Targeted test for antibiotic resistance in clinical Enterobacter species

The currently used microbiological tests for colistin resistance and other antibiotic resistances did not allow accurate conclusions regarding the spread of resistance in differentEnterobacterspecies. This was partly because the taxonomic classification of clinicalEnterobacterisolates was imprecise, and partly because the error rate in determining resistance was high. The large-scale DZIF study has now achieved a breakthrough and clarified the relationships between the numerousEnterobacterspecies as well as optimised resistance testing. To this end, researchers at the Institute of Medical Microbiology of Justus Liebig University Giessen (Deep-iAMR project), together with DZIF scientists at the Research Center Borstel Leibniz Lung Center, analysedEnterobacterisolates collected at German university hospitals over a period of three years.

Using genome-based taxonomic studies,Enterobacter xiangfangensis被发现是最常发生的规范ies in German hospitals: From a data pool of over 3246 isolates worldwide -- representing a collection from over twenty years -- this species accounted for 68.7 percent of allEnterobacterdetected.

Determination of antibiotic resistance profiles using phenotypic assays recommended by the European Committee on Antimicrobial Susceptibility Testing (EUCAST) yielded mixed results with regard to colistin resistance.

"It turned out that many isolates were either not or barely resistant in these tests, even though the bacteria carried all the genes necessary for the expression of colistin resistance," explains the study's first author, Dr. Swapnil Doijad, of Friedrich Schiller University, Jena, Germany. A result that raised questions. The researchers obtained an initial answer by further investigating the isolates in which resistance was not clearly detectable using mass spectrometry.

"Depending on the particularEnterobacterspecies, we detected low levels of modified lipid A, the anchor structure of lipopolysaccharides (LPS) -- a crucial component of the bacterial membrane and required for colistin resistance -- even from bacteria grown in colistin-free medium," comments the co-first author of the study, Dr. Nicolas Gisch of the Research Center Borstel Leibniz Lung Center. "These modifications of lipid A appear to be dependent on the bacterial species and are inherent, meaning their expression is embedded in a more complex regulation and not alone triggered by colistin," he adds.

"The result suggests that there is species-dependent variation in the heteroresistance seen inEnterobacter: In routine test systems, the bacteria are sometimes resistant, sometimes not," explains Dr. Can Imirzalioglu, co-author of the study and Acting Director for Clinical Microbiology and Diagnostics at the Institute of Medical Microbiology of Justus Liebig University Giessen.

Using further sophisticated methods, the authors were able to elucidate the phenomenon of heteroresistance in the genusEnterobacter. "Our analyses revealed that these bacteria have a sensor on their surface that responds to the pH value, i.e., the acidity in the environment, and regulates accordingly, either up or down, the genes required for the expression of colistin resistance," explains Prof. Trinad Chakraborty, senior author and former director of the Institute of Medical Microbiology at Justus Liebig University Giessen. Genetic variations and interactions in this sensing pathway for environmental pH led to species-dependent differences regarding the extent of colistin resistance in the variousEnterobacterspecies in conventional test systems.

Based on these findings, the researchers developed a simple new assay that eliminates heteroresistance effects and allows unambiguous and reliable determination of the true levels of colistin resistance for any isolate. The assay will avoid therapeutic failures when recommending the antibiotic, thereby paving the way for a targeted and economical treatment ofEnterobacterspecies with this reserve antibiotic worldwide. A result that has come about not least through translational collaborations within the DZIF.