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Isolation of Soil Microorganisms Using iChip Technology
Published on: January 10, 2025
Subtyping novel zoonotic pathogen Cryptosporidium chipmunk genotype I
Yaqiong Guo1, Elizabeth Cebelinski2, Christine Matusevich3
1State Key Laboratory of Bioreactor Engineering, School of Resources and Environmental Engineering, East China University of Science and Technology, Shanghai, People's Republic of China Division of Foodborne, Waterborne, and Environmental Diseases, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Abstract:
Cryptosporidium chipmunk genotype I is an emerging zoonotic pathogen in humans. The lack of subtyping tools makes it impossible to determine the role of zoonotic transmission in epidemiology. To identify potential subtyping markers, we sequenced the genome of a human chipmunk genotype I isolate. Altogether, 9,509,783 bp of assembled sequences in 853 contigs were obtained, with an N50 of 117,886 bp and >200-fold coverage. Based on the whole-genome sequence data, two genetic markers encoding the 60-kDa glycoprotein (gp60) and a mucin protein (ortholog of cgd1_470) were selected for the development of a subtyping tool. The tool was used for characterizing chipmunk genotype I in 25 human specimens from four U.S. states and Sweden, one specimen each from an eastern gray squirrel, a chipmunk, and a deer mouse, and 4 water samples from New York. At the gp60 locus, although different subtypes were seen among the animals, water, and humans, the 15 subtypes identified differed mostly in the numbers of trinucleotide repeats (TCA, TCG, or TCT) in the serine repeat region, with only two single nucleotide polymorphisms in the nonrepeat region. Some geographic differences were found in the subtype distribution of chipmunk genotype I from humans. In contrast, only two subtypes were found at the mucin locus, which differed from each other in the numbers of a 30-bp minisatellite repeat. Thus, Cryptosporidium chipmunk genotype I isolates from humans and wildlife are genetically similar, and zoonotic transmission might play a potential role in human infections.
Insights
Cryptosporidium chipmunk genotype I, a zoonotic pathogen, can now be subtyped using new genetic markers. This helps understand its spread from animals to humans, revealing genetic similarities between wildlife and human isolates.
Area of Science:
- Genomics
- Parasitology
- Zoonotic Diseases
Background:
- Cryptosporidium chipmunk genotype I is an emerging zoonotic pathogen.
- Current lack of subtyping tools hinders understanding of zoonotic transmission's epidemiological role.
Purpose of the Study:
- To identify genetic markers for subtyping Cryptosporidium chipmunk genotype I.
- To develop a subtyping tool to investigate zoonotic transmission.
Main Methods:
- Whole-genome sequencing of a human Cryptosporidium chipmunk genotype I isolate.
- Selection and validation of two genetic markers: gp60 and a mucin protein (cgd1_470 ortholog).
- Application of the subtyping tool to human, wildlife, and water samples.
Main Results:
- Genome sequencing yielded 9,509,783 bp in 853 contigs with high coverage.
- Fifteen gp60 subtypes and two mucin subtypes were identified, primarily varying in repeat regions.
- Genetic similarity observed between human and wildlife Cryptosporidium chipmunk genotype I isolates.
Conclusions:
- Developed a novel subtyping tool for Cryptosporidium chipmunk genotype I.
- Findings suggest potential zoonotic transmission plays a role in human infections.
- Genetic similarities support the link between wildlife and human Cryptosporidium chipmunk genotype I strains.
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