Optimizing DNA Extraction Methods for Nanopore Sequencing of Neisseria gonorrhoeae Directly from Urine Samples
Street TL., Barker L., Sanderson ND., Kavanagh J., Hoosdally S., Cole K., Newnham R., Selvaratnam M., Andersson M., Llewelyn MJ., O’Grady J., Crook DW., Eyre DW.
<jats:title>ABSTRACT</jats:title> <jats:p>Empirical gonorrhea treatment at initial diagnosis reduces onward transmission. However, increasing resistance to multiple antibiotics may necessitate waiting for culture-based diagnostics to select an effective treatment. There is a need for same-day culture-free diagnostics that identify infection and detect antimicrobial resistance. We investigated if Nanopore sequencing can detect sufficient <jats:named-content content-type="genus-species">Neisseria gonorrhoeae</jats:named-content> DNA to reconstruct whole genomes directly from urine samples. We used <jats:named-content content-type="genus-species">N. gonorrhoeae</jats:named-content>-spiked urine samples and samples from gonorrhea infections to determine optimal DNA extraction methods that maximize the amount of <jats:named-content content-type="genus-species">N. gonorrhoeae</jats:named-content> DNA sequenced while minimizing contaminating host DNA. In simulated infections, the Qiagen UCP pathogen mini kit provided the highest ratio of <jats:named-content content-type="genus-species">N. gonorrhoeae</jats:named-content> to human DNA and the most consistent results. Depletion of human DNA with saponin increased <jats:named-content content-type="genus-species">N. gonorrhoeae</jats:named-content> yields in simulated infections but decreased yields in clinical samples. In 10 urine samples from men with symptomatic urethral gonorrhea, ≥92.8% coverage of an <jats:named-content content-type="genus-species">N. gonorrhoeae</jats:named-content> reference genome was achieved in all samples, with ≥93.8% coverage breath at ≥10-fold depth in 7 (70%) samples. In simulated infections, if ≥10<jats:sup>4</jats:sup> CFU/ml of <jats:named-content content-type="genus-species">N. gonorrhoeae</jats:named-content> was present, sequencing of the large majority of the genome was frequently achieved. <jats:named-content content-type="genus-species">N. gonorrhoeae</jats:named-content> could also be detected from urine in cobas PCR medium tubes and from urethral swabs and in the presence of simulated <jats:italic>Chlamydia</jats:italic> coinfection. Using Nanopore sequencing of urine samples from men with urethral gonorrhea, sufficient data can be obtained to reconstruct whole genomes in the majority of samples without the need for culture.</jats:p>