# Nosocomial Pneumonia in Georgia: A Focus on Gram-Positive Bacteria and Antimicrobial Resistance

**Authors:** Giorgi Mgeladze, Giorgi Akhvlediani, Shorena Khetsuriani, Giorgi Maisuradze, Vakhtang Robakidze, Shota Mrelashvili, Ani Papiashvili

PMC · DOI: 10.7759/cureus.77710 · 2025-01-20

## TL;DR

This study examines the prevalence and antibiotic resistance of gram-positive bacteria causing hospital-acquired pneumonia in Georgia, emphasizing the need for better infection control and antibiotic use.

## Contribution

The study provides new insights into the local epidemiology and resistance patterns of gram-positive bacteria in Georgia's nosocomial pneumonia cases.

## Key findings

- Staphylococcus aureus was the most common gram-positive pathogen, with high rates of methicillin and macrolide resistance.
- Streptococcus pneumoniae showed nearly complete beta-lactam resistance and significant macrolide and tetracycline resistance.
- Vancomycin-resistant isolates were identified, indicating the emergence of multidrug-resistant strains in Georgia.

## Abstract

Nosocomial pneumonia represents a significant clinical challenge worldwide, and in Georgia, the burden of this healthcare-associated infection is a growing concern. This study investigates the role of gram-positive bacteria in nosocomial pneumonia cases, focusing on their prevalence, antimicrobial resistance patterns, and associated risk factors. A retrospective analysis of 484 clinical samples collected from 397 patients between May 2022 and September 2024 highlights the distribution of pathogens, with a particular emphasis on Staphylococcus aureus and Streptococcus pneumoniae. Among gram-positive pathogens, Staphylococcus aureus was the most prevalent, accounting for 103 cases (21.3%), followed by Streptococcus pneumoniae with 45 cases (9.3%).

The study identifies alarming rates of antimicrobial resistance among gram-positive pathogens. Staphylococcus aureus isolates demonstrated universal penicillinase production (103/103, 100%) and high levels of mecA-mediated methicillin resistance (89/103, 86.4%) and erm-mediated macrolide resistance (74/103, 71.8%). Additionally, notable resistance was observed to tetracycline (93/103, 90.3%), aminoglycosides (31/103, 30.1%), and fluoroquinolones (41/103, 39.8%). Streptococcus pneumoniae isolates exhibited universal penicillinase production (45/45, 100%), with complete beta-lactam resistance found in 42 isolates (42/45, 93.3%), mediated through mutations in the pbp1a, pbp2x, and pbp2b genes. Furthermore, erm(B)-mediated macrolide resistance was observed in 37 isolates (37/45, 82.2%), tetM-mediated tetracycline resistance in 37 isolates (37/45, 82.2%), and fluoroquinolone resistance in 13 isolates (13/45, 28.9%). One isolate of each pathogen demonstrated vancomycin resistance, underscoring the emergence of multidrug-resistant (MDR) strains.

The study underscores the need for stringent infection control measures and rational antibiotic stewardship to mitigate the impact of resistant gram-positive pathogens in Georgian healthcare settings. The findings also stress the importance of continuous surveillance to monitor resistance trends and guide empirical therapy. By exploring the resistance mechanisms and prevalence of gram-positive bacteria in nosocomial pneumonia, this research contributes to a deeper understanding of the local epidemiology and highlights actionable insights for improving patient outcomes.

## Linked entities

- **Genes:** mecA (adaptor protein controlling oligomerization of the AAA+ protein ClpC) [NCBI Gene 936406], ETV5 (ETS variant transcription factor 5) [NCBI Gene 2119], pbp1A (multimodular transpeptidase-transglycosylase PBP 1A) [NCBI Gene 7331562], pbp2x (penicillin-binding protein PBP2X) [NCBI Gene 8154688], pbp2b (penicillin-binding protein PBP2B) [NCBI Gene 8155001], erm(B) (23S rRNA (adenine(2058)-N(6))-methyltransferase Erm(B)) [NCBI Gene 8154416], tet(M) (tetracycline resistance ribosomal protection protein Tet(M)) [NCBI Gene 8154447]
- **Chemicals:** tetracycline (PubChem CID 54675776), vancomycin (PubChem CID 14969)
- **Species:** Staphylococcus aureus (taxon 1280), Streptococcus pneumoniae (taxon 1313)

## Full-text entities

- **Diseases:** Nosocomial Pneumonia (MESH:D000077299), infection (MESH:D007239)
- **Chemicals:** tetracycline (MESH:D013752), fluoroquinolone (MESH:D024841), methicillin (MESH:D008712), beta-lactam (MESH:D047090), macrolide (MESH:D018942), vancomycin (MESH:D014640), aminoglycosides (MESH:D000617)
- **Species:** Homo sapiens (human, species) [taxon 9606], Streptococcus pneumoniae (species) [taxon 1313], Staphylococcus aureus (species) [taxon 1280]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11837978/full.md

---
Source: https://tomesphere.com/paper/PMC11837978