Phylogenetic Analysis Reveals Multiple Lateral Transfers of Adenosine-5′-Phosphosulfate Reductase Genes among Sulfate-Reducing Microorganisms

ABSTRACT Lateral gene transfer affects the evolutionary path of key genes involved in ancient metabolic traits, such as sulfate respiration, even more than previously expected. In this study, the phylogeny of the adenosine-5′-phosphosulfate (APS) reductase was analyzed. APS reductase is a key enzyme in sulfate respiration present in all sulfate-respiring prokaryotes. A newly developed PCR assay was used to amplify and sequence a fragment (∼900 bp) of the APS reductase gene, apsA, from a taxonomically wide range of sulfate-reducing prokaryotes (n = 60). Comparative phylogenetic analysis of all obtained and available ApsA sequences indicated a high degree of sequence conservation in the region analyzed. However, a comparison of ApsA- and 16S rRNA-based phylogenetic trees revealed topological incongruences affecting seven members of the Syntrophobacteraceae and three members of the Nitrospinaceae, which were clearly monophyletic with gram-positive sulfate-reducing bacteria (SRB). In addition, Thermodesulfovibrio islandicus and Thermodesulfobacterium thermophilum, Thermodesulfobacterium commune, and Thermodesulfobacterium hveragerdense clearly branched off between the radiation of the δ-proteobacterial gram-negative SRB and the gram-positive SRB and not close to the root of the tree as expected from 16S rRNA phylogeny. The most parsimonious explanation for these discrepancies in tree topologies is lateral transfer of apsA genes across bacterial divisions. Similar patterns of insertions and deletions in ApsA sequences of donor and recipient lineages provide additional evidence for lateral gene transfer. From a subset of reference strains (n = 25), a fragment of the dissimilatory sulfite reductase genes (dsrAB), which have recently been proposed to have undergone multiple lateral gene transfers (M. Klein et al., J. Bacteriol. 183:6028–6035, 2001), was also amplified and sequenced. Phylogenetic comparison of DsrAB- and ApsA-based trees suggests a frequent involvement of gram-positive and thermophilic SRB in lateral gene transfer events among SRB.

[1]  M. O. Dayhoff A model of evolutionary change in protein , 1978 .

[2]  M. O. Dayhoff,et al.  22 A Model of Evolutionary Change in Proteins , 1978 .

[3]  E. M. Cameron Sulphate and sulphate reduction in early Precambrian oceans , 1982 .

[4]  F. Widdel,et al.  Microbiology and ecology of sulfate-and sulfur-reducing bacteria , 1988 .

[5]  A. Zehnder Biology of anaerobic microorganisms , 1988 .

[6]  D. Lane 16S/23S rRNA sequencing , 1991 .

[7]  S. Goodison,et al.  16S ribosomal DNA amplification for phylogenetic study , 1991, Journal of bacteriology.

[8]  E. Stackebrandt,et al.  Nucleic acid techniques in bacterial systematics , 1991 .

[9]  C. Dahl,et al.  Spectroscopic studies on APS reductase isolated from the hyperthermophilic sulfate-reducing archaebacterium Archaeglobus fulgidus. , 1991, Biochemical and biophysical research communications.

[10]  L. Barton,et al.  Variations in autotrophic life , 1991 .

[11]  William R. Taylor,et al.  The rapid generation of mutation data matrices from protein sequences , 1992, Comput. Appl. Biosci..

[12]  M. Nei,et al.  Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. , 1993, Molecular biology and evolution.

[13]  K. Stetter,et al.  Adenylylsulphate reductase from the sulphate-reducing archaeon Archaeoglobus fulgidus: cloning and characterization of the genes and comparison of the enzyme with other iron-sulphur flavoproteins. , 1994, Microbiology.

[14]  E. Madsen,et al.  Quantitative cell lysis of indigenous microorganisms and rapid extraction of microbial DNA from sediment , 1994, Applied and environmental microbiology.

[15]  B. Schink,et al.  Pure culture and cytological properties of ‘Syntriphobacter wolini’ , 1994 .

[16]  Hideo Matsuda,et al.  fastDNAmL: a tool for construction of phylogenetic trees of DNA sequences using maximum likelihood , 1994, Comput. Appl. Biosci..

[17]  K. Strimmer,et al.  Quartet Puzzling: A Quartet Maximum-Likelihood Method for Reconstructing Tree Topologies , 1996 .

[18]  C. Dahl Insertional gene inactivation in a phototrophic sulphur bacterium: APS-reductase-deficient mutants of Chromatium vinosum. , 1996, Microbiology.

[19]  H. Ochman,et al.  Amelioration of Bacterial Genomes: Rates of Change and Exchange , 1997, Journal of Molecular Evolution.

[20]  C. Dahl,et al.  Towards the phylogeny of APS reductases and sirohaem sulfite reductases in sulfate-reducing and sulfur-oxidizing prokaryotes. , 1997, Microbiology.

[21]  D. M. Ward,et al.  Seasonal distributions of dominant 16S rRNA-defined populations in a hot spring microbial mat examined by denaturing gradient gel electrophoresis , 1997, Applied and environmental microbiology.

[22]  R. Fleischmann,et al.  The complete genome sequence of the hyperthermophilic, sulphate-reducing archaeon Archaeoglobus fulgidus , 1997, Nature.

[23]  K. Stetter,et al.  Archaeoglobus veneficus sp. nov., a novel facultative chemolithoautotrophic hyperthermophilic sulfite reducer, isolated from abyssal black smokers , 1997 .

[24]  E V Koonin,et al.  Evidence for massive gene exchange between archaeal and bacterial hyperthermophiles. , 1998, Trends in genetics : TIG.

[25]  Christof Holliger,et al.  Reductive dechlorination in the energy metabolism of anaerobic bacteria , 1998 .

[26]  M Weizenegger,et al.  Bacterial phylogeny based on comparative sequence analysis (review) , 1998, Electrophoresis.

[27]  H. Ochman,et al.  Molecular archaeology of the Escherichia coli genome. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[28]  B. Patel,et al.  Phenotypic and phylogenetic characterization of dominant culturable methanogens isolated from ricefield soils , 1998 .

[29]  R. Huber,et al.  A dissimilatory sirohaem-sulfite-reductase-type protein from the hyperthermophilic archaeon Pyrobaculum islandicum. , 1998, Microbiology.

[30]  Michael Wagner,et al.  Phylogeny of Dissimilatory Sulfite Reductases Supports an Early Origin of Sulfate Respiration , 1998, Journal of bacteriology.

[31]  C. Friedrich Physiology and genetics of sulfur-oxidizing bacteria. , 1998, Advances in microbial physiology.

[32]  T. Lien,et al.  Dissimilatory sulfite reductase from Archaeoglobus profundus and Desulfotomaculum thermocisternum: phylogenetic and structural implications from gene sequences , 1999, Extremophiles.

[33]  Doolittle Wf Phylogenetic Classification and the Universal Tree , 1999 .

[34]  Michael Wagner,et al.  Diversity of Sulfate-Reducing Bacteria in Oxic and Anoxic Regions of a Microbial Mat Characterized by Comparative Analysis of Dissimilatory Sulfite Reductase Genes , 1999, Applied and Environmental Microbiology.

[35]  L. Orgel,et al.  Phylogenetic Classification and the Universal Tree , 1999 .

[36]  M. Cottrell,et al.  Diversity of Dissimilatory Bisulfite Reductase Genes of Bacteria Associated with the Deep-Sea Hydrothermal Vent Polychaete Annelid Alvinella pompejana , 1999, Applied and Environmental Microbiology.

[37]  Thomas Willhalm,et al.  Software Packages , 2001, Drawing Graphs.

[38]  R. Conrad,et al.  Molecular Analyses of the Methane-Oxidizing Microbial Community in Rice Field Soil by Targeting the Genes of the 16S rRNA, Particulate Methane Monooxygenase, and Methanol Dehydrogenase , 1999, Applied and Environmental Microbiology.

[39]  M. Power,et al.  Monitoring sulfate-reducing bacteria in heterotrophic biofilms , 1999 .

[40]  B. Deplancke,et al.  Molecular Ecological Analysis of the Succession and Diversity of Sulfate-Reducing Bacteria in the Mouse Gastrointestinal Tract , 2000, Applied and Environmental Microbiology.

[41]  I. Beech,et al.  Screening of sulfate-reducing bacteria in colonoscopy samples from healthy and colitic human gut mucosa. , 2000, FEMS microbiology ecology.

[42]  U. Ermler,et al.  Crystallization and preliminary X-ray analysis of adenylylsulfate reductase from Archaeoglobus fulgidus. , 2000, Acta crystallographica. Section D, Biological crystallography.

[43]  Martin Vingron,et al.  Modeling Amino Acid Replacement , 2000, J. Comput. Biol..

[44]  H. Ochman,et al.  Lateral gene transfer and the nature of bacterial innovation , 2000, Nature.

[45]  C. Woese Interpreting the universal phylogenetic tree. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[46]  K. Stetter,et al.  Adenylylsulfate reductases from archaea and bacteria are 1:1 αβ‐heterodimeric iron–sulfur flavoenzymes – high similarity of molecular properties emphasizes their central role in sulfur metabolism , 2000, FEBS letters.

[47]  Yue Wang,et al.  Comparative sequence analyses reveal frequent occurrence of short segments containing an abnormally high number of non-random base variations in bacterial rRNA genes. , 2000, Microbiology.

[48]  Michael Friedrich,et al.  Dissimilatory Sulfite Reductase (Desulfoviridin) of the Taurine-Degrading, Non-Sulfate-Reducing Bacterium Bilophila wadsworthia RZATAU Contains a Fused DsrB-DsrD Subunit , 2001, Journal of bacteriology.

[49]  Linda L. Blackall,et al.  Multiple Lateral Transfers of Dissimilatory Sulfite Reductase Genes between Major Lineages of Sulfate-Reducing Prokaryotes , 2001, Journal of bacteriology.

[50]  S. Whelan,et al.  A general empirical model of protein evolution derived from multiple protein families using a maximum-likelihood approach. , 2001, Molecular biology and evolution.

[51]  M. Schidlowski Antiquity and evolutionary status of bacterial sulfate reduction: Sulfur isotope evidence , 1979, Origins of life.