Abstract

BackgroundIntra-amniotic infection has long been recognized as the leading cause of preterm delivery. Microbial culture is the gold standard for the detection of intra-amniotic infection, but several days are required, and many bacterial species in the amniotic fluid are difficult to cultivate.MethodsWe developed a novel nested-PCR-based assay for detecting Mycoplasma, Ureaplasma, other bacteria and fungi in amniotic fluid samples within three hours of sample collection. To detect prokaryotes, eukaryote-made thermostable DNA polymerase, which is free from bacterial DNA contamination, is used in combination with bacterial universal primers. In contrast, to detect eukaryotes, conventional bacterially-made thermostable DNA polymerase is used in combination with fungal universal primers. To assess the validity of the PCR assay, we compared the PCR and conventional culture results using 300 amniotic fluid samples.ResultsBased on the detection level (positive and negative), 93.3% (280/300) of Mycoplasma, 94.3% (283/300) of Ureaplasma, 89.3% (268/300) of other bacteria and 99.7% (299/300) of fungi matched the culture results. Meanwhile, concerning the detection of bacteria other than Mycoplasma and Ureaplasma, 228 samples were negative according to the PCR method, 98.2% (224/228) of which were also negative based on the culture method. Employing the devised primer sets, mixed amniotic fluid infections of Mycoplasma, Ureaplasma and/or other bacteria could be clearly distinguished. In addition, we also attempted to compare the relative abundance in 28 amniotic fluid samples with mixed infection, and judged dominance by comparing the Ct values of quantitative real-time PCR.ConclusionsWe developed a novel PCR assay for the rapid detection of Mycoplasma, Ureaplasma, other bacteria and fungi in amniotic fluid samples. This assay can also be applied to accurately diagnose the absence of bacteria in samples. We believe that this assay will positively contribute to the treatment of intra-amniotic infection and the prevention of preterm delivery.

Highlights

  • Intra-amniotic infection has long been recognized as the leading cause of preterm delivery [1,2,3], and preterm birth is a major cause of neonatal mortality worldwide [4]

  • Concerning the detection of bacteria other than Mycoplasma and Ureaplasma, 228 samples were negative according to the Polymerase chain reaction (PCR) method, 98.2% (224/228) of which were negative based on the culture method

  • We developed a novel PCR assay for the rapid detection of Mycoplasma, Ureaplasma, other bacteria and fungi in amniotic fluid samples

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Summary

Introduction

Intra-amniotic infection has long been recognized as the leading cause of preterm delivery [1,2,3], and preterm birth is a major cause of neonatal mortality worldwide [4]. A variety of microorganisms have been cultivated from amniotic fluid in pregnancies complicated by preterm birth [1, 11, 12], but in particular, Mycoplasma and Ureaplasma species are the most frequently isolated pathogens in cases with intra-amniotic infection [6, 13,14,15]. Microbial culture of amniotic fluid is recognized as the “gold standard” for the detection of intra-amniotic infection, but several days are usually required to detect bacteria and/or fungi in amniotic fluid samples, and a high percentage of bacterial species in the amniotic fluid are difficult to cultivate [16, 17]. Microbial culture is the gold standard for the detection of intra-amniotic infection, but several days are required, and many bacterial species in the amniotic fluid are difficult to cultivate

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