The trends of isolation and antimicrobial susceptibility of group B Streptococcus in urine culture: a 7-years cross sectional study
DOI:
https://doi.org/10.18203/2320-1770.ijrcog20231555Keywords:
Antimicrobial susceptibility testing, Streptococcus agalactiae, Urine, Urinary tract infectionAbstract
Background: Group B Streptococcus (GBS)/Streptococcus agalactiae (S. agalactiae) is a common rectovaginal colonizer, thereby a potential agent of neonatal and maternal infection. This study estimates the trends of isolation of GBS, its antimicrobial profile in urine culture and the demographic characteristics of these patients over a 7-year period.
Methods: A record-based study was conducted, which included all the urine culture reports of GBS/S. agalactiae from January 2014 to December 2020. The trend of occurrence of GBS bacteriuria, demographic characteristics and antimicrobial susceptibility pattern were analyzed.
Results: Out of 137 urine samples which grew GBS/S. agalactiae, 55(40.15%) were from antenatal women. Most of the isolates were from females (72.26%), with a male preponderance noted among the elderly population (age>60 years). The predominant age group affected were adults between 20 to 59 years. The majority of the isolates (60.58%) were susceptible to all the four tested antibiotics, namely, ciprofloxacin, nitrofurantoin, ampicillin and vancomycin. Ciprofloxacin resistance was observed in 32.85% (45/137) isolates, 5.84% (8/137) isolates were resistant to ampicillin and 2.92% (4/137) were resistant to nitrofurantoin.
Conclusions: All the isolates were susceptible to vancomycin. GBS/S. agalactiae is an important agent of bacteriuria in antenatal women as well as in non-pregnant population, especially the elderly males. Emerging resistance to various group of antibiotics warrants routine susceptibility testing.
Metrics
References
Lancefield RC. A serological differentiation of human and other groups of hemolytic Streptococci. J Exp Med. 1933;57(4):571-95.
Fry RM. Fatal infections by haemolytic Streptococcus group B. The Lancet. 1938;231:199-201.
Schuchat A. Epidemiology of group B streptococcal disease in the United States: shifting paradigms. Clin Microbiol Rev. 1998;11(3):497-513.
Raabe VN, Shane AL. Group B Streptococcus (Streptococcus agalactiae). Microbiol Spectr. 2019;7(2):7-2.
Committee on Obstetric Practice. Prevention of Group B Streptococcal Early-Onset Disease in Newborns: ACOG Committee Opinion, Number 797. Obstet Gynecol. 2020;135:e51-72.
Safari D, Gultom SM, Tafroji W, Azzahidah A, Soesanti F, Khoeri MM, et al. Prevalence, serotype and antibiotic susceptibility of Group B Streptococcus isolated from pregnant women in Jakarta, Indonesia. PLoS ONE. 2021;16(5):e0252328.
Steer PJ, Russell AB, Kochhar S, Cox P, Plumb J, Rao GG. Group B streptococcal disease in the mother and newborn-A review. Eur J Obstet Gynecol Reprod Biol. 2020;252:526-33.
Ulett GC, Webb RI, Ulett KB, Cui X, Benjamin WH, Crowley M, et al. Group B Streptococcus (GBS) urinary tract infection involves binding of GBS to bladder uroepithelium and potent but GBS-specific induction of interleukin 1alpha. J Infect Dis. 2010;201(6):866-70.
Muñoz P, Coque T, Créixems MR, Bernaldo de Quirós JCL, Moreno S, et al. Group B Streptococcus: A Cause of Urinary Tract Infection in Nonpregnant Adults. Clin Infect Dis. 1992;14(2):492-6.
Ulett KB, Benjamin WH, Zhuo F, Xiao M, Kong F, Gilbert GL, et al. Diversity of group B streptococcus serotypes causing urinary tract infection in adults. J Clin Microbiol. 2009;47(7):2055-60.
Rosenberger KD, Seibert A, Hormig S. Asymptomatic GBS bacteriuria during antenatal visits: To treat or not to treat?. Nurse Pract. 2020;45(7):18.
Zhu Y, Lin X-Z. Updates in prevention policies of early-onset group B streptococcal infection in newborns. Pediatr Neonatol. 2021;62(5):465-75.
Goel N, Wattal C, Gujral K, Dhaduk N, Mansukhani C, Garg P. Group B Streptococcus in Indian pregnant women: Its prevalence and risk factors. Indian J. Med. Microbiol. 2020;38(3-4):357-61.
Ashary N, Singh A, Chhabria K, Modi D. Meta-analysis on prevalence of vaginal group B streptococcus colonization and preterm births in India. J Matern-Fetal Neonatal Med. 2022;35(15):2923-31.
Farley MM. Group B streptococcal disease in nonpregnant adults. Clin Infect Dis Off Publ Infect Dis Soc Am. 2001;33(4):556-61.
Farley MM, Harvey RC, Stull T, Smith JD, Schuchat A, Wenger JD, et al. A population-based assessment of invasive disease due to group B Streptococcus in nonpregnant adults. N Engl J Med. 1993;328(25):1807-11.
Muñoz P, Llancaqueo A, Rodríguez-Créixems M, Peláez T, Martin L, Bouza E. Group B streptococcus bacteremia in nonpregnant adults. Arch Intern Med. 1997;157(2):213-6.
Bayer AS, Chow AW, Anthony BF, Guze LB. Serious infections in adults due to group B streptococci: clinical and serotypic characterization. Am J of Med. 1976;61(4):498-503.
Francois Watkins LK, McGee L, Schrag SJ, Beall B, Jain JH, Pondo T, et al. Epidemiology of invasive group B streptococcal infections among nonpregnant adults in the United States, 2008-2016. JAMA Intern Med. 2019;179(4):479-88.
Hayes K, O’Halloran F, Cotter L. A review of antibiotic resistance in Group B Streptococcus: the story so far. Crit Rev Microbiol. 2020;46(3):253-69.
Kimura K, Nishiyama Y, Shimizu S, Wachino J, Matsui M, Suzuki S, et al. Screening for group B streptococci with reduced penicillin susceptibility in clinical isolates obtained between 1977 and 2005. Jpn J Infect Dis. 2013;66(3):222-5.
Seki T, Kimura K, Reid ME, Miyazaki A, Banno H, Jin W, et al. High isolation rate of MDR group B streptococci with reduced penicillin susceptibility in Japan. J Antimicrob Chemother. 2015;70(10):2725-8.
Nagano N, Nagano Y, Toyama M, Kimura K, Shibayama K, Arakawa Y. Penicillin-Susceptible Group B Streptococcal Clinical Isolates with Reduced Cephalosporin Susceptibility. J Clin Microbiol. 2014;52(9):3406-10.
Park C, Nichols M, Schrag SJ. Two cases of invasive vancomycin-resistant group B streptococcus infection. N Engl J Med. 2014;370(9):885-6.