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Updated: Apr 26, 2026

Nanomechanics of Drug-target Interactions and Antibacterial Resistance Detection
Published on: October 25, 2013
vanG element insertions within a conserved chromosomal site conferring vancomycin resistance to Streptococcus
Velusamy Srinivasan1, Benjamin J Metcalf1, Kristen M Knipe2
1Centers for Disease Control and Prevention, Division of Bacterial Diseases, Respiratory Diseases Branch, Atlanta, Georgia, USA.
Abstract:
Three vancomycin-resistant streptococcal strains carrying vanG elements (two invasive Streptococcus agalactiae isolates [GBS-NY and GBS-NM, both serotype II and multilocus sequence type 22] and one Streptococcus anginosus [Sa]) were examined. The 45,585-bp elements found within Sa and GBS-NY were nearly identical (together designated vanG-1) and shared near-identity over an ~15-kb overlap with a previously described vanG element from Enterococcus faecalis. Unexpectedly, vanG-1 shared much less homology with the 49,321-bp vanG-2 element from GBS-NM, with widely different levels (50% to 99%) of sequence identity shared among 44 related open reading frames. Immediately adjacent to both vanG-1 and vanG-2 were 44,670-bp and 44,680-bp integrative conjugative element (ICE)-like sequences, designated ICE-r, that were nearly identical in the two group B streptococcal (GBS) strains. The dual vanG and ICE-r elements from both GBS strains were inserted at the same position, between bases 1328 and 1329, within the identical RNA methyltransferase (rumA) genes. A GenBank search revealed that although most GBS strains contained insertions within this specific site, only sequence type 22 (ST22) GBS strains contained highly related ICE-r derivatives. The vanG-1 element in Sa was also inserted within this position corresponding to its rumA homolog adjacent to an ICE-r derivative. vanG-1 insertions were previously reported within the same relative position in the E. faecalis rumA homolog. An ICE-r sequence perfectly conserved with respect to its counterpart in GBS-NY was apparent within the same site of the rumA homolog of a Streptococcus dysgalactiae subsp. equisimilis strain. Additionally, homologous vanG-like elements within the conserved rumA target site were evident in Roseburia intestinalis. Importance: These three streptococcal strains represent the first known vancomycin-resistant strains of their species. The collective observations made from these strains reveal a specific hot spot for insertional elements that is conserved between streptococci and different Gram-positive species. The two GBS strains potentially represent a GBS lineage that is predisposed to insertion of vanG elements.
Insights
Three vancomycin-resistant streptococcal strains were identified, revealing a conserved insertion hot spot for vanG elements across Gram-positive species. This finding suggests a predisposition in certain group B Streptococcus lineages to vancomycin resistance acquisition.
Area of Science:
- Microbiology
- Genetics
- Antimicrobial Resistance
Background:
- Vancomycin resistance is a growing public health concern.
- Streptococcal species are significant human pathogens.
- Understanding the genetic basis of vancomycin resistance is crucial for developing new treatments.
Purpose of the Study:
- To characterize the genetic elements responsible for vancomycin resistance in three novel streptococcal strains.
- To investigate the insertion sites and mechanisms of vanG element acquisition.
- To identify conserved genomic regions associated with antimicrobial resistance.
Main Methods:
- Whole-genome sequencing of vancomycin-resistant Streptococcus agalactiae and Streptococcus anginosus strains.
- Comparative genomic analysis of vanG and integrative conjugative element (ICE)-like sequences.
- Identification of insertion sites within the RNA methyltransferase (rumA) gene.
Main Results:
- Identified three vancomycin-resistant streptococcal strains, including the first reported for their species.
- Characterized two distinct vanG elements (vanG-1 and vanG-2) and nearly identical ICE-r elements.
- Discovered a conserved insertion hot spot within the rumA gene, shared across streptococci and other Gram-positive bacteria.
- Found that sequence type 22 group B Streptococcus strains harbor related ICE-r derivatives at this site.
Conclusions:
- The identified strains represent novel vancomycin-resistant streptococci.
- A conserved rumA gene locus acts as a hot spot for vanG and ICE-r element insertion.
- Certain group B Streptococcus lineages may be prone to acquiring vancomycin resistance via these elements.
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