Evidence map›Paper›PMID 36315595›Full record

ArticleThe Journal of antimicrobial chemotherapy2022

Development and validation of a resazurin assay for in vitro susceptibility testing of Actinomadura madurae: a common causative agent of actinomycetoma.

S O Abd Algaffar, A Verbon, S A Khalid, W W J van de Sande

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Article in The Journal of antimicrobial chemotherapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

S O Abd AlgaffarFaculty of Pharmacy, University of Science & Technology, Omdurman, Sudan.
A VerbonDepartment of Medical Microbiology and Infectious Diseases, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.
S A KhalidFaculty of Pharmacy, University of Science & Technology, Omdurman, Sudan.ORCID 0000-0002-2511-7040
W W J van de SandeDepartment of Medical Microbiology and Infectious Diseases, Erasmus MC, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID 0000-0002-8652-8783

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesActinomycetoma is a chronic granulomatous disease affecting skin, subcutaneous tissue, fascia, muscle and bones. With increasing resistance against commonly used treatment regimens, susceptibility testing is urgently needed.

methodsWe developed an in vitro susceptibility assay for Actinomadura madurae, one of the common causative agents of actinomycetoma, employing resazurin for endpoint reading. Using this assay, reproducible MICs were determined for the most commonly used antibacterial agents for actinomycetoma treatment. The tested antibacterial agents included trimethoprim/sulfamethoxazole, amikacin, streptomycin, amoxicillin, ceftriaxone, gentamicin, ciprofloxacin, doxycycline, imipenem, linezolid, penicillin G and rifampicin.

resultsFollowing the clinical breakpoints as stated by CLSI, 100% of the tested strains were susceptible to trimethoprim/sulfamethoxazole (MIC 0.03/0.59-1/19 mg/L), amikacin (MIC 0.0078-0.25 mg/L), doxycycline (MIC <0.25-1 mg/L) and linezolid (MIC <0.25-2 mg/L), 90% to ciprofloxacin (MIC <0.25-2 mg/L), 80% to ceftriaxone (MIC <0.5 to >64 mg/L) and imipenem (MIC <0.25-32 mg/L) and only 20% to amoxicillin (MIC <0.5 to >64 mg/L) and rifampicin (MIC 0.5 to >32 mg/L).

conclusionsDeterminations of MICs by visual readings of colour changes versus spectrophotometric readings were comparable. This convenient visual reading has the advantage of feasible implementation in endemic settings.

Indexed as

AmikacinMycetomaActinomaduraAmoxicillinAnti-Bacterial AgentsCeftriaxoneCiprofloxacinDoxycyclineHumansIfosfamideImipenemLinezolidMicrobial Sensitivity TestsOxazinesRifampinTrimethoprim, Sulfamethoxazole Drug CombinationAmikacinAmoxicillinAnti-Bacterial AgentsCeftriaxoneCiprofloxacinDoxycyclineIfosfamideImipenemLinezolidOxazinesresazurinRifampinTrimethoprim, Sulfamethoxazole Drug CombinationXanthenes

Identifiers

PMID36315595
PMCPMC9780526

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.