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Repository series · ncbi-prjeb70279

Genomic insights into the diversity, virulence, and resistance of Group B Streptococcus Clinical isolates from Saudi Arabia

Saudi ArabiaPathogen genomics and infectious diseaseRepository record

Detailed assessment of the population structure of Group B Streptococcus (GBS) among adults is still lacking in Saudi Arabia. Genome sequencing of a representative collection of GBS isolates (n = 89) from colonized and infected adults revealed high genetic diversity, represented by 28 sequence types (STs) and nine distinct serotypes, including uncommon serotypes VII and VIII. The majority of STs (n = 76) belonged to the human-associated clonal complexes (CCs) CC1 (33.71%), CC19 (25.84%), CC17 (11.24%), CC10/CC12 (7.87%), and CC452 (6.74%). Major CCs exhibited intra-lineage serotype diversity, except for hypervirulent CC17, which exclusively expressed serotype III. Virulence profiling revealed that nearly all isolates (94.38%) carried at least one of the four alpha family protein genes (alphaC, alp1, alp2/3, and rib), and 92.13% expressed one of the two serine-rich repeat surface proteins Srr1 or Srr2. In addition, most isolates harbored the pilus island (PI)-2a alone (15.73%) or in combination with PI-1 (62.92%), and those carrying PI-2b alone (10.11%) belonged to CC17. Phylogenetic analysis grouped the sequenced isolates according to CCs and further subdivided them along with their serotypes. Overall, isolates across all CC1 phylogenetic clusters expressed Srr1 and carried the PI-1 and PI-2a loci, but differed in genes encoding alpha-like proteins. CC19 clusters were dominated by the III/rib/srr1/PI-1+PI-2a (43.48%, 10/23) and V/alp1/srr1/PI-1+PI-2a (34.78%, 8/23) lineages, whereas most CC17 isolates (90%, 9/10) had the same III/rib/srr2/P1-2b genetic background. Interestingly, genes encoding the CC17-specific adhesins HvgA and Srr2 were detected in phylogenetically distant isolates belonging to ST1212, suggesting that other highly virulent strains might be circulating within the species. In contrast, the spread of resistance to macrolides and/or lincosamides across all major CCs (n = 48) was associated with the acquisition of erm(B) (62.5%, 30/48), erm(A) (27.1%, 13/48), lsa(C) (8.3%, 4/48), and mef(A) (2.1%, 1/48) genes, whereas resistance to tetracycline was largely mediated by the presence of tet(M) (64.18%, 43/67) and tet(O) (20.9%, 14/67) alone or in combination (13.43%, 9/67). Resistance to erythromycin, gentamicin, levofloxacin, and tetracycline was detected in only three ST19 isolates. These findings underscore the necessity for a more rigorous characterization of GBS isolates causing infections.

Repository interpretation

The accession and its GCC connection are verified. Registration alone does not establish that the broader research programme remains active.

01 / Project overview

What the record establishes.

Geographic scope
Saudi Arabia connection indexed in BioProject metadata
Project type
Repository project
Research domain
Pathogen genomics and infectious disease
Years
2024–
Lifecycle status
repository_recorded
Status basis
Registered in NCBI BioProject on 2024/04/11; operational lifecycle is not asserted.
Status evidence date
2024-04-11
Scale
1 BioProject accession grouped by matching submitter, date, data type and narrative.

02 / Organizations and population

Who and what the project connects.

Lead organizations
King Saudi University
Partner organizations
Not stated
Organism / population
Not stated

03 / Data and access

What exists and how it can be reached.

Data types

  • Other
  • Sequencing
  • Genome

Data access

Public repository metadata with linked data where supplied by the submitter

Identifiers

  • BioProjectPRJEB70279

04 / Evidence and provenance

Why the record is included.

Inclusion basis

Exact country-name match in authoritative NCBI BioProject metadata; repeated submissions are grouped into one Atlas series.

Editorial note

Repository verification confirms the accession and regional connection, not whether the broader research programme remains active.

Sources

  1. primary record source Verified 2026-08-15

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