Antibiotic resistance pattern, capsular types, and molecular characterization of invasive isolates of Streptococcus pneumoniae in the south of Tunisia from 2012 to 2018

S. pneumoniae remains one of the major human pathogens, which can cause various diseases. In developing countries, case fatality rates for invasive pneumococcal diseases remain high, reaching up to 20% for sepsis and 50% for meningitis [2]. In our study, 53.8 and 29.2% of invasive S. pneumoniae isolates were from blood and cerebrospinal fluid, respectively. The most common serotypes were 14, 19F, 3, 6A, 6B, 18C, 19A, 9 V, and 23F, accounting for 77.4% of all isolates. Our findings show that S. pneumoniae serotypes 19A and 3 that cause IPD were in non-meningitis cases. Serotype 19A was more frequently reported in non-meningitis cases than meningitis [29]. Nevertheless, serotype 3 was observed with or without meningitis [3]. The frequencies of serotypes included in PCV7 (55.7%), PCV10 (57.5%), and PCV13 (81.1%) suggest that the 13-valent PCV would be a potentially useful vaccine in Tunisia. In several European countries, before vaccine implementation, the most common serotypes causing invasive pneumococcal diseases were 14, 6B, 19F, and 23F. However, since the introduction of PCV7, serotypes 1, 3, 6A, 7F, and 19A have become the leading cause among the IPD isolates [8]. Our finding was consistent with data previously reported from studies in Singapore, South Korea, and China that showed an increase in serotype 19A among IPD children before the introduction of PCV7 [30,31,32].

Genotyping data using MLST showed high diversity among our isolates. Of 50 different STs, ten clonal complexes and 32 singletons were identified. A total of 43.4% of invasive isolates were closely related to seven of the 43 PMEN clones. These clones were Spain9V-3-ST156 (n = 16), Portugal19F-21-ST177 (n = 13), Netherlands3-31-ST180 (n = 4), Spain23F-1-ST81 (n = 4), Sweden15A-25-ST63 (n = 4), Utah35B-24-ST377 (n = 3), Colombia23F-26-ST338 (n = 1), and Sweeden4-38-ST205 (n = 1). As reported previously, we showed high correlations between serotypes and STs (P < 0.001). The dominant STs, ST179 (14.3%), ST2918 (12.1%), ST386 (5.5%), ST3772 (5.5%), and ST180 (4.4%) were related to serotypes 19F, 14, 6B, 19A and 3, respectively. It is noticeable that serotypes 14 and 9 V were included in the Spain9V-ST156 clone, which has been one of the most successful pneumococcal clones disseminated worldwide before the introduction of PCV-7 [33].

As observed in some countries in the pre-PCV era, the 19A serotype was identified in our population. Nevertheless, the emergence of the 19A serotype was observed worldwide in the post-PCV7 era, particularly in North America and many Asian countries. Mahjoub-Messai reported a clonal expansion of the preexisting penicillin-intermediate ST276 in serotype 19A isolates collected before and after beginning PCV7 vaccination in French children [34]. In Norway, ST3772 and ST276 were detected in 2009, after the introduction of PCV7. ST3772 and ST276 differed only by one locus, ddl. ST276 a single-locus variant of the Denmark14-32-ST230 clone has been identified in the United States and in southern Europe [35, 36]. Of note that S. pneumonia 19A isolates were genetically homogenous and assigned to ST3772. The homogeneous genetic background of 19A and 19F has been reported in the study from multicenter surveillance in China between 2005 and 2011 [31].

We reported for the first time a 6A serotype with ST2105, which was SLV of Sweden15A-25. Based on the PubMLST database, ST2105 was previously reported only in 15A and 19F serotypes.

Among eight isolates of serotype 6B S. pneumoniae, five belonged to ST386, which has already been described as related to the serotype 6B genetic background of the international Poland6B-ST315 clone. In addition, we note that the erythromycin-resistant serotype 6C S. pneumoniae isolate was ST386. The presence of serotypes 6B and 6C for ST386 suggest a potential capsular switch event. Janoir et al. (2014) reported a clonal expansion of macrolide-resistant ST386 within pneumococcal serotype 6C in France [37]. In addition, ST386 showed dramatically increased from 5% of all STs in the early PCV7 period to 77% during the PCV13 period (2010–2011). The emergence of serotype 6C-CC386 lineage was also reported in Brazil after the universal use of PCV [38].

Isolates of serotype 6A were more genetically diverse compared to the other serotypes and were associated with distinct STs including two novel STs. The same diversity was reported by Nurse-Lucas et al. (2016) for the serotypes 19F and 23F [10]. However, our findings showed that 19F and 23F serotypes were allied to three and two STs, respectively.

The sequence types ST179, ST3772, and ST2918 were most frequently associated with erythromycin resistance in Tunisia [39]. Reinert et al. (2005) reported the distribution of sequence types among 82 macrolide-resistant pneumococcal isolates from 11 centers in seven European countries. Twenty-three different MLST types were determined including 19 known STs [40]. Four major antimicrobial-resistant Spanish clones of S. pneumoniae were identified, including Spain23F-1 and Spain9V-3. These clones were described in the early 1980s, and they were the most widespread clones in the world. The clone Spain9V-3-ST156 and the ST143 appear to be responsible for the increase in antibiotic resistance observed in 2002 in Poland [41]. The Spain9V-ST156 clonal complex was the most prevalent clone in invasive penicillin-non-susceptible S. pneumoniae isolates recovered in Poland between 2003 and 2005. In addition, macrolide resistance in France is caused particularly by common ST, ST81, and ST143 [33, 40]. Neves et al. (2018) reported that the serotype 14 variant of ST156 was predominant in the pre-PCV10/13 period, but it was not detected in the post-PCV10/13 period [38]. In our study, three sequence types have been identified for serotype 14 S. pneumoniae isolates: ST2918, ST143, and ST4949. All these STs are related as single or double locus variants of ST156 and ST838. It is noticeable that ST2918 is rarely described in the world; only two serotype 14 S. pneumoniae isolates with ST2918 have been deposited so far on the PubMLST public databases. Recently, Vincent et al. (2019) reported two original cases of neonatal serotype 14 S. pneumoniae isolates belonging to ST2918 [42]. Over the past three decades, the prevalence of S. pneumoniae with reduced susceptibility to penicillin has increased substantially worldwide. Our results show that penicillin resistance is associated with serotypes 14, 19F, 19A, 9A, and 9 V. High doses of β-lactams or treatment with macrolides are used as alternative approaches to overcome these PNSPs. Unfortunately, the extensive use of macrolide may be linked to increasing macrolide resistance in many countries [5, 6, 43]. In Tunisia, resistance to macrolides was very high with a rate of around 70% [13, 15, 16, 39]. In our study, resistance rates to the tested antibiotics of invasive pneumococcal isolates were high, especially for erythromycin (62.3%) and tetracycline (33%). Erythromycin resistance is linked to serotypes 6A and 6B. Recently, analyses of data from 559 epidemiological studies across 104 countries revealed the greatest prevalence of non-susceptibility and resistance for penicillin, macrolides, third-generation cephalosporins, and tetracycline in southeast Asia, east Asia, and Oceania. The high rate of non-susceptibility of macrolides was also reported in high-income Asia-Pacific countries [44].

In our study, the mechanism of resistance to macrolides showed that the enzymatic modification of the MLS binding site was predominant. We noted that 89.4% of the isolates were MLSB phenotype while the efflux mechanism was only 10.6%. Our outcome also confirmed that the majority of isolates (77.3%) exhibited cMLSB phenotype, with iMLSB and M phenotypes observed in 12.1 and 10.6% of the isolates, respectively. cMLSB phenotype is predominant in most European countries and particularly in France, Spain, and Switzerland, whereas the M phenotype predominates in North America, England, and Germany [36]. According to recent studies, the cMLSB phenotype was the most frequent in Tunisia (75.5%) [45]. The macrolide-resistant phenotypes were genotypically confirmed by the presence of ermB (87.5%) and mefE (10.9%) genes. The high prevalence of the ermB gene has also been described in France (90%) and in Belgium (91.5%). In contrast, in the United States and Canada, the mef gene was the most prevalent, exceeding 50% [46]. The widespread dissemination of antibiotic resistance among pneumococci is associated with mobile genetic elements, such as transposons. In our study, the transposon Tn1545 is responsible for the propagation of most resistance to tetracycline and erythromycin (76.6%).

In conclusion, the common serotypes of invasive S. pneumoniae were 14, 19F, and 3 before the introduction of PCV-10 in the national immunization program in April 2019. The most common serotypes in meningitis cases were 19F, 14, 18C, 9 V, 6B, and 6A. For non-meningitis cases, the most frequent serotypes were 14, 3, 19F, 6B, 6A, and 19A. We showed high rates of non-susceptible isolates for penicillin, erythromycin, and tetracycline in the pre-PCV period. Thus, 87.9% of macrolide-resistant invasive isolates harbored the ermB gene. Population structure analysis showed that most serotypes (19F, 14, 6B, 19A, and 23F) are grouped in different clones and CCs as previously described in Tunisia and in European areas, such as Italy, Spain, France, and Poland. The capsular switching event was infrequent in invasive isolates, and it played a minor role in this population. However, this event may be an important source of new variants that may increase in the post-PCVs period. To better evaluate the genetic evolution and to monitor the antimicrobial-resistant and expanding clones, whole genome sequencing will be a necessary tool to use in future studies.

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