Cross-resistance to lincosamides, streptogramins A and pleuromutilins in Streptococcus agalactiae isolates from the USA

• Published in: Journal of antimicrobial chemotherapy 2017-07, Vol.72 (7), p.1886-1892
• Main Authors: Hawkins, Paulina A, Law, Caitlin S, Metcalf, Benjamin J, Chochua, Sopio, Jackson, Delois M, Westblade, Lars F, Jerris, Robert, Beall, Bernard W, McGee, Lesley
• Format: Article
• Language: English
• Subjects: Adult; Anti-Bacterial Agents - pharmacology; Child; Clindamycin - pharmacology; Diterpenes - pharmacology; Drug Resistance, Multiple, Bacterial - genetics; Epidemiological Monitoring; Erythromycin - pharmacology; Female; Humans; Infant; Infant, Newborn; Lincosamides - pharmacology; Microbial Sensitivity Tests; Phenotype; Pleuromutilins; Polycyclic Compounds; Pregnancy; Streptococcal Infections - drug therapy; Streptococcal Infections - epidemiology; Streptococcal Infections - microbiology; Streptococcus agalactiae - drug effects; Streptococcus agalactiae - genetics; Streptococcus agalactiae - isolation & purification; Streptogramins - pharmacology; United States - epidemiology; Young Adult
• ISSN: 0305-7453; 1460-2091
• DOI: 10.1093/jac/dkx077

Streptococcus agalactiae (Group B Streptococcus, GBS) is a leading cause of meningitis, sepsis and pneumonia in neonates in the United States. GBS also causes invasive disease in older infants, pregnant women, children and young adults with underlying medical conditions, and older adults. Resistance to lincosamides in the absence of erythromycin resistance is rare in GBS, but has been previously reported in clinical isolates, both on its own or in combination with resistance to streptogramins A and pleuromutilins (L/LSA/LSAP phenotypes). To retrospectively screen the Active Bacterial Core surveillance (ABCs) GBS isolate collection for these phenotypes in order to identify the causal genetic determinants and determine whether their frequency is increasing. Based on MIC data, 65 (0.31%) isolates susceptible to erythromycin (MIC ≤0.25 mg/L) and non-susceptible to clindamycin (MIC ≥0.5 mg/L) were identified among 21 186 GBS isolates. Genomic DNA was extracted and WGS was performed. The presence of 10 genes previously associated with LSA resistance was investigated by read mapping. Forty-nine (75%) isolates carried the lsa (C) gene and expressed the LSAP phenotype, and 12 (18%) carried both the lnu (B) and lsa (E) genes and expressed the LSAP phenotype. The four remaining isolates were negative for all determinants investigated. While the overall observed frequency of these phenotypes among our GBS isolates was quite low (0.31%), this frequency has increased in recent years. To the best of our knowledge, this is the first time the LSAP phenotype has been reported among GBS isolates from the USA.