2007
DOI: 10.1097/ico.0b013e318060ac3a
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Application of Polymerase Chain Reaction-Based Restriction Fragment Length Polymorphism in Typing Ocular Rapid-Growing Nontuberculous Mycobacterial Isolates From Three Patients With Postoperative Endophthalmitis

Abstract: A clinical suspicion of infection by RGNTM in delayed-onset postoperative endophthalmitis should be considered when resistance to standard therapy is encountered.

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Cited by 27 publications
(22 citation statements)
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“…M. abscessus , while initially categorized as a subspecies of M. chelonae , was determined to be a separate species in 1992 after DNA hybridization studies 2. Given the many biochemical similarities between M. abscessus and M. chelonae , clinical laboratories often fail to distinguish between these organisms at the species level with standard biochemical testing 6–8.…”
Section: Discussionmentioning
confidence: 99%
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“…M. abscessus , while initially categorized as a subspecies of M. chelonae , was determined to be a separate species in 1992 after DNA hybridization studies 2. Given the many biochemical similarities between M. abscessus and M. chelonae , clinical laboratories often fail to distinguish between these organisms at the species level with standard biochemical testing 6–8.…”
Section: Discussionmentioning
confidence: 99%
“…PCR is a rapid, specific, and cost-effective means of identification of RGNTM to the species level that can be performed in parallel with standard biochemical tests;2,6,7 however, it often requires outsourcing to validated laboratories, requiring additional time and resources. Gene sequencing also serves as an effective option for identification of RGNTM 6.…”
Section: Discussionmentioning
confidence: 99%
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“…Culture of vitreous fluid for toxoplasmosis using viral media has been reported to be possible in cases of extensive, diffuse infections. 44 Tuberculous chorioretinitis 45 is potentially confirmable by PCR testing, although higher copy numbers seem to be required than exist in ocular specimens that have not been grown out in culture. 46 PCR protocols optimized for the confirmation of Mycobacterium tuberculosis from cultures rather than from biologic fluids are not efficient diagnostic tools and yield false negatives when applied to ocular specimens.…”
Section: Ancillary Testing To Confirm the Working Diagnosismentioning
confidence: 99%
“…Molecular PCR-based technology has been developed to detect AMB infections, which are relatively faster and more specific compared to traditional microbiological methods 53 . Primers targeting the heat shock protein 65 (hsp65) have been utilized to detect M. fortuitum in postoperative endophthalmitis patients 54 .…”
mentioning
confidence: 99%