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Rabenandrasana, M. A. N.

Publications and source records attributed to Rabenandrasana, M. A. N..

2 recordsLinked to original sources

Antimicrobial Susceptibility Profile of Neisseria gonorrhoeae from Patients Attending a Medical Laboratory, Institut Pasteur de Madagascar between 2014-2020: Phenotypic and Genomic characterization in a Subset of Neisseria gonorrhoeae Isolates.

2The antimicrobial resistance of Neisseria gonorrhoea to all classes of current available antibiotics is a global concern. National surveillance programmes monitoring the susceptibility profiles of Neisseria gonorrhoeae hardly exist in resource constraint settings. Therefore, little is known about the antimicrobial susceptibility profile and associated genetic resistance mechanisms of N. gonorrhoeae in Madagascar. We report susceptibility data of N. gonorrhoeae isolates obtained by the medical laboratory of the Institut Pasteur de Madagascar, from 2014 -2020. In addition, we present data on the antimicrobial resistance mechanisms and antimicrobial resistance profile of a subset of isolates (N=46), including all isolates available of 2020. Over the study period, ceftriaxone resistant isolates exceeding the threshold of 5% in 2017 and 2020, were reported. Of the subset of re-tested isolates, all were found susceptible to ceftriaxone, azithromycin, and spectinomycin. Conversely, all isolates were resistant to ciprofloxacin and the majority was also resistant to penicillin and tetracycline. None of the isolates carried the mosaic penA gene and chromosomal mutations associated to the antibiotic resistance in gyrA, parC, penA, ponA, porB and mtrR genes were detected. The high rate of resistance to Penicillin and Tetracycline is explained by the presence of {beta}-lactamase blaTEM and tetM genes, respectively, a plasmid mediated resistance. We found a high number of circulating multilocus sequence types. Almost half of them were new types, and one of them was among the four most predominant sequence types. Our report provides a detailed dataset obtained through phenotypic and genotypic methods which will serve as baseline for future surveillance of N. gonorrhoeae in our setting, and Madagascar. 1.5 RepositoriesThis Whole Genome Shotgun project has been deposited at DDBJ/ENA/GenBank under the Accession BioProject PRJNA929018. 3 Impact statementNeisseria gonorrhoeae is becoming increasingly resistant to all classes of antibiotics available for infections treatment. Resource constraint settings encounter difficulties in implementing surveillance of the antimicrobial susceptibility of N. gonorrhoeae. We report here antimicrobial susceptibility results from gonorrhoea among patients consulting a medical laboratory in Antananarivo, Madagascar in 2014-2020. We used whole-genome sequencing to identify resistance mechanisms in a subset of isolates including all viable isolates of 2020. We report multilocus sequence types and discuss phenotypes and genotypes according to the phylogenetic analysis of the isolates. The susceptibility results are the first in a decade to be reported. We set the baseline to study further the evolution and transmission of N. gonorrhoeae resistance mechanisms and genotypes in general. Our report will enable improving surveillance of Neisseria gonorrhoeae in Madagascar and Africa. Overall, it will contribute to the global, regional, and national surveillance of N. gonorrhoeae. In addition, it may set a benchmark for implementation in other settings facing barriers implementing phenotypic resistance surveillance of N. gonorrhoeae. 4 Data summaryThe source code of the Tormes pipeline used in this study is also available on Github: https://github.com/nmquijada/tormes. The SRA sequences have been deposited in the NCBI SRA database under accession numbers SRR23260223 and SRR23260193. The genome assemblies can be accessed using the accession numbers: SAMN32949360 - SAMN32949405. The MLST genes of all isolates can be accessed through this link: https://doi.org/10.5281/zenodo.7581537 The Perl scripts used for a quality filtering of the assemblies which is to remove small contigs can be accessed through the following link: https://github.com/Alainnoah/Remove-Small-Contigs-Draft-Assemblies. Genomic analysis with metadata in Pathogenwatch could be accessed with this link: https://pathogen.watch/collection/f7t4wjtjlybh-mdgwhofa A visualization of genomic epidemiology of our isolates with Microreact can be accessed with this link: https://microreact.org/project/7FADQYwhm5h1zJyJTynM6R-unnamed-project A supplementary material in an Excel sheet summarizing the lists of plasmids used for alignment (Table S1), the statistics of the sequences (Table S2), and the minimum inhibitory concentration values of N. gonorrhoeae isolates and their antimicrobial resistance genetic mechanisms (Table S3) is available through this link: https://doi.org/10.6084/m9.figshare.21973511

microbiology↗

Clonal transmission and new mechanism of resistance to trimethoprim-sulfamethoxazole in Stenotrophomonas maltophilia strains isolated in a neonatology unit at Antananarivo, Madagascar, deciphered by whole genome sequence analysis

Stenotrophomonas maltophilia has been recognized as an emerging multidrug resistant organism in hospital settings due to its resistance to a broad range of antimicrobial agents. These include {beta}-lactams and aminoglycosides, afforded by the existence of intrinsic and acquired resistance mechanisms. Trimethoprim/sulfamethoxazole (SXT) is recommended as one of the best treatment choices against S. maltophilia infections; however increasing resistance to SXT has complicated the treatment. From July 2014 to March 2015, individuals and surfaces from a neonatology ward in Antananarivo, Madagascar, were longitudinally followed to assess the transmission of bacteria resistant to antibiotics between neonates, individuals (parents and nurses) and ward environments. Four S. maltophilia strains were successively isolated from a water-tap (N=1), from feces obtained from a newborn (N=1), and nursing staff (N=2). Antimicrobial susceptibility testing and whole genome sequencing were performed on each isolate. Based on coregenome alignment, all strains were identical and belonged to the new sequence type ST-288. They were resistant to trimethoprim-sulfamethoxazole, carbapenems and intermediate to levofloxacin. Each isolate carried the aadB, strA, strB and sul1 genes located in a class I integron but variants of the dfrA gene were absent. We assessed by PROVEAN analysis the single nucleotide mutations found in folA, folC and folM genes and only the mutation in folA (A114T:GCC[->]ACC) has an effect on the activity of trimethoprim. Our findings demonstrated the prolonged presence of SXT-resistant S. maltophilia in a clinical setting with consecutive transfers from the environment to a newborn and staff based on the isolation dates. We also hypothesized that single nucleotide mutations in folA could be responsible for trimethoprim resistance.

microbiology↗