First complete genome sequence and comparative analysis of Salmonella enterica subsp. diarizonae serovar 61:k:1,5,(7) indicates host adaptation traits to sheep

• Published in: Gut pathogens Vol. 11; no. 1; pp. 48 - 8
• Main Authors: Uelze, Laura, Borowiak, Maria, Deneke, Carlus, Jacobs, Cécile, Szabó, István, Tausch, Simon H, Malorny, Burkhard
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 14.10.2019; BioMed Central; BMC
• Subjects: Adaptability (Psychology); Adaptation; Analysis; Antibiotics; Chromosomes; Comparative analysis; Deoxyribonucleic acid; Diarrhea; DNA; DNA sequencing; Drug resistance; Genetic aspects; Genetic research; Genetic testing; Genome Report; Genomes; Genomic islands; Genomics; Host-adaptation; Infection; Medical research; Novels; Nucleotide sequence; Pathogenicity; Pipelines; Pseudogenes; Rhinitis; Salmonella; Salmonella enterica; Salmonella enterica subsp. diarizonae; Sheep; Technology; United States > US; Germany; Host-adaptation; Sheep; Pseudogenes; Salmonella enterica subsp. diarizonae
• ISSN: 1757-4749; 1757-4749
• DOI: 10.1186/s13099-019-0330-9

The subsp. serovar 61:k:1,5,(7) (SASd) has been found to be host-adapted to sheep, with a high prevalence in sheep herds worldwide. Infections are usually sub-clinical, however the serovar has the potential to cause diarrhea, abortions and chronic proliferative rhinitis. Although occurrence and significance of SASd infections in sheep have been extensively studied, the genetic mechanism underlying this unusual host-adaptation have remained unknown, due to a lack of (a) available high-quality genome sequence(s). We utilized Nanopore and Illumina sequencing technologies to generate a de novo assembly of the 4.88-Mbp complete genome sequence of the SASd strain 16-SA00356, isolated from the organs of a deceased sheep in 2016. We annotated and analyzed the genome sequence with the aim to gain a deeper understanding of the genome characteristics associated with its pathogenicity and host adaptation to sheep. Overall, we found a number of interesting genomic features such as several prophage regions, a VirB4/D4 plasmid and novel genomic islands. By comparing the genome of 16-SA00356 to other serovars we found that SASd features an increased number of pseudogenes as well as a high level of genomic rearrangements, both known indicators of host-adaptation. With this sequence, we provide the first complete and closed genome sequence of a SASd strain. With this study, we provide an important basis for an understanding of the genetic mechanism that underlie pathogenicity and host adaptation of SASd to sheep.