Within-Host and Population Transmission of blaOXA-48 in K. pneumoniae and E. coli

Publication date

2015

Authors

Haverkate, Manon R
Dautzenberg, Mirjam J D
Ossewaarde, Tjaco J M
van der Zee, Anneke
den Hollander, Jan G
Troelstra, Annet
Bonten, Marc J M
Bootsma, M.ISNI 0000000396969686

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Abstract

During a large hospital outbreak of OXA-48 producing bacteria, most K. pneumoniaeOXA-48 isolates were phenotypically resistant to meropenem or imipenem, whereas most E. coliOXA-48 isolates were phenotypically susceptible to these antibiotics. In the absence of molecular gene-detection E. coliOXA-48 could remain undetected, facilitating cross-transmission and horizontal gene transfer of blaOXA-48. Based on 868 longitudinal molecular microbiological screening results from patients carrying K. pneumoniaeOXA-48 (n = 24), E. coliOXA-48 (n = 17), or both (n = 40) and mathematical modelling we determined mean durations of colonisation (278 and 225 days for K. pneumoniaeOXA-48 and E. coliOXA-48, respectively), and horizontal gene transfer rates (0.0091/day from K. pneumoniae to E. coli and 0.0015/day vice versa). Based on these findings the maximum effect of horizontal gene transfer of blaOXA-48 originating from E. coliOXA-48 on the basic reproduction number (R0) is 1.9%, and it is, therefore, unlikely that phenotypically susceptible E. coliOXA-48 will contribute significantly to the spread of blaOXA-48.

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Haverkate, M R, Dautzenberg, M J D, Ossewaarde, T J M, van der Zee, A, den Hollander, J G, Troelstra, A, Bonten, M J M & Bootsma, M C J 2015, 'Within-Host and Population Transmission of blaOXA-48 in K. pneumoniae and E. coli', PLoS One, vol. 10, no. 10, pp. e0140960. https://doi.org/10.1371/journal.pone.0140960