1996
DOI: 10.1016/0166-0934(95)01903-0
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Multiplex polymerase chain reaction for adenovirus and herpes simplex virus in eye swabs

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Cited by 37 publications
(32 citation statements)
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“…Consistent with what was reported in the early optimization experiments, detection in foods was more sensitive with the monoplex than with the multiplex NASBA system. Indeed, some investigators have found that the amplification efficiency of one target may decrease by 1 to 3 log 10 in the presence of excess competitive target (13,21). The reduced detection sensitivity of electrochemiluminescence compared to dot blot hybridization may be explained by differences in temperature and time used in the hybridization protocols or differences in the mechanisms and chemistries upon which detection of positive signals was based.…”
Section: Discussionmentioning
confidence: 99%
“…Consistent with what was reported in the early optimization experiments, detection in foods was more sensitive with the monoplex than with the multiplex NASBA system. Indeed, some investigators have found that the amplification efficiency of one target may decrease by 1 to 3 log 10 in the presence of excess competitive target (13,21). The reduced detection sensitivity of electrochemiluminescence compared to dot blot hybridization may be explained by differences in temperature and time used in the hybridization protocols or differences in the mechanisms and chemistries upon which detection of positive signals was based.…”
Section: Discussionmentioning
confidence: 99%
“…Some affected patients revisited the casualty department repeatedly while awaiting viral culture results and therefore represented a potential infection source. More rapid diagnostic tests, for example, radioimmune dot blot testing and PCR, have been argued for by previous researchers, [19][20][21][22] with potential benefits in reducing the degree of spread of the viral transmission. This audit supports their findings.…”
Section: Discussionmentioning
confidence: 99%
“…Spread is via droplet or direct contact. The majority of virology departments currently use viral isolation by the culture of conjunctival swab samples to confirm infection, while the uptake of more rapid virological confirmation techniques [1][2][3][19][20][21][22] has been slow because of the increased cost and expertise required for their implementation.…”
Section: Introductionmentioning
confidence: 99%
“…Then the DNA products used for polymerase chain reaction PCR technique, the adenovirus primers (P1 -5' GCCGCAGTGGTCTTACATGCACATC 3', P2 -5' CAGCACGCCGCGGATGTCAAGT 3') were designed according to the DNA sequence of the hexon region of adenoviruses types 2 and 5. This pair of primers amplifies a fragment of 300 bp from the hexon gene of many serotypes 22 . The PCR reaction was carried out as described elsewhere…”
Section: Methodsmentioning
confidence: 99%