Comparative Genomic Analysis of Three Strains of Ehrlichia ruminantium Reveals an Active Process of Genome Size Plasticity

Author:

Frutos Roger1,Viari Alain2,Ferraz Conchita3,Morgat Anne24,Eychenié Sophie3,Kandassamy Yane1,Chantal Isabelle1,Bensaid Albert1,Coissac Eric2,Vachiery Nathalie1,Demaille Jacques3,Martinez Dominique1

Affiliation:

1. CIRAD-Emvt, TA30/G, Campus International de Baillarguet, 34398 Montpellier Cedex 5, France

2. Inria Rhône-Alpes—Projet HELIX, 655 Av. de l'Europe, 38330 Montbonnot-Saint Martin, France

3. Centre de Séquençage Génomique, IGH-CNRS-UPR 1142, 141 rue de la Cardonille, 34396 Montpellier Cedex 5, France

4. Swiss Institute of Bioinformatics, Swiss-Prot Group, 1 rue Michel, Servet, CH-1211 Geneva 4, Switzerland

Abstract

ABSTRACT Ehrlichia ruminantium is the causative agent of heartwater, a major tick-borne disease of livestock in Africa that has been introduced in the Caribbean and is threatening to emerge and spread on the American mainland. We sequenced the complete genomes of two strains of E. ruminantium of differing phenotypes, strains Gardel (Erga; 1,499,920 bp), from the island of Guadeloupe, and Welgevonden (Erwe; 1,512,977 bp), originating in South Africa and maintained in Guadeloupe in a different cell environment. Comparative genomic analysis of these two strains was performed with the recently published parent strain of Erwe (Erwo) and other Rickettsiales ( Anaplasma , Wolbachia , and Rickettsia spp.). Gene order is highly conserved between the E. ruminantium strains and with A. marginale . In contrast, there is very little conservation of gene order with members of the Rickettsiaceae . However, gene order may be locally conserved, as illustrated by the tuf operons. Eighteen truncated protein-encoding sequences (CDSs) differentiate Erga from Erwe / Erwo, whereas four other truncated CDSs differentiate Erwe from Erwo. Moreover, E. ruminantium displays the lowest coding ratio observed among bacteria due to unusually long intergenic regions. This is related to an active process of genome expansion/contraction targeted at tandem repeats in noncoding regions and based on the addition or removal of ca. 150-bp tandem units. This process seems to be specific to E. ruminantium and is not observed in the other Rickettsiales .

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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