S'abonner

Population-based resistance of Mycobacterium tuberculosis isolates to pyrazinamide and fluoroquinolones: results from a multicountry surveillance project - 21/09/16

Doi : 10.1016/S1473-3099(16)30190-6 
Matteo Zignol, DrMD a, , Anna S Dean, PhD a, Natavan Alikhanova, MD b, Sönke Andres, PhD c, Andrea Maurizio Cabibbe, BA d, Daniela Maria Cirillo, MD d, Andrei Dadu, MD e, Andries Dreyer, MD f, Michèle Driesen, MSc g, Christopher Gilpin, PhD a, Rumina Hasan, MD h, Zahra Hasan, PhD h, Sven Hoffner, PhD i, j, Ashaque Husain, MD k, Alamdar Hussain, BA l, Nazir Ismail, MD f, m, Mostofa Kamal, MD n, Mikael Mansjö, BA o, Lindiwe Mvusi, MD p, Stefan Niemann, PhD c, Shaheed V Omar, PhD f, Ejaz Qadeer, MD q, Leen Rigouts, PhD g, r, Sabine Ruesch-Gerdes, PhD c, Marco Schito, PhD s, Mehriban Seyfaddinova, BA b, Alena Skrahina, MD t, Sabira Tahseen, MD l, William A Wells, PhD u, Ya Diul Mukadi, MD u, Michael Kimerling, MD v, Katherine Floyd, PhD a, Karin Weyer, PhD a, Mario C Raviglione, MD a
a Global Tuberculosis Programme, World Health Organization, Geneva, Switzerland 
b Scientific Research Institute of Lung Diseases, Baku, Azerbaijan 
c National and Supranational Reference Laboratory for Mycobacterium, Borstel, Germany 
d IRCCS San Raffaele Scientific Institute, Milan, Italy 
e Regional Office for Europe, World Health Organization, Copenhagen, Denmark 
f National Institute for Communicable Diseases, Sandringham, South Africa 
g Mycobacteriology Unit, Institute of Tropical Medicine, Antwerp, Belgium 
h Department of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan 
i Department of Microbiology, Public Health Agency of Sweden, Solna, Sweden 
j Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden 
k National Tuberculosis Control Programme, Dhaka, Bangladesh 
l National Tuberculosis Reference Laboratory, National Tuberculosis Control Programme, Islamabad, Pakistan 
m University of Pretoria, Pretoria, South Africa 
n National Institute of Diseases of the Chest and Hospital, Dhaka, Bangladesh 
o Department of Microbiology, Public Health Agency of Sweden, Solna, Sweden 
p Tuberculosis Control and Management, National Department of Health, Pretoria, South Africa 
q National Tuberculosis Control Programme, Ministry of National Health Services, Regulation and Coordination, Islamabad, Pakistan 
r Biomedical Sciences, Antwerp University, Antwerp, Belgium 
s Critical Path Institute, Tucson, AZ, USA 
t Republican Research and Practical Centre for Pulmonology and Tuberculosis, Minsk, Belarus 
u Bureau for Global Health, US Agency for International Development, Washington, DC, USA 
v KNCV Tuberculosis Foundation, The Hague, Netherlands 

* Correspondence to: Dr Matteo Zignol, Global Tuberculosis Programme, World Health Organization, Geneva, Switzerland Correspondence to: Dr Matteo Zignol Global Tuberculosis Programme World Health Organization Geneva Switzerland

Summary

Background

Pyrazinamide and fluoroquinolones are essential antituberculosis drugs in new rifampicin-sparing regimens. However, little information about the extent of resistance to these drugs at the population level is available.

Methods

In a molecular epidemiology analysis, we used population-based surveys from Azerbaijan, Bangladesh, Belarus, Pakistan, and South Africa to investigate resistance to pyrazinamide and fluoroquinolones among patients with tuberculosis. Resistance to pyrazinamide was assessed by gene sequencing with the detection of resistance-conferring mutations in the pncA gene, and susceptibility testing to fluoroquinolones was conducted using the MGIT system.

Findings

Pyrazinamide resistance was assessed in 4972 patients. Levels of resistance varied substantially in the surveyed settings (3·0–42·1%). In all settings, pyrazinamide resistance was significantly associated with rifampicin resistance. Among 5015 patients who underwent susceptibility testing to fluoroquinolones, proportions of resistance ranged from 1·0–16·6% for ofloxacin, to 0·5–12·4% for levofloxacin, and 0·9–14·6% for moxifloxacin when tested at 0·5 μg/mL. High levels of ofloxacin resistance were detected in Pakistan. Resistance to moxifloxacin and gatifloxacin when tested at 2 μg/mL was low in all countries.

Interpretation

Although pyrazinamide resistance was significantly associated with rifampicin resistance, this drug may still be effective in 19–63% of patients with rifampicin-resistant tuberculosis. Even though the high level of resistance to ofloxacin found in Pakistan is worrisome because it might be the expression of extensive and unregulated use of fluoroquinolones in some parts of Asia, the negligible levels of resistance to fourth-generation fluoroquinolones documented in all survey sites is an encouraging finding. Rational use of this class of antibiotics should therefore be ensured to preserve its effectiveness.

Funding

Bill & Melinda Gates Foundation, United States Agency for International Development, Global Alliance for Tuberculosis Drug Development.

Le texte complet de cet article est disponible en PDF.

Plan


© 2016  The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY license. Publié par Elsevier Masson SAS. Tous droits réservés.
Ajouter à ma bibliothèque Retirer de ma bibliothèque Imprimer
Export

    Export citations

  • Fichier

  • Contenu

Vol 16 - N° 10

P. 1185-1192 - octobre 2016 Retour au numéro
Article précédent Article précédent
  • Reducing unnecessary antibiotic use in the neonatal intensive care unit (SCOUT): a prospective interrupted time-series study
  • Joseph B Cantey, Phillip S Wozniak, Jessica E Pruszynski, Pablo J Sánchez
| Article suivant Article suivant
  • Global burden of drug-resistant tuberculosis in children: a mathematical modelling study
  • Peter J Dodd, Charalambos Sismanidis, James A Seddon

Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.

Déjà abonné à cette revue ?

Mon compte


Plateformes Elsevier Masson

Déclaration CNIL

EM-CONSULTE.COM est déclaré à la CNIL, déclaration n° 1286925.

En application de la loi nº78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés, vous disposez des droits d'opposition (art.26 de la loi), d'accès (art.34 à 38 de la loi), et de rectification (art.36 de la loi) des données vous concernant. Ainsi, vous pouvez exiger que soient rectifiées, complétées, clarifiées, mises à jour ou effacées les informations vous concernant qui sont inexactes, incomplètes, équivoques, périmées ou dont la collecte ou l'utilisation ou la conservation est interdite.
Les informations personnelles concernant les visiteurs de notre site, y compris leur identité, sont confidentielles.
Le responsable du site s'engage sur l'honneur à respecter les conditions légales de confidentialité applicables en France et à ne pas divulguer ces informations à des tiers.


Tout le contenu de ce site: Copyright © 2024 Elsevier, ses concédants de licence et ses contributeurs. Tout les droits sont réservés, y compris ceux relatifs à l'exploration de textes et de données, a la formation en IA et aux technologies similaires. Pour tout contenu en libre accès, les conditions de licence Creative Commons s'appliquent.