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High Subtelomeric GC Content in the Genome of a Zoonotic Species

Overview
Journal Microb Genom
Specialties Genetics
Microbiology
Date 2023 Jul 3
PMID 37399068
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Abstract

is a zoonotic species causing cryptosporidiosis in humans in addition to its natural hosts dogs and other fur animals. To understand the genetic basis for host adaptation, we sequenced the genomes of from dogs, minks, and foxes and conducted a comparative genomics analysis. While the genomes of have similar gene contents and organisations, they (~41.0 %) and (39.6 %) have GC content much higher than other spp. (24.3-32.9 %) sequenced to date. The high GC content is mostly restricted to subtelomeric regions of the eight chromosomes. Most of these GC-balanced genes encode specific proteins that have intrinsically disordered regions and are involved in host-parasite interactions. Natural selection appears to play a more important role in the evolution of codon usage in GC-balanced , and most of the GC-balanced genes have undergone positive selection. While the identity in whole genome sequences between the mink- and dog-derived isolates is 99.9 % (9365 SNVs), it is only 96.0 % (362 894 SNVs) between them and the fox-derived isolate. In agreement with this, the fox-derived isolate possesses more subtelomeric genes encoding invasion-related protein families. Therefore, the change in subtelomeric GC content appears to be responsible for the more GC-balanced genomes, and the fox-derived isolate could represent a new species.

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References
1.
Roberts C, Roberts F, Henriquez F, Akiyoshi D, Samuel B, Richards T . Evidence for mitochondrial-derived alternative oxidase in the apicomplexan parasite Cryptosporidium parvum: a potential anti-microbial agent target. Int J Parasitol. 2004; 34(3):297-308. DOI: 10.1016/j.ijpara.2003.11.002. View

2.
Menon V, Okhuysen P, Chappell C, Mahmoud M, Meng Q, Doddapaneni H . Fully resolved assembly of Cryptosporidium parvum. Gigascience. 2022; 11. PMC: 8848321. DOI: 10.1093/gigascience/giac010. View

3.
Bouzid M, Hunter P, Chalmers R, Tyler K . Cryptosporidium pathogenicity and virulence. Clin Microbiol Rev. 2013; 26(1):115-34. PMC: 3553671. DOI: 10.1128/CMR.00076-12. View

4.
Smarda P, Bures P, Horova L, Leitch I, Mucina L, Pacini E . Ecological and evolutionary significance of genomic GC content diversity in monocots. Proc Natl Acad Sci U S A. 2014; 111(39):E4096-102. PMC: 4191780. DOI: 10.1073/pnas.1321152111. View

5.
Feng Y, Li N, Roellig D, Kelley A, Liu G, Amer S . Comparative genomic analysis of the IId subtype family of Cryptosporidium parvum. Int J Parasitol. 2017; 47(5):281-290. PMC: 5774651. DOI: 10.1016/j.ijpara.2016.12.002. View