2019
DOI: 10.1016/j.mcp.2019.101451
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A novel approach for detection of brucella using a real-time recombinase polymerase amplification assay

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Cited by 9 publications
(4 citation statements)
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“…A dual PCR was established for distinguishing the B. suis vaccine strain S2 and B. suis biovar 1 among 76 field isolates representing all the common Brucella species and biovars, as well as four Brucella vaccine strains (104M, A19, S19, and M5) [89]. Qin et al developed a real-time recombinase polymerase amplification assay for the detection of Brucella, suggesting that this method could successfully distinguish 18 representative Brucella strains and four Brucella vaccine strains, including S2, A19, S19, and M5 [90]. Based on the genome-wide core-SNP typing platform, the B. suis vaccine strain S2 was discriminated from 54 B. suis strains with the accumulation of the highest number of SNPs [30,91] and using MLVA, Jiang et al identified the B. suis vaccine strain S2 isolate from cattle in China [23].…”
Section: Surveillance Of S2 Vaccine Immunizationmentioning
confidence: 99%
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“…A dual PCR was established for distinguishing the B. suis vaccine strain S2 and B. suis biovar 1 among 76 field isolates representing all the common Brucella species and biovars, as well as four Brucella vaccine strains (104M, A19, S19, and M5) [89]. Qin et al developed a real-time recombinase polymerase amplification assay for the detection of Brucella, suggesting that this method could successfully distinguish 18 representative Brucella strains and four Brucella vaccine strains, including S2, A19, S19, and M5 [90]. Based on the genome-wide core-SNP typing platform, the B. suis vaccine strain S2 was discriminated from 54 B. suis strains with the accumulation of the highest number of SNPs [30,91] and using MLVA, Jiang et al identified the B. suis vaccine strain S2 isolate from cattle in China [23].…”
Section: Surveillance Of S2 Vaccine Immunizationmentioning
confidence: 99%
“…Qin et al. developed a real‐time recombinase polymerase amplification assay for the detection of Brucella , suggesting that this method could successfully distinguish 18 representative Brucella strains and four Brucella vaccine strains, including S2, A19, S19, and M5 [90]. Based on the genome‐wide core‐SNP typing platform, the B. suis vaccine strain S2 was discriminated from 54 B .…”
Section: Surveillance Of S2 Vaccine Immunizationmentioning
confidence: 99%
“…Detection of the H9-subtype of Avian influenza virus by RPA LFD assay with 10 × more sensitivity than conventional RT-PCR has also been documented (Wang et al 2019). Several other significant animal diseases for which RPA-LFD assays have been developed include detection of Porcine circovirus type 2 (PCV-2) (Yang et al 2017b), PPRV (Yang et al 2017c), ASFV (Miao et al 2019), Porcine deltacoronavirus (PDCoV) (Gao et al 2020), Pasteurella multocida (Zhao et al 2019), Bovine viral diarrhoea virus (BVDV) (Hou et al 2018a), Bovine ephemeral fever virus (BEFV) (Hou et al 2018b), Mycoplasma bovis (Zhao et al 2018), Infectious bovine rhinotracheitis virus (IBRV) (Hou et al 2017), FMDV (Wang et al 2018b), Brucella species (Qin et al 2019), PRRSV (Wang et al 2017) and LSDV (Shalaby et al 2016). The use of RPA-LFD assay in diagnostic application is therefore becoming a molecular tool of choice for the rapid, specific, and cost-effective approach for identification of animal diseases in laboratory settings as well as in field conditions.…”
Section: Nucleic Acid-based Detection Systemsmentioning
confidence: 99%
“…A total of 52 Brucella field strains were detected by real-time PCR and RPA in parallel, and compared with real-time PCR, the sensitivity of the RPA assay was 94%. Thus, this RPA assay may be a rapid, sensitive, and specific tool for the prevention and control of Brucellosis [80].…”
Section: Diagnosis Of Brucellosismentioning
confidence: 99%