disease virus (FMDV) in different geographic locations of Tanzania. Epithelial tissues and fluids (n = 364) were collected from cattle exhibiting oral and foot vesicular lesions suggestive of FMD and submitted for routine FMD diagnosis. The analysis of these samples collected during the period of 2002 and 2010 was performed by serotype-specific antigen capture ELISA to determine the presence of FMDV. The results of this study indicated that 167 out of 364 (46.1%) of the samples contained FMDV antigen. Of the 167 positive samples, 37 (28.4%) were type O, 7 (4.1%) type A, 45 (21.9%) SAT 1 and 79 (45.6%) SAT 2. Two FMDV serotypes (O and SAT 2) were widely distributed throughout Tanzania whilst SAT 1 and A types were only found in the Eastern zone. Our findings suggest that serotypes A, O, SAT 1 and SAT 2 prevail in Tanzania and are associated with the recent FMD outbreaks. The lack of comprehensive animal movement records and inconsistent vaccination programmes make it difficult to determine the exact source of FMD outbreaks or to trace the transmission of the disease over time. Therefore, further collection and analysis of samples from domestic and wild animals are being undertaken to investigate the genetic and antigenic characteristics of the circulating strains, so that a rational method to control FMD in Tanzania and the neighbouring countries can be recommended.


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