2012
DOI: 10.1016/j.biologicals.2011.12.011
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Evaluation of a rapid immunochromatographic diagnostic test for the detection of rabies from brain material of European mammals

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Cited by 48 publications
(49 citation statements)
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“…The availability of simple, accurate and affordable alternatives to the DFAT, such as rabies antigen rapid diagnostic tests (RDTs) [2629], would be a useful adjunct to current surveillance methods in rural Lao PDR. However, a recent study has highlighted diagnostic problems with these tests [30] and therefore rabies antigen RDTs results should be interpreted with caution and may only be useful for surveillance purposes rather than for acute diagnosis and patient management (i.e., post-exposure prophylaxis).…”
Section: Discussionmentioning
confidence: 99%
“…The availability of simple, accurate and affordable alternatives to the DFAT, such as rabies antigen rapid diagnostic tests (RDTs) [2629], would be a useful adjunct to current surveillance methods in rural Lao PDR. However, a recent study has highlighted diagnostic problems with these tests [30] and therefore rabies antigen RDTs results should be interpreted with caution and may only be useful for surveillance purposes rather than for acute diagnosis and patient management (i.e., post-exposure prophylaxis).…”
Section: Discussionmentioning
confidence: 99%
“…The detection of infectious particles in brain homogenate was performed using RTCIT on neuroblastoma cells with an incubation period of 48 hours at 37°C as previously described [21]. The conventional hnRT-PCR was performed with universal rabies primers JW12-JW6 as previously described [19].…”
Section: Methodsmentioning
confidence: 99%
“…Primers targeting the nucleoprotein gene were applied in a two-step RT-PCR. RT was performed with Invitrogen SuperScript® III Reverse Transcriptase (Thermo Fisher Scientific) with the primer LYSSA-NMA (5′-ATGTAACACCYCTACAATG-‘3) that is modified from primer JW12 in [34]. …”
Section: Case Presentationmentioning
confidence: 99%
“…The forward primer, LYSSA-NMB (5′-ATGTAACACCYCTACAATGGA-‘3) was used in two separate PCR reactions with either LYSSA-NGA (5’-TGACTCCAGTTRGCRCACAT-‘3) or LYSSA-NGC (5’-GGGTACTTGTACTCATAYTGRTC-‘3) as reverse primers, yielding amplicons of 612 bp and 108 bp respectively. The primers are modified from the primers JW12, JW6 and SB1 in [34] respectively. Amplicons were separated on 1% agarose gel at 90 V for 90 min and visualized by DNA Gel Loading Dye (Thermo Fisher Scientific).…”
Section: Case Presentationmentioning
confidence: 99%