Mahamat O. O., Tidjani A., Lounnas Manon, Hide M., Benavides J., Somasse C., Ouedraogo A. S., Sanou S., Carriere C., Banuls Anne-Laure, Jean-Pierre H., Dumont Y., Godreuil S. (2019). Fecal carriage of extended-spectrum beta-lactamase-producing Enterobacteriaceae in hospital and community settings in Chad. Antimicrobial Resistance and Infection Control, 8 (1), art. 169 [7 p.]. ISSN 2047-2994.
Titre du document
Fecal carriage of extended-spectrum beta-lactamase-producing Enterobacteriaceae in hospital and community settings in Chad
Année de publication
2019
Auteurs
Mahamat O. O., Tidjani A., Lounnas Manon, Hide M., Benavides J., Somasse C., Ouedraogo A. S., Sanou S., Carriere C., Banuls Anne-Laure, Jean-Pierre H., Dumont Y., Godreuil S.
Source
Antimicrobial Resistance and Infection Control, 2019,
8 (1), art. 169 [7 p.] ISSN 2047-2994
Background Fecal carriage of extended-spectrum beta-lactamase-producing Enterobacteriaceae (ESBL-PE) remains poorly documented in Africa. The objective of this study was to determine the prevalence of ESBL-PE fecal carriage in Chad. Methods In total, 200 fresh stool samples were collected from 100 healthy community volunteers and 100 hospitalized patients from January to March 2017. After screening using ESBL-selective agar plates and species identification by MALDI-TOF mass spectrometry, antibiotic susceptibility was tested using the disk diffusion method, and ESBL production confirmed with the double-disc synergy test. The different ESBL genes in potential ESBL-producing isolates were detected by PCR and double stranded DNA sequencing. Escherichia coli phylogenetic groups were determined using a PCR-based method. Results ESBL-PE fecal carriage prevalence was 44.5% (51% among hospitalized patients vs 38% among healthy volunteers; p < 0.05). ESBL-producing isolates were mostly Escherichia coli (64/89) and Klebsiella pneumoniae (16/89). PCR and sequencing showed that 98.8% (87/89) of ESBL-PE harbored bla(CTX-M) genes: bla(CTX-M-15) in 94.25% (82/87) and bla(CTX-M)-(14) in 5.75% (5/87). Phylogroup determination by quadruplex PCR indicated that ESBL-producing E. coli isolates belonged to group A (n = 17; 27%), C (n = 17; 27%), B2 (n = 9; 14%), B1 (n = 8; 13%), D (n = 8; 13%), E (n = 1; 1.6%), and F (n = 1; 1.6%). The ST131 clone was identified in 100% (9/9) of E. coli B2 strains. Conclusions The high fecal carriage rate of ESBL-PE associated with CTX-M-15 in hospital and community settings of Chad highlights the risk for resistance transmission between non-pathogenic and pathogenic bacteria.
Plan de classement
Santé : généralités [050]
;
Biotechnologies [084]
Description Géographique
TCHAD
Localisation
Fonds IRD [F B010077299]
Identifiant IRD
fdi:010077299
