# Physicochemical and microbiome changes in queso Crema de Chiapas during ripening

**Authors:** Blanca Nayelli Ocampo Morales, Arturo Hernández Montes, Karel Estrada, Ernestina Valadez Moctezuma, Guadalupe Nevárez-Moorillón, Guadalupe Nevárez-Moorillón, Guadalupe Nevárez-Moorillón, Guadalupe Nevárez-Moorillón

PMC · DOI: 10.1371/journal.pone.0323038 · 2026-01-07

## TL;DR

This study tracks how the cheese Crema de Chiapas changes during ripening, focusing on its chemical and microbial shifts.

## Contribution

The study reveals how microbial diversity and physicochemical properties evolve during cheese ripening using metagenomic and qPCR analyses.

## Key findings

- Protein content influenced sample differentiation more than other properties during ripening.
- Microbial diversity shifted with ripening, showing reduced bacterial, fungal, and yeast populations.
- Potentially pathogenic microorganisms were not detected at biologically relevant levels.

## Abstract

The dynamic changes in the physicochemical, microbiological, and metagenomic profiles of Crema de Chiapas cheese were evaluated across three ripening stages (2, 29, and 58 days). Although the main physicochemical properties —including fat content— remained remarkably stable, salt and protein levels showed noticeable variation throughout ripening. Protein content had the strongest influence on sample differentiation across ripening stages in unsupervised multivariate models, enabling the clustering of microbial diversity according to maturation time. A clear shift in microbial diversity was detected, marked by a reduction in bacterial genera and a concurrent decline in fungal and yeast populations as ripening advanced. The predominant bacterial genera throughout ripening were Streptococcus, Lactobacillus, and Lactococcus. While Streptococcus and Lactobacillus increased over time, Lactococcus exhibited the opposite trend. Metagenomic analysis revealed a decrease in Candida etchellsii and a concomitant increase in Candida tropicalis as ripening progressed. Quantitative PCR (qPCR) confirmed the presence of C. etchellsii at T1 (Ct = 7.22) and C. tropicalis at T3 (Ct = 9.84). The presence of three additional bacterial genera—Chryseobacterium, Aeromonas, and Enterobacter—identified by next-generation sequencing (NGS), was also assessed by qPCR. Chryseobacterium was detected at T2 (Ct = 3.26), whereas Aeromonas and Enterobacter were absent across all stages. Collectively, these findings suggest that potentially pathogenic microorganisms were not present at biologically relevant levels.

## Linked entities

- **Species:** Streptococcus (taxon 1301), Lactobacillus (taxon 1578), Lactococcus (taxon 1357), Candida tropicalis (taxon 5482), Chryseobacterium (taxon 59732), Aeromonas (taxon 642), Enterobacter (taxon 547)

## Full-text entities

- **Chemicals:** salt (MESH:D012492)
- **Species:** Starmerella etchellsii (species) [taxon 45547], Chryseobacterium (genus) [taxon 59732], Aeromonas (genus) [taxon 642], Candida tropicalis (species) [taxon 5482], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Lactococcus (lactic streptococci, genus) [taxon 1357], Streptococcus (genus) [taxon 1301], Enterobacter (genus) [taxon 547], Lactobacillus (genus) [taxon 1578]

## Figures

18 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12779153/full.md

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Source: https://tomesphere.com/paper/PMC12779153