In mice, the genetic background of the host organism itself may play an underappreciated role in the sharing of resistance between bacteria, said researchers.
Genetic makeup of the host organism was found to influence the transfer of plasmids, revealed new findings published in mSphere. Bacteria share the genes responsible for antibiotic resistance through circular pieces of DNA called plasmids, but the //process of their transfer in the host is complex. The researchers hope to identify new ways to stop the spread of antibiotic resistance, which kills tens of thousands of people every year in the United States alone. "The human gut has millions of bacteria," said microbiologist Melha Mellata, Ph.D., at Iowa State University in Ames, Iowa. "If an AR plasmid is introduced into our gut through contaminated food or by another means, it will quickly spread to other gut bacteria, which will generate bacteria resistant to treatments with antibiotics." To stop that from happening, she said, researchers need to know what factors trigger or reduce the transfer of plasmids.
‘In the gastrointestinal tract of host animals, bacteria can exchange the genes responsible for antibiotic resistance (AR) via small, circular chunks of DNA called plasmids. ’
This week in mSphere, an open-access journal of the American Society for Microbiology, Mellata and her colleagues published findings that suggest the genetic background of the host organism itself may play an underappreciated role in the sharing of resistance between bacteria, at least in mice. The researchers analyzed how AR-associated plasmids were transferred from one microbe to another in two genetically different groups of mice. Both groups started with the same population of gut microbes and were fed the same diet in the same environment. The researchers found that the plasmids transferred successfully in some mice but not in others, which meant that AR didn't spread in the same way in all groups. That observation led the researchers to run further analyses, which suggested that the microbial transactions could be attributed to genetic factors in the mice themselves, as well as the complexity of the gut microbiota.
"There is something in the host's genes that can amplify this transfer," said Mellata, who led the study.
Mellata and her colleagues used a strain of Salmonella known to harbor large plasmids that make the bacterium resistant to treatment with streptomycin and tetracycline, two common antibiotics. Previous studies by other researchers have confirmed that these plasmids can transfer to Escherichia coli.
But those previous experiments were conducted in bacterial cultures. For the new study, Mellata's group studied how the plasmids spread to E. coli in the animals themselves. A better understanding of how resistance spreads requires examining what's going on in the host gastrointestinal tract, she said. "We need to study this issue through the lens of the host's complex environment, since in reality this is how this phenomenon happens."
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Mellata's group is now following up on the experiment by trying to identify the specific genetic host factors that can trigger the plasmid transfer. She hopes those findings can lead to a new way to stop the spread of antibiotic resistance. "If we can target those specific host factors, we can reduce the plasmid transfer, which will prevent the emergence of new antibiotic-resistant strains," she said.
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Source-Eurekalert