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Antimicrobial resistance and heterogeneity of Neisseria gonorrhoeae isolated from patients attending sexually transmitted infection clinics in Lusaka, Zambia.

Publication ,  Journal Article
Sarenje, KL; van Zwetselaar, M; Kumburu, H; Sonda, T; Mmbaga, B; Ngalamika, O; Maimbolwa, MC; Siame, A; Munsaka, S; Kwenda, G
Published in: BMC genomics
March 2024

Antimicrobial resistance (AMR) of Neisseria gonorrhoeae is a threat to public health as strains have developed resistance to antimicrobials available for the treatment of gonorrhea. Whole genome sequencing (WGS) can detect and predict antimicrobial resistance to enhance the control and prevention of gonorrhea. Data on the molecular epidemiology of N. gonorrhoeae is sparse in Zambia. This study aimed to determine the genetic diversity of N. gonorrhoeae isolated from patients attending sexually transmitted infection (STI) clinics in Lusaka, Zambia.A cross-sectional study that sequenced 38 N. gonorrhoeae isolated from 122 patients with gonorrhea from 2019 to 2020 was conducted. The AMR profiles were determined by the E-test, and the DNA was extracted using the NucliSens easyMaG magnetic device. Whole genome sequencing was performed on the Illumina NextSeq550 platform. The Bacterial analysis pipeline (BAP) that is readily available at: https://cge.cbs.dtu.dk/services/CGEpipeline-1.1 was used for the identification of the species, assembling the genome, multi-locus sequence typing (MLST), detection of plasmids and AMR genes. Phylogeny by single nucleotide polymorphisms (SNPs) was determined with the CCphylo dataset.The most frequent STs with 18.4% of isolates each were ST7363, ST1921 and ST1582, followed by ST1583 (13%), novel ST17026 (7.9%), ST1588 (7.9%), ST1596 (5.3%), ST11181 (5.3%), ST11750 (2.6/%) and ST11241 (2.6%) among the 38 genotyped isolates. The blaTeM-1B and tetM (55%) was the most prevalent combination of AMR genes, followed by blaTeM-1B (18.4%), tetM (15.8%), and the combination of blaTeM-1B, ermT, and tetL was 2.6% of the isolates. The AMR phenotypes were predicted in ciprofloxacin, penicillin, tetracycline, azithromycin, and cefixime. The combination of mutations 23.7% was gryA (S91F), parC (E91G), ponA (L421) and rpsJ (V57M), followed by 18.4% in gyrA (S91F), ponA (L421P), rpsJ (V57M), and 18.4% in gyrA (D95G, S91F), ponA (L421P), and rpsJ (V57M). The combinations in gyrA (D95G, S91F) and rpsJ (V57M), and gyrA (D95G, S91F), parC (E91F), ponA (L421P) and rpsJ (V57M) were 13.2% each of the isolates. Plasmid TEM-1 (84.2%), tetM (15.8%), and gonococcal genetic island (GGI) was detected in all isolates.This study revealed remarkable heterogeneity of N. gonorrhoeae with blaTEM-1, tetM, ponA, gyrA, and parC genes associated with high resistance to penicillin, tetracycline, and ciprofloxacin demanding revision of the standard treatment guidelines and improved antimicrobial stewardship in Zambia.

Published In

BMC genomics

DOI

EISSN

1471-2164

ISSN

1471-2164

Publication Date

March 2024

Volume

25

Issue

1

Start / End Page

290

Related Subject Headings

  • Zambia
  • Tetracycline
  • Penicillins
  • Neisseria gonorrhoeae
  • Multilocus Sequence Typing
  • Microbial Sensitivity Tests
  • Humans
  • Gonorrhea
  • Drug Resistance, Bacterial
  • Cross-Sectional Studies
 

Citation

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Sarenje, K. L., van Zwetselaar, M., Kumburu, H., Sonda, T., Mmbaga, B., Ngalamika, O., … Kwenda, G. (2024). Antimicrobial resistance and heterogeneity of Neisseria gonorrhoeae isolated from patients attending sexually transmitted infection clinics in Lusaka, Zambia. BMC Genomics, 25(1), 290. https://doi.org/10.1186/s12864-024-10155-y
Sarenje, Kelvin Lutambo, Marco van Zwetselaar, Happiness Kumburu, Tolbert Sonda, Blandina Mmbaga, Owen Ngalamika, Margaret C. Maimbolwa, Amon Siame, Sody Munsaka, and Geoffrey Kwenda. “Antimicrobial resistance and heterogeneity of Neisseria gonorrhoeae isolated from patients attending sexually transmitted infection clinics in Lusaka, Zambia.BMC Genomics 25, no. 1 (March 2024): 290. https://doi.org/10.1186/s12864-024-10155-y.
Sarenje KL, van Zwetselaar M, Kumburu H, Sonda T, Mmbaga B, Ngalamika O, et al. Antimicrobial resistance and heterogeneity of Neisseria gonorrhoeae isolated from patients attending sexually transmitted infection clinics in Lusaka, Zambia. BMC genomics. 2024 Mar;25(1):290.
Sarenje, Kelvin Lutambo, et al. “Antimicrobial resistance and heterogeneity of Neisseria gonorrhoeae isolated from patients attending sexually transmitted infection clinics in Lusaka, Zambia.BMC Genomics, vol. 25, no. 1, Mar. 2024, p. 290. Epmc, doi:10.1186/s12864-024-10155-y.
Sarenje KL, van Zwetselaar M, Kumburu H, Sonda T, Mmbaga B, Ngalamika O, Maimbolwa MC, Siame A, Munsaka S, Kwenda G. Antimicrobial resistance and heterogeneity of Neisseria gonorrhoeae isolated from patients attending sexually transmitted infection clinics in Lusaka, Zambia. BMC genomics. 2024 Mar;25(1):290.
Journal cover image

Published In

BMC genomics

DOI

EISSN

1471-2164

ISSN

1471-2164

Publication Date

March 2024

Volume

25

Issue

1

Start / End Page

290

Related Subject Headings

  • Zambia
  • Tetracycline
  • Penicillins
  • Neisseria gonorrhoeae
  • Multilocus Sequence Typing
  • Microbial Sensitivity Tests
  • Humans
  • Gonorrhea
  • Drug Resistance, Bacterial
  • Cross-Sectional Studies