The contribution of local animal populations to human drug resistant Salmonella infections may previously have been overstated

Genomic study shows that Salmonella populations in humans and animals living side by side are more different than expected

The contribution of local animal populations to human drug resistant Salmonella infections may previously have been overstated

salmonellatree.jpgDOI: 10.1126/science.1240578
This is the first time that the numbers of human-to-animal and animal-to-human transitions of a zoonotic pathogen have been estimated in this way. Our results have indicated that the cross-species spillover between local animals and humans of Salmonella Typhimurium DT104 is less than has been previously thought.

A new study has shown that, contrary to popular belief, local domestic animals are unlikely to be the major source of antibiotic-resistant Salmonella in humans. The result comes from a detailed study of DNA from more than 370 Salmonella samples collected over a 22-year period.

By studying the genetic variation in the Salmonella bacteria and their drug resistance genes, researchers found that distinguishable bacterial populations exist in human and animal populations living side by side. Antibiotic resistance is considered to be one of the most important dangers to human health, threatening to make many treatments to common infections ineffective. By comparing the genomes of Salmonella in humans and animals the researchers have provided important new insights into the likely sources and spread of antibiotic resistant infections. First, the Salmonella bacteria largely remained within their original host populations and second, there were more varied combinations of drug resistance in the human-infecting bacteria.

Salmonella infection is a global issue, with approximately 94 million people contracting gastroenteritis or food poisoning each year. The combined annual cost in the United States and European Union is estimated to be more than £4 billion ($6 billion). This public health issue is exacerbated further by antibiotic resistance, which can lead to more complicated and protracted illness in patients and increased treatment costs.

"For the first time we've determined in detail and on a large scale how Salmonella strains taken from humans and animals in the same setting and over the same time period relate to each other. Our genomic data reveal how the Salmonella bacteria spread during the course of a long-term epidemic. We found that people have a more diverse source of infection and antibiotic resistance than just the local animals, pointing towards alternative sources."

Dr Alison Mather, first author on the study, from the Wellcome Trust Sanger Institute

The team sequenced DNA from 373 samples from humans and animals infected with Salmonella Typhimurium DT104 over a 22-year period, mainly from Scotland, but also from other countries. This is the largest study of its type; whole genome DNA sequencing delivers the highest level of resolution possible to examine how closely related the bacteria are, enabling the team to unravel the details of this epidemic.

The team discovered that, contrary to much current thinking, the populations of Salmonella in humans and animals were distinguishable. They also found that the estimated number of times that the bacteria had jumped from animals to humans (and vice versa) was remarkably low. In addition, there was greater diversity in antibiotic resistance genes in salmonellae isolated from humans. Taken together, these findings suggest that the contribution of local animal populations to human infections with S. Typhimurium DT104 may previously have been overstated.

"This is a study that uses the latest genomic approaches and a unique collection of samples to address a significant public health problem. Our data provide a very simple message, challenging the established view that local animals are the predominant source of Salmonella infections in Scotland. This finding will reinvigorate discussions on the sources of antibiotic-resistant Salmonella infections in humans in other environments."

Professor Nicholas Thomson, senior author from the Wellcome Trust Sanger Institute

The team speculate that international travel and imported foods may be major sources of antibiotic-resistant strains of Salmonella. However, to understand fully the routes of infection and find ways to prevent it, further research into other bacteria and other environments will be needed.

"Discovering that the animal and human populations of Salmonella were as distinguishable as they were was a great surprise to us. This finding in no way undermines the importance of prudent antimicrobial use in all species. But our study does demonstrate that greater effort needs to be focused on understanding the natural history of the pathogens and on identifying the major sources of resistance in our global ecosystems."

Professor Stuart Reid, co-author from the Royal Veterinary College

Notes to Editors
  • Distinguishable epidemics of multidrug-resistant Salmonella Typhimurium DT104 in different hosts.

    Mather AE, Reid SW, Maskell DJ, Parkhill J, Fookes MC et al.

    Science (New York, N.Y.) 2013;341;6153;1514-7


Funding for the research came from, the William Stewart Fellowship at the University of Glasgow, Wellcome Trust grant 098051, funding from the European Union Seventh Framework Programme [FP7/2007-2013] under ERC Grant agreement no. 260864, National Institutes of Health R01 grants AI107034 and HG006139 and National Science Foundation grant DMS-1264153.

Participating Centres
  • Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK.
  • Royal Veterinary College, North Mymms, Hatfield, UK.
  • Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
  • Scottish Salmonella Shigella and Clostridium difficile Reference Laboratory, Stobhill Hospital, Glasgow, UK.
  • National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Canada.
  • Animal Health and Veterinary Laboratories Agency, Weybridge, UK.
  • Gastrointestinal Bacteria Reference Unit, Public Health England, Colindale, London, UK.
  • Pathogen Genomics Center, National Institute of Infectious Diseases, Tokyo, Japan.
  • Bacterial and Parasitic Disease Research Division, National Institute of Animal Health, Ibaraki,Japan.
  • Department of Bacteriology I, National Institute of Infectious Diseases, Tokyo, Japan.
  • Departments of Biomathematics and Human Genetics, David Geffen School of Medicine at UCLA, and Department of Biostatistics, UCLA Fielding School of Public Health, University of California, Los Angeles, USA.
  • Department of Microbiology and Immunology, Rega Institute, KU Leuven, Leuven, Belgium.
  • Boyd Orr Centre for Population and Ecosystem Health, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
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