» Articles » PMID: 27716100

Temporal Trends of β-haemolytic Streptococcal Osteoarticular Infections in Western Norway

Overview
Journal BMC Infect Dis
Publisher Biomed Central
Date 2016 Oct 8
PMID 27716100
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Beta-haemolytic streptococci are important contributors to the global burden of osteoarticular infections (OAI). Knowledge on the disease traits specific for streptococcal OAI, however, remains scarce. We wished to explore temporal trends of OAI caused by Group A Streptococci (GAS), Group B Streptococci (GBS) and Group C and G Streptococci (GCGS), and furthermore, to describe the associated host and pathogen characteristics.

Methods: All cases of microbiologically verified β-haemolytic streptococcal OAI in Health Region Bergen, Norway, in the period 1999-2013 were retrospectively identified. Clinical data were extracted from medical records. Microbial isolates were submitted to antibiotic susceptibility testing and molecular typing.

Results: A total of 24 GAS, 45 GBS and 42 GCGS acute OAI were identified. The cumulative incidence of GCGS OAI, but not GAS or GBS OAI, increased significantly from the first to the last 5-year period (IRR 5.7, p = 0.0003), with the annual incidence peaking at 1.9/100 000 in 2013. GAS OAI generally produced the most acute and severe clinical presentation, whereas GBS and GCGS predominantly affected the elderly, and were significantly associated with the presence of host risk factors of systemic and focal origin, respectively.

Conclusions: We found a significantly increasing incidence of GCGS OAI, likely related to the presence of host susceptibility factors, including prosthetic material and pre-existing joint disease. With an increasing application of therapeutic and diagnostic bone and joint procedures, the rising trend of OAI caused by GCGS is likely to continue. Sustained epidemiological attentiveness to GCGS seems warranted.

Citing Articles

Integrative genomic, virulence, and transcriptomic analysis of emergent subspecies (SDSE) type isolates causing human infections.

Eraso J, Olsen R, Long S, Gadd R, Boukthir S, Faili A mBio. 2024; 15(11):e0257824.

PMID: 39417630 PMC: 11559094. DOI: 10.1128/mbio.02578-24.


Genomic epidemiology of subsp. strains causing invasive disease in Norway during 2018.

Kaci A, Jonassen C, Skrede S, Sivertsen A, Steinbakk M, Oppegaard O Front Microbiol. 2023; 14:1171913.

PMID: 37485526 PMC: 10361778. DOI: 10.3389/fmicb.2023.1171913.


Analysis of the Genomics and Mouse Virulence of an Emergent Clone of Streptococcus dysgalactiae Subspecies .

Beres S, Olsen R, Long S, Eraso J, Boukthir S, Faili A Microbiol Spectr. 2023; :e0455022.

PMID: 36971562 PMC: 10100674. DOI: 10.1128/spectrum.04550-22.


Streptococcus dysgalactiae Bloodstream Infections, Norway, 1999-2021.

Oppegaard O, Glambek M, Skutlaberg D, Skrede S, Sivertsen A, Kittang B Emerg Infect Dis. 2023; 29(2):260-267.

PMID: 36692331 PMC: 9881787. DOI: 10.3201/eid2902.221218.


Transcriptomic analysis of Streptococcus agalactiae periprosthetic joint infection.

Cho H, Masters T, Greenwood-Quaintance K, Johnson S, Jeraldo P, Chia N Microbiologyopen. 2021; 10(6):e1256.

PMID: 34964296 PMC: 8678771. DOI: 10.1002/mbo3.1256.


References
1.
Choi S, Rasmussen M, Hubisz M, Gronau I, Stanhope M, Siepel A . Replacing and additive horizontal gene transfer in Streptococcus. Mol Biol Evol. 2012; 29(11):3309-20. PMC: 3472495. DOI: 10.1093/molbev/mss138. View

2.
Dubost J, Soubrier M, De Champs C, Ristori J, Sauvezie B . Streptococcal septic arthritis in adults. A study of 55 cases with a literature review. Joint Bone Spine. 2004; 71(4):303-11. DOI: 10.1016/S1297-319X(03)00122-2. View

3.
Imohl M, Reinert R, Ocklenburg C, van der Linden M . Epidemiology of invasive Streptococcus pyogenes disease in Germany during 2003-2007. FEMS Immunol Med Microbiol. 2010; 58(3):389-96. DOI: 10.1111/j.1574-695X.2010.00652.x. View

4.
Schattner A, Vosti K . Bacterial arthritis due to beta-hemolytic streptococci of serogroups A, B, C, F, and G. Analysis of 23 cases and a review of the literature. Medicine (Baltimore). 1998; 77(2):122-39. DOI: 10.1097/00005792-199803000-00004. View

5.
Colavite P, Sartori A . Septic arthritis: immunopathogenesis, experimental models and therapy. J Venom Anim Toxins Incl Trop Dis. 2014; 20:19. PMC: 4017707. DOI: 10.1186/1678-9199-20-19. View