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Lack of resistance to macrolides in Mycoplasma genitalium detected in South African pregnant women

BACKGROUND: Azithromycin regimens have been considered first-line treatment for Mycoplasma genitalium (M. genitalium), a sexually transmitted infection (STI) associated with adverse pregnancy outcomes. However, recent years have seen rapid emergence of macrolide resistance in M. genitalium as a resu...

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Autores principales: Naicker, Meleshni, Singh, Ravesh, van der Westhuizen, Donald, Tinarwo, Partson, Abbai, Nathlee S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447758/
https://www.ncbi.nlm.nih.gov/pubmed/34549049
http://dx.doi.org/10.4102/sajid.v36i1.209
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author Naicker, Meleshni
Singh, Ravesh
van der Westhuizen, Donald
Tinarwo, Partson
Abbai, Nathlee S.
author_facet Naicker, Meleshni
Singh, Ravesh
van der Westhuizen, Donald
Tinarwo, Partson
Abbai, Nathlee S.
author_sort Naicker, Meleshni
collection PubMed
description BACKGROUND: Azithromycin regimens have been considered first-line treatment for Mycoplasma genitalium (M. genitalium), a sexually transmitted infection (STI) associated with adverse pregnancy outcomes. However, recent years have seen rapid emergence of macrolide resistance in M. genitalium as a result of widespread administration of azithromycin. Currently, there are limited data on macrolide resistance in pregnant women from KwaZulu-Natal (KZN), South Africa. This study investigated the prevalence of M. genitalium and emerging patterns of macrolide resistance in pregnant women from KZN. METHODS: This was a sub-study of a larger study which involved laboratory-based detection of STIs in pregnant women. In the main study, pregnant women provided urine samples for detection of STIs. For this study, deoxyribose nucleic acid (DNA) extracted from stored urine was used to determine emerging macrolide resistance by amplification of the 23S ribosomal ribonucleic acid (rRNA) gene of M. genitalium by polymerase chain reaction (PCR) and sequencing of amplicons to identify mutations associated with resistance. The Allplex™ MG & AziR assay was used as a confirmatory assay. RESULTS: The prevalence of M. genitalium in pregnant women was 5.9% (13 out of 221). Sequencing of PCR amplicons did not reveal the presence of the A2059G and A2058G mutations associated with macrolide resistance. These findings were confirmed by the Allplex™ MG & AziR assay. CONCLUSION: Despite the lack of resistance to macrolides in this study population, continued antimicrobial resistance surveillance for M. genitalium in pregnant women is important because azithromycin is now part of the South African national STI syndromic management guidelines for vaginal discharge syndrome.
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spelling pubmed-84477582021-09-20 Lack of resistance to macrolides in Mycoplasma genitalium detected in South African pregnant women Naicker, Meleshni Singh, Ravesh van der Westhuizen, Donald Tinarwo, Partson Abbai, Nathlee S. S Afr J Infect Dis Original Research BACKGROUND: Azithromycin regimens have been considered first-line treatment for Mycoplasma genitalium (M. genitalium), a sexually transmitted infection (STI) associated with adverse pregnancy outcomes. However, recent years have seen rapid emergence of macrolide resistance in M. genitalium as a result of widespread administration of azithromycin. Currently, there are limited data on macrolide resistance in pregnant women from KwaZulu-Natal (KZN), South Africa. This study investigated the prevalence of M. genitalium and emerging patterns of macrolide resistance in pregnant women from KZN. METHODS: This was a sub-study of a larger study which involved laboratory-based detection of STIs in pregnant women. In the main study, pregnant women provided urine samples for detection of STIs. For this study, deoxyribose nucleic acid (DNA) extracted from stored urine was used to determine emerging macrolide resistance by amplification of the 23S ribosomal ribonucleic acid (rRNA) gene of M. genitalium by polymerase chain reaction (PCR) and sequencing of amplicons to identify mutations associated with resistance. The Allplex™ MG & AziR assay was used as a confirmatory assay. RESULTS: The prevalence of M. genitalium in pregnant women was 5.9% (13 out of 221). Sequencing of PCR amplicons did not reveal the presence of the A2059G and A2058G mutations associated with macrolide resistance. These findings were confirmed by the Allplex™ MG & AziR assay. CONCLUSION: Despite the lack of resistance to macrolides in this study population, continued antimicrobial resistance surveillance for M. genitalium in pregnant women is important because azithromycin is now part of the South African national STI syndromic management guidelines for vaginal discharge syndrome. AOSIS 2021-01-15 /pmc/articles/PMC8447758/ /pubmed/34549049 http://dx.doi.org/10.4102/sajid.v36i1.209 Text en © 2021. The Authors https://creativecommons.org/licenses/by/4.0/Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Original Research
Naicker, Meleshni
Singh, Ravesh
van der Westhuizen, Donald
Tinarwo, Partson
Abbai, Nathlee S.
Lack of resistance to macrolides in Mycoplasma genitalium detected in South African pregnant women
title Lack of resistance to macrolides in Mycoplasma genitalium detected in South African pregnant women
title_full Lack of resistance to macrolides in Mycoplasma genitalium detected in South African pregnant women
title_fullStr Lack of resistance to macrolides in Mycoplasma genitalium detected in South African pregnant women
title_full_unstemmed Lack of resistance to macrolides in Mycoplasma genitalium detected in South African pregnant women
title_short Lack of resistance to macrolides in Mycoplasma genitalium detected in South African pregnant women
title_sort lack of resistance to macrolides in mycoplasma genitalium detected in south african pregnant women
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447758/
https://www.ncbi.nlm.nih.gov/pubmed/34549049
http://dx.doi.org/10.4102/sajid.v36i1.209
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