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Assessing Microbial Community Diversity Using Amplicon Length Heterogeneity Polymerase Chain Reaction
Author(s) -
Mills DeEtta K.,
Entry James A.,
Gillevet Patrick M.,
Mathee Kalai
Publication year - 2007
Publication title -
soil science society of america journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.836
H-Index - 168
eISSN - 1435-0661
pISSN - 0361-5995
DOI - 10.2136/sssaj2006.0147
Subject(s) - amplicon , biology , hypervariable region , environmental dna , polymerase chain reaction , computational biology , microbial population biology , microbial ecology , ribosomal rna , evolutionary biology , metagenomics , ecology , amplicon sequencing , gene , genetics , 16s ribosomal rna , biodiversity , bacteria
It is thought that a microbial community is an assemblage of organisms, genes, and gene functions. Transient, acute signals such as excessive nutrient loads or disturbance and chronic signals such as seasonal temperature or rainfall impact the total environmental system. The goal of many microbial ecologists is to determine if a finely resolved study of microbial dynamics can be used as a large‐scale biosensor to follow diversity patterns in the environment. With the development of new genomic tools, community‐level studies have been designed that can interrogate the finer details of the biological components of a given habitat. Amplicon length heterogeneity polymerase chain reaction (LH‐PCR) interrogates the hypervariable domains of the ribosomal small‐subunit genes and separates these domains based on the naturally occurring sequence lengths of DNA. The amplicons are phylogenetically relevant in that the various amplicons generated can be directly associated with specific taxonomic sequences archived in the databases. The application of the LH‐PCR technique as a monitoring tool for microbial ecology has been shown to enhance and extend the current understanding of the dynamics of microbial communities in their specific environments.