» Articles » PMID: 21209889

Environmental Shaping of Sponge Associated Archaeal Communities

Overview
Journal PLoS One
Date 2011 Jan 7
PMID 21209889
Citations 30
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Archaea are ubiquitous symbionts of marine sponges but their ecological roles and the influence of environmental factors on these associations are still poorly understood.

Methodology/principal Findings: We compared the diversity and composition of archaea associated with seawater and with the sponges Hymeniacidon heliophila, Paraleucilla magna and Petromica citrina in two distinct environments: Guanabara Bay, a highly impacted estuary in Rio de Janeiro, Brazil, and the nearby Cagarras Archipelago. For this we used metagenomic analyses of 16S rRNA and ammonia monooxygenase (amoA) gene libraries. Hymeniacidon heliophila was more abundant inside the bay, while P. magna was more abundant outside and P. citrina was only recorded at the Cagarras Archipelago. Principal Component Analysis plots (PCA) generated using pairwise unweighted UniFrac distances showed that the archaeal community structure of inner bay seawater and sponges was different from that of coastal Cagarras Archipelago. Rarefaction analyses showed that inner bay archaeaoplankton were more diverse than those from the Cagarras Archipelago. Only members of Crenarchaeota were found in sponge libraries, while in seawater both Crenarchaeota and Euryarchaeota were observed. Although most amoA archaeal genes detected in this study seem to be novel, some clones were affiliated to known ammonia oxidizers such as Nitrosopumilus maritimus and Cenarchaeum symbiosum.

Conclusion/significance: The composition and diversity of archaeal communities associated with pollution-tolerant sponge species can change in a range of few kilometers, probably influenced by eutrophication. The presence of archaeal amoA genes in Porifera suggests that Archaea are involved in the nitrogen cycle within the sponge holobiont, possibly increasing its resistance to anthropogenic impacts. The higher diversity of Crenarchaeota in the polluted area suggests that some marine sponges are able to change the composition of their associated archaeal communities, thereby improving their fitness in impacted environments.

Citing Articles

Holobiont dysbiosis or acclimatation? Shift in the microbial taxonomic diversity and functional composition of a cosmopolitan sponge subjected to chronic pollution in a Patagonian bay.

Gastaldi M, Pankey M, Svendsen G, Medina A, Firstater F, Narvarte M PeerJ. 2024; 12:e17707.

PMID: 39184395 PMC: 11344537. DOI: 10.7717/peerj.17707.


High microbiome and metabolome diversification in coexisting sponges with different bio-ecological traits.

Mazzella V, DellAnno A, Etxebarria N, Gonzalez-Gaya B, Nuzzo G, Fontana A Commun Biol. 2024; 7(1):422.

PMID: 38589605 PMC: 11001883. DOI: 10.1038/s42003-024-06109-5.


Uncovering the Microbial Diversity of Two Exotic Calcareous Sponges.

Ribeiro B, Padua A, Francesco Rodrigues de Oliveira B, Puccinelli G, da Costa Fernandes F, Laport M Microb Ecol. 2022; 85(2):737-746.

PMID: 35234997 DOI: 10.1007/s00248-022-01980-3.


Characterization of archaeal symbionts of sponges from the coral reef ecosystems of the Gulf of Mannar, Southeast coast of India.

Chekidhenkuzhiyil J, Anas A, Thomas P, Tharakan B, Nair S Saudi J Biol Sci. 2021; 28(7):3783-3788.

PMID: 34220232 PMC: 8241630. DOI: 10.1016/j.sjbs.2021.03.054.


Friends or Foes-Microbial Interactions in Nature.

Weiland-Brauer N Biology (Basel). 2021; 10(6).

PMID: 34199553 PMC: 8229319. DOI: 10.3390/biology10060496.


References
1.
Kimura M . A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol. 1980; 16(2):111-20. DOI: 10.1007/BF01731581. View

2.
Andrade L, Gonzalez A, Araujo F, Paranhos R . Flow cytometry assessment of bacterioplankton in tropical marine environments. J Microbiol Methods. 2003; 55(3):841-50. DOI: 10.1016/j.mimet.2003.08.002. View

3.
Otto T, Vasconcellos E, Gomes L, Moreira A, Degrave W, Mendonca-Lima L . ChromaPipe: a pipeline for analysis, quality control and management for a DNA sequencing facility. Genet Mol Res. 2008; 7(3):861-71. DOI: 10.4238/vol7-3x-meeting04. View

4.
Hallam S, Konstantinidis K, Putnam N, Schleper C, Watanabe Y, Sugahara J . Genomic analysis of the uncultivated marine crenarchaeote Cenarchaeum symbiosum. Proc Natl Acad Sci U S A. 2006; 103(48):18296-301. PMC: 1643844. DOI: 10.1073/pnas.0608549103. View

5.
Saitou N, Nei M . The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol. 1987; 4(4):406-25. DOI: 10.1093/oxfordjournals.molbev.a040454. View