Differentiation of biosolids from animal faecal material using the 16s ribosomal RNA genetic markers of gastrointestinal anaerobic bacteria

Recombinant DNA techniques were evaluated for their usefulness in distinguishing biosolids from faecal material of cow, kangaroo and sheep. It involved PCR amplification using published priming sequences, and restriction site profiling of amplified DNA across the 16S rRNA gene of anaerobic gastroin...

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Main Authors: Ho, K., Pritchard, Deborah, Penney, N.
Format: Conference Paper
Published: International Water Association 2007
Subjects:
Online Access:http://www.awa.asn.au/
http://hdl.handle.net/20.500.11937/24871
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author Ho, K.
Pritchard, Deborah
Penney, N.
author_facet Ho, K.
Pritchard, Deborah
Penney, N.
author_sort Ho, K.
building Curtin Institutional Repository
collection Online Access
description Recombinant DNA techniques were evaluated for their usefulness in distinguishing biosolids from faecal material of cow, kangaroo and sheep. It involved PCR amplification using published priming sequences, and restriction site profiling of amplified DNA across the 16S rRNA gene of anaerobic gastrointestinal bacteria, Bacteroides spp and Bifidobacteria spp. Of the three Bacteroides spp primer pairs, two were useful for cow faecal material though at lower annealing temperatures were also applicable to biosolids and sheep faecal material. The third primer pair was specific only for biosolids. All three primer pairs were not able to PCR-amplify Bacteroides spp sequences in faecal material of kangaroo. Of the three Bifidobacteria spp primer pairs, one was useful for sheep faecal material though at lower annealing temperature was also applicable to biosolids and cow and kangaroo faecal material. The Bifidobacterium angulatum specific primer pair enabled the PCR detection of anaerobes only in biosolids and in faecal material of kangaroo. The third, a Bifidobacterium catenulatum specific primer pair was suitable for faecal material of cow and at lower annealing temperatures was also applicable to the sample from sheep. For some primer sets, PCR amplification alone could not differentiate biosolids from other faecal samples. However, this could be resolved by digesting amplified DNA with the appropriate restriction enzymes. Overall, our evaluations show that recombinant DNA techniques have the potential to distinguish biosolids from other sources of faecal material, including that from kangaroo.
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institution Curtin University Malaysia
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publishDate 2007
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spelling curtin-20.500.11937-248712017-10-02T02:27:38Z Differentiation of biosolids from animal faecal material using the 16s ribosomal RNA genetic markers of gastrointestinal anaerobic bacteria Ho, K. Pritchard, Deborah Penney, N. Bacteroides spp Bifidobacteria spp kangaroo biosolids 16S rRNA gene Recombinant DNA techniques were evaluated for their usefulness in distinguishing biosolids from faecal material of cow, kangaroo and sheep. It involved PCR amplification using published priming sequences, and restriction site profiling of amplified DNA across the 16S rRNA gene of anaerobic gastrointestinal bacteria, Bacteroides spp and Bifidobacteria spp. Of the three Bacteroides spp primer pairs, two were useful for cow faecal material though at lower annealing temperatures were also applicable to biosolids and sheep faecal material. The third primer pair was specific only for biosolids. All three primer pairs were not able to PCR-amplify Bacteroides spp sequences in faecal material of kangaroo. Of the three Bifidobacteria spp primer pairs, one was useful for sheep faecal material though at lower annealing temperature was also applicable to biosolids and cow and kangaroo faecal material. The Bifidobacterium angulatum specific primer pair enabled the PCR detection of anaerobes only in biosolids and in faecal material of kangaroo. The third, a Bifidobacterium catenulatum specific primer pair was suitable for faecal material of cow and at lower annealing temperatures was also applicable to the sample from sheep. For some primer sets, PCR amplification alone could not differentiate biosolids from other faecal samples. However, this could be resolved by digesting amplified DNA with the appropriate restriction enzymes. Overall, our evaluations show that recombinant DNA techniques have the potential to distinguish biosolids from other sources of faecal material, including that from kangaroo. 2007 Conference Paper http://hdl.handle.net/20.500.11937/24871 http://www.awa.asn.au/ International Water Association fulltext
spellingShingle Bacteroides spp
Bifidobacteria spp
kangaroo
biosolids
16S rRNA gene
Ho, K.
Pritchard, Deborah
Penney, N.
Differentiation of biosolids from animal faecal material using the 16s ribosomal RNA genetic markers of gastrointestinal anaerobic bacteria
title Differentiation of biosolids from animal faecal material using the 16s ribosomal RNA genetic markers of gastrointestinal anaerobic bacteria
title_full Differentiation of biosolids from animal faecal material using the 16s ribosomal RNA genetic markers of gastrointestinal anaerobic bacteria
title_fullStr Differentiation of biosolids from animal faecal material using the 16s ribosomal RNA genetic markers of gastrointestinal anaerobic bacteria
title_full_unstemmed Differentiation of biosolids from animal faecal material using the 16s ribosomal RNA genetic markers of gastrointestinal anaerobic bacteria
title_short Differentiation of biosolids from animal faecal material using the 16s ribosomal RNA genetic markers of gastrointestinal anaerobic bacteria
title_sort differentiation of biosolids from animal faecal material using the 16s ribosomal rna genetic markers of gastrointestinal anaerobic bacteria
topic Bacteroides spp
Bifidobacteria spp
kangaroo
biosolids
16S rRNA gene
url http://www.awa.asn.au/
http://hdl.handle.net/20.500.11937/24871