7 : Molecular Diagnosis of Infectious Diseases Flashcards

(34 cards)

1
Q

T or F
Nucleic Acid Amplification Techniques can overcome low sensitivity to improve the specificity of conventional phenotypic tests

A

True

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2
Q

T or F
Nucleic Acid Amplification Techniques provide early diagnosis for proper treatment with potential reduction in mortality and morbidity

A

True

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3
Q

It is a cartridge-based PCR

A

Cepheid GeneXpert®

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4
Q

It is a testing platform that is used for gastrointestinal, respiratory, and cerebrospinal organisms

A

Biofire® Filmarray®

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5
Q

It is a testing platform (microarray) that detects multiple pathogens within 1 chip and is more expensive
(e.g. : 1 chip = multiple pathogens)

A

Biofire® Filmarray®

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6
Q

It is a testing platform that uses FRET and hydrolysis probes such as quencher & reporter

A

Roche COBAS® TaqMan®

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7
Q

It is a viral loading system used to detect HIV, HBV, & HCV

A

Roche COBAS® TaqMan®

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8
Q

It is a testing platform used to detect HPV HR and uses Scorpion detection

A

Seegene Anyplex™ II

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9
Q

It is a testing platform used to detect HPV HR and uses Scorpion detection

A

Seegene Anyplex™ II

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10
Q

These are are ideal
primer targets for amplification
from all bacterial species and remain stable despite evolution

A

Conserved regions

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11
Q

In diagnosis with sequencing, measuring the degree of divergence is observed within ____ rRNA molecule

A

16s rRNA

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12
Q

In diagnosis with sequencing, the _________ sequence obtained is compared to a database containing sequences of known microorganisms

A

signature sequence

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13
Q

T or F
In diagnosis with sequencing, the number of similar nucleotide bases between sequences is used to calculate the percent identify and ascertain the identification of the microorganisms

A

True

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14
Q

T or F

The rRNA genes and their intergenic regions found in bacteria are commonly used for prokaryotic phylogenetic studies.

A

True

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15
Q

The small-subunit rRNA
molecule is a fragment
with a sedimentation
coefficient of 16S and is
encoded by a roughly
________ gene.

A

1542-bp gene

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16
Q

It known as bet subunit of RNA polymerase

17
Q

It is a DNA target known as manganese-dependent superoxide dismutase

18
Q

It is a DNA target also known as elongation factor Tu

19
Q

What are the common,y used OCR targets for detection of Bartonella spp. under molecular characterization of isolated from cultures?

A
  • citrate synthase gltA
  • B-subunit if RNA polymerase rpob
  • 16s-23s internal transcribed spacer ITS
  • 16s ribosomal RNA gene 16s
  • Riboflavin synthase ribC
  • NADH dehydrogenase gamma subunit nuoG
  • Cell division protein fitsZ
  • Heat shock protein groEL
20
Q

What are the common,y used OCR targets for detection of Bartonella spp. under direct molecular detection from blood/tissues/arthropods?

A
  • mtRNA ssrA
  • 16s-23s Internal transcribes spacer ITS
  • B-subunit of RNA polymerase rpoB
21
Q

Recently applied techniques include NGS and proteomic (includes pathogens)
approaches is used to detect what spp?

A

Borellia spp.

22
Q

In detecting Chlamydia trachomatis, the molecular genotyping of the gene _______ can be performed by using
restriction fragment length polymorphism on PCR products
(from: culture isolates or clinical specimens)

23
Q

What are the 9 polymorphic membrane protein genes that can can be used for detecting and typing Chlamydia trachomatis?

24
Q

The highly conserved genome of C. trachomatis cab be use
for _________ target systems.

25
In detecting *C. trachomatis*, analysis of variable numbers of tandem repeats in **three loci** combined with __________ can bring a significantly higher diversity index than by using ompA alone.
ompA sequencing
26
What are the toxin genes of *Clostridium difficile*?
- tcdA - tcdB - tcdC117
27
What are the two tests that can be used for detecting toxigenic genes of *Clostridium difficile*?
- Multiplex PCR - Isothermal helicase-dependent amplification
28
What are the binary toxin genes of *Clistridium difficile*?
- cdtA - cdtB
29
It is a one-step, rapid, and specific screening method for *C. difficile* toxin genes and allow an evaluation of the pathogenic potential of *C. difficile.*
Multiplex PCR
30
What are the two tests that can be used to detect *M. pneumoniae* RNA which can be used in **monoplex** and **multiplex** format
Conventional and Real-time NAATs
31
It is an assay that has been applied to detect *M. pneumoniae* in clinical specimens using **P1 sequences** for primers in direct comparison to real-time PCR.
LAMP Assay (Loop-mediated isothermal amplification)
32
It is an assay that can be used to detect point mutations in all three positions of the 23s rRNA gene
Multiplex real-time PCR
33
What are the 3 positions of the 23s rRNA gene that can be detected by using multiplex relaxation-time PCR and are related to the **macrolide resistance** on all clinical samples that are positive for *M. pneumoniae* in the *repMp1* real-time PCR assay
- 2063 - 2064 - 2617
34
What is the target gene in *M. pneumoniae*?
repMp1