The DOI matches its Crossref record; 91 of the 92 references it cites were found in a registry or an index.
Prevalence of mutations associated with resistance to macrolides and fluoroquinolones in Mycoplasma genitalium: a systematic review and meta-analysis
Open accessAbstract
BACKGROUND Mycoplasma genitalium is now recognised as an important bacterial sexually transmitted infection. We summarised data from studies of mutations associated with macrolide and fluoroquinolone resistance in M genitalium to establish the prevalence of resistance. We also investigated temporal trends in resistance and aimed to establish the association between resistance and geographical location. METHODS In this systematic review and meta-analysis, we searched PubMed, Embase, and MEDLINE for studies that included data for the prevalence of mutations associated with macrolide and fluoroquinolone resistance in M genitalium published in any language up to Jan 7, 2019. We defined prevalence as the proportion of M genitalium samples positive for key mutations associated with azithromycin resistance (23S rRNA gene, position 2058 or 2059) or moxifloxacin resistance (S83R, S83I, D87N, or D87Y in parC), or both, among all M genitalium samples that were successfully characterised. We used random-effects meta-analyses to calculate summary estimates of prevalence. Subgroup and meta-regression analyses by WHO region and time period were done. This study was registered with PROSPERO, number CRD42016050370. RESULTS Overall, 59 studies from 21 countries met the inclusion criteria for our study: 57 studies of macrolide resistance (8966 samples), 25 of fluoroquinolone resistance (4003 samples), and 22 of dual resistance to macrolides and fluoroquinolones (3280 samples). The summary prevalence of mutations associated with macrolide resistance among M genitalium samples was 35·5% (95% CI 28·8-42·5); prevalence increased from 10·0% (95% CI 2·6-20·1%) before 2010, to 51·4% (40·3-62·4%) in 2016-17 (p<0·0001). Prevalence of mutations associated with macrolide resistance was significantly greater in samples in the WHO Western Pacific and Americas regions than in those from the WHO European region. The overall prevalence of mutations associated with fluoroquinolone resistance in M genitalium samples was 7·7% (95% CI 4·5-11·4%). Prevalence did not change significantly over time, but was significantly higher in the Western Pacific region than in the European region. Overall, the prevalence of both mutations associated with macrolide resistance and those associated with fluoroquinolone resistance among M genitalium samples was 2·8% (1·3-4·7%). The prevalence of dual resistance did not change significantly over time, and did not vary significantly by geographical region. INTERPRETATION Global surveillance and measures to optimise the efficacy of treatments-including resistance-guided strategies, new antimicrobials, and antimicrobial combination approaches-are urgently needed to ensure cure in a high proportion of M genitalium infections and to prevent further spread of resistant strains. FUNDING Australian National Health and Medical Research Council.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“A systematic review of 59 studies found that the prevalence of mutations linked to macrolide resistance rose from 10% to 51% between the years prior to 2010 and the years 2016–2017 in Mycoplasma genitalium (34).”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Shamseer, L., Moher, D., Clarke, M., Ghersi, D., Liberati, A., Petticrew, M., Shekelle, P., Stewart, L. A., & the PRISMA-P Group (2015) · BMJ · doi:10.1136/bmj.g7647 · Cited by 13,120
Hoy, D., Brooks, P., Woolf, A., Blyth, F., March, L., Bain, C., Baker, P., Smith, E., & Buchbinder, R. (2012) · Journal of Clinical Epidemiology · doi:10.1016/j.jclinepi.2011.11.014 · Cited by 2,555
Wi, T., Lahra, M. M., Ndowa, F. J., Bala, M., Dillon, J. R., Ramón-Pardo, P., Eremin, S., BOLAN, G. A., & Unemo, M. (2017) · PLoS Medicine · doi:10.1371/journal.pmed.1002344 · Cited by 621
Self-citationMycoplasma genitalium: from Chrysalis to Multicolored Butterfly
TAYLOR‐ROBINSON, D., & Jensen, J. S. (2011) · Clinical Microbiology Reviews · doi:10.1128/cmr.00006-11 · Cited by 536
Self-citationMycoplasma genitalium Infection and Female Reproductive Tract Disease: A Meta-analysis
Lis, R., Rowhani‐Rahbar, A., & Manhart, L. E. (2015) · Clinical Infectious Diseases · doi:10.1093/cid/civ312 · Cited by 458
2016 European guideline on Mycoplasma genitalium infections
Jensen, J. S., Cusini, M., Gomberg, M. A., et al. (2016) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/jdv.13849 · Cited by 343
Self-citationJensen, J. S., Bradshaw, C. S., Tabrizi, S. N., et al. (2008) · Clinical Infectious Diseases · doi:10.1086/593188 · Cited by 338
Self-citationUK national guideline for the management of gonorrhoea in adults, 2011
Bignell, C., Fitzgerald, M. G., & (Guideline Development Group) (2011) · International Journal of STD & AIDS · doi:10.1258/ijsa.2011.011267 · Cited by 269
Baumann, L., Cina, M., Egli-Gany, D., Goutaki, M., Halbeisen, F. S., Lohrer, G.-R., Ali, H., Scott, P., & Low, N. N. (2018) · Sexually Transmitted Infections · doi:10.1136/sextrans-2017-053384 · Cited by 253
Self-citation
Research works printed but not linked: 2
- Murray, 2020, Moxifloxacin and sitafloxacin treatment failure in Mycoplasma genitalium infection: association with parC mutation G248T (S83I) and concurrent gyrA utations, J Infect Dis, 221, 1017
- Jensen, 2016, 2016 European guideline on Mycoplasma genitalium infections, J Eur Acad Dermatol Venereol, 30, 1650, 10.1111/jdv.13849 · DOI
Cited by
Sorted by citations
Items 201–269 of 269
Simos, P., & Stewart, A. G. (2022) · Internal Medicine Journal · doi:10.1111/imj.15684 · Cited by 2
Waites, K. B., Xiao, L., & Dybvig, K. F. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-818619-0.00122-2 · Cited by 2
Individualised treatment of sexually transmitted infections by rapid molecular assays
Murray, G. L., Sweeney, E. L., & Bradshaw, C. S. (2024) · Microbiology Australia · doi:10.1071/ma24035 · Cited by 2
Self-citationToh, E. C., Gao, X., Williams, J. A., et al. (2022) · IUScholarWorks (Indiana University) · doi:10.1097/olq.0000000000001509 · Cited by 1
“Macrolide resistance occurs through selection of single nucleotide polymorphisms at positions A2058 and A2059 (Escherichia coli numbering) in domain V of the MG 23S rRNA gene, termed macrolide resistance-mediating mutations (MRMs); a recent meta-analysis showed a rapid increase in MRM prevalence from <10% before 2010…”
BackgroundLeng, X., Zhu, R., Ao, X., et al. (2025) · Infection and Drug Resistance · doi:10.2147/idr.s489403 · Cited by 1
“17,18 Notably, macrolide resistance appears to be more prevalent in specimens from MSM 16,19 , with reported rates as high as 95.4% in France, 20 79.9% in Berlin, 21 88.4% in Belgium, 22 84.2–89.7% in Australia 4,23 and 70.6–80.0% in America.”
InfluentialIncreasing incidence of Mycoplasma genitalium is driven by people living with HIV and PrEP users
Rossotti, R., Nava, A., D’Amico, F., Baiguera, C., Fanti, D., Inglese, E., Raimondi, A., Bana, N. B., Spelzini, F., Bini, M., et al. (2025) · International Journal of STD & AIDS · doi:10.1177/09564624251315782 · Cited by 1
Rincón-Quintero, A., Daviña‐Núñez, C., Pintos‐Fonseca, A. D. M., et al. (2025) · Sexually Transmitted Infections · doi:10.1136/sextrans-2025-056524 · Cited by 1
“13 14 Likewise, the emergence and expansion of sexually transmitted MDR shigel-losis among MSM is a global public health problem.”
Nagase, Y., Hayakawa, K., Kubo, T., et al. (2025) · Journal of Infection and Chemotherapy · doi:10.1016/j.jiac.2025.102775 · Cited by 1
Performance of Allplex TM MG & AziR Assay for Detecting Macrolide-Resistant Mycoplasma genitalium
Lee, G., Seo, Y., Lim, D.-H., et al. (2025) · Journal of Korean Medical Science · doi:10.3346/jkms.2025.40.e285 · Cited by 1
Son, J.-G., Kim, N., Oh, H. S., et al. (2025) · Journal of Korean Medical Science · doi:10.3346/jkms.2025.40.e337 · Cited by 1
“6,8 13 Given the recent trends in resistance, strategies such as post-treatment follow-up NAAT to confirm microbial clearance might be considered.”
Llaca-Díaz, J. M., & Casillas-Vega, N. G. (2026) · Archivio Italiano di Urologia e Andrologia · doi:10.4081/aiua.2026.14694 · Cited by 1
“Macrolide resistance explains empirical azithromycin treatment failures and symptom recurrence (18).”
InfluentialSuperbugs Neisseria gonorrhoeae und Mycoplasma genitalium
Kogler, A., Chromy, D., & Sadoghi, B. (2026) · Die Dermatologie · doi:10.1007/s00105-026-05650-0 · Cited by 1
Lim, H.-J., Hong, Y.-T., Baek, S.-H., et al. (2026) · Microorganisms · doi:10.3390/microorganisms14030665 · Cited by 1
“…of resistance-guided management requires timely, accurate, and population-specific data on the distribution of resistance-associated mutations [13,16], and in several regions, including Korea, comprehensive and current surveillance data from routine clinical practice remain limited [16,22].”
InfluentialA clinical case of ineffective treatment of infection caused by Mycoplasma genitalium
Negasheva, E. S., Frigo, N. V., Эйдельштейн, И. А., et al. (2026) · Russian Journal of Clinical Dermatology and Venereology · doi:10.17116/klinderma20262501131 · Cited by 1
Dirks, J. A. M. C., van Loo, I. H. M., Dukers–Muijrers, N. H. T. M., et al. (2022) · Sexually Transmitted Diseases · doi:10.1097/olq.0000000000001752 · Cited by 1
“Prevalence of antimicrobial resistance in MG, especially of macrolides, is rapidly increasing.(3) Coinfections of MG with other bacterial STIs have been frequently reported, of which coinfections with Chlamydia trachomatis (CT) are most commonly described, where ~10% of CT-positive women are also MG-positive.”
BackgroundHakre, S., Sanders‐Buell, E., Casimier, R. O., O’Sullivan, A. M., Peel, S. A., Tovanabutra, S., Scott, P. T., & Okulicz, J. F. (2024) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofae407 · Cited by 1
“%) did not vary markedly over time [42].”
BackgroundMycoplasma genitalium retrospective audit of Northern Territory isolates from 2022
Proudmore, K., Gunathilake, M., Crawford, L. C., et al. (2024) · Communicable Diseases Intelligence · doi:10.33321/cdi.2024.48.43 · Cited by 1
Zhang, R., Chung, S. L., Lee, S. S., & Wong, N. S. (2025) · AIDS · doi:10.1097/qad.0000000000004219 · Cited by 1
Mycoplasma genitalium, en route vers la multirésistance !
Pereyre, S., & Bébéar, C. (2021) · Revue Francophone des Laboratoires · doi:10.1016/s1773-035x(21)00066-6 · Cited by 1
Waites, K. B., & Bébéar, C. (2023) · ClinMicroNow · doi:10.1002/9781683674849.mcm0065 · Cited by 1
Detection of Human Mycoplasmas and Ureaplasmas from Clinical Specimens by Culture and PCR
Bébéar, C., & Waites, K. B. (2023) · ClinMicroNow · doi:10.1002/9781683674849.cmph0017 · Cited by 1
Mycoplasma genitalium İnfeksiyonları, Tanı ve Tedavide Güncel Yaklaşımlar
Işık, M. C., & Zarakolu, P. (2022) · Flora the Journal of Infectious Diseases and Clinical Microbiology · doi:10.5578/flora.20229702
Shah, S. S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-75608-2.00197-x
Kisina, V. I., Romanova, I. V., & Guschin, A. E. (2022) · Russian Journal of Clinical Dermatology and Venereology · doi:10.17116/klinderma202221061784
Argamasilla, A. A. T., Jordán, J. M., & Moreno‐Docón, A. (2023) · Enfermedades infecciosas y microbiologia clinica (English ed ) · doi:10.1016/j.eimce.2022.04.015
Progress in the Treatment of Mycoplasma genitalium Infection
王, 芋. (2023) · Advances in Clinical Medicine · doi:10.12677/acm.2023.13122663
Engage, L. D. L., Lê, A.-S., Labbé, A., et al. (2023) · Relevé des maladies transmissibles au Canada · doi:10.14745/ccdr.v49i1112a03f
Adawiyah, R. A., Vodstrcil, L. A., Bradshaw, C. S., Fairley, C. K., Zhang, L., & Ong, J. J. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4673221
Self-citationAntimicrobial resistance in genital Mycoplasmas infections
Ciccarese, G., Serviddio, G., Herzum, A., et al. (2024) · Indian Journal of Medical Microbiology · doi:10.1016/j.ijmmb.2024.100533
Palmeiro, A. G., Duarte, S., Barreto, M. R., et al. (2024) · Actas Dermo-Sifiliográficas · doi:10.1016/j.ad.2023.03.018
Non‐Syphilitic Bacterial Sexually Transmitted Diseases
Kinghorn, G. R., & Gupta, N. K. (2024) · doi:10.1002/9781119709268.rook030
Palmeiro, A. G., Duarte, S., Barreto, M. R., et al. (2024) · Actas Dermo-Sifiliográficas · doi:10.1016/j.ad.2024.03.028
Lê, A.-S., Labbé, A., Fourmigue, A., et al. (2024) · doi:10.32920/25461097
Lê, A.-S., Labbé, A., Fourmigue, A., et al. (2024) · doi:10.32920/25461097.v1
Llata, E., Tromble, E., Schumacher, C. M., et al. (2024) · Sexually Transmitted Diseases · doi:10.1097/olq.0000000000001975
Hakre, S., Sanders‐Buell, E., Casimier, R. O., O’Sullivan, A. M., Peel, S. A., Tovanabutra, S., Scott, P. T., & Okulicz, J. F. (2024) · medRxiv · doi:10.1101/2024.04.24.24306271
Sexually Transmitted Infections in People with Human Immunodeficiency Virus
Tuan, J., Goheen, M. M., Trebelcock, W. L., & Dunne, D. (2024) · Infectious Disease Clinics of North America · doi:10.1016/j.idc.2024.04.007
Waites, K. B., Ambalavanan, N., & Viscardi, R. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-79525-8.00030-5
Barazzetti, F. H., Schörner, M. A., Ribeiro, J. A., et al. (2024) · Jornal Brasileiro de Doenças Sexualmente Transmissíveis · doi:10.5327/dst-2177-8264-2024361423
Efficacy and Tolerability of Minocycline and Metronidazole for Treatment of Mycoplasma GenitaliumPreprint
Htaik, K., Vodstrcil, L. A., Plummer, E. L., et al. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.5068599
Self-citationWaites, K. B., & Bébéar, C. (2023) · ClinMicroNow · doi:10.1002/9781683670438.mcm0065
Detection of Human Mycoplasmas and Ureaplasmas from Clinical Specimens by Culture and PCR
Bébéar, C., & Waites, K. B. (2023) · ClinMicroNow · doi:10.1002/9781683670438.cmph0017
The Missing Piece: Pelvic and Abdominal Pain in a 40-Year-Old Cisgender Female
Samoriski, C. M., & DiMarco, D. (2025) · Infectious Diseases in Clinical Practice · doi:10.1097/ipc.0000000000001445
Moreno‐Flores, A., Domínguez-Landesa, M., Fernández, L. S., et al. (2025) · Enfermedades infecciosas y microbiologia clinica (English ed ) · doi:10.1016/j.eimce.2025.03.012
Barairo, N., Singh, A. E., Peterson, S. W., et al. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.01553-25
Development and clinical evaluation of a novel SHERLOCK test for Mycoplasma genitalium
Omachi, R., Imai, K., Sato, A., et al. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.00445-25
Bashorun, A. O., Kotei, L., Jallow, A. F., Jawla, O., Richard-Ugwuadu, E. U., Jagana, M., Bah, L., Bah, A. T., Conteh, K., Jallow, M. S. K., et al. (2025) · PLoS ONE · doi:10.1371/journal.pone.0332842
“Macrolide resistance-associated mutations (MRAMs), predominantly associated with 23S rRNA gene mutations at A2058 and A2059, and quinolone resistance-associated mutations (QRAMs), predominantly associated with parC gene mutations (ParC S83 and D87 codons) will be measured [44–46].”
Маджарова, О. А., Тишурова, Т. В., Эйдельштейн, И. А., et al. (2025) · Репродуктивное здоровье Восточная Европа · doi:10.34883/pi.2025.15.5.015
Butcher, R., Jarju, S., Obayemi, D., Bashorun, A. O., Vasileva, H., Bransbury-Hare, H., Agboghoroma, O., Drammeh, L., Holland, M. J., Harding-Esch, E., et al. (2023) · Figshare · doi:10.6084/m9.figshare.23682150
Miller, A. K., Bennett, S. J., & Stone, O. R. (2021) · Bulletin of pioneering researches of medical and clinical science · doi:10.51847/lt1g3p9xmi
Cheng, Q., Watts, C. G., Adawiyah, R. A., Guy, R., Ong, J. J., Bradshaw, C. S., & Wiseman, V. L. (2026) · Scientific Reports · doi:10.1038/s41598-026-36992-3
“The resistance to fluoroquinolone in Australia is also rising (from 10.5 to 34.5%), likely due to the increasing use of the fluoroquinolone moxifloxacin to treat increasing numbers of macrolide resistant infections 24,25 .”
InfluentialSelf-citationAMR surveillance in Canada: Insights from the 2025 Priority Pathogen List
Abdesselam, K., Muchaal, P. K., Mishra, A., et al. (2026) · PLoS ONE · doi:10.1371/journal.pone.0341133
“While Mycoplasma genitalium is not yet included in WHO’s lists, it is categorized in the CDC’s “Watch” tier, though this assessment is based on the 2019 report, and more recent data suggest increasing global concern due to rising macrolide and fluoroquinolone resistance [56,57].”
InfluentialTreatment Approaches for Refractory Mycoplasma genitalium Infection
Tenney, R., Portillo, E., Bacic, D., et al. (2026) · Open Forum Infectious Diseases · doi:10.1093/ofid/ofag031
“However, rising macrolide, fluoroquinolone, and tetracycline resistance has eroded first and second-line options from an already limited pool of possible choices, pushing refractory M. genitalium from an exception to an expectation [4].”
Qiu, X., Chen, B., Chen, J. M., et al. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1787520
“This fi nding aligns with and extends the rationale for “ sequential therapy ” advocated in settings of high macrolide resistance (Machalek et al., 2020).”
Chen, H., Wu, Z., Yang, Q., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-9183112/v1
Matthews, L. G., Vodstrcil, L. A., Wild, N. L., et al. (2026) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiag251
“…our geographic and economic proximity to epicenters of antimicrobial resistance has significant implications for M. genitalium management in Australia, and particularly at MSHC, which receives frequent attendance by clients whose infections were acquired in Japan, China, and Korea [3, 4, 30].”
Self-citationRossotti, R., Baiguera, C., Bernasconi, D. P., Bana, N. B., Nava, A., Cavazza, G., Burastero, G. J., Rezzonico, L. F., Simoncini, E., Gennaro, E. D., et al. (2026) · Clinical Infectious Diseases · doi:10.1093/cid/ciag317
Syrym, N. S., Yespembetov, B., Kokanov, S. K., Куралбаевич, Н. А., Bulatov, Y. A., Abdimukhtar, A. R., Toleukhan, A. T., Serikbay, Y., Terebay, A. A., Anarbekova, A. M., et al. (2026) · Pathogens · doi:10.3390/pathogens15060559
“Macrolide resistance frequently exceeds 50–60% and may reach over 80% in certain populations, while fluoroquinolone resistance and dual resistance are also increasing [37–40].”
InfluentialМаджарова, О. А., Эйдельштейн, И. А., Абельская, И. С., et al. (2026) · Лабораторная диагностика Восточная Европа · doi:10.34883/pi.2026.15.2.001
Pongchaikul, P., Warintaksa, P., Jenjaroenpun, P., Opasawatchai, A., Settacomkul, R., Vivithanaporn, P., Hadratchai, S., Singsnaeh, A., Thaipisuttikul, I., Wongsurawat, T., et al. (2026) · Clinical Microbiology Reviews · doi:10.1128/cmr.00070-26
“…review and meta-analysis of 57 studies (8,966 samples from 21 countries) demonstrated that macrolide resistance-associated mutations in Mycoplasma genitalium rose from approximately 10% before 2010 to over 51% by 2016–2017, with the highest prevalence in the Western Pacific and Americas (138).”
InfluentialDrug resistance of Mycoplasma genitalium: mechanism and regional distribution
Ouyang, Y., Zhang, Y., Zhang, Y., et al. (2026) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2026.1789671
Chen, H., Wu, Z., Yang, Q., et al. (2026) · Current Microbiology · doi:10.1007/s00284-026-05065-z
“However, apart from a few cases that lead to genital tract infections and neonatal infections [1], most individuals do not develop any disease [2].”
Negasheva, E. S., Frigo, N. V., Попова, Е. С., et al. (2026) · Russian Journal of Clinical Dermatology and Venereology · doi:10.17116/klinderma202625041603
Kwon, H.-J., Jang, J., Han, J.-B., et al. (2026) · Pathogens · doi:10.3390/pathogens15090971
“MG is an established sexually transmitted pathogen associated with non-gonococcal urethritis in men and with cervicitis and pelvic inflammatory disease in women, and antimicrobial resistance complicates treatment [7–11].”
Raccagni, A. R., Micheli, G., Lolatto, R., et al. (2026) · Sexually Transmitted Infections · doi:10.1136/sextrans-2026-057137
Cetatean, R., Foschi, C., Lazzarotto, T., et al. (2026) · International Journal of STD & AIDS · doi:10.1177/09564624261498927
Barazzetti, F. H., Schörner, M. A., Filho, V. B., et al. (2026) · Revista do Instituto de Medicina Tropical de São Paulo · doi:10.1590/s1678-9946202668070
Metadata
- Authors
- Machalek, D. A., Tao, Y., Shilling, H., Jensen, J. S., Unemo, M., Murray, G., Chow, E. P. F., Low, N., Garland, S. M., Vodstrcil, L. A., Fairley, C. K., Hocking, J. S., Zhang, L., & Bradshaw, C. S.
- Affiliations
- Royal Women's Hospital (AU)
- The Alfred Hospital (AU)
- Statens Serum Institut (DK)
- Örebro University (SE)
- University of Bern (CH)
- The University of Melbourne (AU)
- Corresponding author
- Machalek, Dorothy A
- ORCID
- Venue
- The Lancet Infectious Diseases
- Publisher
- Elsevier BV
- Published
- 2020-11
- Volume
- 20
- Issue
- 11
- Pages
- 1302-1314
- ISSN
- 1473-3099 (ISSN-L)
- OpenAlex
- W3038888845
- Semantic Scholar
- 121969556aa4999049ccb6b492ce88b5ce6d7302
- Cited by
- 273
- References
- 92
- Citations by year
- 2026: 22 · 2025: 32 · 2024: 56 · 2023: 61 · 2022: 50 · 2021: 36 · 2020: 16
- FWCI
- 4.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Lancet Infectious Diseases (publishedVersion)
- PubMed (publishedVersion)
- UNSWorks (UNSW Sydney) (submittedVersion, cc-by-nc-nd)
- BORIS (University Library Bern) (submittedVersion, cc-by-nc-nd)
- Open Access CRIS of the University of Bern
- Funders
- Australian Government
- Nabriva Therapeutics
- Department of Industry, Innovation and Science, Australian Government
- Seqirus
- Medical Research Council
- National Health and Medical Research Council (568971)
- Topics
- Life Sciences › Immunology and Microbiology › Microbiology › Reproductive tract infections research
- Life Sciences › Immunology and Microbiology › Microbiology › Microbial infections and disease research
- Health Sciences › Medicine › Microbiology (medical) › Antibiotic Resistance in Bacteria
- Keywords
- Mycoplasma genitalium, macrolide resistance, fluoroquinolone resistance, antimicrobial resistance, 23S rRNA mutations, parC mutations, azithromycin resistance, moxifloxacin resistance, dual resistance, sexually transmitted infections, prevalence trends, WHO regions, resistance trends, antimicrobial susceptibility testing
- MeSH terms
- Moxifloxacin, Anti-Bacterial Agents, Carrier Proteins, Female, Humans, Male, Mutation, Mycoplasma Infections, RNA, Ribosomal, 23S, Transferases, Sexually Transmitted Diseases, Bacterial, Prevalence, Azithromycin, Polymorphism, Single Nucleotide, Drug Resistance, Bacterial, Mycoplasma genitalium
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review