The type IV secretion system of Patescibacteria is homologous to the bacterial monoderm conjugation machinery

The Candidate Phyla Radiation, also known as <i>Patescibacteria</i>, represents a vast and diverse division of bacteria that has come to light via culture-independent 'omics' technologies. Their limited biosynthetic capacity, along with evidence of their growth as obligate epibionts on other bacteria, suggests a broad reliance on host organisms for their survival. Nevertheless, our understanding of the molecular mechanisms governing their metabolism and lifestyle remains limited. The type IV secretion system (T4SS) represents a superfamily of translocation systems with a wide range of functional roles. T4SS genes have been identified in the <i>Patescibacteria</i> class <i>Saccharimonadia</i> as essential for their epibiotic growth. In this study, we used a comprehensive bioinformatics approach to investigate the diversity and distribution of T4SS within <i>Patescibacteria</i>. The phylogenetic analysis of the T4SS signature protein VirB4 suggests that most of these proteins cluster into a distinct monophyletic group with a shared ancestry to the MPF<sub>FATA</sub> class of T4SS. This class is found in the conjugative elements of <i>Firmicutes</i>, <i>Actinobacteria</i>, <i>Tenericutes</i> and <i>Archaea</i>, indicating a possible horizontal gene transfer from these monoderm micro-organisms to <i>Patescibacteria</i>. We identified additional T4SS components near <i>virB4</i>, particularly those associated with the MPF<sub>FATA</sub> class, as well as homologues of other T4SS classes, such as VirB2-like pilins, and observed their varied arrangements across different <i>Patescibacteria</i> classes. The absence of a relaxase in most of these T4SS clusters suggests that the system has been co-opted for other functions in <i>Patescibacteria</i>. The proximity of T4SS components to the origin of replication (gene <i>dnaA</i>) in some <i>Patescibacteria</i> suggests a potential mechanism for increased expression. The broad ubiquity of a phylogenetically distinct T4SS, combined with its chromosomal location, underscores the significance of T4SS in the biology of <i>Patescibacteria</i>.

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Publication Details

Journal
Microbial Genomics
Published
2025-05-23
DOI
https://doi.org/10.1099/mgen.0.001409
Citations
1
Primary Topic
Protist diversity and phylogeny
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article
Field-Weighted Citation Impact
0.81

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article

The type IV secretion system of Patescibacteria is homologous to the bacterial monoderm conjugation machinery

Pedro J. Cabello‐Yeves, Maria Pilar Garcillán-Barcia, Francisco Rodríguez‐Valera, José M. Haro-Moreno et al.
1 citations
Microbial Genomics
Protist diversity and phylogeny
0.81
article

The type IV secretion system of Patescibacteria is homologous to the bacterial monoderm conjugation machinery

Pedro J. Cabello‐Yeves, Maria Pilar Garcillán-Barcia, Francisco Rodríguez‐Valera, José M. Haro-Moreno, María del Mar Quiñonero‐Coronel
article en
1 citations

Abstract

The Candidate Phyla Radiation, also known as <i>Patescibacteria</i>, represents a vast and diverse division of bacteria that has come to light via culture-independent 'omics' technologies. Their limited biosynthetic capacity, along with evidence of their growth as obligate epibionts on other bacteria, suggests a broad reliance on host organisms for their survival. Nevertheless, our understanding of the molecular mechanisms governing their metabolism and lifestyle remains limited. The type IV secretion system (T4SS) represents a superfamily of translocation systems with a wide range of functional roles. T4SS genes have been identified in the <i>Patescibacteria</i> class <i>Saccharimonadia</i> as essential for their epibiotic growth. In this study, we used a comprehensive bioinformatics approach to investigate the diversity and distribution of T4SS within <i>Patescibacteria</i>. The phylogenetic analysis of the T4SS signature protein VirB4 suggests that most of these proteins cluster into a distinct monophyletic group with a shared ancestry to the MPF<sub>FATA</sub> class of T4SS. This class is found in the conjugative elements of <i>Firmicutes</i>, <i>Actinobacteria</i>, <i>Tenericutes</i> and <i>Archaea</i>, indicating a possible horizontal gene transfer from these monoderm micro-organisms to <i>Patescibacteria</i>. We identified additional T4SS components near <i>virB4</i>, particularly those associated with the MPF<sub>FATA</sub> class, as well as homologues of other T4SS classes, such as VirB2-like pilins, and observed their varied arrangements across different <i>Patescibacteria</i> classes. The absence of a relaxase in most of these T4SS clusters suggests that the system has been co-opted for other functions in <i>Patescibacteria</i>. The proximity of T4SS components to the origin of replication (gene <i>dnaA</i>) in some <i>Patescibacteria</i> suggests a potential mechanism for increased expression. The broad ubiquity of a phylogenetically distinct T4SS, combined with its chromosomal location, underscores the significance of T4SS in the biology of <i>Patescibacteria</i>.

Microbial GenomicsVol. 11(5)
Universitat de Miguel Hernández d'Elx (ES), Universidad de Cantabria (ES), Consejo Superior de Investigaciones Científicas (ES), University of Warwick (GB), Instituto de Biomedicina y Biotecnología de Cantabria (ES)
Fundación Alfonso Martín Escudero, UK Research and Innovation, Ministerio de Economía y Competitividad, Ministerio de Ciencia e Innovación, Ministerio de Asuntos Económicos y Transformación Digital, Gobierno de España, HORIZON EUROPE Framework Programme, Agencia Estatal de Investigación, H2020 Marie Skłodowska-Curie Actions
Life in Land
Openalex Percentile: Top 28%
Protist diversity and phylogeny
0.81
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