<HashMap><database>GEO</database><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Non-coding RNA profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE333874</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Small RNA sequencing reveals placental miRNAs linked to congenital transmission of Trypanosoma cruzi</name><description>Background: Congenital transmission remains an important source of new Chagas disease cases. This study aimed to identify placental microRNAs (miRNAs) associated with congenital transmission of Trypanosoma cruzi. Methods: Placental samples from T. cruzi-infected mothers were classified according to congenital transmission status and analyzed by small RNA sequencing. Differential expression was assessed using DESeq2 with Benjamini-Hochberg false discovery rate correction. Nine candidate miRNAs were subsequently assessed by RT-qPCR. Results: Small RNA sequencing was performed in 31 placental samples, including 13 from transmitting mothers and 18 from non-transmitting mothers. hsa-miR-155-5p was the only miRNA significantly upregulated in placentas from transmitting mothers after multiple-testing correction and was selected as a candidate for further validation. Seven additional miRNAs (hsa-miR-193a-5p, hsa-miR-187-3p, hsa-miR-512-5p, hsa-miR-515-5p, hsa-miR-526a-5p, hsa-miR-99b-3p, and hsa-miR-455-5p) were selected based on nominal p-value, expression abundance, and differences in mean normalized counts between groups. RT-qPCR assessment in 15 placental samples, including 5 from transmitting mothers and 10 from non-transmitting mothers, showed higher normalized expression of hsa-miR-193a-5p and hsa-miR-187-3p in transmitting mothers.Conclusion: Placental miRNA profiling identified hsa-miR-155-5p, hsa-miR-193a-5p, and hsa-miR-187-3p as candidates for further investigation in congenital transmission of T. cruzi. These findings require confirmation in larger cohorts.</description><dates><publication>2026/06/04</publication></dates><accession>GSE333874</accession><cross_references><GSM>GSM9776360</GSM><GSM>GSM9776367</GSM><GSM>GSM9776345</GSM><GSM>GSM9776368</GSM><GSM>GSM9776346</GSM><GSM>GSM9776365</GSM><GSM>GSM9776366</GSM><GSM>GSM9776363</GSM><GSM>GSM9776364</GSM><GSM>GSM9776361</GSM><GSM>GSM9776362</GSM><GSM>GSM9776349</GSM><GSM>GSM9776347</GSM><GSM>GSM9776369</GSM><GSM>GSM9776348</GSM><GSM>GSM9776370</GSM><GSM>GSM9776371</GSM><GSM>GSM9776356</GSM><GSM>GSM9776357</GSM><GSM>GSM9776354</GSM><GSM>GSM9776355</GSM><GSM>GSM9776374</GSM><GSM>GSM9776352</GSM><GSM>GSM9776353</GSM><GSM>GSM9776375</GSM><GSM>GSM9776350</GSM><GSM>GSM9776372</GSM><GSM>GSM9776373</GSM><GSM>GSM9776351</GSM><GSM>GSM9776358</GSM><GSM>GSM9776359</GSM><GPL>24676</GPL><GSE>333874</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>