- Research article
- Open Access
Molecular characteristics of erythromycin-resistant Streptococcus pneumoniaefrom pediatric patients younger than five years in Beijing, 2010
BMC Microbiologyvolume 12, Article number: 228 (2012)
Streptococcus pneumoniae is the main pathogen that causes respiratory infections in children younger than five years. The increasing incidence of macrolide- and tetracycline-resistant pneumococci among children has been a serious problem in China for many years. The molecular characteristics of erythromycin-resistant pneumococcal isolates that were collected from pediatric patients younger than five years in Beijing in 2010 were analyzed in this study.
A total of 140 pneumococcal isolates were collected. The resistance rates of all isolates to erythromycin and tetracycline were 96.4% and 79.3%, respectively. Of the 135 erythromycin-resistant pneumococci, 91.1% were non-susceptible to tetracycline. In addition, 30.4% of the erythromycin-resistant isolates expressed both the ermB and mef genes, whereas 69.6% expressed the ermB gene but not the mef gene. Up to 98.5% of the resistant isolates exhibited the cMLSB phenotype, and Tn6002 was the most common transposon present in approximately 56.3% of the resistant isolates, followed by Tn2010, with a proportion of 28.9%. The dominant sequence types (STs) in all erythromycin-resistant S. pneumoniae were ST271 (11.9%), ST81 (8.9%), ST876 (8.9%), and ST320 (6.7%), whereas the prevailing serotypes were 19F (19.3%), 23F (9.6%), 14 (9.6%), 15 (8.9%), and 6A (7.4%). The 7-valent pneumococcal conjugate vaccine (PCV7) and 13-valent pneumococcal conjugate vaccine (PCV13) coverage of the erythromycin-resistant pneumococci among the children younger than five years were 45.2% and 62.2%, respectively. ST320 and serotype 19A pneumococci were common in children aged 0 to 2 years. CC271 was the most frequent clonal complex (CC), which accounts for 24.4% of all erythromycin-resistant isolates.
The non-invasive S. pneumoniae in children younger than five years in Beijing presented high and significant resistance rates to erythromycin and tetracycline. The expressions of ermB and tetM genes were the main factors that influence pneumococcal resistance to erythromycin and tetracycline, respectively. Majority of the erythromycin-resistant non-invasive isolates exhibited the cMLSB phenotype and carried the ermB, tetM, xis, and int genes, suggesting the spread of the transposons of the Tn916 family. PCV13 provided higher serotype coverage in the childhood pneumococcal diseases caused by the erythromycin-resistant isolates better than PCV7. Further long-term surveys are required to monitor the molecular characteristics of the erythromycin-resistant S. pneumoniae in children.
Streptococcus pneumoniae, the main pathogen that causes respiratory infections in children younger than five years, can cause various pneumococcal diseases, such as otitis media, sinusitis, pneumonia, meningitis, pleurisy, and bacteremia. Pneumococcal disease has been a major public health problem worldwide. In 2005, the World Health Organization (WHO) estimated that 1.6 million people die of pneumococcal diseases annually, of which the deaths of 0.7 million to 1 million were children younger than five years .
Antibiotics are often the first treatment of choice for pneumococcal infections. However, the increasing resistance of S. pneumoniae to various antibiotics, including macrolides and tetracyclines, makes pneumococcal infections difficult to treat especially in children and in regions like China. The resistance rate of S. pneumoniae to erythromycin and to tetracycline among children younger than five years in Beijing ranged from 87% to 94% and above 80%, respectively . Pneumococcal macrolide resistance is mediated by two major mechanisms, namely, target modification by a ribosomal methylase encoded by the ermB gene and drug efflux encoded by the mef gene. In S. pneumoniae, the tetracycline resistance is a result of the acquisition of one of the two genes, tetM or tetO, both of which encode ribosome protection proteins [3, 4]. Pneumococcal resistance to erythromycin and tetracycline is frequently associated with the insertion of the ermB gene into the transposons of the Tn916 or Tn917 family (Tn6002, Tn2010, Tn3872, Tn1545, and Tn6003) that contains the tetM gene.
Resistant-clonal isolates are distributed in different countries and regions, which results in the spread of bacterial resistance. The molecular epidemiological monitoring network (http://spneumoniae.mlst.net/pmen/) has published 43 international clones of S. pneumoniae, among which the clones of serotypes 6A, 6B, 14, 15A, 19A, 19F, 23F, and 35B were found to be associated with bacterial resistance. Thus, a study on the molecular epidemiology of S. pneumoniae for children in one region is beneficial to monitor pneumococal-resistant clones.
Studies on the characteristics of erythromycin-resistant S. pneumoniae in China are rare. Thus, the present study focuses on analyzing the phenotypic and genotypic characteristics of erythromycin-resistant pneumococcal isolates from pediatric patients in Beijing in 2010 as well as their respective relationships.
A total of 140 S. pneumoniae isolates were collected from the nasopharyngeal swabs of pediatric patients younger than five years with upper respiratory infections in the Beijing Children’s Hospital in 2010 after their parents or legal guardians have given their consent. The study was approved by the Ethics Committee of the Beijing Children’s Hospital, and all procedures were performed in accordance with the Helsinki Declaration . The isolates were identified based on the typical colony morphology, Gram staining, optochin sensitivity test (Oxoid Company, Britain), and Omni serum assay (Statens Serum Institut, Copenhagen, Denmark). Only one isolate was selected from the same subject. Of the 140 S. pneumoniae isolates, 57 were obtained from pediatric patients aged 0 to 2 years (≤2 years old) and 83 from those aged 2 years to 5 years (>2 but ≤5 years old).
Antibiotic susceptibility testing
The E-test (AB Biodisk, Sweden) method was performed to determine the antibiotic susceptibility of the 140 pneumococcal isolates to erythromycin and tetracycline according to the guidelines established by the Clinical and Laboratory Standards Institute (CLSI). The CLSI 2010 criteria  for minimum inhibitory concentrations (MICs) were applied to classify the susceptible, intermediate, or resistant isolates with the following breakpoints: erythromycin, ≤0.25 μg/mL, 0.5 μg/mL, and ≥1 μg/mL; and tetracycline, ≤2 μg/mL, 4 μg/mL, and ≥8 μg/mL, respectively. ATCC49619 was used as the quality control strain and was included in each set of tests to ensure accurate results.
Macrolide resistance phenotype
Macrolide resistance phenotyping was performed via double-disk diffusion using standard disks of erythromycin (15 μg) and clindamycin (2 μg) (Oxoid Company, Britain). A blunting of the clindamycin inhibition zone adjacent to the erythromycin disk (“D zone”) indicated the presence of the inducible macrolide-resistant phenotype (iMLSB), whereas the absence of blunting indicated the presence of the constitutive macrolide-resistant phenotype (cMLSB). The M macrolide phenotype was characterized by clindamycin susceptibility with no blunting of the inhibition zone around the clindamycin disk.
Chromosomal DNA was isolated from the overnight cultures of the isolates that were grown on 5% trypticase soy agar by using the DNA Mini Kit (SBS Genetech, Beijing) according to the manufacturer’s instructions.
Detection of genes and related transposons
The macrolide-resistance genes ermB and mef were detected using polymerase chain reaction (PCR) with oligonucleotide primers specific for each gene as described in the previous studies . The PCR products of the mef genes were digested with BamHI to distinguish the mefA and mefE gene subclasses .
The Tn916 and Tn917 transposon-related genes (int, xis, tnpA, and tnpR), the tetracycline-resistance gene tetM, and the promoter of the aph3’-III gene were detected by PCR using the primers described in previous studies [9–13]. The resistance gene combinations related to the different presumed transposons were Tn6002 (ermB, tetM, int, and xis), Tn2010 (ermB, tetM, int, xis, and mefE), Tn3872 (ermB, tetM, tnpA, and tnpR), Tn1545, or Tn6003 (ermB, tetM, int, xis, and aph3’-III).
Multi locus sequence typing (MLST)
The housekeeping genes aroE, gdh, gki, recP, spi, xpt, and ddl were amplified via PCR . The sequences of each of the seven loci were compared with those of all known alleles at the loci as well as with the STs in the database of the pneumococcal multi locus sequence typing (MLST) website (http://spneumoniae.mlst.net). New allelic numbers or new ST numbers were assigned by the curator of the pneumococcal MLST website. The eBURST v3 software (http://spneumoniae.mlst.net/eburst/) was used to investigate the relationships between the isolates and to assign a clonal complex (CC) based on the stringent group definition of six out of seven shared alleles.
Pneumococcal serotyping was performed through the Quellung reaction by using Pneumotest kits and type-specific antisera (Statens Serum Institut, Copenhagen, Denmark) for the erythromycin-resistant isolates as previously described . The isolates that reacted negatively were non-typeable. The PCV7 and PCV13 coverage was estimated by calculating the percentage of isolates that expressed the serotypes included in the vaccine.
The data from the antibiotic susceptibility testing were set up and analyzed using the WHONET 5.3 software, which was recommended by the WHO. The χ2-test and the Fisher’s accurate probability tests were performed using the SPSS version 13.0 software to compare proportions. Differences with P < 0.05 were considered statistically significant.
The susceptibility and MICs to erythromycin and tetracycline of 140 pneumococcal isolates that were collected among children of different ages are presented in Table 1. Based on the CLSI 2010 criteria, the resistance rate of all isolates to erythromycin was 96.4% (135/140), whereas the susceptibility rate was merely 2.9% (4/140). Up to 98.5% (133/135) of the erythromycin-resistant pneumococcal isolates exhibited high MICs (>256 μg/mL). The erythromycin resistance rates between children aged 0 to 2 years and 2 to 5 years were all above 94.0%, with 54 and 81 isolates, respectively. No significant difference was found between the two age groups (P > 0.05). The total resistance rate of all the isolates to tetracycline reached 79.3% (111/140). No difference was also found in tetracycline resistance between children aged 0 to 2 years and 2 to 5 years (P > 0.05). A total of 110 (78.6%) isolates were resistant to both erythromycin and tetracycline, and 91.1% (123/135) of the erythromycin-resistant strains were non-susceptible (intermediate and resistant) to tetracycline.
Detection of resistance genes and phenotype
All 135 erythromycin-resistant isolates were detected for macrolide- and tetracycline-resistance genes as well as macrolide-resistant phenotype. Almost 30.4% isolates expressed both the ermB and mef genes, whereas 69.6% were positive for the ermB gene but negative for the mef gene. The resistant isolates had no different carrying proportions of both the ermB and mef genes, as well as only ermB, between the two aforementioned pediatric age groups (P > 0.05) (Table 2). All mef-positive isolates carried the mefE gene. Among the erythromycin-resistant pneumococcal isolates, all the 123 tetracycline-resistant and intermediate isolates carried the tetM gene. However, eight of the 12 tetracycline-susceptible isolates carried the tetM gene. Up to 98.5% (133/135) of the resistant isolates exhibited the cMLSB phenotype, but only two isolates expressed the M phenotype. No iMLSB phenotype was found among the resistant isolates.
Among the 135 erythromycin-resistant pneumococci, 76 isolates (56.3%) contained ermB, tetM, int, and xis genes related to Tn6002. 39 isolates (28.9%) were detected for the presence of ermB, tetM, int, xis, and mefE genes, carrying the transposon of Tn2010. Seven isolates (5.2%) were positive for the ermB, tetM, tnpA, and tnpR genes related to Tn3872. Eight isolates (5.9%) containing the ermB, tetM, int, and xis genes were also positive for the promoter of the aph3’-III gene related to Tn1545/6003 via PCR, of which only two isolates had the mefE gene. The int, xis, tnpA, tnpR, aph3’-III, and mefE genes were not detected in the remaining five isolates (3.7%) (Figure 1).
Multi locus sequence typing
A total of 62 STs were found in the erythromycin-resistant S. pneumoniae, of which 28 STs were newly assigned, via MLST analysis. Of the new STs, 19 types were novel combinations of known alleles (ST6875, ST6946, and ST7746 to ST7762). Up to 9 profiles (ST7763 to ST7770 and ST7869) contained 10 new alleles, namely, aroE236, gdh353, gki353, gki354, gki355, recP207, recP208, spi332, spi338, and ddl512. The four predominant STs of all resistant pneumococci were ST271 (11.9%, 16/135), ST81 (8.9%, 12/135), ST876 (8.9%, 12/135), and ST320 (6.7%, 9/135) (Figure 2). Of the common STs, the proportion of ST320 was higher among children aged 0 to 2 years than that of the other age group (P < 0.05). However, the percentage of the other STs, such as ST81, ST236, ST271, ST876, ST386, and ST2572, did not show any difference between the two age groups (P > 0.05). The eBURST analysis results showed 9 CCs and 36 singletons (Figure 3). CC271 was the most frequent CC, with a proportion of 24.4% (33/135) among the resistant isolates.
Serotyping and vaccine coverage
Among the 135 erythromycin-resistant pneumococci, 121 isolates (89.6%) could be serotyped, of which the prevailing five serotypes were 19F (19.3%), 23F (9.6%), 14 (9.6%), 15 (8.9%), and 6A (7.4%), which accounted for 54.8% (74/135). The pneumococcal isolates of serotype 19A were significantly common among children aged 0 to 2 years than that of 2 to 5 years (P < 0.05). However, the pneumococcal isolates of the other serotypes were not different between the two age groups (P > 0.05). The PCV13 coverage for the erythromycin-resistant isolates was 62.2% (84/135). This value was higher than that of PCV7 (45.2%, 61/135) among all children younger than five years as well as the children aged 0 to 2 years (P < 0.05). The PCV7 coverage of children aged 2 to 5 years was significantly higher than that of 0 to 2 years (P < 0.05). However, no difference in PCV13 coverage was observed among these two age groups (P > 0.05) (Figure 4).
Relations of sequence types, serotypes, resistance genes, and transposons
Several associations were observed between the STs, serotypes, macrolide-resistance genes, as well as Tn916- and Tn917-related transposons for the erythromycin-resistant pneumococcal isolates (Table 3). The dominant ST of the serotype 19F isolates was ST271, followed by ST236. On the other hand, that of the serotype 14, 23F, and 6B isolates was ST876, ST81, and ST386, respectively. The ST of all the serotype 19A pneumococci was ST320. All isolates of CC271, which was identified as serotype 19F and 19A, carried two macrolide-resistance genes, ermB and mefE. However, the mefE gene was not found among the isolates of other CCs, such as CC2754, CC230, CC3173, CC3397, CC6202, and CC855. Tn6002 was distributed among the isolates of seven CCs except for CC271 and CC3173, among which the dominant transposons were Tn2010 and Tn3872, respectively. Tn1545/6003 was found in the isolates of ST180, ST271, ST320, ST505, ST2572, ST7759, ST7760, and ST7768.
S. pneumoniae is a Gram-positive encapsulated diplococcus and is often transmitted by direct contact with respiratory secretions from the infected and healthy carriers. The disease develops by contiguous spread to the sinuses or the middle ear, aspiration into the lower respiratory tract, which causes pneumonia, or by invasion into the bloodstream with or without the seeding of secondary sites. According to the 2000 Chinese census data, an estimated 260,768 (113,000 to 582,382) pneumonia and 902 (114 to 4,463) meningitis cases were caused by S. pneumoniae. The estimated deaths from S. pneumoniae pneumonia and meningitis were 10,703 (4,638 to 23,904) and 75 (10 to 370), respectively . This result indicates that pneumococcal diseases are a significant health problem among children in China.
Pneumococcal resistance to antimicrobials, such as macrolides and tetracyclines, is a serious and rapidly growing problem worldwide. In the Asian Network for Surveillance of Resistant Pathogen study, Song et al.  demonstrated that Asian regions had the highest levels of S. pneumoniae antibiotic resistance. A total of 59.3% of erythromycin-resistant pneumococcal isolates were observed in Asian countries. Vietnam had the highest resistance rate, followed by Taiwan, Korea, Hong Kong, and the hinterlands of China . The erythromycin resistance rate of S. pneumoniae in 1998 to 1999 in Beijing was 71.0% , which was much higher than that in 1996 to 1997 . Pneumococci data of hospitalized pediatric patients with respiratory infections showed 85.7% erythromycin resistance in Shanghai  and 92.1% in Chongqing . In the present study, the erythromycin resistance rate of S. pneumoniae was higher at 96.4%, and most of the isolates had high MICs (>256 μg/mL), which indicated an increasing trend of pneumococcal erythromycin resistance in the hinterlands of China. Geographical variations were observed in the phenotypic and genotypic characteristics of erythromycin-resistant S. pneumoniae. The ermB gene was the most common mechanism for erythromycin resistance in the hinterlands of China, Taiwan, Sri Lanka, and Korea, similar to the results of this study for the children in Beijing. However, the mef gene was more common in Hong Kong, Singapore, Thailand, and Malaysia . In Europe, the ermB gene was the dominant macrolide-resistance gene, especially in France, Spain, Switzerland, and Poland. On the other hand, the mef gene was common in Greece and Germany . In the present study, the MLSB phenotype was the predominant phenotype among the erythromycin-resistant pneumococcal isolates, which was in accordance with previous studies in China [23, 24]. However, the M phenotype was more prevalent than the MLSB phenotype in other countries, such as in Canada and in the United Kingdom [9, 25].
The resistance of S. pneumoniae to tetracycline was also significantly high in China, which was similar to that of erythromycin. This result may be related to the abuse of tetracycline in agriculture and edible animals. A multi-center research on the antibiotic resistance of S. pneumoniae involving four cities in China revealed that 82.1% of pneumococcal isolates were tetracycline-resistant among 1-month-old to 5-year-old children with acute upper respiratory infections . The tetracycline non-susceptible rate among the invasive erythromycin-resistant pneumococcal isolates collected in Australia was 75.5% . This value was lower than the non-invasive erythromycin-resistant isolates in the current study. The present study, in addition to previous ones [10, 11, 27], proved that the tetM gene was responsible for tetracycline resistance in S. pneumoniae. In the present study, we found that the eight pneumococcal isolates with the tetM gene were susceptible to tetracycline. Amezaga et al.  identified a 10 bp deletion in the sequence of the tetM gene of one tetracycline-susceptible isolate. This result was relative to the tetM sequence in tetracycline-resistant isolates. Thus, further studies are necessary.
Tetracycline resistance is associated with erythromycin resistance in pneumococcal isolates, which are transmitted by the transposons of the Tn916 or Tn917 family including Tn6002, Tn2010, Tn3872, Tn1545, and Tn6003. Tn6002, which was first detected in Streptococcus cristatus, originated from the insertion of an ermB-containing DNA fragment into Tn916, which carries the tetM gene [28, 29]. Our study showed that Tn6002 was more common among erythromycin-resistant isolates in Beijing children, which accounts for 56.3%. In addition, Tn2010 is a composite element of adding the mefE gene on the basis of Tn6002, with a proportion of 28.9% in the present study. Tn3872 results from the insertion of the ermB-containing Tn917 transposon  into Tn916. Tn1545 and Tn6003 have similar compositions; they both contain the kanamycin resistance gene aph3’-III aside from the erythromycin- and tetracycline-resistance determinants ermB and tetM. In this study, the transposons Tn3872 and Tn1545/Tn6003 were rare at approximately 11.1%, indicating that Tn3872 and Tn1545/Tn6003 were not the main factors for erythromycin and tetracycline resistance in Beijing children. Moreover, we also found five pneumococcal isolates without transposon determinants that carried the ermB and tetM genes or only ermB gene. Further studies are necessary to verify if these five isolates contain unknown transposons.
Three conjugate vaccines, namely, PCV7, PCV10, and PCV13, were introduced to prevent pneumococcal infections in children. PCV13 included serotypes 1, 3, 5, 6A, 7F, and 19A plus the PCV7 serotypes 4, 6B, 9V, 14, 18C, 19F, and 23F. In this study, the serotypes 23F, 19F, 14, and 6B were common among S. pneumoniae from Beijing children younger than five years. This result was similar with the previous studies in China [20, 32, 33], but different from that of the other European countries, in which the serotypes 1, 3, 6A, 7F, and 19A were common among pneumococcal isolates . Since the introduction of PCV7, the incidence of pneumococcal disease because of PCV7-serotypes has significantly declined in many countries. However, several countries have reported an increased rate of pneumococcal disease in non-PCV7 serotypes. This phenomenon, termed ‘replacement’, is associated with specific pneumococcal serotypes or clones . In China, the PCV7-serotypes were more popular among children for two reasons: first, PCV7 has been on the market for only four years in China since 2008. Second, only about 1% of Chinese children use PCV7 for their routine pneumococcal immunization. We found that the PCV13 coverage of the erythromycin-resistant isolates was higher than that of PCV7 among all children younger than five years as well as the children aged 0 to 2 years because of the high rates of serotypes 3, 6A, and 19A. Moreover, the PCV7 coverage of children aged 2 to 5 years was also significant higher than that of children aged 0 to 2 years. All these results indicate that PCV13 controls the pneumococcal diseases caused by the erythromycin-resistant isolates better than PCV7 for children, especially those younger than two years.
Maiden et al.  introduced the MLST approach to monitor the epidemiology of bacteria based on multi locus enzyme electrophoresis. Enright and Spratt were the first to apply MLST for pneumococcal studies . The MLST database enables the global sharing of data and helps in the exchange of data between different laboratories. Thus, it can be used to monitor the molecular epidemiology of S. pneumoniae worldwide. In the present study, the prevalent STs were ST271, ST81, ST876, and ST320. In Shanghai, ST236 and ST271 were the most common STs for S. pneumoniae. ST320, ST271, and ST876 were the prevalent types among the invasive pneumococcal isolates collected from 11 cities in China . In Norway, the frequent STs were ST199, ST176, and ST36 among the isolates collected from the children attending daycare centers . Several associations were found between STs, serotypes, and macrolide-resistance genes in this study. The dominant STs of the serotype 19F, 14, 23F, and 6B isolates were ST271, ST876, ST81, and ST386, respectively. ST320 was more common in children aged 0 to 2 years than in other age groups and all were from the serotype 19A pneumococci. Notably, ST320 was found to be the predominant type among pneumococcal serotype 19A isolates from ten Asian countries . This suggests that ST320 has an important function in pneumococcal diseases in children. The ST320 clone of serotype 19A is expected to be more prevalent worldwide because of the wide use of PCV7. A systematic study showed that Taiwan19F-14 was one of the two dominant clones for erythromycin-resistant isolates in Asian regions . Taiwan19F-14 (ST236), a multidrug-resistant pneumococcal molecular epidemiology network clone and one of the most main clones causing invasive pneumococcal diseases in Asian countries , was associated with seven STs in this study, ST236, ST271, ST320, ST1464, ST6993, ST7758, and ST7766. ST236 is a single locus variant of ST271 and a double locus variant of ST320. According to eBURST analysis, both ST271 and ST320 belong to CC271, which was the most common CC observed in this study. CC271 emerged in the United States after the introduction of PCV7, and expressed both the ermB and mef genes , as shown in the present study.
S. pneumoniae in children younger than five years in Beijing presented high and significant resistance rates to erythromycin and tetracycline. The ermB and tetM genes were the main factors for pneumococcal erythromycin and tetracycline resistance, respectively. Majority of the erythromycin-resistant isolates exhibited the cMLSB phenotype and carries the ermB, tetM, xis, and int genes, which suggested the spread of the transposons of the Tn916 family. PCV13 provided higher serotype coverage in the childhood pneumococcal diseases caused by the erythromycin-resistant isolates better than PCV7. The incidence of erythromycin-resistant S. pneumoniae among children is continuously increasing; thus, further long-term studies of their molecular characteristics are necessary.
World Health Organization (WHO): Pneumococcal conjugate vaccine for childhood immunization--WHO position paper. Wkly Epidemiol Rec. 2007, 82 (12): 93-104.
Yu S, Yao K, Shen X, Zhang W, Liu X, Yang Y: Serogroup distribution and antimicrobial resistance of nasopharyngeal isolates of Streptococcus pneumoniae among Beijing children with upper respiratory infections (2000–2005). Eur J Clin Microbiol Infect Dis. 2008, 27 (8): 649-655. 10.1007/s10096-008-0481-y.
Widdowson CA, Klugman KP, Hanslo D: Identification of the tetracycline resistance gene, tet(O), in Streptococcus pneumoniae. Antimicrob Agents Chemother. 1996, 40 (12): 2891-2893.
Widdowson CA, Klugman KP: The molecular mechanisms of tetracycline resistance in the pneumococcus. Microb Drug Resist. 1998, 4 (1): 79-84. 10.1089/mdr.1998.4.79.
World Medical Association (WMA): WMA Declaration of Helsinki-Ethical Principles for Medical Research Involving Human Subjects. 1964, the 18th World Medical Association: Helsinki, Finland
Clinical and Laboratory Standards Institute (CLSI): Performance Standards for antimicrobial susceptibility testing; Twentieth Informational Supplement. 2010, Wayne, PA: Clinical and Laboratory Standards Institute, M100–S20
Sutcliffe J, Grebe T, Tait-Kamradt A, Wondrack L: Detection of erythromycin-resistant determinants by PCR. Antimicrob Agents Chemother. 1996, 40 (11): 2562-2566.
Montanari MP, Mingoia M, Cochetti I, Varaldo PE: Phenotypes and genotypes of erythromycin-resistant pneumococci in Italy. J Clin Microbiol. 2003, 41 (1): 428-431. 10.1128/JCM.41.1.428-431.2003.
Amezaga MR, Carter PE, Cash P, McKenzie H: Molecular epidemiology of erythromycin resistance in Streptococcus pneumoniae isolates from blood and noninvasive sites. J Clin Microbiol. 2002, 40 (9): 3313-3318. 10.1128/JCM.40.9.3313-3318.2002.
Doherty N, Trzcinski K, Pickerill P, Zawadzki P, Dowson CG: Genetic diversity of the tet(M) gene in tetracycline-resistant clonal lineages of Streptococcus pneumoniae. Antimicrob Agents Chemother. 2000, 44 (11): 2979-2984. 10.1128/AAC.44.11.2979-2984.2000.
Izdebski R, Sadowy E, Fiett J, Grzesiowski P, Gniadkowski M, Hryniewicz W: Clonal diversity and resistance mechanisms in tetracycline-nonsusceptible Streptococcus pneumoniae isolates in Poland. Antimicrob Agents Chemother. 2007, 51 (4): 1155-1163. 10.1128/AAC.01384-06.
Poyart C, Quesne G, Acar P, Berche P, Trieu-Cuot P: Characterization of the Tn916-like transposon Tn3872 in a strain of abiotrophia defectiva (Streptococcus defectivus) causing sequential episodes of endocarditis in a child. Antimicrob Agents Chemother. 2000, 44 (3): 790-793. 10.1128/AAC.44.3.790-793.2000.
Trzcinski K, Cooper BS, Hryniewicz W, Dowson CG: Expression of resistance to tetracyclines in strains of methicillin-resistant Staphylococcus aureus. J Antimicrob Chemother. 2000, 45 (6): 763-770. 10.1093/jac/45.6.763.
Enright MC, Spratt BG: A multilocus sequence typing scheme for Streptococcus pneumoniae: identification of clones associated with serious invasive disease. Microbiology. 1998, 144 (Pt 11): 3049-3060.
Sorensen UB: Typing of pneumococci by using 12 pooled antisera. J Clin Microbiol. 1993, 31 (8): 2097-2100.
Chen Y, Deng W, Wang SM, Mo QM, Jia H, Wang Q, Li SG, Li X, Yao BD, Liu CJ, et al: Burden of Pneumonia and Meningitis Caused by Streptococcus pneumoniae in China among Children under 5 Years of Age: A Systematic Literature Review. PLoS One. 2011, 6 (11): e27333-10.1371/journal.pone.0027333.
Song JH, Jung SI, Ko KS, Kim NY, Son JS, Chang HH, Ki HK, Oh WS, Suh JY, Peck KR, et al: High prevalence of antimicrobial resistance among clinical Streptococcus pneumoniae isolates in Asia (an ANSORP study). Antimicrob Agents Chemother. 2004, 48 (6): 2101-2107. 10.1128/AAC.48.6.2101-2107.2004.
Song JH, Chang HH, Suh JY, Ko KS, Jung SI, Oh WS, Peck KR, Lee NY, Yang Y, Chongthaleong A, et al: Macrolide resistance and genotypic characterization of Streptococcus pneumoniae in Asian countries: a study of the Asian Network for Surveillance of Resistant Pathogens (ANSORP). J Antimicrob Chemother. 2004, 53 (3): 457-463. 10.1093/jac/dkh118.
Lee NY, Song JH, Kim S, Peck KR, Ahn KM, Lee SI, Yang Y, Li J, Chongthaleong A, Tiengrim S, et al: Carriage of antibiotic-resistant pneumococci among Asian children: a multinational surveillance by the Asian Network for Surveillance of Resistant Pathogens (ANSORP). Clin Infect Dis. 2001, 32 (10): 1463-1469. 10.1086/320165.
Zhao GM, Black S, Shinefield H, Wang CQ, Zhang YH, Lin YZ, Lu JL, Guo YF, Jiang QW: Serotype distribution and antimicrobial resistance patterns in Streptococcus pneumoniae isolates from hospitalized pediatric patients with respiratory infections in Shanghai, China. Pediatr Infect Dis J. 2003, 22 (8): 739-742. 10.1097/01.inf.0000078373.54515.40.
Chen J, Liu L, Wang G, Chen Y, Luo Z, Huang Y, Fu Z, Yang Y, Liu E: Correlation between usage of macrolide antibiotic and resistance of Streptococcus pneumoniae clinic isolates from Chongqing children’s hospital. Pediatr Pulmonol. 2009, 44 (9): 917-921. 10.1002/ppul.21081.
Reinert RR, Ringelstein A, van der Linden M, Cil MY, Al-Lahham A, Schmitz FJ: Molecular epidemiology of macrolide-resistant Streptococcus pneumoniae isolates in Europe. J Clin Microbiol. 2005, 43 (3): 1294-1300. 10.1128/JCM.43.3.1294-1300.2005.
Shen X, Lu Q, Ye Q, Zhang G, Yu S, Zhang H, Deng Q, Yang Y: Prevalence of antimicrobial resistance of Streptococcus pneumoniae in Chinese children: four hospitals surveillance. Chin Med J (Engl). 2003, 116 (9): 1304-1307.
Wang M, Zhang Y, Zhu D, Wang F: Prevalence and phenotypes of erythromycin-resistant Streptococcus pneumoniae in Shanghai, China. Diagn Microbiol Infect Dis. 2001, 39 (3): 187-189. 10.1016/S0732-8893(01)00217-6.
Powis J, McGeer A, Green K, Vanderkooi O, Weiss K, Zhanel G, Mazzulli T, Kuhn M, Church D, Davidson R, et al: In vitro antimicrobial susceptibilities of Streptococcus pneumoniae clinical isolates obtained in Canada in 2002. Antimicrob Agents Chemother. 2004, 48 (9): 3305-3311. 10.1128/AAC.48.9.3305-3311.2004.
Xu X, Cai L, Xiao M, Kong F, Oftadeh S, Zhou F, Gilbert GL: Distribution of serotypes, genotypes, and resistance determinants among macrolide-resistant Streptococcus pneumoniae isolates. Antimicrob Agents Chemother. 2010, 54 (3): 1152-1159. 10.1128/AAC.01268-09.
Shen X, Yang H, Yu S, Yao K, Wang Y, Yuan L, Yang Y: Macrolide-resistance mechanisms in Streptococcus pneumoniae isolates from Chinese children in association with genes of tetM and integrase of conjugative transposons 1545. Microb Drug Resist. 2008, 14 (2): 155-161. 10.1089/mdr.2008.0773.
Brenciani A, Bacciaglia A, Vecchi M, Vitali LA, Varaldo PE, Giovanetti E: Genetic elements carrying erm(B) in Streptococcus pyogenes and association with tet(M) tetracycline resistance gene. Antimicrob Agents Chemother. 2007, 51 (4): 1209-1216. 10.1128/AAC.01484-06.
Cochetti I, Tili E, Vecchi M, Manzin A, Mingoia M, Varaldo PE, Montanari MP: New Tn916-related elements causing erm(B)-mediated erythromycin resistance in tetracycline-susceptible pneumococci. J Antimicrob Chemother. 2007, 60 (1): 127-131. 10.1093/jac/dkm120.
Tomich PK, An FY, Clewell DB: Properties of erythromycin-inducible transposon Tn917 in Streptococcus faecalis. J Bacteriol. 1980, 141 (3): 1366-1374.
McDougal LK, Tenover FC, Lee LN, Rasheed JK, Patterson JE, Jorgensen JH, LeBlanc DJ: Detection of Tn917-like sequences within a Tn916-like conjugative transposon (Tn3872) in erythromycin-resistant isolates of Streptococcus pneumoniae. Antimicrob Agents Chemother. 1998, 42 (9): 2312-2318.
Yao K, Shen X, Yul S, Lu Q, Deng L, Ye Q, Zhang H, Deng Q, Hu Y, Yang Y: Antimicrobial resistance and serotypes of nasopharyngeal strains of Streptococcus pneumoniae in Chinese children with acute respiratory infections. J Int Med Res. 2007, 35 (2): 253-267.
Yao KH, Wang LB, Zhao GM, Zheng YJ, Deng L, Huang JF, Wang JX, Zhao RZ, Deng QL, Hu YH, et al: Pneumococcal serotype distribution and antimicrobial resistance in Chinese children hospitalized for pneumonia. Vaccine. 2011, 29 (12): 2296-2301. 10.1016/j.vaccine.2011.01.027.
Isaacman DJ, McIntosh ED, Reinert RR: Burden of invasive pneumococcal disease and serotype distribution among Streptococcus pneumoniae isolates in young children in Europe: impact of the 7-valent pneumococcal conjugate vaccine and considerations for future conjugate vaccines. Int J Infect Dis. 2010, 14 (3): e197-e209. 10.1016/j.ijid.2009.05.010.
Reinert RR: The antimicrobial resistance profile of Streptococcus pneumoniae. Clin Microbiol Infect. 2009, 15 (Suppl 3): 7-11.
Maiden MC, Bygraves JA, Feil E, Morelli G, Russell JE, Urwin R, Zhang Q, Zhou J, Zurth K, Caugant DA, et al: Multilocus sequence typing: a portable approach to the identification of clones within populations of pathogenic microorganisms. Proc Natl Acad Sci U S A. 1998, 95 (6): 3140-3145. 10.1073/pnas.95.6.3140.
Yang F, Xu XG, Yang MJ, Zhang YY, Klugman KP, McGee L: Antimicrobial susceptibility and molecular epidemiology of Streptococcus pneumoniae isolated from Shanghai, China. Int J Antimicrob Agents. 2008, 32 (5): 386-391. 10.1016/j.ijantimicag.2008.05.004.
Qian J, Yao K, Xue L, Xie G, Zheng Y, Wang C, Shang Y, Wang H, Wan L, Liu L, et al: Diversity of pneumococcal surface protein A (PspA) and relation to sequence typing in Streptococcus pneumoniae causing invasive disease in Chinese children. Eur J Clin Microbiol Infect Dis. 2011, 31 (3): 217-223.
Vestrheim DF, Hoiby EA, Aaberge IS, Caugant DA: Phenotypic and genotypic characterization of Streptococcus pneumoniae strains colonizing children attending day-care centers in Norway. J Clin Microbiol. 2008, 46 (8): 2508-2518. 10.1128/JCM.02296-07.
Shin J, Baek JY, Kim SH, Song JH, Ko KS: Predominance of ST320 among Streptococcus pneumoniae serotype 19A isolates from 10 Asian countries. J Antimicrob Chemother. 2011, 66 (5): 1001-1004. 10.1093/jac/dkr048.
Ko KS, Song JH: Evolution of erythromycin-resistant Streptococcus pneumoniae from Asian countries that contains erm(B) and mef(A) genes. J Infect Dis. 2004, 190 (4): 739-747. 10.1086/422156.
McGee L, McDougal L, Zhou J, Spratt BG, Tenover FC, George R, Hakenbeck R, Hryniewicz W, Lefévre JC, Tomasz A, et al: Nomenclature of major antimicrobial-resistant clones of Streptococcus pneumoniae defined by the pneumococcal molecular epidemiology network. J Clin Microbiol. 2001, 39 (7): 2565-2571. 10.1128/JCM.39.7.2565-2571.2001.
The study was financially supported by the Construction of Platform for Research and Development Technology of Innovative Drugs, a grant from the Science and Technology Department of China (Grant No. 2011ZX09302) and the Beijing Guidance Teacher Technology Grant for Excellent Doctoral Thesis of 2009 for Tutor Yong-hong Yang from Capital Medical University (Grant No. PXM2010-014226-07-000060).
LZ and XM conducted the laboratory work, performed the analysis, wrote the draft, and are the co-first authors for the same contributions of this study. WG, KY, AS, and SY provided the bacterial isolates and laboratory supplies. YY planned the study. All authors read and approved the final manuscript.
Lin Zhou, Xiang Ma contributed equally to this work.