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. 2025 Jul 1;15(1):20369.
doi: 10.1038/s41598-025-08200-1.

Molecular identification and diversity of gastrointestinal apicomplexan protozoa in pigs in the Republic of Korea

Affiliations

Molecular identification and diversity of gastrointestinal apicomplexan protozoa in pigs in the Republic of Korea

Subin Lee et al. Sci Rep. .

Abstract

The genera Cryptosporidium, Eimeria, and Cystoisospora cause gastrointestinal diseases in pigs that can lead to economic losses in the pig industry. Despite their importance, the molecular epidemiology and species diversity of these parasites remain poorly understood. Therefore, this study aimed to investigate the distribution and diversity of these genera Cryptosporidium, Eimeria, and Cystoisospora in pigs in Korea and to evaluate their potential influencing factors, including geographical location and season. A total of 700 fecal samples were collected from 103 pig farms between May 2020 and February 2023. PCR identified the genera Cryptosporidium, Eimeria, and Cystoisospora in 49 (7.0%), 24 (3.4%), and 6 (0.9%) samples, respectively. At the farm level, 43 (41.8%) out of 103 farms had at least one pig infected with these parasites. According to the region, Eimeria spp. showed the highest prevalence in Gyeongsangnam-do (8.5%; 17/200) with a statistically significant difference. Seasonal analysis revealed a statistically significant difference for Eimeria spp. with higher prevalence in summer (6.4%; 15/233) and winter (4.7%; 7/149). Phylogenetic analyses revealed Cryptosporidium (Cr.) scrofarum and Cr. suis, and confirmed the presence of Eimeria (E.) debliecki, E. perminuta, E. spinosa, and E. suis, as well as Eimeria sp. genotype 1-4. All Cystoisospora (Cy.) positive samples were confirmed as Cy. suis. This study examined the nationwide distribution of the genera Cryptosporidium, Eimeria, and Cystoisospora in pigs in Korea, providing molecular evidence of these parasites. The results improve our understanding of the distribution and diversity of apicomplexan protozoa in pigs in Korea. Notably, Cr. scrofarum and Cr. suis identified in this study are known to infect humans, indicating potential zoonotic risks. These findings highlight the importance of continued surveillance to mitigate economic losses on the pig industry and to address public health concerns.

Keywords: Cryptosporidium; Cystoisospora; Eimeria; Apicomplexan protozoa; Pig; Prevalence.

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Conflict of interest statement

Declarations. Competing interest: The authors declare no competing interests. Ethical approval and consent to participate: Ethical review and approval were waived for this study, due to the study focused on post-slaughter samples.

Figures

Fig. 1
Fig. 1
Map of Korea showing the sampling region of pig fecal samples. The prevalence of Cryptosporidium, Eimeria, and Cystoisospora were determined by PCR. GW, Gangwon-do; GG, Gyeonggi-do; CB, Chungcheongbuk-do; CN, Chungcheongnam-do; JB, Jeollabuk-do; JN, Jeollanam-do; GB, Gyeongsangbuk-do; GN, Gyeongsangnam-do. No positive cases were identified in Gangwon-do and Chungcheongbuk-do. The map was originally created by Ksiom and adapted by Kwj2772 (Public domain, via Wikimedia Commons), and was subsequently modified using Microsoft Paint (Microsoft Corporation, Redmond, WA, USA).
Fig. 2
Fig. 2
Phylogenetic tree of 18S rRNA gene of Cryptosporidium spp. To construct the phylogenetic tree, the neighbor joining method was used with 1000 bootstrap replications. The bootstrap values less than 50 were omitted. The sequences analyzed in this tree were obtained from the GenBank databases. The sequences identified in this study are indicated with bold and arrows.
Fig. 3
Fig. 3
Phylogenetic tree of 18S rRNA gene of Eimeria spp. To construct the phylogenetic tree, the neighbor joining method was used with 1000 bootstrap replications. The bootstrap values less than 50 were omitted. The sequences analyzed in this tree were obtained from the GenBank databases. The sequences identified in this study are indicated with bold and arrows.
Fig. 4
Fig. 4
Phylogenetic tree of internal transcribed spacer 1 of Cystoisospora spp. To construct the phylogenetic tree, the neighbor joining method was used with 1000 bootstrap replications. The bootstrap values less than 50 were omitted. The sequences analyzed in this tree were obtained from the GenBank databases. The sequences identified in this study are indicated with bold and arrows.

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