A multiplex fluorescence-based loop-mediated isothermal amplification assay for identifying chicken parvovirus, chicken infectious anaemia virus, and fowl aviadenovirus serotype 4

References

• Aonuma, H., Yoshimura, A., Kobayashi, T., Okado, K., Badolo, A., Nelson, B., Kanuka, H. & Fukumoto, S. (2010). A single fluorescence-based LAMP reaction for identifying multiple parasites in mosquitoes. Experimental Parasitology, 125, 179–183.
   PubMed Web of Science ®Google Scholar
• Brown Jordan, A., Blake, L., Bisnath, J., Ramgattie, C., Carrington, C.V. & Oura, C.A.L. (2019). Identification of four serotypes of fowl adenovirus in clinically affected commercial poultry co-infected with chicken infectious anaemia virus in Trinidad and Tobago. Transboundary and Emerging Diseases, 66, 1341–1348.
   PubMed Web of Science ®Google Scholar
• Chen, C., Zhao, Q., Guo, J., Li, Y. & Chen, Q. (2017). Identification of methicillin-resistant Staphylococcus aureus (MRSA) using simultaneous detection of mecA, nuc, and femB by loop-mediated isothermal amplification (LAMP). Current Microbiology, 74, 965–971.
   PubMed Web of Science ®Google Scholar
• Duan, Y.B., Yang, Y., Wang, J.X., Chen, C.J., Steinberg, G., Fraaije, B.A. & Zhou, M.G. (2018). Simultaneous detection of multiple benzimidazole-resistant beta-tubulin variants of Botrytis cinerea using loop-mediated isothermal amplification. Plant Disease, 102, 2016–2024.
   PubMed Web of Science ®Google Scholar
• Fan, Q., Xie, Z., Xie, L., Liu, J., Pang, Y., Deng, X., Xie, Z., Peng, Y. & Wang, X. (2012). A reverse transcription loop-mediated isothermal amplification method for rapid detection of bovine viral diarrhea virus. Journal of Virological Methods, 186, 43–48.
   PubMed Web of Science ®Google Scholar
• Fan, Q., Xie, Z., Xie, Z., Xie, L., Huang, J., Zhang, Y., Zeng, T., Zhang, M., Wan, S., Luo, S., Liu, J. & Deng, X. (2018). Development of duplex fluorescence-based loop-mediated isothermal amplification assay for detection of Mycoplasma bovis and bovine herpes virus 1. Journal of Virological Methods, 261, 132–138.
   PubMed Web of Science ®Google Scholar
• Hermann, J., Koski, D., Taylor, S. & Gatewood, D. (2012). Evaluation of the analytical sensitivity of a polymerase chain reaction assay for the detection of chicken infectious anemia virus in avian vaccines. Biologicals, 40, 266–269.
   PubMed Web of Science ®Google Scholar
• Huynh, L.T.M., Nguyen, G.V., Do, L.D., Dao, T.D., Le, T.V., Vu, N.T. & Cao, P.T.B. (2020). Chicken infectious anaemia virus infections in chickens in northern Vietnam: epidemiological features and genetic characterization of the causative agent. Avian Pathology, 49, 5–14.
   PubMed Web of Science ®Google Scholar
• Iseki, H., Alhassan, A., Ohta, N., Thekisoe, O.M., Yokoyama, N., Inoue, N., Nambota, A., Yasuda, J. & Igarashi, I. (2007). Development of a multiplex loop-mediated isothermal amplification (mLAMP) method for the simultaneous detection of bovine Babesia parasites. Journal of Microbiological Methods, 71, 281–287.
   PubMed Web of Science ®Google Scholar
• Kim, M.J. & Kim, H.Y. (2018). Direct duplex real-time loop mediated isothermal amplification assay for the simultaneous detection of cow and goat species origin of milk and yogurt products for field use. Food Chemistry, 246, 26–31.
   PubMed Web of Science ®Google Scholar
• Kisary, J., Avalosse, B., Miller-Faures, A. & Rommelaere, J. (1985). The genome structure of a new chicken virus identifies it as a parvovirus. Journal of General Virology, 66, 2259–2263.
   PubMed Web of Science ®Google Scholar
• Kisary, J., Nagy, B. & Bitay, Z. (1984). Presence of parvoviruses in the intestine of chickens showing stunting syndrome. Avian Pathology, 13, 339–343.
   PubMed Web of Science ®Google Scholar
• Koo, B.S., Lee, H.R., Jeon, E.O., Han, M.S., Min, K.C., Lee, S.B., Bae, Y.J., Cho, S.H., Mo, J.S., Kwon, H.M., Sung, H.W., Kim, J.N. & Mo, I.P. (2015). Genetic characterization of three novel chicken parvovirus strains based on analysis of their coding sequences. Avian Pathology, 44, 28–34.
   PubMed Web of Science ®Google Scholar
• Li, P.H., Zheng, P.P., Zhang, T.F., Wen, G.Y., Shao, H.B. & Luo, Q.P. (2017a). Fowl adenovirus serotype 4: epidemiology, pathogenesis, diagnostic detection, and vaccine strategies. Poultry Science, 96, 2630–2640.
   PubMed Web of Science ®Google Scholar
• Li, S., Fang, M., Zhou, B., Ni, H., Shen, Q., Zhang, H., Han, Y., Yin, J., Chang, W., Xu, G. & Cao, G. (2011). Simultaneous detection and differentiation of dengue virus serotypes 1–4, Japanese encephalitis virus, and West Nile virus by a combined reverse-transcription loop-mediated isothermal amplification assay. Virology Journal, 8, 360.
   PubMed Web of Science ®Google Scholar
• Li, Y., Hu, Y., Cui, S., Fu, J., Wang, Y., Cui, Z., Fang, L., Chang, S. & Zhao, P. (2017b). Molecular characterization of chicken infectious anemia virus from contaminated live-virus vaccines. Poultry Science, 96, 1045–1051.
   PubMed Web of Science ®Google Scholar
• Lin, F., Liu, L., Hao, G.J., Sheng, P.C., Cao, Z., Zhou, Y., Lv, P., Xu, T., Shen, J. & Chen, K. (2018). The development and application of a duplex reverse transcription loop-mediated isothermal amplification assay combined with a lateral flow dipstick method for Macrobrachium rosenbergii nodavirus and extra small virus isolated in China. Molecular and Cellular Probes, 40, 1–7.
   PubMed Web of Science ®Google Scholar
• Liu, N., Zou, D., Dong, D., Yang, Z., Ao, D., Liu, W. & Huang, L. (2017). Development of a multiplex loop-mediated isothermal amplification method for the simultaneous detection of Salmonella spp. and Vibrio parahaemolyticus. Scientific Reports, 7, 45601.
   PubMed Web of Science ®Google Scholar
• Liu, X.L., Zhao, X.T., Muhammad, I., Ge, B.B. & Hong, B. (2014). Multiplex reverse transcription loop-mediated isothermal amplification for the simultaneous detection of CVB and CSVd in chrysanthemum. Journal of Virological Methods, 210, 26–31.
   PubMed Web of Science ®Google Scholar
• Nanayakkara, I.A. & White, I.M. (2019). Demonstration of a quantitative triplex LAMP assay with an improved probe-based readout for the detection of MRSA. The Analyst, 144, 3878–3885.
   PubMed Web of Science ®Google Scholar
• Niu, D., Feng, J., Duan, B., Shi, Q., Li, Y., Chen, Z., Ma, L., Liu, H. & Wang, Y. (2022). Epidemiological survey of avian adenovirus in China from 2015 to 2021 and the genetic variability of highly pathogenic FAdV-4 isolates. Infection, Genetics and Evolution, 101, 105277.
   PubMed Web of Science ®Google Scholar
• Notomi, T., Okayama, H., Masubuchi, H., Yonekawa, T., Watanabe, K., Amino, N. & Hase, T. (2000). Loop-mediated isothermal amplification of DNA. Nucleic Acids Research, 28, E63.
   PubMed Web of Science ®Google Scholar
• Nunez, L.F.N., Santander-Parra, S.H., De la Torre, D.I., Sa, L.R.M., Buim, M.R., Astolfi-Ferreira, C.S. & Piantino Ferreira, A.J. (2020). Molecular characterization and pathogenicity of chicken parvovirus (ChPV) in specific pathogen-free chicks infected experimentally. Pathogens (basel, Switzerland), 9, 606.
   PubMed Web of Science ®Google Scholar
• Smieja, M., Mahony, J.B., Goldsmith, C.H., Chong, S., Petrich, A. & Chernesky, M. (2001). Replicate PCR testing and probit analysis for detection and quantitation of Chlamydia pneumoniae in clinical specimens. Journal of Clinical Microbiology, 39, 1796–1801.
   PubMed Web of Science ®Google Scholar
• Su, Q., Li, Y., Meng, F., Cui, Z., Chang, S. & Zhao, P. (2018). Newcastle disease virus-attenuated vaccine co-contaminated with fowl adenovirus and chicken infectious anemia virus results in inclusion body hepatitis-hydropericardium syndrome in poultry. Veterinary Microbiology, 218, 52–59.
   PubMed Web of Science ®Google Scholar
• Su, Q., Meng, F., Li, Y., Zhang, Y., Zhang, Z., Cui, Z., Chang, S. & Zhao, P. (2019). Chicken infectious anemia virus helps fowl adenovirus break the protection of maternal antibody and cause inclusion body hepatitis-hydropericardium syndrome in layers after using co-contaminated Newcastle disease virus-attenuated vaccine. Poultry Science, 98, 621–628.
   PubMed Web of Science ®Google Scholar
• Sun, J., Zhang, Y., Gao, S., Yang, J., Tang, Y. & Diao, Y. (2019). Pathogenicity of fowl adenovirus serotype 4 (FAdV-4) in chickens. Infection, Genetics and Evolution, 75, 104017.
   PubMed Web of Science ®Google Scholar
• Tanner, N.A., Zhang, Y. & Evans, T.C., Jr. (2012). Simultaneous multiple target detection in real-time loop-mediated isothermal amplification. Biotechniques, 53, 81–89.
   PubMed Web of Science ®Google Scholar
• Techera, C., Marandino, A., Tomas, G., Grecco, S., Hernandez, M., Hernandez, D., Panzera, Y. & Perez, R. (2021). Origin, spreading and genetic variability of chicken anaemia virus. Avian Pathology, 50, 311–320.
   PubMed Web of Science ®Google Scholar
• Vagnozzi, A.E., Espinosa, R., Cheng, S., Brinson, D., O'Kane, P., Wilson, J. & Zavala, G. (2018). Study of dynamic of chicken infectious anaemia virus infection: which sample is more reliable for viral detection? Avian Pathology, 47, 489–496.
   PubMed Web of Science ®Google Scholar
• Vera-Hernandez, P.F., Morales-Garzon, A., Cortes-Espinosa, D.V., Galiote-Flores, A., Garcia-Barrera, L.J., Rodriguez-Galindo, E.T., Toscano-Contreras, A., Lucio-Decanini, E. & Absalon, A.E. (2016). Clinicopathological characterization and genomic sequence differences observed in a highly virulent fowl aviadenovirus serotype 4. Avian Pathology, 45, 73–81.
   PubMed Web of Science ®Google Scholar
• Wang, L.C., Huang, D. & Chen, H.W. (2016). Simultaneous subtyping and pathotyping of avian influenza viruses in chickens in Taiwan using reverse transcription loop-mediated isothermal amplification and microarray. Journal of Veterinary Medical Science, 78, 1223–1228.
   PubMed Web of Science ®Google Scholar
• Xie, Z., Luo, S., Xie, L., Liu, J., Pang, Y., Deng, X., Xie, Z., Fan, Q. & Khan, M.I. (2014). Simultaneous typing of nine avian respiratory pathogens using a novel GeXP analyzer-based multiplex PCR assay. Journal of Virological Methods, 207, 188–195.
   PubMed Web of Science ®Google Scholar
• Yamazaki, W., Mioulet, V., Murray, L., Madi, M., Haga, T., Misawa, N., Horii, Y. & King, D.P. (2013). Development and evaluation of multiplex RT-LAMP assays for rapid and sensitive detection of foot-and-mouth disease virus. Journal of Virological Methods, 192, 18–24.
   PubMed Web of Science ®Google Scholar
• Yuming, F., Sheng, Y., Wenyu, D., Shihong, C., Wenfeng, L., Wenjing, H., Xiaowen, L., El-Ashram, S., Mei, K., Jinyue, G., Xuelian, Z., Zhili, L. & Shujian, H. (2020). Molecular characterization and phylogenetic analysis of fowl adenovirus serotype-4 from Guangdong Province, China. Veterinary World, 13, 981–986.
   PubMed Web of Science ®Google Scholar
• Zhang, L., Zhang, Y., Li, Q., Yang, X., Zhang, H. & Chen, H. (2016). Diagnosis and preventive treatment of fowl adenovirus-4 infection. Anhui Agricultural Science Bulletin, 22, 116–122.
   Google Scholar
• Zhang, Y., Feng, B., Xie, Z., Deng, X., Zhang, M., Xie, Z., Xie, L., Fan, Q., Luo, S., Zeng, T., Huang, J. & Wang, S. (2020). Epidemiological surveillance of parvoviruses in commercial chicken and turkey farms in Guangxi, Southern China, during 2014–2019. Frontiers in Veterinary Science, 7, 561371.
   PubMed Web of Science ®Google Scholar
• Zhang, Y., Xie, Z., Deng, X., Xie, Z., Xie, L., Zhang, M., Luo, S., Fan, Q., Huang, J., Zeng, T. & Wang, S. (2019). Molecular characterization of parvovirus strain GX-Tu-PV-1, isolated from a Guangxi turkey. Microbiology Resource Announcements, 8, e00152-19.
   PubMed Web of Science ®Google Scholar