Antimicrobial Resistance of Neisseria Gonorrhoeae in a Newly Implemented Surveillance Program in Uganda: Surveillance Report.


Journal

JMIR public health and surveillance
ISSN: 2369-2960
Titre abrégé: JMIR Public Health Surveill
Pays: Canada
ID NLM: 101669345

Informations de publication

Date de publication:
10 06 2020
Historique:
received: 15 11 2019
accepted: 20 04 2020
revised: 18 04 2020
entrez: 11 6 2020
pubmed: 11 6 2020
medline: 13 4 2021
Statut: epublish

Résumé

Neisseria gonorrhoeae (commonly known as gonorrhea) has developed resistance to all first-line therapy in Southeast Asia. East Africa has historically had absent or rudimentary gonorrhea surveillance programs and, while the existence of antimicrobial-resistant gonorrhea is recognized, the extent of its resistance is largely unknown. In 2016, the World Health Organization's Enhanced Gonococcal Antimicrobial Surveillance Program (EGASP) was initiated in Uganda to monitor resistance trends. This study characterizes gonorrhea and antibiotic resistance in a large surveillance program of men with urethral discharge syndrome from Kampala, Uganda. Men attending sentinel clinics with urethritis provided demographic information, behavior data, and a urethral swab in line with the World Health Organization's EGASP protocols for culture, identification, and antibiotic-sensitivity testing using 2 methods-disk diffusion (Kirby-Bauer test) and Etest (BioMérieux Inc). A subset of samples underwent detailed antimicrobial resistance testing. Of 639 samples collected from September 2016 to February 2018, 400 (62.6%) were culture-positive though 414 (64.8%) had microscopic evidence of gonorrhea. The mean age of the men from whom the samples were collected was 26.9 (SD 9.6) years and 7.2% (46/639) reported having HIV. There was high-level resistance to ciprofloxacin, tetracycline, and penicillin (greater than 90%) by Kirby-Bauer disk diffusion and 2.1% (4/188) had reduced azithromycin sensitivity by Etest. Of the early isolates that underwent detailed characterization, 60.3% (70/116) were culture-positive, 94% (66/69) isolates were either ciprofloxacin-resistant or ciprofloxacin-intermediate by Etest, 96% (65/68) were azithromycin-sensitive, and 96% (66/69) were gentamicin-sensitive. Resistance profiles were comparable between methods except for ceftriaxone (disk diffusion: 68/69, 99%; Etest: 67/69, 97%) and for gentamicin (disk diffusion: 2/8, 25%; Etest: 66/69, 96%) sensitivity. This is the first report from a systematic gonorrhea surveillance program in Uganda. Findings demonstrated resistance or increased minimum inhibitory concentration to all key antigonococcal antibiotics. There was evidence of poor antibiotic stewardship, near-universal resistance to several antibiotics, and emerging resistance to others. Individuals in the population sampled were at exceptionally high risk of STI and HIV infection requiring intervention. Ongoing surveillance efforts to develop interventions to curtail antimicrobial-resistant gonorrhea are needed.

Sections du résumé

BACKGROUND
Neisseria gonorrhoeae (commonly known as gonorrhea) has developed resistance to all first-line therapy in Southeast Asia. East Africa has historically had absent or rudimentary gonorrhea surveillance programs and, while the existence of antimicrobial-resistant gonorrhea is recognized, the extent of its resistance is largely unknown. In 2016, the World Health Organization's Enhanced Gonococcal Antimicrobial Surveillance Program (EGASP) was initiated in Uganda to monitor resistance trends.
OBJECTIVE
This study characterizes gonorrhea and antibiotic resistance in a large surveillance program of men with urethral discharge syndrome from Kampala, Uganda.
METHODS
Men attending sentinel clinics with urethritis provided demographic information, behavior data, and a urethral swab in line with the World Health Organization's EGASP protocols for culture, identification, and antibiotic-sensitivity testing using 2 methods-disk diffusion (Kirby-Bauer test) and Etest (BioMérieux Inc). A subset of samples underwent detailed antimicrobial resistance testing.
RESULTS
Of 639 samples collected from September 2016 to February 2018, 400 (62.6%) were culture-positive though 414 (64.8%) had microscopic evidence of gonorrhea. The mean age of the men from whom the samples were collected was 26.9 (SD 9.6) years and 7.2% (46/639) reported having HIV. There was high-level resistance to ciprofloxacin, tetracycline, and penicillin (greater than 90%) by Kirby-Bauer disk diffusion and 2.1% (4/188) had reduced azithromycin sensitivity by Etest. Of the early isolates that underwent detailed characterization, 60.3% (70/116) were culture-positive, 94% (66/69) isolates were either ciprofloxacin-resistant or ciprofloxacin-intermediate by Etest, 96% (65/68) were azithromycin-sensitive, and 96% (66/69) were gentamicin-sensitive. Resistance profiles were comparable between methods except for ceftriaxone (disk diffusion: 68/69, 99%; Etest: 67/69, 97%) and for gentamicin (disk diffusion: 2/8, 25%; Etest: 66/69, 96%) sensitivity.
CONCLUSIONS
This is the first report from a systematic gonorrhea surveillance program in Uganda. Findings demonstrated resistance or increased minimum inhibitory concentration to all key antigonococcal antibiotics. There was evidence of poor antibiotic stewardship, near-universal resistance to several antibiotics, and emerging resistance to others. Individuals in the population sampled were at exceptionally high risk of STI and HIV infection requiring intervention. Ongoing surveillance efforts to develop interventions to curtail antimicrobial-resistant gonorrhea are needed.

Identifiants

pubmed: 32519969
pii: v6i2e17009
doi: 10.2196/17009
pmc: PMC7315362
doi:

Substances chimiques

Anti-Bacterial Agents 0
Ciprofloxacin 5E8K9I0O4U
Ceftriaxone 75J73V1629
Spectinomycin 93AKI1U6QF
Cefixime 97I1C92E55
Tetracycline F8VB5M810T
Penicillin G Q42T66VG0C

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e17009

Subventions

Organisme : NIBIB NIH HHS
ID : U54 EB007958
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI007291
Pays : United States

Informations de copyright

©Meklit Workneh, Matthew M Hamill, Francis Kakooza, Emmanuel Mande, Jessica Wagner, Olive Mbabazi, Rodney Mugasha, Henry Kajumbula, Richard Walwema, Jonathan Zenilman, Patrick Musinguzi, Peter Kyambadde, Mohammed Lamorde, Yukari C Manabe. Originally published in JMIR Public Health and Surveillance (http://publichealth.jmir.org), 10.06.2020.

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Auteurs

Meklit Workneh (M)

Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, MD, United States.

Matthew M Hamill (MM)

Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, MD, United States.

Francis Kakooza (F)

Infectious Disease Institute, Kampala, Uganda.

Emmanuel Mande (E)

Infectious Disease Institute, Kampala, Uganda.

Jessica Wagner (J)

Bayview Pediatric Unit, Johns Hopkins University, Baltimore, MD, United States.

Olive Mbabazi (O)

Infectious Disease Institute, Kampala, Uganda.

Rodney Mugasha (R)

Infectious Disease Institute, Kampala, Uganda.

Henry Kajumbula (H)

Infectious Disease Institute, Kampala, Uganda.

Richard Walwema (R)

Infectious Disease Institute, Kampala, Uganda.

Jonathan Zenilman (J)

Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, MD, United States.

Patrick Musinguzi (P)

AIDS Control Program, Division of Sexually Transmitted Infections, Ministry of Health, Kampala, Uganda.

Peter Kyambadde (P)

AIDS Control Program, Division of Sexually Transmitted Infections, Ministry of Health, Kampala, Uganda.

Mohammed Lamorde (M)

Infectious Disease Institute, Kampala, Uganda.

Yukari C Manabe (YC)

Division of Infectious Diseases, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Infectious Disease Institute, Kampala, Uganda.

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Classifications MeSH