» Articles » PMID: 20511433

Diversity, Abundance, and Spatial Distribution of Sediment Ammonia-oxidizing Betaproteobacteria in Response to Environmental Gradients and Coastal Eutrophication in Jiaozhou Bay, China

Overview
Date 2010 Jun 1
PMID 20511433
Citations 62
Authors
Affiliations
Soon will be listed here.
Abstract

Ongoing anthropogenic eutrophication of Jiaozhou Bay offers an opportunity to study the influence of human activity on bacterial communities that drive biogeochemical cycling. Nitrification in coastal waters appears to be a sensitive indicator of environmental change, suggesting that function and structure of the microbial nitrifying community may be associated closely with environmental conditions. In the current study, the amoA gene was used to unravel the relationship between sediment aerobic obligate ammonia-oxidizing Betaproteobacteria (Beta-AOB) and their environment in Jiaozhou Bay. Protein sequences deduced from amoA gene sequences grouped within four distinct clusters in the Nitrosomonas lineage, including a putative new cluster. In addition, AmoA sequences belonging to three newly defined clusters in the Nitrosospira lineage were also identified. Multivariate statistical analyses indicated that the studied Beta-AOB community structures correlated with environmental parameters, of which nitrite-N and sediment sand content had significant impact on the composition, structure, and distribution of the Beta-AOB community. Both amoA clone library and quantitative PCR (qPCR) analyses indicated that continental input from the nearby wastewater treatment plants and polluted rivers may have significant impact on the composition and abundance of the sediment Beta-AOB assemblages in Jiaozhou Bay. Our work is the first report of a direct link between a sedimentological parameter and the composition and distribution of the sediment Beta-AOB and indicates the potential for using the Beta-AOB community composition in general and individual isolates or environmental clones in the Nitrosomonas oligotropha lineage in particular as bioindicators and biotracers of pollution or freshwater or wastewater input in coastal environments.

Citing Articles

Nitrite improved nitrification efficiency and enriched ammonia-oxidizing archaea and bacteria in the simultaneous nitrification and denitrification process.

Xiang Y, Zhou T, Deng S, Shao Z, Liu Y, He Q Water Res X. 2023; 21:100204.

PMID: 38098882 PMC: 10719579. DOI: 10.1016/j.wroa.2023.100204.


Biogeography of ammonia oxidizers in New England and Gulf of Mexico salt marshes and the potential importance of comammox.

Bernhard A, Beltz J, Giblin A, Roberts B ISME Commun. 2023; 1(1):9.

PMID: 36717686 PMC: 9723745. DOI: 10.1038/s43705-021-00008-0.


Effects of Co-Inoculated with and on the Structure and Functional Genes of Soybean Rhizobacteria Community.

Xing P, Zhao Y, Guan D, Li L, Zhao B, Ma M Genes (Basel). 2022; 13(11).

PMID: 36360159 PMC: 9689485. DOI: 10.3390/genes13111922.


Effects of Land Use on the Soil Microbial Community in the Songnen Grassland of Northeast China.

Liu G, Bai Z, Cui G, He W, Kongling Z, Ji G Front Microbiol. 2022; 13:865184.

PMID: 35879955 PMC: 9307977. DOI: 10.3389/fmicb.2022.865184.


Lake microbiome and trophy fluctuations of the ancient hemp rettery.

Iwanska O, Latoch P, Suchora M, Pidek I, Huber M, Bubak I Sci Rep. 2022; 12(1):8846.

PMID: 35614182 PMC: 9132974. DOI: 10.1038/s41598-022-12761-w.


References
1.
Bernhard A, Tucker J, Giblin A, Stahl D . Functionally distinct communities of ammonia-oxidizing bacteria along an estuarine salinity gradient. Environ Microbiol. 2007; 9(6):1439-47. DOI: 10.1111/j.1462-2920.2007.01260.x. View

2.
Acinas S, Marcelino L, Klepac-Ceraj V, Polz M . Divergence and redundancy of 16S rRNA sequences in genomes with multiple rrn operons. J Bacteriol. 2004; 186(9):2629-35. PMC: 387781. DOI: 10.1128/JB.186.9.2629-2635.2004. View

3.
Limpiyakorn T, Shinohara Y, Kurisu F, Yagi O . Communities of ammonia-oxidizing bacteria in activated sludge of various sewage treatment plants in Tokyo. FEMS Microbiol Ecol. 2005; 54(2):205-17. DOI: 10.1016/j.femsec.2005.03.017. View

4.
Dang H, Zhang X, Sun J, Li T, Zhang Z, Yang G . Diversity and spatial distribution of sediment ammonia-oxidizing crenarchaeota in response to estuarine and environmental gradients in the Changjiang Estuary and East China Sea. Microbiology (Reading). 2008; 154(Pt 7):2084-2095. DOI: 10.1099/mic.0.2007/013581-0. View

5.
Nicolaisen M, Ramsing N . Denaturing gradient gel electrophoresis (DGGE) approaches to study the diversity of ammonia-oxidizing bacteria. J Microbiol Methods. 2002; 50(2):189-203. DOI: 10.1016/s0167-7012(02)00026-x. View