Influence of Sub-Inhibitory Dosage of Cefotaxime on Multidrug Resistant Staphylococcus haemolyticus Isolated from Sick Neonatal Care Unit.
Madhurima ChakrabortyTaniya BardhanManjari BasuBornali BhattacharjeePublished in: Antibiotics (Basel, Switzerland) (2022)
Staphylococcus haemolyticus has emerged to be a frequently encountered late-onset sepsis pathogen among newborn infants. Critical care of neonates involves substantial usage of antibiotics and these pathogens are often exposed to sub-optimal doses of antibiotics which can augment maintenance of selection determinants and a range of physiological effects, prime among them being biofilm formation. Therefore, in this study, the outcome of a sub-inhibitory dosage of a commonly prescribed third-generation antibiotic, cefotaxime (CTX), on multidrug resistant (MDR) S. haemolyticus , was investigated. A total of 19 CTX-resistant, MDR and 5 CTX-susceptible strains isolated from neonates were included. Biofilm-forming abilities of S. haemolyticus isolates in the presence of sub-optimal CTX (30 μg/mL) were determined by crystal violet assays and extracellular DNA (eDNA) quantitation. CTX was found to significantly enhance biofilm production among the non-susceptible isolates ( p -value Wilcoxintest -0.000008) with an increase in eDNA levels ( p -value Wilcoxintest -0.000004). Further, in the absence of antibiotic selection in vitro, populations of MDR isolates, JNM56C1 and JNM60C2 remained antibiotic non-susceptible after >500 generations of growth. These findings demonstrate that sub-optimal concentration of CTX induces biofilm formation and short-term non-exposure to antibiotics does not alter non-susceptibility among S. haemolyticus isolates under the tested conditions.
Keyphrases
- biofilm formation
- multidrug resistant
- klebsiella pneumoniae
- candida albicans
- pseudomonas aeruginosa
- gram negative
- escherichia coli
- staphylococcus aureus
- drug resistant
- late onset
- acinetobacter baumannii
- genetic diversity
- early onset
- ms ms
- healthcare
- intensive care unit
- quality improvement
- low birth weight
- circulating tumor
- pain management
- septic shock
- nucleic acid