Analysis of virulence factors and antibiotic resistance genes in group B streptococcus from clinical samples

Abstract Background Streptococcus agalacticae (Group B Streptococcus, GBS) is one of the most important causative agents of serious infections among neonates. This study was carried out to identify antibiotic resistance and virulence genes associated with GBS isolated from pregnant women. Methods A...

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Main Authors: Raymond Mudzana, Rooyen T. Mavenyengwa, Muchaneta Gudza-Mugabe
Format: Article
Language:English
Published: BMC 2021-01-01
Series:BMC Infectious Diseases
Subjects:
PCR
Online Access:https://doi.org/10.1186/s12879-021-05820-6
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spelling doaj-7d385f4ca9f8434d9d3e89e0e8bb02bb2021-01-31T12:14:30ZengBMCBMC Infectious Diseases1471-23342021-01-0121111110.1186/s12879-021-05820-6Analysis of virulence factors and antibiotic resistance genes in group B streptococcus from clinical samplesRaymond Mudzana0Rooyen T. Mavenyengwa1Muchaneta Gudza-Mugabe2Department of Medical Microbiology, National Polio Laboratory, University of Zimbabwe College of Health SciencesDepartment of Medical Microbiology, National Polio Laboratory, University of Zimbabwe College of Health SciencesFaculty of Health Sciences, Institute of Infectious Diseases and Molecular Medicine, University of Cape TownAbstract Background Streptococcus agalacticae (Group B Streptococcus, GBS) is one of the most important causative agents of serious infections among neonates. This study was carried out to identify antibiotic resistance and virulence genes associated with GBS isolated from pregnant women. Methods A total of 43 GBS isolates were obtained from 420 vaginal samples collected from HIV positive and negative women who were 13–35 weeks pregnant attending Antenatal Care at Chitungwiza and Harare Central Hospitals in Zimbabwe. Identification tests of GBS isolates was done using standard bacteriological methods and molecular identification testing. Antibiotic susceptibility testing was done using the modified Kirby-Bauer method and E-test strips. The boiling method was used to extract DNA and Polymerase Chain Reaction (PCR) was used to screen for 13 genes. Data was fed into SPSS 24.0. Results Nine distinct virulence gene profiles were identified and hly-scpB-bca-rib 37.2% (16/43) was common. The virulence genes identified were namely hly 97.8% (42/43), scpB 90.1% (39/43), bca 86.0% (37/43), rib 69.8% (30/43) and bac 11.6% (5/43). High resistance to tetracycline 97.7% (42/43) was reported followed by 72.1% (31/43) cefazolin, 69.8% (30/43) penicillin G, 58.1% (25/43) ampicillin, 55.8% (24/43) clindamycin, 46.5% (20/43) ceftriaxone, 34.9% (15/43) chloramphenicol, and 30.2% (13/43) for both erythromycin and vancomycin using disk diffusion. Antibiotic resistance genes among the resistant and intermediate-resistant isolates showed high frequencies for tetM 97.6% (41/42) and low frequencies for ermB 34.5% (10/29), ermTR 10.3% (3/29), mefA 3.4% (1/29), tetO 2.4% (1/42) and linB 0% (0/35). The atr housekeeping gene yielded 100% (43/43) positive results, whilst the mobile genetic element IS1548 yielded 9.3% (4/43). Conclusion The study showed high prevalence of hly, scpB, bca and rib virulence genes in S. agalactiae strains isolated from pregnant women. Tetracycline resistance was predominantly caused by the tetM gene, whilst macrolide resistance was predominantly due to the presence of erm methylase, with the ermB gene being more prevalent. Multi-drug resistance coupled with the recovery of resistant isolates to antimicrobial agents such as penicillins indicates the importance of GBS surveillance and susceptibility tests. It was also observed that in vitro phenotypic resistance is not always accurately predicted by resistance genotypes.https://doi.org/10.1186/s12879-021-05820-6Group B streptococcusVirulence genesAntibiotic resistance genesPCRZimbabwe
collection DOAJ
language English
format Article
sources DOAJ
author Raymond Mudzana
Rooyen T. Mavenyengwa
Muchaneta Gudza-Mugabe
spellingShingle Raymond Mudzana
Rooyen T. Mavenyengwa
Muchaneta Gudza-Mugabe
Analysis of virulence factors and antibiotic resistance genes in group B streptococcus from clinical samples
BMC Infectious Diseases
Group B streptococcus
Virulence genes
Antibiotic resistance genes
PCR
Zimbabwe
author_facet Raymond Mudzana
Rooyen T. Mavenyengwa
Muchaneta Gudza-Mugabe
author_sort Raymond Mudzana
title Analysis of virulence factors and antibiotic resistance genes in group B streptococcus from clinical samples
title_short Analysis of virulence factors and antibiotic resistance genes in group B streptococcus from clinical samples
title_full Analysis of virulence factors and antibiotic resistance genes in group B streptococcus from clinical samples
title_fullStr Analysis of virulence factors and antibiotic resistance genes in group B streptococcus from clinical samples
title_full_unstemmed Analysis of virulence factors and antibiotic resistance genes in group B streptococcus from clinical samples
title_sort analysis of virulence factors and antibiotic resistance genes in group b streptococcus from clinical samples
publisher BMC
series BMC Infectious Diseases
issn 1471-2334
publishDate 2021-01-01
description Abstract Background Streptococcus agalacticae (Group B Streptococcus, GBS) is one of the most important causative agents of serious infections among neonates. This study was carried out to identify antibiotic resistance and virulence genes associated with GBS isolated from pregnant women. Methods A total of 43 GBS isolates were obtained from 420 vaginal samples collected from HIV positive and negative women who were 13–35 weeks pregnant attending Antenatal Care at Chitungwiza and Harare Central Hospitals in Zimbabwe. Identification tests of GBS isolates was done using standard bacteriological methods and molecular identification testing. Antibiotic susceptibility testing was done using the modified Kirby-Bauer method and E-test strips. The boiling method was used to extract DNA and Polymerase Chain Reaction (PCR) was used to screen for 13 genes. Data was fed into SPSS 24.0. Results Nine distinct virulence gene profiles were identified and hly-scpB-bca-rib 37.2% (16/43) was common. The virulence genes identified were namely hly 97.8% (42/43), scpB 90.1% (39/43), bca 86.0% (37/43), rib 69.8% (30/43) and bac 11.6% (5/43). High resistance to tetracycline 97.7% (42/43) was reported followed by 72.1% (31/43) cefazolin, 69.8% (30/43) penicillin G, 58.1% (25/43) ampicillin, 55.8% (24/43) clindamycin, 46.5% (20/43) ceftriaxone, 34.9% (15/43) chloramphenicol, and 30.2% (13/43) for both erythromycin and vancomycin using disk diffusion. Antibiotic resistance genes among the resistant and intermediate-resistant isolates showed high frequencies for tetM 97.6% (41/42) and low frequencies for ermB 34.5% (10/29), ermTR 10.3% (3/29), mefA 3.4% (1/29), tetO 2.4% (1/42) and linB 0% (0/35). The atr housekeeping gene yielded 100% (43/43) positive results, whilst the mobile genetic element IS1548 yielded 9.3% (4/43). Conclusion The study showed high prevalence of hly, scpB, bca and rib virulence genes in S. agalactiae strains isolated from pregnant women. Tetracycline resistance was predominantly caused by the tetM gene, whilst macrolide resistance was predominantly due to the presence of erm methylase, with the ermB gene being more prevalent. Multi-drug resistance coupled with the recovery of resistant isolates to antimicrobial agents such as penicillins indicates the importance of GBS surveillance and susceptibility tests. It was also observed that in vitro phenotypic resistance is not always accurately predicted by resistance genotypes.
topic Group B streptococcus
Virulence genes
Antibiotic resistance genes
PCR
Zimbabwe
url https://doi.org/10.1186/s12879-021-05820-6
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