Abstract
Human infections with Salmonella enterica subspecies enterica serovar Senftenberg are often associated with exposure to poultry flocks, farm environments, or contaminated food. The recent emergence of multidrug-resistant isolates has raised public health concerns. In this study, comparative genomics and phenotypic analysis were used to characterize 14 Salmonella Senftenberg clinical isolates recovered from multiple outbreaks in Shenzhen and Shanghai, China, between 2002 and 2011. Single-nucleotide polymorphism analyses identified two phylogenetically distinct clades of S. Senftenberg, designated SC1 and SC2, harboring variations in Salmonella pathogenicity island 1 (SPI-1) and SPI-2 and exhibiting distinct biochemical and phenotypic signatures. Although the two variants shared the same serotype, the SC2 isolates of sequence type 14 (ST14) harbored intact SPI-1 and -2 and hence were characterized by possessing efficient invasion capabilities. In contrast, the SC1 isolates had structural deletion patterns in both SPI-1 and -2 that correlated with an impaired capacity to invade cultured human cells and also the year of their isolation. These atypical SC1 isolates also lacked the capacity to produce hydrogen sulfide. These findings highlight the emergence of atypical Salmonella Senftenberg variants in China and provide genetic validation that variants lacking SPI-1 and regions of SPI-2, which leads to impaired invasion capacity, can still cause clinical disease. These data have identified an emerging public health concern and highlight the need to strengthen surveillance to detect the prevalence and transmission of nontyphoidal Salmonella species.
Original language | English (US) |
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Pages (from-to) | 2014-2022 |
Number of pages | 9 |
Journal | Journal of Clinical Microbiology |
Volume | 54 |
Issue number | 8 |
DOIs | |
State | Published - May 25 2016 |
Bibliographical note
KAUST Repository Item: Exported on 2020-10-01Acknowledgements: This work, including the efforts of Qinghua Hu, was funded by The National
Science Foundation of China (81071433). This work, including the
efforts of Qinghua Hu, was funded by China National Science and Technology
Major Project Foundation (2012ZX10004215-003-005 and
2016ZX10004215-005-005). This work, including the efforts of Qinghua
Hu, was funded by Shenzhen Public Service Platform of Pathogenic Microorganisms
Repository. This work, including the efforts of Arnab Pain,
was funded by Faculty Baseline Research Funds (KAUST-BRF).