# Proteomic signatures of cervical mucus associated with fertility in Bali heifers (Bos javanicus): Implications for biomarker-based selection in artificial insemination programs

**Authors:** Muhammad Yusuf, Abdul Latief Toleng, Hasrin Hasrin, Abdullah Baharun, Athhar Manabi Diansyah, Santoso Santoso, Rahmat Rahmat, Andi Muhammad Alfian, Masturi Masturi, Sahiruddin Sahiruddin, Muhammad Fajar Amrullah, Ahmad Alfaruqi Syahrandi Adam, Miftahul Jannah

PMC · DOI: 10.14202/vetworld.2026.135-148 · 2026-01-14

## TL;DR

This study identifies specific proteins in cervical mucus linked to fertility in Bali heifers, offering new biomarkers to improve artificial insemination success.

## Contribution

The study provides the first proteomic analysis of cervical mucus in relation to fertility in Bali cattle, identifying novel biomarkers for improved artificial insemination.

## Key findings

- Thirteen proteins showed significant differential abundance between good and poor cervical mucus groups.
- NT5E, lactoferrin, and SCGB1D were enriched in good mucus, while CFI, haptoglobin, and MUC5AC were enriched in poor mucus.
- NT5E, CFI, and haptoglobin demonstrated excellent discriminative performance for fertility status.

## Abstract

Despite strong adaptive traits, the reproductive efficiency of Bali cattle (Bos javanicus) remains suboptimal, with low conception rates following artificial insemination (AI). Cervical mucus (CM) is a critical factor in sperm transport and fertilization; however, its molecular basis in relation to fertility has not been elucidated in this indigenous breed. This study aimed to characterize the proteomic profile of CM in Bali heifers and to identify protein biomarkers associated with fertility-related mucus quality.

The study was conducted between February and August 2024 in South Sulawesi, Indonesia. Forty clinically healthy Bali heifers (2–3 years old) were sampled during natural oestrus and divided into good CM (GCM; n = 20) and poor CM (PCM; n = 20) groups using a validated five-parameter biophysical scoring system. CM proteins were extracted and analyzed using one-dimensional sodium dodecyl sulfate–polyacrylamide gel electrophoresis followed by liquid chromatography–tandem mass spectrometry. High-confidence protein identification was achieved at <1% false discovery rate, and differential abundance was evaluated using Benjamini–Hochberg correction (p < 0.05). Functional enrichment, correlation analysis with mucus traits, and receiver-operating-characteristic (ROC) analyses with cross-validation were performed.

Significant differences (p < 0.05) were observed between GCM and PCM groups for appearance, viscosity, spinnbarkeit, and ferning pattern, while pH did not differ. A total of 52 proteins were identified after quality control, of which 13 showed significant differential abundance. GCM was characterized by higher levels of NT5E, lactoferrin, SCGB1D, and lactotransferrin, whereas PCM showed enrichment of complement factor I (CFI), haptoglobin (HP), MUC5AC, FAIM2, TIMP2, PEBP4, SAA3, GRP, and IGL. Functional enrichment analysis indicated anti-inflammatory and epithelial-protective pathways in GCM, in contrast to complement activation, proteolysis, and oxidative remodeling in PCM. ROC analysis demonstrated excellent discriminative performance for NT5E (GCM) and CFI and haptoglobin (PCM), each achieving an area under the curve of 1.00 in this cohort.

This study offers the first proteomic evidence connecting CM composition to fertility-related traits in Bali heifers. NT5E, CFI, and HP stand out as promising biomarkers for fertility screening, providing a molecular framework to improve AI efficiency and selection strategies in indigenous cattle.

## Linked entities

- **Genes:** NT5E (5'-nucleotidase ecto) [NCBI Gene 4907], SCGB1D (secretoglobin, family 1D, member 2) [NCBI Gene 338419], CFI (complement factor I) [NCBI Gene 3426], HP (haptoglobin) [NCBI Gene 3240], MUC5AC (mucin 5AC, oligomeric mucus/gel-forming) [NCBI Gene 4586], FAIM2 (Fas apoptotic inhibitory molecule 2) [NCBI Gene 23017], TIMP2 (TIMP metallopeptidase inhibitor 2) [NCBI Gene 7077], PEBP4 (phosphatidylethanolamine binding protein 4) [NCBI Gene 157310], SAA3P (serum amyloid A3, pseudogene) [NCBI Gene 6290], GRP (gastrin releasing peptide) [NCBI Gene 2922], IGL (immunoglobulin lambda locus) [NCBI Gene 3535]
- **Proteins:** NT5E (5'-nucleotidase ecto), tf.S (transferrin S homeolog), SCGB1D (secretoglobin, family 1D, member 2), CFI (complement factor I), MUC5AC (mucin 5AC, oligomeric mucus/gel-forming), FAIM2 (Fas apoptotic inhibitory molecule 2), TIMP2 (TIMP metallopeptidase inhibitor 2), PEBP4 (phosphatidylethanolamine binding protein 4), SAA3P (serum amyloid A3, pseudogene), GRP (gastrin releasing peptide), IGL (immunoglobulin lambda locus)
- **Species:** Bos javanicus (taxon 9906)

## Full-text entities

- **Diseases:** inflammatory (MESH:D007249), GCM (MESH:D002575)
- **Chemicals:** polyacrylamide (MESH:C016679), sulfate (MESH:D013431), sodium (MESH:D012964)
- **Species:** Bos javanicus (banteng, species) [taxon 9906], Bos taurus (bovine, species) [taxon 9913]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12975713/full.md

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Source: https://tomesphere.com/paper/PMC12975713