Beta-Haemolytic Group A, C and G Streptococcal Infections in Southern Hungary: A 10-Year Population-Based Retrospective Survey (2008–2017) and a Review of the Literature

Introduction

Pyogenic β-hemolytic streptococci (consisting of Streptococcus pyogenes [Group A Streptococcus; GAS], S. agalactiae [Group B Streptococcus], S. dysgalactiae subsp. equisimilis (SDSE; relevant in human disease) and S. dysgalactiae subsp. dysgalactiae (SDSD; relevant in animal disease) [Group C and Group G Streptococcus; GCS and GGS]) are some of the most important Gram-positive bacterial pathogens in human medicine, especially in the paediatric population.^1–5 Streptococci were classified according to the Lancefield-grouping, a system based on the composition of the cell wall antigens;⁶ although some believe that this classification has outlived its usefulness in the era of whole genome sequencing (WGS), Lancefield-grouping is still frequently used in routine clinical practice.⁷

GAS and GCS/GGS species are taxonomically very close, with a 72% sequence similarity; in addition, these bacteria share many virulence factors (eg, the M protein, encoded by the emm genes, surface proteins, fibronectin (Fn)-binding proteins, streptolysin S and streptolysin O).^8–11 Due to their pronounced tissue tropism, GAS and GCS/GGS isolates frequently occur as colonizers of the skin, oropharynx, alimentary tract and genito-urinary region.¹² In fact, a recent meta-analysis has reported that the prevalence of GAS carriage in children was 12%, while other report concluded that GCS/GGS carriage in all age groups was around 4%; however, carriage rates may vary greatly based on seasonality and different geographical regions.^13,14 Nevertheless, they are also highly pathogenic, capable of causing a wide spectrum of illnesses, being an important factor of morbidity and mortality.¹⁵ Mild manifestations may include tonsillo-pharyngitis (“strep throat”), wound infections and impetigo,¹⁶ while severe infections, such as scarlet fever,¹⁷ endophthalmitis,¹⁸ mastoiditis,¹⁹ septic arthritis,²⁰ osteomyelitis,²¹ necrotizing fasciitis,²² puerperal infections,²³ bacteremia and sepsis,²⁴ meningitis,²⁵ endocarditis,²⁶ and streptococcal toxic shock syndrome (STSS)²⁷ may also occur. In addition, clinicians must take into consideration the emergence of post-streptococcal manifestations, such as rheumatic fever, rheumatic heart disease, glomerulonephritis and other immune-mediated complications.²⁸

Although effective therapy is available, invasive streptococcal infections are associated with a significant disease burden, estimated at >500,000 worldwide deaths annually.^29–32 In the United States, GAS is responsible for 1–2.5 million cases of tonsillo-pharyngitis, 12,000–25,000 invasive infections and around 1250–2000 deaths, according to the CDC database. While the importance of GAS in human infections is well-known, the importance of GCS/GGS species has only been studied extensively in recent times.³³ This may be attributed to novel technical developments in clinical microbiology, in addition to the growing number of people in immunocompromised state, at higher risk for GCS/GGS infections.³⁴ Several reports have highlighted the role of GCS/GGS in severe, invasive infections: in fact, GCS/GGS are responsible for 80% of invasive infections caused by non-GAS and non-GBS β-hemolytic streptococci, and in some countries, their incidence approaches that of invasive GAS infections.^35,36 Many authors have also suggested the phenomenon of epidemiological differentiation between patients affected by GAS and GCS/GGS infections, ie, the incidence of GCS/GGS infections is reported to be higher among adult patients, both in tonsillo-pharyngitis and in invasive infections, and the resistance levels associated with GCS/GGS infections have also been reported to be higher.^37,38

The long-term surveillance of streptococcal infections is important for clinical medicine and for public health purposes; however, the availability of reports from Hungary and Central/Eastern Europe is scarce. In the present study, we report the epidemiological characteristics of pharyngitis and invasive infections caused by GAS and GCS/GGS in Southern Hungary over a 10-year surveillance period (2008–2017).

Materials and Methods

Study Site and Population

The present retrospective study was carried out using epidemiological data/demographics and microbiological data collected between the period of 2008.01.01 and 2017.12.31 at the Institute of Clinical Microbiology (University of Szeged). The Institute acts as the affiliated diagnostic laboratory for the Albert Szent-Györgyi Clinical Center (ASCC), the principal primary- and tertiary-care teaching hospital in Southern Hungary and also receives microbiological samples from community-based healthcare-professionals in the region.³⁹ The Clinical Center is equipped has a bed capacity of 1820 beds (1465 acute and 355 chronic beds, respectively), according to the data of the Hungarian National Health Insurance Fund (NEAK).⁴⁰ The population of the region has decreased from 417,456 to 399,012 during the respective 10-year period, based on Eurostat data for the region. As high as 27.5% of the population lives in rural areas, while the majority of the population lives in cities/towns.

Data Collection

Electronic search in the records of the MedBakter laboratory information system (LIS) for samples positive for GAS, GCS and GGS was conducted by the authors (M.G., Á.M. and A.L.). Age and sex of the patients, date of sample submission, sample type and indication for sample submission (including preliminary diagnoses) were collected.³⁹ During data analysis, affected patients were differentiated to two age groups: 0–17 year-olds and 18 and over, based on Oppegaard et al.³⁸ Retrospective chart review of the affected patients was not performed; therefore, the incidence of chronic sequelae such as acute rheumatic fever, rheumatic heart disease or poststreptococcal glomerulonephritis was not assessed.⁴¹

Due to the very low number of group C streptococci and the fact that β-haemolytic group C and G streptococci causing human infections most frequently belong to the species SDSE, these bacteria were treated as one group (GCGS) for statistical purposes, based on Oppegaard et al.³⁸ GAS and GCGS bacteria were categorized into two groups, namely tonsillo-pharyngitis-causing GAS/GCGS (pGAS and pGCGS) and GAS/GCGS causing invasive infections (iGAS and iGCGS). Cases of iGAS and iGCGS were defined as the isolation of a Group A or Group C/G Streptococcus from a sterile site (eg, blood, cerebrospinal fluid, pleural fluid, peritoneal fluid, pericardial fluid, surgical aspirate, bone, joint fluid, or internal body site) or from a wound culture accompanied by necrotizing fasciitis (NF) or streptococcal toxic shock syndrome (STSS), based on the criteria established by Rudolph et al.⁴¹ Repeatedly positive cultures with the same organism identified within 30 days of initial isolation were considered to be from a single episode.⁴¹ Isolates considered as contaminants during microbiological analysis were excluded from the study. As an external control for our data, the incidence of scarlet fever (erythrogenic toxin-producing GAS; which is a reportable illness in Hungary) was collected from the National Bacteriological Surveillance database of the National Institute of Public Health (NNK) for the period of 2008–2017. Rates were expressed as x/100,000 persons.

Bacterial Identification

Processing of clinical samples submitted to the Institute of Clinical Microbiology was carried out according to guidelines for routine clinical bacteriology. Isolates were cultured on Columbia agar plates containing 5% sheep blood (bioMérieux, Marcy-l’Étoile, France) and stored in Todd Hewitt broth (bioMérieux, Marcy-l’Étoile, France) with glycerol in a −80°C freezer. All isolates have initially been identified based on macroscopic appearance after 24 h (β-hemolysis, colony size), Gram-staining results and bacitracin sensitivity, which was followed-up by hippurate test, pyrrolidonylarylamidase (PYR) test (Remel, Lenexa, KS, USA) and slide agglutination test kit for Lancefield antigen grouping (Slidex Strepto-Kit, bioMerieux, Marcy-l’Étoile, France).^38,41 After 2013, this was complemented by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS; Bruker Daltonics, Bremen, Germany). The methodology of sample preparation and the technical details for MALDI-TOF MS measurements were described elsewhere.^42,43 The MALDI Biotyper RTC 3.1 software (Bruker Daltonics, Germany) and the MALDI Biotyper Library 3.1 were used for spectrum analysis. Identification was considered reliable on species-level, if the log(score) values were ≥2.300. If there was a discrepancy between the identification and the agglutination test results, the identification results were taken into consideration (ie, irrespective of the outcome of the agglutination test, if an isolate was identified as S. pyogenes, it was grouped as GAS, and if an isolate was identified as S. dysgalactiae subsp. equisimilis, it was grouped as GCGS).

Antibiotic Susceptibility Testing

Antimicrobial susceptibility testing (AST) was performed using the Kirby–Bauer disk diffusion method (Liofilchem, Abruzzo, Italy) on Mueller–Hinton agar plates complemented with 5% defibrinated horse blood and 20 mg/L β-NAD (MH-F), based on EUCAST laboratory standards.⁴⁴ The following antibiotic disks were used: benzyl-penicillin (1 IU; susceptibility to β-lactams was inferred from this test), erythromycin (15 µg), clindamycin (2 µg), norfloxacin (10 µg; susceptibility to quinolones was inferred from this test), trimethoprim-sulfamethoxazole (1.25–23.75 µg), tetracycline (30 µg), vancomycin (5 µg) and linezolid (10 µg). Inducible clindamycin resistance was detected using the erythromycin-clindamycin D test; these strains were also reported as resistant to clindamycin. Interpretation of results was carried out using EUCAST clinical breakpoints.⁴⁴ During data analysis, intermediately susceptible results were grouped with and reported as resistant. Streptococcus pneumoniae ATCC 49619 was used as a quality control strain.

Statistical Analysis

Statistical analyses, including the descriptive analysis (means or medians with ranges and percentages to characterize data) and statistical tests (Χ²-tests) were performed with IBM SPSS Statistics for Windows 24.0 (IBM Corp., Armonk, NY, USA). P values <0.05 were considered statistically significant.

Ethical Considerations

Our research complies with the Declaration of Helsinki (1964) and its amendments. The study was deemed exempt from ethics review by the Institutional Review Board of the University of Szeged, as anonymity and the privacy of the patients was maintained during data collection and the collected data were handled confidentially. Informed consent was not required due to the retrospective nature of the review. Data on the epidemiology of scarlet fever were freely available from the National Bacteriological Surveillance database of the National Institute of Public Health; therefore, no approval was required for their use.

Results

Epidemiology of GAS/GCGS Isolates Throughout the Study Period

Over the 10-year study period (January 2008 through December 2017), 1554 cases of streptococcal tonsillo-pharyngitis and 1104 cases of invasive streptococcal infections were detected (Table 1). Tonsillo-pharyngitis cases were predominantly caused by GAS (95.5%; n=1484), with 148.4±31.9 cases/year (ranging between 108 cases, ie, 26.5/100,000 persons in 2009, and 216 cases, ie, 44.1/100,000 persons in 2010), GCGS corresponded to a minority of pharyngitis cases (4.5%; n=70), with 8.0±3.6 cases/year (ranging between 1 case, ie, 0.2/100,000 persons in 2011, and 12 cases, ie, 2.9/100,000 cases in 2012). Similarly, GAS were the more common pathogens in invasive infections as well; however, their dominance was not as pronounced as in pharyngitis. GAS isolates constituted 77.9% (n=861), with 84.0±26.5 cases/year (ranging between 51 cases, ie, 12.5/100,000 persons in 2016, and 128 cases, ie, 31.4/100,000 persons in 2011). GCGS isolates were relevant in 22.1% (n=243) of cases, with 22.6±18.9 cases/year (ranging between 3 cases, ie, 0.73/100,000 persons in 2010, and 50 cases, ie, 12.3/100,000 persons in 2014) (Table 1). The annual distribution of GAS/GCGS isolates causing tonsillo-pharyngitis and invasive infections is presented in Figures 1–4. The incidence and rate of pGAS and pGCGS isolates was relatively constant between 2012 and 2017 (Figures 1 and 2). The incidence of iGAS reached a peak in 2011, while a steady decrease was seen, beginning from 2012 (Figure 3); on the other hand, the incidence of iGCGS isolates increased continuously throughout the study period (Figure 4) pGCGS and iGCGS isolates were statistically more common in the second half (2013–2017) of the study period. Statistically significant differences were observed based on sex (pGCGS were more frequent in females) and age (pGCGS were more frequent in patients aged 0–17 years) (Table 1).

Table 1 Epidemiology, Age and Gender-Distribution of Group A and Group C/G Streptococcal Infections Causing Pharyngitis and Invasive Infections, 2008–2017

Figure 1 Incidence and rates of pGAS isolates during the study period, 2008–2017.

Figure 2 Incidence and rates of pGCGS isolates during the study period, 2008–2017.

Figure 3 Incidence and rates of iGAS isolates during the study period, 2008–2017.

Figure 4 Incidence and rates of iGCGS isolates during the study period, 2008–2017.

Seasonal variation was observed in the incidence of both types of streptococcal infections: pGAS was most common in the period between December and February (35.0%), while the peak of pGCGS was seen a bit later, between January and March (29.5%). Peak incidence of iGAS infections were also detected between December and February (31.7%), with a smaller peak during summer months (June–August; 18.4%). In contrast, the incidence of iGCGS showed a peak during summer months (June–August; 33.2%), while a winter peak was not observed. To put our local results in a national context, the incidence of GAS and GCGS infections was compared to the incidence of scarlet fever between 2008 and 2017: the average number of scarlet fever cases in Hungary was 2972.2±617.2/year (ranging between 2356 cases, ie, 24.1/100,000 persons in 2009, and 4411 cases, ie, 45.1/100,000 persons in 2017).

The average age of the affected patients in the various groups was the following: pGAS: 13.2±13.1 years and pGCGS: 21.0±15.0 years (p=0.039), iGAS: 49.1±12.8 years and iGCGS: 58.7±18.5 years (p>0.05). The distribution of GAS/GCGS isolates causing pharyngitis and invasive infections among patients 0–17 years and in adult patients is presented in Table 1.

iGAS isolates originated from abscesses (47.1%), blood culture samples (24.1%), surgical samples (16.7%), biopsies (4.6%), pleural fluid (3.5%), pus (2.0%), synovial fluid (1.3%) and CSF samples (0.7%). In contrast, iGCGS isolates mainly originated from blood culture samples (53.8%), abscesses (22.9%), surgical samples (12.3%), synovial fluid (5.1%), pleural fluid (3.7%), pus (1.8%) and CSF samples (0.4%).

Antibiotic Resistance of GAS/GCGS Isolates Throughout the Study Period

The susceptibility-testing results of GAS and GCGS isolates over the 10-year study period are presented in Table 2. All respective isolates were susceptible to benzyl-penicillin (ie, all β-lactam antibiotics), tetracycline (ie, also susceptible to doxycycline, minocycline, tigecycline), vancomycin and linezolid. Nevertheless, overall resistance levels of erythromycin (10.5% for GAS, 21.4% for GCGS) and clindamycin (9.2% for GAS, 17.2% for GCGS) were significantly higher in GCGS isolates, while resistance levels for norfloxacin (ie, fluoroquinolone antibiotics) were higher in Group A isolates (13.5% for GAS, 6.9% for GCGS). There were no statistically significant differences seen in the resistance levels of GAS and GCGS isolates between the 2008–2012 and 2013–2017 time periods (data not shown).

Table 2 Antibiotic Resistance Levels of Group A and Group C/G Streptococcal Infections Causing Pharyngitis and Invasive Infections, 2008–2017

Discussion

A total of 1554 cases of streptococcal tonsillo-pharyngitis and 1104 cases of invasive streptococcal infections were noted in Southern Hungary; although the majority of isolates still belonged to GAS, the steady increase in the isolation rates of GCGS isolates were shown in Southern Hungary, which is consistent with the worldwide reports (GCS: 2–7%, GGS: 0.1–2.5%), showing an increase in the GCS/GGS-related disease burden. Although the incidence of iGCGS isolates were proportionally higher in patients aged 18 and older, pronounced epidemiological differentiation towards adult patients, similar to what has been shown in previous reports in the literature; in contrast, this tendency was not verified for pGCGS isolates whatsoever. Nonetheless, resistance levels were consistently higher in GCGS isolates (with the exception of quinolones), with has been noted in previous publications. Although many international studies from the last 5–10 years have noted the increase in the isolation frequency of GCGS isolates (which occurred from 2013 in our local settings), this coincided with the introduction of the MALDI-TOF MS in routine diagnostics. It is unclear whether this increase reflects true epidemiological changes (associated with the ageing population and the higher number of patients with risk factors for iCGCS infections) or rather, a technical change in diagnostics – which may have also distorted the results of other studies reporting an increased incidence.^{4,27,37,38,41} As there are no other reports available from the other regions of Hungary, it is also hard to ascertain the possible role of a geographical component.

Although the majority of GAS and GCS/GGS isolates remain exquisitely sensitive to penicillin in vitro,⁴⁵ the clinical management of severe, invasive β-haemolytic streptococcal infections remain challenging.⁴⁶ While penicillin is still considered as the first-choice drug for uncomplicated streptococcal infections, they have been proven ineffective in invasive infections.⁴⁷ In fact, based on the recommendations of the Infectious Diseases Society of America, penicillin should be used in combination with a protein synthesis inhibitor (eg, clindamycin) in these clinical cases.⁴⁸ The use of clindamycin for life-threatening invasive infections was shown to reduce mortality rates.⁴⁹ Patients with penicillin-allergy (where these patients may also have cross-reactions with cephalosporins and carbapenems) must also be considered during the choice of therapy.^50,51 In case of patients with penicillin allergy, macrolides, lincosamides and fluoroquinolones are considered as relevant therapeutic alternatives.⁵² However, one of the most concerning developments include the description of penicillin-resistance in boh GAS⁵³ and SDSE⁵⁴ isolates, linked to a pbp2x mutation; additionally, a report provided evidence of a large clonal population of GAS with sub-clinical β-lactam tolerance (associated with a similar pbp2x mutation) in Iceland.⁵⁵

Based on the data mentioned above, the relevance of protein-synthesis inhibitor antibiotics in the therapy of these infections should be stressed further. Increased resistance in GAS and GCS/GGS isolates towards macrolides and clindamycin has been reported in many countries, eg, macrolide-resistance in GAS was shown to be 22.8% in Greece, 32.8% in Spain, 40% in Bulgaria and Belgium and may be as high as 95% in China.⁵⁶ The steady increase in resistance was demonstrated in the US, where erythromycin/clindamycin resistance was 14/13% in 2015, 16/15% in 2016 and 23/22% in 2017, respectively (based on the CDC database). In addition, erythromycin-resistant GAS was associated with 5400 cases and 450 extra deaths in 2017. Macrolide resistance is either mediated by target site modification (rRNA methylases; the expression of which may be constitutive [cMLS] or inducible [iMLS]) or the overexpression of efflux pumps (mefA gene) and is related to the M phenotype.^56,57 Currently, emm cluster typing (which groups emm types into 48 different clusters on the basis of their structural properties of the M protein).⁵⁸ Similar to the emergence of fluoroquinolone-resistant S. pneumoniae, resistant GAS isolates are also increasingly reported; the main mechanism associated with these isolates are the mutations of gyrA and parC genes.⁵⁹ The emergence of resistance in GAS has been associated with the extensive use of relevant antibiotics in the country.⁶⁰ When it comes to antibiotic consumption, Hungary is among the countries with low consumption levels quantitatively; however, consumption levels of macrolides, lincosamides and streptogramins (J01F; 2.8 defined daily doses/1000 inhabitants per day) and quinolones (J01M; 2.3 defined daily doses/1000 inhabitants per day) in the country is among the highest in Europe.⁶¹ This phenomenon may explain the rate of resistance in Southern Hungary in GAS and GCS/GGS isolates.

In the following section, a concise summary of the most relevant epidemiological studies will be presented to put our results in context with findings in the international literature. In a study by Ekelund et al in Denmark, GAS infections were the most numerous (40%) among invasive infections between 1999 and 2002, followed by GGS (32%), GBS (23%) and GCS (6%). The overall mortality in this study was 21%, with most of the GCS/GGS affecting patients (74%) with predisposing factors.³⁷ Later on, a nationwide study by Lambertsen et al between 2005 and 2011 pointed out the increase in the incidence of laboratory-confirmed GAS, GBS, GCS and GGS infections (3.1, 2.3, 0.9 and 2.6 per 100 000 persons, respectively), compared to the previous study.⁶² Zaoutis et al reported the incidence of GCS/GGS in acute pharyngitis over a 12-month period in Philadelphia, USA: 17.7% of pharyngitis cases were non-GAS, and the average age of patients was 6 years.⁶³ In a prospective study by Steer et al, the epidemiology of invasive GAS over a 2-year period in Fiji was assessed; all-age incidence was 9.9 cases/100,000 population per year, while the case-fatality rate was 32.0%. In addition, they have shown that invasive GAS infections were the most common in patients over 65 years of age.⁵ In a Spanish study by Montes et al, the prevalence of GAS isolates was studied during 1998–2009;⁶⁴ incidence of invasive disease was 3.1 for children and 1.9 for adults per 100,000 inhabitants, and 17%, 8.9% and 13% of isolates were resistant to erythromycin, ciprofloxacin and tetracycline, respectively.⁶⁴ Invasive GAS infections were assessed in Germany between 2003 and 2007 by Imöhl et al;⁶⁵ out of n=586 isolates, susceptibility to penicillin G and levofloxacin was 100%, while resistance to tetracycline, clarithromycin and clindamycin was 11.6%, 5.5% and 1.2%. Clinical manifestations included sepsis (40.1%), necrotizing fasciitis (20.8%) and streptococcal toxic shock syndrome (16.6%).⁶⁵ Darenberg et al provided epidemiological results for invasive GAS infections for Sweden corresponding to 2002–2004.⁶⁶ The incidence was 3.0 cases per 100,000 population, 11% of the patients developed TSS, while 9.5% developed necrotizing fasciitis; the overall mortality rate was 14.5%. Ho et al assessed the resistance levels of invasive and non-invasive GAS isolates between 1995 and 1998;⁶⁷ resistance levels to erythromycin and tetracycline were high (32% and 53%). Rantala et al provided a population-based study, corresponding to the period between 1995 and 2004, during which 18 cases of GCS and 128 GGS bacteremia were identified.⁶⁸

Harris et al carried out a 14-year-long study in Australia, assessing bacteraemia caused by beta-haemolytic streptococci: GAS isolates were the most common (49%), with GCS/GGS isolates showing a modest, but significant, increase over time. Significant differences were no observed in the mortality rates between the different beta-haemolytic streptococci infections.⁶⁹ Wong et al reported n=73 invasive GGS infections in a New York community hospital over a 5-year period; the mean age of patients was 53 years, and the average length of stay for all patients with GGS was 9.4 days, with longer stays for those with underlying diabetes mellitus (14.6 days).⁷⁰ Bruun et al studied the incidence of GCS/GGS necrotizing soft tissue infections in Norway (2000–2009):⁷¹ they have reported a mean annual incidence rate of 1.4 per 100 000, with a mortality rate of 33%, compared to 11% in the GAS group. Hashikawa et al characterized GCS/GGS causing toxic shock syndrome (STSS) in Japan, finding that all STSS-causing isolates had a close genetic relationship.⁷² Slyvetsky et al showed that 15% of bacteremia caused by β-hemolytic Streptococcus was GGS, with a mortality rate of 15%.³⁵ Loubinoux et al characterized n=182 isolates of SDSE from invasive and non-invasive infections between 2006 and 2010; resistance to macrolides was 26.4%, while resistance to tetracycline was 34.6%.⁷³

During a 15-year-long surveillance period, Oppegaard et al³⁸ assessed the incidence of invasive and non-invasive GAS, GCS and GGS isolates in Western Norway: the distribution of invasive isolates was 58% GAS, 5% GCS and 37% GGS, respectively. The incidence of all isolates increased with patient age, a male dominance was observed, and a seasonal variation was shown, similarly to our study. The incidence of invasive GCGS infections increased from 1.4 to 6.3 per 100,000 persons from the beginning to the end of the study period, while GAS infections showed marked fluctuations (2.7–8.3 per 100,000 persons).³⁸ As a part of the Arctic Investigations Program (AIP), Rudolph et al surveyed the incidence of invasive GAS infections in Alaska between 2001 and 2013.⁴¹ Resistance to tetracycline, erythromycin, and clindamycin were relatively low (11.0%, 5.8% and 1.2%, respectively) with an observed incidence of 5.8 cases per 100,000 persons; the mortality rate was 10.7%, overall. In a large collaborative study (by the Strep-EURO Study Group) involving 11 European countries, the emergence of severe S. pyogenes infections was surveyed between 2003 and 2004;⁷⁴ the reported incidence was 3/100,000 population, which higher incidences in the northern European countries, while the 7-day mortality rate was 19% (44% for patients with STSS). This European study has also highlighted the seasonal variation in invasive GAS infections, which coincided in almost all participating countries. The epidemiology of invasive GAS infections was assessed on a national level by the CDC: between 2000 and 2004, the incidence was 3.5 cases/100,000 persons with an overall mortality rate of 13.7% (36.0% for STSS and 24.0% for necrotizing fasciitis).⁷⁵ The continuation of this study in 2005–2012 saw a slight increase in overall incidence (3.8 cases/100,000 persons) and a decrease in mortality rate (11.7%; mortality rate in patients aged 65 and over: 9.4/100 000).⁷⁶ M typing and the molecular characterization of resistance-determinants in a national setting has important public health implications; nevertheless, there is a scarcity of data on the molecular epidemiology of streptococci in Hungary. This scarcity was not improved by the fact that Hungary was not among the participating members of the Strep-EURO group study.⁷⁷ The most recent data available are from the early 2000s: Gattringer et al characterized n=191 S. pyogenes isolates originating from Hungary. In their report, 3.7% of the isolates were resistant to macrolides (mainly due to mefA and ermTR genes) and 30.5% were resistant to tetracycline (the large volume of prophylactic tetracycline use may have contributed to this rate).⁷⁸ Additionally, Krucsó et al characterized n=26 invasive GAS isolates from Hungary with molecular biological methods during 2004–2005: the following emm types were the most numerous: emm1 (50%), emm80 (19.2%); however, other M types were also described in these isolates (emm4, emm28, emm66, emm81.1, emm82 and emm84).⁷⁹

Limitations of the Study

Some limitation of our study should be addressed: i) the study design is retrospective and there was scarce clinical data available due to the inability to access the medical records of the individual patients. ii) for this reason, the association of relevant risk factors, underlying illnesses (apart from age and inpatient/outpatient status) and studies infections could not be performed (however, attempts were made to discard/exclude isolates with little or no clinical relevance). iii) our study is subject of selection bias, ie, it reports the results from a tertiary-care hospital, corresponding to patients with more severe conditions or underlying illnesses. iv) the CDC has recently identified SDSE isolates containing Group A antigens; as the uncertainty of misidentification regarding the presence of such isolates could not be excluded using our methods, this must also be noted as a limitation. v) data on emm typing or M typing could have strengthened the relevance of our results in an international context; however, due to the prolonged study period, lacking technical capabilities, monetary constraints and the overwhelming number of isolates to be tested, our study did not include this. vi) the molecular characterization of resistance determinants (eg, macrolide, quinolone resistance) in the individual isolates and erm typing were not performed as a part of this study for reasons mentioned in point v).

Conclusions

In our study, the epidemiology and resistance levels were assessed among Groups A, C and G β-haemolytic streptococci in Southern Hungary, over a long surveillance period. While there was undoubtedly an increase in the isolation rate of GCGS isolates, associations with patients characteristics are still unclear. The rates of resistance to macrolides and clindamycin are a cause for concern (especially among GCGS isolates); however, resistance levels are still relatively low, compared to Southern European countries. Due to the constant burden of β-haemolytic streptococcal diseases, the continuous surveillance of GAS and GCGS infections in both tonsillo-pharyngitis and in invasive infections is warranted.