Development and evaluation of silver amplification immunochromatography kit for foot-and-mouth disease virus antigen detection

•A silver amplification immunochromatography was developed for FMDV antigen detection.•FMDV-Ag SAI increased the sensitivity of conventional immunochromatographic assay.•FMDV-Ag SAI was able to detect specific antigen even in saliva samples.•FMDV-Ag SAI was evaluated with various clinical samples fr...

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Published inJournal of Virological Methods Vol. 275; p. 113736
Main Authors Morioka, Kazuki, Urayama, Kana, Wada, Atsuhiko, Yoshida, Kazuo, Kato, Tomoko, Kitano, Rie, Nishi, Tatsuya, Kanno, Toru, Yamada, Manabu, Yamakawa, Makoto, Ulziibat, Gelermaa, Makino, Yoshihiko, Nakamura, Kentaro, Hojo, Eri, Matsumoto, Takashi, Fukai, Katsuhiko
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.01.2020
Elsevier BV
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Abstract •A silver amplification immunochromatography was developed for FMDV antigen detection.•FMDV-Ag SAI increased the sensitivity of conventional immunochromatographic assay.•FMDV-Ag SAI was able to detect specific antigen even in saliva samples.•FMDV-Ag SAI was evaluated with various clinical samples from an outbreak. A silver amplification immunochromatography (SAI) kit for the detection of all seven serotypes of foot-and-mouth disease virus (FMDV)—FMDV-Ag SAI—was developed using the monoclonal antibody 1H5 recognizing the highly conserved N terminus region of VP2. The FMDV-Ag SAI can be used under conditions of high biosecurity containment as it does not require any apparatus. The FMDV-Ag SAI exhibited 10–100 times higher sensitivity against the five serotypes (O, A, Asia1, C, and SAT1) and similar sensitivity against SAT2 and SAT3, compared with the Svanodip® FMDV-Ag kit immunochromatography kit. The Svanodip kit showed inhibitory results with several saliva samples but not with the FMDV-Ag SAI kit. In a validation study using clinical samples (n = 132; vesicular epithelium = 92, vesicular lesion swabs = 20, saliva = 20) in Mongolia, the sensitivity of FMDV-Ag SAI in comparison with real-time reverse transcription-polymerase chain reaction revealed the following data: vesicular epithelium, 85.4% (76/89); vesicular lesion swab, 46.7% (7/17); and saliva, 36.8% (7/19). No cross-reactivity with the non-FMDV vesicular-forming viruses and taxonomically related viruses of the Picornaviridae family occurred. The FMDV-Ag SAI is a highly sensitive diagnostic tool that enables pen-side diagnosis without requiring the use of any equipment.
AbstractList •A silver amplification immunochromatography was developed for FMDV antigen detection.•FMDV-Ag SAI increased the sensitivity of conventional immunochromatographic assay.•FMDV-Ag SAI was able to detect specific antigen even in saliva samples.•FMDV-Ag SAI was evaluated with various clinical samples from an outbreak. A silver amplification immunochromatography (SAI) kit for the detection of all seven serotypes of foot-and-mouth disease virus (FMDV)—FMDV-Ag SAI—was developed using the monoclonal antibody 1H5 recognizing the highly conserved N terminus region of VP2. The FMDV-Ag SAI can be used under conditions of high biosecurity containment as it does not require any apparatus. The FMDV-Ag SAI exhibited 10–100 times higher sensitivity against the five serotypes (O, A, Asia1, C, and SAT1) and similar sensitivity against SAT2 and SAT3, compared with the Svanodip® FMDV-Ag kit immunochromatography kit. The Svanodip kit showed inhibitory results with several saliva samples but not with the FMDV-Ag SAI kit. In a validation study using clinical samples (n = 132; vesicular epithelium = 92, vesicular lesion swabs = 20, saliva = 20) in Mongolia, the sensitivity of FMDV-Ag SAI in comparison with real-time reverse transcription-polymerase chain reaction revealed the following data: vesicular epithelium, 85.4% (76/89); vesicular lesion swab, 46.7% (7/17); and saliva, 36.8% (7/19). No cross-reactivity with the non-FMDV vesicular-forming viruses and taxonomically related viruses of the Picornaviridae family occurred. The FMDV-Ag SAI is a highly sensitive diagnostic tool that enables pen-side diagnosis without requiring the use of any equipment.
A silver amplification immunochromatography (SAI) kit for the detection of all seven serotypes of foot-and-mouth disease virus (FMDV)-FMDV-Ag SAI-was developed using the monoclonal antibody 1H5 recognizing the highly conserved N terminus region of VP2. The FMDV-Ag SAI can be used under conditions of high biosecurity containment as it does not require any apparatus. The FMDV-Ag SAI exhibited 10-100 times higher sensitivity against the five serotypes (O, A, Asia1, C, and SAT1) and similar sensitivity against SAT2 and SAT3, compared with the Svanodip® FMDV-Ag kit immunochromatography kit. The Svanodip kit showed inhibitory results with several saliva samples but not with the FMDV-Ag SAI kit. In a validation study using clinical samples (n = 132; vesicular epithelium = 92, vesicular lesion swabs = 20, saliva = 20) in Mongolia, the sensitivity of FMDV-Ag SAI in comparison with real-time reverse transcription-polymerase chain reaction revealed the following data: vesicular epithelium, 85.4% (76/89); vesicular lesion swab, 46.7% (7/17); and saliva, 36.8% (7/19). No cross-reactivity with the non-FMDV vesicular-forming viruses and taxonomically related viruses of the Picornaviridae family occurred. The FMDV-Ag SAI is a highly sensitive diagnostic tool that enables pen-side diagnosis without requiring the use of any equipment.A silver amplification immunochromatography (SAI) kit for the detection of all seven serotypes of foot-and-mouth disease virus (FMDV)-FMDV-Ag SAI-was developed using the monoclonal antibody 1H5 recognizing the highly conserved N terminus region of VP2. The FMDV-Ag SAI can be used under conditions of high biosecurity containment as it does not require any apparatus. The FMDV-Ag SAI exhibited 10-100 times higher sensitivity against the five serotypes (O, A, Asia1, C, and SAT1) and similar sensitivity against SAT2 and SAT3, compared with the Svanodip® FMDV-Ag kit immunochromatography kit. The Svanodip kit showed inhibitory results with several saliva samples but not with the FMDV-Ag SAI kit. In a validation study using clinical samples (n = 132; vesicular epithelium = 92, vesicular lesion swabs = 20, saliva = 20) in Mongolia, the sensitivity of FMDV-Ag SAI in comparison with real-time reverse transcription-polymerase chain reaction revealed the following data: vesicular epithelium, 85.4% (76/89); vesicular lesion swab, 46.7% (7/17); and saliva, 36.8% (7/19). No cross-reactivity with the non-FMDV vesicular-forming viruses and taxonomically related viruses of the Picornaviridae family occurred. The FMDV-Ag SAI is a highly sensitive diagnostic tool that enables pen-side diagnosis without requiring the use of any equipment.
A silver amplification immunochromatography (SAI) kit for the detection of all seven serotypes of foot-and-mouth disease virus (FMDV)-FMDV-Ag SAI-was developed using the monoclonal antibody 1H5 recognizing the highly conserved N terminus region of VP2. The FMDV-Ag SAI can be used under conditions of high biosecurity containment as it does not require any apparatus. The FMDV-Ag SAI exhibited 10-100 times higher sensitivity against the five serotypes (O, A, Asia1, C, and SAT1) and similar sensitivity against SAT2 and SAT3, compared with the Svanodip® FMDV-Ag kit immunochromatography kit. The Svanodip kit showed inhibitory results with several saliva samples but not with the FMDV-Ag SAI kit. In a validation study using clinical samples (n = 132; vesicular epithelium = 92, vesicular lesion swabs = 20, saliva = 20) in Mongolia, the sensitivity of FMDV-Ag SAI in comparison with real-time reverse transcription-polymerase chain reaction revealed the following data: vesicular epithelium, 85.4% (76/89); vesicular lesion swab, 46.7% (7/17); and saliva, 36.8% (7/19). No cross-reactivity with the non-FMDV vesicular-forming viruses and taxonomically related viruses of the Picornaviridae family occurred. The FMDV-Ag SAI is a highly sensitive diagnostic tool that enables pen-side diagnosis without requiring the use of any equipment.
ArticleNumber 113736
Author Morioka, Kazuki
Fukai, Katsuhiko
Yoshida, Kazuo
Hojo, Eri
Matsumoto, Takashi
Wada, Atsuhiko
Kitano, Rie
Ulziibat, Gelermaa
Kato, Tomoko
Nakamura, Kentaro
Yamada, Manabu
Yamakawa, Makoto
Makino, Yoshihiko
Kanno, Toru
Urayama, Kana
Nishi, Tatsuya
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  givenname: Gelermaa
  surname: Ulziibat
  fullname: Ulziibat, Gelermaa
  organization: Viral Animal Disease Diagnostic Division, State Central Veterinary Laboratory, Ulaanbaatar, 17024, Khan-Uul district, 53/03, Mongolia
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  surname: Makino
  fullname: Makino, Yoshihiko
  organization: In Vitro Diagnostic Division, Medical System Business Division FUJIFILM Corporation, Nishiazabu 2-26-30 Minatoku, Tokyo, 106-8620, Japan
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  surname: Nakamura
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  surname: Matsumoto
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  email: fukai@affrc.go.jp
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Keywords Antigen detection
Foot-and-mouth disease virus
Immunochromatography
Silver amplification
Language English
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Snippet •A silver amplification immunochromatography was developed for FMDV antigen detection.•FMDV-Ag SAI increased the sensitivity of conventional...
A silver amplification immunochromatography (SAI) kit for the detection of all seven serotypes of foot-and-mouth disease virus (FMDV)-FMDV-Ag SAI-was developed...
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StartPage 113736
SubjectTerms Animals
Antigen detection
Antigens, Viral
Antigens, Viral - isolation & purification
Cattle
Cattle Diseases
Cattle Diseases - diagnosis
Cell Line
Chromatography, Affinity
Chromatography, Affinity - instrumentation
Foot-and-Mouth Disease
Foot-and-Mouth Disease - diagnosis
Foot-and-Mouth Disease Virus
Foot-and-Mouth Disease Virus - classification
Foot-and-Mouth Disease Virus - isolation & purification
Immunochromatography
Reagent Kits, Diagnostic
Sensitivity and Specificity
Serogroup
Silver
Silver - chemistry
Silver amplification
Title Development and evaluation of silver amplification immunochromatography kit for foot-and-mouth disease virus antigen detection
URI https://dx.doi.org/10.1016/j.jviromet.2019.113736
https://cir.nii.ac.jp/crid/1873398392425039744
https://www.ncbi.nlm.nih.gov/pubmed/31669454
https://www.proquest.com/docview/2310721198
Volume 275
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