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. 2022 Nov 4;15(1):408.
doi: 10.1186/s13071-022-05533-y.

The microbial community associated with Parascaris spp. infecting juvenile horses

Affiliations

The microbial community associated with Parascaris spp. infecting juvenile horses

Jennifer L Cain et al. Parasit Vectors. .

Abstract

Background: Parasitic nematodes, including large roundworms colloquially known as ascarids, affect the health and well-being of livestock animals worldwide. The equine ascarids, Parascaris spp., are important parasites of juvenile horses and the first ascarids to develop widespread anthelmintic resistance. The microbiota has been shown to be an important factor in the fitness of many organisms, including parasitic nematodes, where endosymbiotic Wolbachia have been exploited for treatment of filariasis in humans.

Methods: This study used short-read 16S rRNA sequences and Illumina sequencing to characterize and compare microbiota of whole worm small intestinal stages and microbiota of male and female intestines and gonads. Diversity metrics including alpha and beta diversity, and the differential abundance analyses DESeq2, ANCOM-BC, corncob, and metagenomeSeq were used for comparisons.

Results: Alpha and beta diversity of whole worm microbiota did not differ significantly between groups, but Simpson alpha diversity was significantly different between female intestine (FI) and male gonad (MG) (P= 0.0018), and Shannon alpha diversity was significantly different between female and male gonads (P = 0.0130), FI and horse jejunum (HJ) (P = 0.0383), and FI and MG (P= 0.0001). Beta diversity (Fig. 2B) was significantly different between female and male gonads (P = 0.0006), male intestine (MI) and FG (P = 0.0093), and MG and FI (P = 0.0041). When comparing organs, Veillonella was differentially abundant for DESeq2 and ANCOM-BC (p < 0.0001), corncob (P = 0.0008), and metagenomeSeq (P = 0.0118), and Sarcina was differentially abundant across four methods (P < 0.0001). Finally, the microbiota of all individual Parascaris spp. specimens were compared to establish shared microbiota between groups.

Conclusions: Overall, this study provided important information regarding the Parascaris spp. microbiota and provides a first step towards determining whether the microbiota may be a viable target for future parasite control options.

Keywords: Ascarid; Equine parasite; Nematode; Parascaris; Parasite; Parasite microbiota.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Diversity metrics, phylum relative abundance (RA), and shared genera for whole worm microbiota. A Mean RA of the five most abundant phyla, where error bars represent 95% confidence intervals. B Principal coordinate analysis plot based on Bray–Curtis dissimilarities. C Alpha diversity box plot showing both Shannon and Simpson alpha diversity, where • denotes outliers. D Venn diagram showing number of shared genera between groups. F female, M male, I immature, H horse
Fig. 2
Fig. 2
Diversity metrics, phylum relative abundance (RA), and shared genera for whole worm microbiota. A Mean RA of the five most abundant phyla, where error bars represent 95% confidence intervals. B Principal coordinate analysis plot based on Bray–Curtis dissimilarities. C Alpha diversity box plot showing both Shannon and Simpson alpha diversity, where • denotes outliers, and the same letters indicate significant differences. D Venn diagram showing number of shared genera between groups. FG female gonad, FI female intestine, HJ horse jejunum, MG male gonad, MI male intestine
Fig. 3
Fig. 3
Shared microbiota heat plots showing genera with prevalence > 20% and relative abundance > 0.05% for A female parasites, B immature parasites, and C male parasites
Fig. 4
Fig. 4
Shared microbiota heat plots showing genera with prevalence > 20% and relative abundance > 0.05% for A female gonad, B female intestine, C male gonad, and D male intestine

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