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Indian J Med Res 124, July 2006, pp 99-104 Serotype distribution of Streptococcus pneumoniae isolates from ophthalmic & systemic infections & of commensal origin Upendra K. Kar, Gita Satpathy, N. Nayak, B.K. Das* & S.K. Panda** Department of Ocular Microbiology, Dr R. P. Center for Ophthalmic Sciences, Departments of *Microbiology & **Pathology, All India Institute of Medical Sciences, New Delhi, India Received April 26, 2005 Background & objectives: Information regarding serotype distributions of Streptococcus pneumoniae causing ophthalmic infections is scanty. This study was therefore undertaken to determine the antimicrobial susceptibility status and serotypes of S. pneumoniae isolated from various ophthalmic infections and to compare with those isolated from systemic infections and commensal nasopharyngeal flora. Methods: Thirty eight of S. pneumoniae isolates from ophthalmic infections, 9 from systemic infections and 14 from the nasopharynx of apparently healthy school children were biochemically characterized and tested for in vitro antimicrobial susceptibity to various antibiotics. Serotyping of these 61 isolates was done by a rapid co-agglutination method. Results: All the 61 isolates were sensitive to oxacillin (penicillin) and susceptibility against other antimicrobials was variable. No multidrug resistance was observed. The 38 ophthalmic isolates were distributed in 15 different serotypes. Most prevalent serotypes were 14, followed by 8 and 19F. The 9 systemic and 14 commensal. isolates of S. pneumoniae were distributed in 7 and 11 serotypes respectively. Three of the systemic and six of the commensal serotypes were observed in ophthalmic infections whereas four of the commensal serotypes were observed in systemic infections. Interpretation & conclusion: Resistance to penicillin was not observed. In ophthalmic infections, a wide range of serotypes of S. pneumoniae were observed. More than half of the commensal serotypes obtained in the study as well as majority of the systemic serotypes were observed in ophthalmic infections. Key words Commensals - in vitro antimicrobial susceptibility - ophthalmic infections - serotyping - Streptococcus pneumoniae systemic infections 99 100 INDIAN J MED RES, JULY 2006 Streptococcus pneumoniae is an important pathogen in ophthalmic infections like infective keratitis, dachryocystitis and conjunctivitis 1-4. In India, S. pneumoniae is the most common bacterial cause of dachryocystitis, which if left untreated, leads to nasolachrymal duct blockage with grave sequelae 1,3 . S. pneumoniae has been shown to constitute 11.74 per cent of all bacterial isolates causing ocular infections in a study on school children in Delhi5. S. pneumoniae is also the cause of community acquired bacterial pneumonia, a substantial proportion of bacterial meningitis, otitis media and sinusitis worldwide6. There are more than 90 serotypes of S. pneumoniae described till date8. Of these, only a limited number of serotypes are responsible for majority of the infection, against which the currently available 23 valent capsular polysaccharide vaccine is designed6,7. Some of the serotypes involved in eye infections may be different from those associated with systemic infections 8. Moreover up to 77 per cent of healthy individuals including children carry S. pneumoniae as normal flora in the nasopharynx9,10. Due to the anatomical proximity of the eye to nasopharynx it is plausible that some of the commensal serotypes may be involved in some of the ocular infections. We studied 61 well characterized isolates of S. pneumoniae (38 from various ophthalmic infections, 9 from systemic infections and 14 commensal isolates from normal nasopharynx) for in vitro antimicrobial susceptibility pattern and serotype determination by co-agglutination (COA) method. Material & Methods Isolation and characterization of Streptococcus pneumoniae: Thirty-eight consecutive isolates of S. pneumoniae ophthalmic isolates with no selection bias included in this study were from patients attending the outpatient department of Dr Rajendra Prasad Ophthalmic Centre for Ophthalmic Sciences, All India Institute of Medical Sciences (AIIMS), New Delhi from January 2002 to June 2003. The clinical diagnoses were; dachryocystitis: 28 [18 were <12 yr of age (10 M and 8 F) and remaining 10 were 16-81 yr of age (6 M and 4 F)], infective keratitis: 7 (4 M and 3 F) 7-70 yr of age, sporadic conjunctivitis: 2 and panophthalamitis: 1. The systemic isolates of S. pneumoniae were from 9 patients with pneumococcal infections (4 with pneumonia, 3 with meningitis, and 2 with septicaemia) attending AIIMS hospital. Fourteen commensal S. pneumoniae isolates were collected from the nasopharynx of 30 apparently healthy school children (5-10 yr of age) from Delhi. After detailed clinical examination and obtaining informed consent, specimens with sterile cotton tipped swabs were collected from lachrymal canaliculus, cornea, and conjunctiva of patients with dachryocystitis, infective keratitis and conjunctivitis respectively. Pleural fluid, sputum and cerebrospinal fluid were collected from patients suffering from pneumonia and meningitis respectively. Five ml of blood was collected aseptically from the patients of septicaemia. Nasopharyngeal swabs were collected from 30 apparently healthy school children. However, ethical clearance was not required. The specimens were cultured on tryptic soy agar (TSA) plates supplemented with 5 per cent sheep blood (for blood culture in 50 ml of tryptic soy broth which was subcultured into plates after 48 h) and incubated at 37 0C for 18-24 h in an atmosphere of 5 per cent CO 2 . a-haemolytic colonies with morphology suggestive of S. pneumoniae in Gram stain were subcultured to a fresh plate with an KAR et al: SEROTYPE DISTRIBUTION OF S. PNEUMONIAE optochin disk (5 mg/6 mm), (Difco Laboratories, Detroit, USA) and were incubated at 370C for another 18-24 h. Isolates that exhibited an inhibition zone of about 14 mm around the optochin disk and were showing both bile-solubility and capability to ferment inulin were identified as S. pneumoniae. Antimicrobial susceptibility testing: The isolates were tested for antimicrobial susceptibility with antibiotic impregnated discs (Hi-Media, Mumbai, India) against oxacillin (20 µg for penicillin), tetracycline (30 µg), erythromycin (15 µg), chloramphenicol (30 µg), co-trimoxazole (1.25/23.75 µg), ciprofloxacin (5 µg), gentamicin (100 µg), cephalexin (30 µg) and vancomycin (30 µg), using Kirby Bauer’s disc diffusion method11. The inhibition zone was measured and interpreted according to the recommendations of the National Committee for Clinical Laboratory Standards12. Serotyping of the S. pneumoniae isolates: The isolates were sent to India CLEN infectious diseases Reference Laboratory, Vellore, for serotyping. The serotyping was carried out by a rapid co-agglutination method using 12 pooled S. pneumoniae antisera from Statens Serum Institut, Copenhagen, Denmark 13. 101 Results & Discussion High incidence of pneumococcal infections and emergence of multidrug resistance are the major reasons for continuous epidemiological surveillance. In the present study, majority of S. pneumoniae isolates from eye infections were from patients with dachryocystitis 73.6 per cent, followed by infective keratitis (18.4%) and sporadic conjunctivitis (5.2%). All isolates were uniformly sensitive to oxacillin (penicillin) (Table I), though intermediate resistance to penicillin amongst ophthalmic isolates was reported from south India 8. Resistances to the other antibiotics tested were variable i.e., co-trimoxazole (75.4%), ciprofloxacin (29.5%), cephalexin (22.9%), tetracycline (26.22%), chloramphenicol (6.5%), gentamicin (6.5%), erythromycin (1.6%). No multidrug resistant isolates were noted. However, 65 per cent of the ophthalmic isolates, and almost all of the systemic isolates were resistant to co-trimoxazole, which is extensively used as a first line treatment for pneumococcal infections. Majority of the ophthalmic isolates were sensitive to ciprofloxacin whereas the same was not observed for systemic and commensal isolates. Table I. Isolation source and antimicrobial susceptibility of 61 Streptococcus pneumoniae isolates Antibiotics Ophthalmic (38) S I Penicillin (20 µg) 38 Co-trimoxazole (1.25/23.75 µg) 10 Ciprofloxacin (5 µg) Systemic (9) Commensal (14) R S I R S I R 0 0 9 0 0 14 0 0 3 25 0 1 8 1 0 13 19 15 4 2 2 5 1 4 9 Cephalexin(30 µg) 29 4 5 5 0 4 9 0 5 Tetracycline (30 µg) 33 2 3 3 4 2 9 2 3 Chloramphenicol (30 µg) 36 0 2 9 0 0 12 0 2 Gentamicin (100 µg) 28 6 4 8 1 0 14 0 0 Erythromycin (15 µg) 37 0 1 9 0 0 14 0 0 Vancomycin (30 µg) 30 8 0 8 1 0 12 2 0 S, sensitive; I, intermediate; R, resistant 102 INDIAN J MED RES, JULY 2006 Serotyping still remains the most import epidemiological typing method 7,8, because currently available vaccine is dependent on serotype distribution of the strains causing major diseases6,14. Certain serotypes of S. pneumoniae are more frequently associated with specific types of infections 6,15 . Even though information regarding serotype distribution of S. pneumoniae is available for both commensal and systemic isolates, such information is limited for the ophthalmic infections from different geographical regions. In the present study, of the 38 ophthalmic isolates, 36 could be typed into 15 serotypes and two were non-typeable. The 28 isolates from dachryocystitis and the 7 isolates from keratitis were distributed in 14 and 5 serotypes respectively (Table II). Serotype 14 was found to be most prevalent (n=6) followed by 8 (n=5) and 19 F (n=4) which correlates with an earlier report suggesting 6A was more prevalent serotype in ophthalmic infection 8. Five of the serotypes i.e., 14, 34, 22, 23A, and 23B were observed in both the studies 8. An earlier study at our hospital reported that 19 of 20 ophthalmic isolates were typeable into serotypes 3, 6, 8, 28, 29, 45, 21 and 18 1. Of these only serotypes 18F and 28 were observed in the present study. It is believed that serotypes of S. pneumoniae causing a particular infection in a geographical location may change over a period of time and this is of interest for epidemiological purposes. All the serotypes observed in keralitits were also in dachryocystitis. The serotypes observed in panophthalamitis (serotype 14) and conjunctivitis (serotypes 33) were also observed in dachryocystitis. This suggests that the same serotypes may be responsible for different types of ocular infections. We did not observe non typable isolates from conjuctivitis, though it is commonly reported from Europe and other parts of the world4. The 9 isolates from systemic infections and 14 commensal isolates from the nasopharynx were distributed in 7 and 11 serotypes respectively (Table III). Serotypes 1 and 4 were isolated from 2 patients each from systemic infections. These have been reported as the predominant serotypes in systemic from India14,15. Three of the systemic serotypes (8, 19 F and 23 A) were also observed in ophthalmic infections. Only two serotypes i.e., 19 F, 23 A were observed amongst the isolates from all the studied sites. Table III. Serotype distribution of systemic and commensal Streptococcus pneuminiae isolates Source Serogroup/type No. of isolates Table II. Serotype distribution of ophthalmic Streptococcus pneuminiae isolates Pneumonia and meningitis 1 1 (each) Source Serogroup/type No. of isolates Pneumonia 8 1 Dachryocystitis 14 5 Pneumonia 15 A 1 Dachryocystitis 8, 34 3 (each) Dachryocystitis 18F, 19F, 22, 23A 2 (each) Pneumonia 19 F 1 Dachryocystitis 10, 11, 16, 17, 1 (each) Meningitis and septicaemia 4 1 (each) Meningitis 6 1 Septicaemia 23A 1 23B, 28, 33 Dachryocystitis Non-typeable 2 Corneal ulcer 8, 19F 2 (each) Corneal ulcer 10, 17, 33 1 (each) Commensal 11,23A,34 2 (each) Conjunctivitis 31,33 1 (each) Commensal 6A,6B, 16, 18F, 19F, 1 (each) Pan-ophthalmitis 14 1 Commensal 4, 18C, 39 1 (each) KAR et al: SEROTYPE DISTRIBUTION OF S. PNEUMONIAE From the 11 serotypes of commensal isolates, 6 (11, 16, 18F, 19F, 23A, 34) were observed in ophthalmic infections (dachryocystitis and keratitis) and 3 were seen in systemic infections. Because of the anatomical proximity, the commensal isolates may be frequently associated with ophthalmic infections8. Some of the commensal serotypes 6, 11, 19, and 23 observed in this study, were also reported in the nasopharynx of normal healthy children in other Indian studies16,17. In conclusion, no specific serotype of S. pneumoniae was found to have any special predilection to cause eye infection. However, majority of the nasopharyngeal isolates were observed in ophthalmic infections suggesting a role for anatomical proximity. Acknowledgment The authors thank Dr M.K. Lalitha, Department of Clinical Microbiology, Christian Medical College and Hospital, Vellore, for serotyping of the isolates, Prof. S Ghose ,the faculties and resident doctors of Dr RP Centre for Ophthalmic Sciences for clinical specimens. This study was funded by an Ad-hoc research grant from Indian Council of Medical Research (ICMR), New Delhi. 103 5. Kumar R, Mehra M, Dabas P, Kamlesh, Raha R. A study of ocular infections amongst primary school children in Delhi. J Commun Dis 2004; 36 : 121-6. 6. Obaro S, Adegbola R. The pneumococcus: carriage, disease and conjugate vaccine. J Med Microbiol 2002; 51 : 98-104. 7. Dot C, Lousily C, Gosling P, Binge E. Phenotypic and genetic diversity of invasive pneumococcal isolates recovered from French children. J Clin Microbial 2002; 40 : 2994-8. 8. Mathews MS, Savanna A, Manchurian A, Maharaja S, Lalitha MK. Streptococcus pneumoniae from ophthalmic infections: serotype distribution and penicillin susceptibility. Deign Microbial Infect Dis 2000; 36 : 81-4. 9. Regev-Yochay G, Raz M, Dagan R, Porat N, Shainberg B, Pinco E, et al. Nasopharyngeal carriage of Streptococcus pneumoniae by adults and children in community and family settings. Clin Infect Dis 2004; 38 : 632-9. 10. Jain A, Kumar P, Awasthi S. High nasopharyngeal carriage of drug resistant Streptococcus pneumoniae and Haemophilus influenzae in north Indian school children. Trop Med Int Health 2005; 10 : 234-9. 11. Bauer AW, Kirby WMM, Sherris JC, Turck M. Antibiotic susceptibility testing by a standardized single disk method. Am J Clin Pathol 1966; 45 : 493-6. References 1. Mahajan VM, Bareja U, Prakash K, Ghose S. Pneumococci in ocular disease of children and their treatment. Ann Trop Paediatr 1987; 7 : 270-3. 2. Parmar P, Salman A, Kalavathy CM, Jesudasan CA, Thomas PA. Pneumococcal keratitis: a clinical profile. Clin Experiment Ophthalmol 2003; 31 : 44-7. 3. Aasuri MK, Reddy MK, Sharma S, Rao GN. Co-occurrence of pneumococcal keratitis and dachryocystitis. Cornea 1999; 18 : 273-6. 4. Berrón S, Fenoll A, Ortega M, Arellano N, Casal J. Analysis of the genetic structure of nontypeable pneumococcal strains isolates from conjuctiva. Clin Microbiol 2005; 43 : 1694-8. 12. Performance standards for antimicrobial susceptibility testing: 12th information supplement, vol.22, no.1, NCCLS. M100-S12/ISBN1-56238-4511-6/ISSN 0273-3099. 13. Lalitha MK, Thomas K, Kumar RS, Steinhoff MC. Serotyping of Streptococcus pneumoniae b y coagglutination with 12 pooled antisera. J Clin Microbiol 1999; 37 : 263-5. 14. Hausdorff WP, Bryant J, Paradiso PR, Siber GR. Which pneumococcal serogroups cause the most invasive disease: implications for conjugate vaccine formulation and use, part I. Clin Infect Dis 2000; 30 : 100-21. 15. Invasive Bacterial Infection Surveillence (IBIS) Group and International Clinical Epidemiology Network 104 INDIAN J MED RES, JULY 2006 (INCLEN). Prospective multi-center hospital surveillance of Streptococcal disease in India. Lancet 1999; 353 : 1216-21. 16. Coles CL, Kanungo R, Rahmathullah L,Thulasiraj RD, Katz J, Santosham M, et al. Pneumococcal nasopharyngeal colonization in young south Indian infants. Pediatr Infect Dis J 2001; 20 : 289-95. 17. Jebaraj R, Cherian T, Raghupathy P, Brahmadathan KN, Lalitha MK, Thomas K, et al. Nasopharyngeal colonization of infants in southern India with Streptococcus pneumoniae. Epidemiol Infect 1999; 123 : 383-8. Reprint requests: Dr Gita Satpathy, Professor, Ocular Microbiology, Dr R.P. Center for Ophthalmic Sciences All India Institute of Medical Sciences (AIIMS), Ansari Nagar, New Delhi 110029, India e-mail: gita.satpathy@ gmail.com