Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant

Autores
Harms, Gerda; Layton, Alice C.; Dionisi, Hebe Monica; Gregory, Igrid R.; Garrett, Victoria M.; Hawkins, Shawn A.; Robinson, Kevin G.; Sayler, Gary S.
Año de publicación
2003
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Real-time PCR assays using TaqMan or Molecular Beacon probes were developed and optimized for the quantification of total bacteria, the nitrite-oxidizing bacteria Nitrospira, and Nitrosomonas oligotropha-like ammonia oxidizing bacteria (AOB) in mixed liquor suspended solids (MLSS) from a municipal wastewater treatment plant (WWTP) using a single-sludge nitrification process. The targets for the real-time PCR assays were the 16S rRNA genes (16S rDNA) for bacteria and Nitrospira spp. and the amoA gene for N. oligotropha. A previously reported assay for AOB 16S rDNA was also tested for its application to activated sludge. The Nitrospira 16S rDNA, AOB 16S rDNA, and N. oligotropha-like amoA assays were log-linear over 6 orders of magnitude and the bacterial 16S rDNA real-time PCR assay was log-linear over 4 orders of magnitude with DNA standards. When these real-time PCR assays were applied to DNA extracted from MLSS, dilution of the DNA extracts was necessary to prevent PCR inhibition. The optimal DNA dilution range was broad for the bacterial 16S rDNA (1000-fold) and Nitrospira 16S rDNA assays (2500-fold) but narrow for the AOB 16S rDNA assay (10-fold) and N. oligotropha-like amoA real-time PCR assay (5-fold). In twelve MLSS samples collected over one year, mean cell per L values were 4.3 ± 2.0 × 1011 for bacteria, 3.7 ± 3.2 × 1010 for Nitrospira, 1.2 ± 0.9 × 1010 for all AOB, and 7.5 ± 6.0 × 109 for N. oligotropha-like AOB. The percent of the nitrifying population was 1.7% N. oligotropha-like AOB based on the N. oligotropha amoA assay, 2.9% total AOB based on the AOB 16S rDNA assay, and 8.6% nitrite-oxidizing bacteria based on the Nitrospira 16S rDNA assay. Ammonia-oxidizing bacteria in the wastewater treatment plant were estimated to oxidize 7.7 ± 6.8 fmol/hr/cell based on the AOB 16S rDNA assay and 12.4 ± 7.3 fmol/hr/cell based on the N. oligotropha amoA assay.
Fil: Harms, Gerda. University of Tennessee; Estados Unidos
Fil: Layton, Alice C.. University of Tennessee; Estados Unidos
Fil: Dionisi, Hebe Monica. University of Tennessee; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Gregory, Igrid R.. University of Tennessee; Estados Unidos
Fil: Garrett, Victoria M.. University of Tennessee; Estados Unidos
Fil: Hawkins, Shawn A.. University of Tennessee; Estados Unidos
Fil: Robinson, Kevin G.. University of Tennessee; Estados Unidos
Fil: Sayler, Gary S.. University of Tennessee; Estados Unidos
Materia
NITRIFYING BACTERIA
REAL-TIME PCR
MUNICIPAL WASTEWATER TREATMENT PLANT
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/98939

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network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plantHarms, GerdaLayton, Alice C.Dionisi, Hebe MonicaGregory, Igrid R.Garrett, Victoria M.Hawkins, Shawn A.Robinson, Kevin G.Sayler, Gary S.NITRIFYING BACTERIAREAL-TIME PCRMUNICIPAL WASTEWATER TREATMENT PLANThttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Real-time PCR assays using TaqMan or Molecular Beacon probes were developed and optimized for the quantification of total bacteria, the nitrite-oxidizing bacteria Nitrospira, and Nitrosomonas oligotropha-like ammonia oxidizing bacteria (AOB) in mixed liquor suspended solids (MLSS) from a municipal wastewater treatment plant (WWTP) using a single-sludge nitrification process. The targets for the real-time PCR assays were the 16S rRNA genes (16S rDNA) for bacteria and Nitrospira spp. and the amoA gene for N. oligotropha. A previously reported assay for AOB 16S rDNA was also tested for its application to activated sludge. The Nitrospira 16S rDNA, AOB 16S rDNA, and N. oligotropha-like amoA assays were log-linear over 6 orders of magnitude and the bacterial 16S rDNA real-time PCR assay was log-linear over 4 orders of magnitude with DNA standards. When these real-time PCR assays were applied to DNA extracted from MLSS, dilution of the DNA extracts was necessary to prevent PCR inhibition. The optimal DNA dilution range was broad for the bacterial 16S rDNA (1000-fold) and Nitrospira 16S rDNA assays (2500-fold) but narrow for the AOB 16S rDNA assay (10-fold) and N. oligotropha-like amoA real-time PCR assay (5-fold). In twelve MLSS samples collected over one year, mean cell per L values were 4.3 ± 2.0 × 1011 for bacteria, 3.7 ± 3.2 × 1010 for Nitrospira, 1.2 ± 0.9 × 1010 for all AOB, and 7.5 ± 6.0 × 109 for N. oligotropha-like AOB. The percent of the nitrifying population was 1.7% N. oligotropha-like AOB based on the N. oligotropha amoA assay, 2.9% total AOB based on the AOB 16S rDNA assay, and 8.6% nitrite-oxidizing bacteria based on the Nitrospira 16S rDNA assay. Ammonia-oxidizing bacteria in the wastewater treatment plant were estimated to oxidize 7.7 ± 6.8 fmol/hr/cell based on the AOB 16S rDNA assay and 12.4 ± 7.3 fmol/hr/cell based on the N. oligotropha amoA assay.Fil: Harms, Gerda. University of Tennessee; Estados UnidosFil: Layton, Alice C.. University of Tennessee; Estados UnidosFil: Dionisi, Hebe Monica. University of Tennessee; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Gregory, Igrid R.. University of Tennessee; Estados UnidosFil: Garrett, Victoria M.. University of Tennessee; Estados UnidosFil: Hawkins, Shawn A.. University of Tennessee; Estados UnidosFil: Robinson, Kevin G.. University of Tennessee; Estados UnidosFil: Sayler, Gary S.. University of Tennessee; Estados UnidosAmerican Chemical Society2003-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/98939Harms, Gerda; Layton, Alice C.; Dionisi, Hebe Monica; Gregory, Igrid R.; Garrett, Victoria M.; et al.; Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant; American Chemical Society; Environmental Science & Technology; 37; 2; 1-2003; 343-3510013-936XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1021/es0257164info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/es0257164info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-11-05T09:50:28Zoai:ri.conicet.gov.ar:11336/98939instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-11-05 09:50:28.344CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
title Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
spellingShingle Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
Harms, Gerda
NITRIFYING BACTERIA
REAL-TIME PCR
MUNICIPAL WASTEWATER TREATMENT PLANT
title_short Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
title_full Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
title_fullStr Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
title_full_unstemmed Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
title_sort Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant
dc.creator.none.fl_str_mv Harms, Gerda
Layton, Alice C.
Dionisi, Hebe Monica
Gregory, Igrid R.
Garrett, Victoria M.
Hawkins, Shawn A.
Robinson, Kevin G.
Sayler, Gary S.
author Harms, Gerda
author_facet Harms, Gerda
Layton, Alice C.
Dionisi, Hebe Monica
Gregory, Igrid R.
Garrett, Victoria M.
Hawkins, Shawn A.
Robinson, Kevin G.
Sayler, Gary S.
author_role author
author2 Layton, Alice C.
Dionisi, Hebe Monica
Gregory, Igrid R.
Garrett, Victoria M.
Hawkins, Shawn A.
Robinson, Kevin G.
Sayler, Gary S.
author2_role author
author
author
author
author
author
author
dc.subject.none.fl_str_mv NITRIFYING BACTERIA
REAL-TIME PCR
MUNICIPAL WASTEWATER TREATMENT PLANT
topic NITRIFYING BACTERIA
REAL-TIME PCR
MUNICIPAL WASTEWATER TREATMENT PLANT
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Real-time PCR assays using TaqMan or Molecular Beacon probes were developed and optimized for the quantification of total bacteria, the nitrite-oxidizing bacteria Nitrospira, and Nitrosomonas oligotropha-like ammonia oxidizing bacteria (AOB) in mixed liquor suspended solids (MLSS) from a municipal wastewater treatment plant (WWTP) using a single-sludge nitrification process. The targets for the real-time PCR assays were the 16S rRNA genes (16S rDNA) for bacteria and Nitrospira spp. and the amoA gene for N. oligotropha. A previously reported assay for AOB 16S rDNA was also tested for its application to activated sludge. The Nitrospira 16S rDNA, AOB 16S rDNA, and N. oligotropha-like amoA assays were log-linear over 6 orders of magnitude and the bacterial 16S rDNA real-time PCR assay was log-linear over 4 orders of magnitude with DNA standards. When these real-time PCR assays were applied to DNA extracted from MLSS, dilution of the DNA extracts was necessary to prevent PCR inhibition. The optimal DNA dilution range was broad for the bacterial 16S rDNA (1000-fold) and Nitrospira 16S rDNA assays (2500-fold) but narrow for the AOB 16S rDNA assay (10-fold) and N. oligotropha-like amoA real-time PCR assay (5-fold). In twelve MLSS samples collected over one year, mean cell per L values were 4.3 ± 2.0 × 1011 for bacteria, 3.7 ± 3.2 × 1010 for Nitrospira, 1.2 ± 0.9 × 1010 for all AOB, and 7.5 ± 6.0 × 109 for N. oligotropha-like AOB. The percent of the nitrifying population was 1.7% N. oligotropha-like AOB based on the N. oligotropha amoA assay, 2.9% total AOB based on the AOB 16S rDNA assay, and 8.6% nitrite-oxidizing bacteria based on the Nitrospira 16S rDNA assay. Ammonia-oxidizing bacteria in the wastewater treatment plant were estimated to oxidize 7.7 ± 6.8 fmol/hr/cell based on the AOB 16S rDNA assay and 12.4 ± 7.3 fmol/hr/cell based on the N. oligotropha amoA assay.
Fil: Harms, Gerda. University of Tennessee; Estados Unidos
Fil: Layton, Alice C.. University of Tennessee; Estados Unidos
Fil: Dionisi, Hebe Monica. University of Tennessee; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Gregory, Igrid R.. University of Tennessee; Estados Unidos
Fil: Garrett, Victoria M.. University of Tennessee; Estados Unidos
Fil: Hawkins, Shawn A.. University of Tennessee; Estados Unidos
Fil: Robinson, Kevin G.. University of Tennessee; Estados Unidos
Fil: Sayler, Gary S.. University of Tennessee; Estados Unidos
description Real-time PCR assays using TaqMan or Molecular Beacon probes were developed and optimized for the quantification of total bacteria, the nitrite-oxidizing bacteria Nitrospira, and Nitrosomonas oligotropha-like ammonia oxidizing bacteria (AOB) in mixed liquor suspended solids (MLSS) from a municipal wastewater treatment plant (WWTP) using a single-sludge nitrification process. The targets for the real-time PCR assays were the 16S rRNA genes (16S rDNA) for bacteria and Nitrospira spp. and the amoA gene for N. oligotropha. A previously reported assay for AOB 16S rDNA was also tested for its application to activated sludge. The Nitrospira 16S rDNA, AOB 16S rDNA, and N. oligotropha-like amoA assays were log-linear over 6 orders of magnitude and the bacterial 16S rDNA real-time PCR assay was log-linear over 4 orders of magnitude with DNA standards. When these real-time PCR assays were applied to DNA extracted from MLSS, dilution of the DNA extracts was necessary to prevent PCR inhibition. The optimal DNA dilution range was broad for the bacterial 16S rDNA (1000-fold) and Nitrospira 16S rDNA assays (2500-fold) but narrow for the AOB 16S rDNA assay (10-fold) and N. oligotropha-like amoA real-time PCR assay (5-fold). In twelve MLSS samples collected over one year, mean cell per L values were 4.3 ± 2.0 × 1011 for bacteria, 3.7 ± 3.2 × 1010 for Nitrospira, 1.2 ± 0.9 × 1010 for all AOB, and 7.5 ± 6.0 × 109 for N. oligotropha-like AOB. The percent of the nitrifying population was 1.7% N. oligotropha-like AOB based on the N. oligotropha amoA assay, 2.9% total AOB based on the AOB 16S rDNA assay, and 8.6% nitrite-oxidizing bacteria based on the Nitrospira 16S rDNA assay. Ammonia-oxidizing bacteria in the wastewater treatment plant were estimated to oxidize 7.7 ± 6.8 fmol/hr/cell based on the AOB 16S rDNA assay and 12.4 ± 7.3 fmol/hr/cell based on the N. oligotropha amoA assay.
publishDate 2003
dc.date.none.fl_str_mv 2003-01
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/98939
Harms, Gerda; Layton, Alice C.; Dionisi, Hebe Monica; Gregory, Igrid R.; Garrett, Victoria M.; et al.; Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant; American Chemical Society; Environmental Science & Technology; 37; 2; 1-2003; 343-351
0013-936X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/98939
identifier_str_mv Harms, Gerda; Layton, Alice C.; Dionisi, Hebe Monica; Gregory, Igrid R.; Garrett, Victoria M.; et al.; Real-time PCR quantification of nitrifying bacteria in a municipal wastewater treatment plant; American Chemical Society; Environmental Science & Technology; 37; 2; 1-2003; 343-351
0013-936X
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1021/es0257164
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/es0257164
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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