Rapid, sensitive, and discriminating identification of Naegleria spp. by real-time PCR and melting-curve analysis
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作者:
Robinson, Bret S.
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S Australia Water Corp, Australian Water Qual Ctr, Salisbury, SA 5108, AustraliaS Australia Water Corp, Australian Water Qual Ctr, Salisbury, SA 5108, Australia
Robinson, Bret S.
[1
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Monis, Paul T.
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S Australia Water Corp, Australian Water Qual Ctr, Salisbury, SA 5108, AustraliaS Australia Water Corp, Australian Water Qual Ctr, Salisbury, SA 5108, Australia
Monis, Paul T.
[1
]
Dobson, Phillip J.
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S Australia Water Corp, Australian Water Qual Ctr, Salisbury, SA 5108, AustraliaS Australia Water Corp, Australian Water Qual Ctr, Salisbury, SA 5108, Australia
Dobson, Phillip J.
[1
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[1] S Australia Water Corp, Australian Water Qual Ctr, Salisbury, SA 5108, Australia
The free-living amoeboflagellate genus Naegleria includes one pathogenic and two potentially pathogenic species (Naegleria fowleri, Naegleria italica, and Naegleria australiensis) plus numerous benign organisms. Monitoring of bathing water, water supplies, and cooling systems for these pathogens requires a timely and reliable method for identification, but current DNA sequence-based methods identify only N. fowleri or require full sequencing to identify other species in the genus. A novel closed-tube method for distinguishing thermophilic Naegleria species is presented, using a single primer set and the DNA intercalating dye SYTO9 for real-time PCR and melting-curve analysis of the 5.8S ribosomal DNA gene and flanking noncoding spacers (ITS1, ITS2). Collection of DNA melting data at close temperature intervals produces highly informative melting curves with one or more recognizable melting peaks, readily distinguished for seven Naegleria species and the related Willaertia magna. Advantages over other methods used to identify these organisms include its comprehensiveness (encompassing all species tested to date), simplicity (no electrophoresis required to verify the product), and sensitivity (unambiguous identification from DNA equivalent to one cell). This approach should be applicable to a wide range of microorganisms of medical importance.
机构:
Cent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, EnglandCent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, England
Logan, JMJ
Edwards, KJ
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Cent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, EnglandCent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, England
Edwards, KJ
Saunders, NA
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Cent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, EnglandCent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, England
Saunders, NA
Stanley, J
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Cent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, EnglandCent Publ Hlth Lab, Div Virus Reference, Mol Biol Unit, London NW9 5HT, England
机构:
Zayed Mil Hosp, Div Microbiol, Dept Pathol & Lab Med, Abu Dhabi, U Arab EmiratesZayed Mil Hosp, Div Microbiol, Dept Pathol & Lab Med, Abu Dhabi, U Arab Emirates
Alfaresi, Mubarak
Elkosh, Abida
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Zayed Mil Hosp, Div Microbiol, Dept Pathol & Lab Med, Abu Dhabi, U Arab EmiratesZayed Mil Hosp, Div Microbiol, Dept Pathol & Lab Med, Abu Dhabi, U Arab Emirates