curvetl curvetr
Contact Us image
header
curvebl curvebr
curvetl curvetr
Member login
Side Menu

Anaerobes
Fungi / Yeasts
Gram Positive
Gram Negative

headergif

Scientific Publications - Gram Positive

headergif

Gram postitive Isolate Test Samples Gene Specificity Sensitivity Reference
AbiotrophiaA. defectivaFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%99%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
BacillusBacillus. spp.DNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA Microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
DiphtheroidsDiphtheroidsDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA Microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
EnterococcusE. faecalisRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 100% ; 3 CFU/ml 85%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
EnterococcusE. faeciumRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 100% ; 3 CFU/ml 65%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
EnterococcusE. faecalisDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
EnterococcusE. faeciumDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
EnterococcusE. casseliflavusDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA Microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
EnterococcusE. faecalisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
EnterococcusE. faeciumFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
EnterococcusE. faecalisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
EnterococcusE. faeciumLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
GemellaG. haemolysansPCRreference microorganismsgroEL96.1% (sequence identity)No percentage givenUse of groESL as a Target for Identification of Abiotrophia, Granulicatella, and Gemella Species, Wei-Chun Hung, JOURNAL OF CLINICAL MICROBIOLOGY, Oct. 2010,Vol. 48,No. 10, p. 3532-3538
GemellaG. haemolysansPCRreference microorganismsgroES97.8% (sequence identity)No percentage givenUse of groESL as a Target for Identification of Abiotrophia, Granulicatella, and Gemella Species, Wei-Chun Hung, JOURNAL OF CLINICAL MICROBIOLOGY, Oct. 2010,Vol. 48,No. 10, p. 3532-3538
GemellaG. morbillorumPCRreference microorganismsgroEL96.1% (sequence identity)No percentage givenUse of groESL as a Target for Identification of Abiotrophia, Granulicatella, and Gemella Species, Wei-Chun Hung, JOURNAL OF CLINICAL MICROBIOLOGY, Oct. 2010,Vol. 48,No. 10, p. 3532-3538
GemellaG. morbillorumPCRreference microorganismsgroES97.8% (sequence identity)No percentage givenUse of groESL as a Target for Identification of Abiotrophia, Granulicatella, and Gemella Species, Wei-Chun Hung, JOURNAL OF CLINICAL MICROBIOLOGY, Oct. 2010,Vol. 48,No. 10, p. 3532-3538
GranulicatellaG. adiacensFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%99%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
GranulicatellaG. balaenopteraeFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
GranulicatellaG. elegansFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
GranulicatellaG. paraadiacensFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
LactobacillusL. coleohominisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
ListeriaL. monocytogenesDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-42
ListeriaL. monocytogenesDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
ListeriaL. monocytogenesRT-PCRCSF16S rRNA54.0%, this specificity does not reflect the true percentage,100%Rapid detection of eight causative pathogens for the diagnosis of bacterial meningitis by real-time PCR, Naoko Chiba et al., J Infect Chemother (2009) 15:92-98
RothiaR. mucilaginosaPCRreference microorganisms16S rRNA geneNo percentage givenNo percentage givenMolecular Identification of Clinical Rothia Isolates from Human Patients: Proposal of a Novel Rothia Species, Rothia arfidiae sp. nov., Kwan Soo Ko, Journal of Bacteriology and Virology 2009. Vol. 39,No. 3 p.159 - 164
StaphylococcusS. aureusRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 100% ; 3 CFU/ml 75%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
StaphylococcusS. epidermidisRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 75% ; 3 CFU/ml 0%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
StaphylococcusS. haemolyticusRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 50% ; 3 CFU/ml 0%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
StaphylococcusS. aureusDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-34
StaphylococcusS. epidermidisDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-35
StaphylococcusS. capitisDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-60
StaphylococcusS. lugdunensisDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-61
StaphylococcusS. haemolyticus, DNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-62
StaphylococcusS. hominisDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-63
StaphylococcusS. saprophyticusDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-64
StaphylococcusS. warneriDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-65
StaphylococcusS. xylosusDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-66
StaphylococcusS. aureusDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StaphylococcusS. epidermidisDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StaphylococcusCoagulase negativeDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA Microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StaphylococcusS. aureusFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StaphylococcusS. epidermidisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StaphylococcusS. haemolyticusFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StaphylococcusS. aureusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StaphylococcusS. epidermidisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StaphylococcusS. haemolyticusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StaphylococcusS. aureusqRT-PCRnasopharyngeal secretionsmecANo percentage givenNo percentage givenQuantitative reverse transcription-PCR assay for the rapid detection of methicillin-resistant Staphylococcus aureus, M. Wada et al., Journal of Applied Microbiology ISSN 1364-5072 (2009)
StaphylococcusS. aureusqRT-PCRnasopharyngeal secretionsSpaNo percentage givenNo percentage givenQuantitative reverse transcription-PCR assay for the rapid detection of methicillin-resistant Staphylococcus aureus, M. Wada et al., Journal of Applied Microbiology ISSN 1364-5072 (2009)
StaphylococcusS. aureusRT-PCRCSFSpa54.0%, this specificity does not reflect the true percentage,100%Rapid detection of eight causative pathogens for the diagnosis of bacterial meningitis by real-time PCR, Naoko Chiba et al., J Infect Chemother (2009) 15:92-98
StaphylococcusS. epidermidisPCRblood cultureto amplify a 124bp fragment specific for S. epidermidisNo percentage givenNo percentage givenStaphylococcus aureus, Staphylococcus epidermidis and Staphylococcus haemolyticus: Methicillin-resistant isolates are detected directly in blood cultures by multiplex PCR, Eliezer M. et al., MicrobiologicalResearch 165 (2010) 243?249
StreptococcusS. agalactiaeRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 92% ; 3 CFU/ml 10%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
StreptococcusS. mitisRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 100% ; 3 CFU/ml 65%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
StreptococcusS. pneumoniaeRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 100% ; 3 CFU/ml 30%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
StreptococcusS. pyogenesRT-multiplex PCRblood cultureInternal transcribed spacer regions (ITS)98.80%100 CFU/ml 100% ; 30 CFU/ml 67% ; 3 CFU/ml 0%A multiplex real-time PCR assay for rapid detection and differentiation of 25 bacterial and fungal pathogens from whole blood samples, Lutz Eric Lehmann et al., Med Microbiol Immunol (2008) 197:313-324
StreptococcusS. pyogenesDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-36
StreptococcusS. agalactiaeDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-37
StreptococcusS. dysgalactiae subspecies equisimilisDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-38
StreptococcusS. pneumoniaeDNA-based microarray (Prove-It Sepsis Assay)blood culturegyrB, parE, mecA98.80%94.70%Accurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päi Tissari et al., Lancet 2010; 375: 224-39
StreptococcusS. pneumoniaeDNA-based microarrayblood culturemecA98.80%No percentage givenAccurate and rapid identification of bacterial species from positive blood cultures with a DNA-based microarray platform: an observational study, Päivi Tissari et al., Lancet 2010; 375: 224-30
StreptococcusS. suisRT-qPCRblood cultureGDHNo percentage givenNo percentage givenCharacterization of Streptococcus suis serotype 2 blood infections using RT-qPCR to quantify glutamate dehydrogenase copy numbers, Weijun Yang et al., Journal of Microbiological Methods 83 (2010) 326-329
StreptococcusS. anginosusDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. mitisDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. sanguisDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. mutansDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. oralisDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. pneumoniaeDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. Group BDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA Microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. Group CDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA Microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. Group GDNA-based micro-arrayreference microorganismsbacterial 23S ribosomal DNA (rDNA) and 16S-23S intergenic spacer region (ISR)No percentage given93%DNA Microarray-based identification of bacterial and fungal pathogens in bloodstream infections, Seung Min Yoo et al., Molecular and Cellular Probes 24 (2010) 44-52
StreptococcusS. gordoniiFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. mitisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. sanguisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. suisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. vestibularisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. oralisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. pneumoniaeFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. mitisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. perorisFISH (Fluorescence in situ hybridisation)blood culture16S rRNA99.00%98.65%Fluorescence in situ hybridisation (FISH) accelerates identification of Gram-positive cocci in positive blood cultures, Dorothee Maria Gescher et al., International Journal of Antimicrobial Agents 32S (2008) S51-S59
StreptococcusS. intermedius16S rRNA gene sequencingblood culture16S rRNANo percentage givenNo percentage givenIdentification of oral bacteria in blood cultures by conventional versus molecular methods, Farah K. Bahrani-Mougeot, ORAL MEDICINE, Vol. 105No. 6 June 2008
StreptococcusS. mitis16S rRNA gene sequencingblood culture16S rRNANo percentage givenNo percentage givenIdentification of oral bacteria in blood cultures by conventional versus molecular methods, Farah K. Bahrani-Mougeot, ORAL MEDICINE, Vol. 105No. 6 June 2008
StreptococcusS. agalactiaeLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. anginosusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. constellatusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. gordoniiLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. intermediusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. pyogenesLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. salivariusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. sanguisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. vestibularisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. mitisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. mutansLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. oralisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. pneumoniaeLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. capraeLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. cristatusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. epidermidisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. hominisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. parasanguinisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. saprophyticusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. - Viridans groupLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. bovisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. capitisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. cohniiLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. haemolyticusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. lugdunensisLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. milleriLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. pasteuriLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. thermophilusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. warneriLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. xylosusLightCycler® SeptiFast test MGRADEblood culture16S-23S and 18S-109 5.8S ITS region of rRNA genes93.50%85%Multiplex PCR allows rapid and accurate diagnosis of bloodstream infections in newborns and children with suspected sepsis, Barbara Lucignano et al., J. Clin. Microbiol. doi:10.1128/JCM.02460-10 published online ahead of print on 6 April 2011
StreptococcusS. pneumoniaeRT-PCRnasopharyngeal secretionspneumolysin gene of S.pneumoniaecompared to culture:96%100%Quantitative Detection of Streptococcus pneumoniae in Nasopharyngeal Secretions by Real-Time PCR, Oliver Greiner et al., journal of clinical microbiology, Sept. 2001, vol. 39, no.9, p. 3129-3134
StreptococcusS. agalactiaeRT-PCRCSFdltS54.0%, this specificity does not reflect the true percentage,100%Rapid detection of eight causative pathogens for the diagnosis of bacterial meningitis by real-time PCR, Naoko Chiba et al., J Infect Chemother (2009) 15:92-98
StreptococcusS. pneumoniaeRT-PCRCSFlytA54.0%, this specificity does not reflect the true percentage,100%Rapid detection of eight causative pathogens for the diagnosis of bacterial meningitis by real-time PCR, Naoko Chiba et al., J Infect Chemother (2009) 15:92-98
StreptococcusHemolytic Streptococci group A (Streptoccus pyogenes)Antigen detection testThroat swabGAHBS antigen>95%60-96%Impact on antibiotic prescription of rapid antigen detection testing in acute pharyngitis in adults: a randomised clinical trial, Lior, C. et al., 2011, 6, 244-251
StaphylococcusMethicilline Resistant Staphylococcus aureus (MRSA)Flow cytometry using a Peptide Nucleic Acid Probe"Bacterial suspension (0,5 McF)""Higher grow rate in presence of oxacilline, side scatter, Fluorescence intensity"100.00%96.00%Rapid identification of Staphylococcus aureus and Methicilline Resistante by Flow Cytometry Using a Peptide Nucleic Acid Probe, Nab K. Shrestha et al., Journal of Clinical Microbiology 2011; 49: 3383-3385
StaphylococcusMethicilline Sensitive Staphylococcus aureusFlow cytometry using a Peptide Nucleic Acid Probe"Bacterial suspension (0,5 McF)"Lower grow rate in presence of oxacilline100.00%96.00%Rapid identification of Staphylococcus aureus and Methicilline Resistante by Flow Cytometry Using a Peptide Nucleic Acid Probe, Nab K. Shrestha et al., Journal of Clinical Microbiology 2011; 49: 3383-3385
EnterococcusE. faecalisPNA FISH techniqueBlood cultureSpecies-specific ribosomal RNA (rRNA)100%95%A 1.5h Procedure for Identification of Enterococcus Species Directly from Blood Cultures, Margu A. Morgan et al., Jove 2011; 48: 10379/2616.
EnterococcusEnterococcus speciesPNA FISH techniqueBlood cultureSpecies-specific ribosomal RNA (rRNA)100%95%A 1.5h Procedure for Identification of Enterococcus Species Directly from Blood Cultures, Margu A. Morgan et al., Jove 2011; 48: 10379/2616.
StaphylococcusS. aureusStaphylococcus Quick FISHBlood cultureSpecies-specific ribosomal RNA (rRNA)99.50%89.50%Multicenter Evaluation of the Staphylococcus QuickFISH Method for Simultaneous Identification of Staphylococcus aureus and Coagulase-Negative Staphylococci Directly from Blood Culture Bottles in Less than 30 Minutes, K. Deck, M. et al., Journal of Clinical Microbiology 2012; 50: 1994-1998.
StaphylococcusCoagulase-negative StaphylococciStaphylococcus Quick FISHBlood cultureSpecies-specific ribosomal RNA (rRNA)98.80%89.50%Multicenter Evaluation of the Staphylococcus QuickFISH Method for Simultaneous Identification of Staphylococcus aureus and Coagulase-Negative Staphylococci Directly from Blood Culture Bottles in Less than 30 Minutes, K. Deck, M. et al., Journal of Clinical Microbiology 2012; 50: 1994-1998.
More Information Here
7thframeworklogo The TEMPOtest-QC project has received funding from the European Community's Seventh Framework Programme [FP7/2007-2013] under grant agreement no 241742 EUFlag
curvebl curvebr