Best among the key molecular diagnostic markers of bacterial vaginosis

被引:0
作者
Deng, Tongyang [1 ]
Song, Xiangquan [2 ]
Liao, Qiumei [4 ]
Zheng, Ying [3 ]
Sun, Hong [1 ]
Zhang, Lianzhen [1 ]
Chen, Xuejia [5 ]
机构
[1] Tongde Hosp Zhejiang Prov, Dept Lab Med, Hangzhou, Peoples R China
[2] Hangzhou Xihu Dist Hosp Tradit Chinese & Western M, Dept Lab, Hangzhou, Peoples R China
[3] Tongde Hosp Zhejiang Prov, Dept Obstet & Gynecol, Hangzhou, Peoples R China
[4] Tongde Hosp Zhejiang Prov, Dept Rehabil Med, Hangzhou, Peoples R China
[5] Hangzhou Hosp Tradit Chinese Med, Dept Obstet & Gynecol, Hangzhou, Peoples R China
关键词
Bacterial vaginosis; Molecular diagnostic marker; Lactobacillus crispatus; Gardnerella vaginalis; Fannyhessea vaginae; GARDNERELLA-VAGINALIS; GRAM STAIN; ATOPOBIUM-VAGINAE; PRETERM DELIVERY; PCR ASSAY; WOMEN; VALIDATION; COLONIZATION; MICROBIOME; CRITERIA;
D O I
10.1186/s13568-025-01847-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To assess bacterial vaginosis (BV)-related primary molecular diagnostic markers of Lactobacillus crispatus, Gardnerella vaginalis, Fannyhessea vaginae, bacterial vaginosis-associated bacteria 2 (BVAB-2), Megasphaera-1 and Megasphaera-2 and to discover molecular diagnostic indicators of BV with the most economic value for the efficient diagnosis of BV.All vaginal secretion specimens, including 122 BV-positive cases and 130 BV-negative controls were collected. First, quantitative polymerase chain reaction (PCR) was used to determine the levels of above the six bacteria. Then, the detection rates, sensitivity, specificity, diagnostic threshold, and receiver operating characteristic (ROC) curve were compared. Megasphaera-1 and Megasphaera-2 were detected in the BV-positive group, with a low detection rate of 35.25% and 19.67% respectively. The sensitivity and specificity of the above four bacteria were 95.90%/72.31%, 82.79%/92.48%, 72.13%/95.38%, and 56.56%/94.62% respectively, using the cut-off value for the diagnosis of BV. When combinations of L. crispatus with G. vaginalis, F. vaginae, and BVAB-2 were performed respectively, their sensitivity and specificity were 99.29%/97.79%, 98.86%/98.72%, and 98.22%/98.51% in sequence.It is difficult to diagnose BV using only one species, however, combinations of L. crispatus with G. vaginalis or F. vaginae showed a better diagnostic effect, particularly with the combination of L. crispatus and G. vaginalis.
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页数:9
相关论文
共 46 条
[41]   SELECTIVE DIFFERENTIAL HUMAN-BLOOD BILAYER MEDIA FOR ISOLATION OF GARDNERELLA (HEMOPHILUS) VAGINALIS [J].
TOTTEN, PA ;
AMSEL, R ;
HALE, J ;
PIOT, P ;
HOLMES, KK .
JOURNAL OF CLINICAL MICROBIOLOGY, 1982, 15 (01) :141-147
[42]  
van de Wijgert DHHM, 2008, JAIDS-J ACQ IMM DEF, V48, P203, DOI 10.1097/QAI.0b013e3181743936
[43]   The Vaginal Microbiota: What Have We Learned after a Decade of Molecular Characterization? [J].
van de Wijgert, Janneke H. H. M. ;
Borgdorff, Hanneke ;
Verhelst, Rita ;
Crucitti, Tania ;
Francis, Suzanna ;
Verstraelen, Hans ;
Jespers, Vicky .
PLOS ONE, 2014, 9 (08)
[44]   Emended description of Gardnerella vaginalis and description of Gardnerella leopoldii sp. nov., Gardnerella piotii sp. nov. and Gardnerella swidsinskii sp. nov., with delineation of 13 genomic species within the genus Gardnerella [J].
Vaneechoutte, Mario ;
Guschin, Alexander ;
Van Simaey, Leen ;
Gansemans, Yannick ;
Van Nieuwerburgh, Filip ;
Cools, Piet .
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY, 2019, 69 (03) :679-687
[45]   Cloning of 16S rRNA genes amplified from normal and disturbed vaginal microflora suggests a strong association between Atopobium vaginae, Gardnerella vaginalis and bacterial vaginosis [J].
Verhelst, R ;
Verstraelen, H ;
Claeys, G ;
Verschraegen, G ;
Delanghe, J ;
Van Simaey, L ;
De Ganck, C ;
Temmerman, M ;
Vaneechoutte, M .
BMC MICROBIOLOGY, 2004, 4 (1)
[46]   Quantitative PCR Assessments of Bacterial Species in Women with and without Bacterial Vaginosis [J].
Zozaya-Hinchliffe, Marcela ;
Lillis, Rebecca ;
Martin, David H. ;
Ferris, Michael J. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2010, 48 (05) :1812-1819