2017
DOI: 10.1016/j.diagmicrobio.2016.11.013
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Development of a multiplex taqMan real-time PCR assay for typing of Mycoplasma pneumoniae based on type-specific indels identified through whole genome sequencing

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Cited by 7 publications
(9 citation statements)
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“…[ 11 ] as a type 1-specific insertion sequence consisting of genes encoding hypothetical proteins and a single tRNA gene. Three small indels (13–15 bp) previously identified as unique to either type 1 or type 2 isolates [ 54 ] were confirmed in all newly sequenced genomes (n = 67). To confirm the apparent absence of these segments was not due to lack of Illumina sequencing reads, we performed multiple sequence alignments of only closed genomes (n = 34) ( Table 1 ).…”
Section: Resultssupporting
confidence: 55%
“…[ 11 ] as a type 1-specific insertion sequence consisting of genes encoding hypothetical proteins and a single tRNA gene. Three small indels (13–15 bp) previously identified as unique to either type 1 or type 2 isolates [ 54 ] were confirmed in all newly sequenced genomes (n = 67). To confirm the apparent absence of these segments was not due to lack of Illumina sequencing reads, we performed multiple sequence alignments of only closed genomes (n = 34) ( Table 1 ).…”
Section: Resultssupporting
confidence: 55%
“…P1 typing. The specimens that were PCR positive for M. pneumoniae were classified into two main genomic groups corresponding to P1 types 1 and 2 using a multiplex real-time PCR assay for detection of type-specific short genomic regions identified through whole-genome sequencing as previously described (47).…”
Section: Methodsmentioning
confidence: 99%
“…Mycoplasma pneumoniae is also a significant cause of respiratory diseases including CAP for all ages [153]. Mycoplasma pneumoniae pneumonia may be altered by the level of host cell-mediated immunity [154].…”
Section: Neutrophils In Infectious Pneumoniamentioning
confidence: 99%