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Identification of Cultivable Bacteria in Amniotic Fluid Using Cervicovaginal Fluid Protein Microarray in Preterm
Seung Mi Lee1,2, Kyo Hoon Park3,4, Subeen Hong1,5
1Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, South Korea.
Abstract:
We aimed to identify cervicovaginal fluid (CVF) protein biomarkers of microbial invasion of the amniotic cavity (MIAC) in women with preterm premature rupture of membranes (PPROM), using an antibody microarray. This retrospective cohort study included 99 consecutive women with singleton pregnancies and PPROM (23-33 weeks) who underwent amniocentesis and who gave CVF samples. CVF proteomes from the MIAC (n = 20) versus non-MIAC groups (n = 20) were comparatively profiled by an antibody microarray using a nested case-control study design. The seven candidate biomarkers of interest were validated in the total cohort (n = 99) by enzyme-linked immunosorbent assays (ELISA). For comparison with candidate markers, amniotic fluid (AF) white blood cell (WBC) count was also measured. The primary outcome measure was MIAC (defined as positive AF culture). Thirty of the proteins studied exhibited significant intergroup differences. Measurements of the total cohort with ELISA confirmed a significant increase in the levels of CVF IL-8, lipocalin-2, MIP-1α, MMP-9, and TIMP-1 in women with MIAC, independent of gestational age at sampling. A combined, non-invasive model was developed by using a stepwise regression procedure, which included CVF IL-8 and CVF MMP-9 (area under the curve [AUC] = 0.763), and this AUC was comparable with the AUC of AF WBC. Using protein-antibody microarray technology, we found several novel, independent, non-invasive biomarkers to identify MIAC in women with PPROM: IL-8, lipocalin-2, MIP-1α, MMP-9, and TIMP-1. Furthermore, the combined non-invasive model (IL-8 and MMP-9) was a useful independent predictor for MIAC with good discriminatory power, similar to AF WBC count.
Insights
Cervicovaginal fluid (CVF) protein biomarkers, including IL-8 and MMP-9, can non-invasively identify microbial invasion of the amniotic cavity (MIAC) in women with preterm premature rupture of membranes (PPROM). This discovery offers a new diagnostic approach for PPROM complications.
Area of Science:
- Obstetrics and Gynecology
- Infectious Diseases
- Biomarker Discovery
Background:
- Preterm premature rupture of membranes (PPROM) is a leading cause of preterm birth.
- Microbial invasion of the amniotic cavity (MIAC) is a major complication of PPROM, associated with adverse neonatal outcomes.
- Accurate and early diagnosis of MIAC is crucial for timely intervention.
Purpose of the Study:
- To identify cervicovaginal fluid (CVF) protein biomarkers for detecting microbial invasion of the amniotic cavity (MIAC) in women with PPROM.
- To evaluate the diagnostic performance of these biomarkers, individually and in combination, compared to amniotic fluid white blood cell (AF WBC) count.
Main Methods:
- A retrospective cohort study involving 99 women with PPROM.
- Proteomic profiling of CVF using antibody microarray in a nested case-control design (MIAC vs. non-MIAC groups).
- Validation of candidate biomarkers using enzyme-linked immunosorbent assays (ELISA) and comparison with AF WBC count.
Main Results:
- Thirty proteins showed significant differences between MIAC and non-MIAC groups.
- ELISA confirmed elevated levels of CVF IL-8, lipocalin-2, MIP-1α, MMP-9, and TIMP-1 in women with MIAC.
- A combined non-invasive model of CVF IL-8 and CVF MMP-9 demonstrated good discriminatory power (AUC=0.763), comparable to AF WBC count.
Conclusions:
- Novel, non-invasive CVF protein biomarkers (IL-8, lipocalin-2, MIP-1α, MMP-9, TIMP-1) can identify MIAC in women with PPROM.
- A combined model using CVF IL-8 and MMP-9 is a valuable predictor of MIAC, offering a promising diagnostic tool.
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