2012
DOI: 10.1371/journal.pone.0034931
|View full text |Cite
|
Sign up to set email alerts
|

Counting Mycobacteria in Infected Human Cells and Mouse Tissue: A Comparison between qPCR and CFU

Abstract: Due to the slow growth rate and pathogenicity of mycobacteria, enumeration by traditional reference methods like colony counting is notoriously time-consuming, inconvenient and biohazardous. Thus, novel methods that rapidly and reliably quantify mycobacteria are warranted in experimental models to facilitate basic research, development of vaccines and anti-mycobacterial drugs. In this study we have developed quantitative polymerase chain reaction (qPCR) assays for simultaneous quantification of mycobacterial a… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

2
26
0

Year Published

2012
2012
2023
2023

Publication Types

Select...
8
2

Relationship

0
10

Authors

Journals

citations
Cited by 45 publications
(29 citation statements)
references
References 22 publications
2
26
0
Order By: Relevance
“…Although this variable does not only represent true bacterial viability, but also bacterial burden determined by the differences in culture and PCR sensitivity, the fact is that it might roughly indicate the amounts of live bacteria that are available for transmission according to PTB form. In any case, the results presented in this study would provide a reference of what can be expected in terms of infectivity if the lengthy and labor-intensive traditional isolation methods are replaced by the faster molecular PCR tests (Pathak et al, 2012). From a clinical and epidemiological perspective, the distribution of each of these two PTB forms through age seems to point out to different levels of production damage .…”
Section: Discussionmentioning
confidence: 78%
“…Although this variable does not only represent true bacterial viability, but also bacterial burden determined by the differences in culture and PCR sensitivity, the fact is that it might roughly indicate the amounts of live bacteria that are available for transmission according to PTB form. In any case, the results presented in this study would provide a reference of what can be expected in terms of infectivity if the lengthy and labor-intensive traditional isolation methods are replaced by the faster molecular PCR tests (Pathak et al, 2012). From a clinical and epidemiological perspective, the distribution of each of these two PTB forms through age seems to point out to different levels of production damage .…”
Section: Discussionmentioning
confidence: 78%
“…The total unbound lipid extracts from before the biphasic separation were subjected to MALDI-TOF MS. Two microliters of the lipid extract was dried on a steel MALDI-TOF MS sample target on a heat plate at 45°C. This was overlain with the matrix solution (1 l of saturated ␣-cyano-4-hydroxycinnamic acid [CHCA] in (18,19). We chose to do qPCR of the 16S rRNA gene because it is highly conserved and only a single copy exists in the M. abscessus genome.…”
Section: Multilocus Genotyping Of the Clinical Isolatesmentioning
confidence: 99%
“…However, only platable, replicating bacteria are detected. Additionally, the plating method has considerable technical variation, and other methods need to be considered for enumerating bacteria in complex samples (149). In infected cells the multiplicity of infection varies with infection efficiency and replication post-infection, and mycobacterial load varies considerably in human lesions (150).…”
Section: Direct Quantification Of Mycobacterial Proteins In Infected mentioning
confidence: 99%