Evidence map›Paper›PMID 41580762›Full record

ArticleParasites & vectors2026

Population structure and zoonotic potential of Cryptosporidium parvum in Italy inferred using a multi-locus sequence typing scheme.

Marianna Ascierto, Antonio Di Grazia, Francesco Celani, Nicoletta D'Avino, Luciana Petrullo, Maria Grazia Coppola, Simone M Cacciò

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Article in Parasites & vectors, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Marianna AsciertoUOC Microbiology and Virology, Azienda dei Colli of Naples, "D. Cotugno" Hospital, Naples, Italy.
Antonio Di GraziaDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Francesco CelaniDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy.
Nicoletta D'AvinoIstituto Zooprofilattico Sperimentale delle Marche e dell'umbria, Perugia, Italy.
Luciana PetrulloUOC Microbiology and Virology, Azienda dei Colli of Naples, "D. Cotugno" Hospital, Naples, Italy.
Maria Grazia CoppolaUOC Microbiology and Virology, Azienda dei Colli of Naples, "D. Cotugno" Hospital, Naples, Italy.
Simone M CacciòDepartment of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy. simone.caccio@iss.it.

Funding

European Commission 773830
6 · The paper itself

Abstract

backgroundThe genetic variability of a large collection of European samples of the zoonotic pathogen Cryptosporidium parvum has been recently explored on the basis of a novel multi-locus sequence typing (MLST) scheme. In this work, we assessed the usefulness of this scheme to type C. parvum samples from Italy, a country where this pathogen is widespread and associated with human infections.

methodsPolymerase chain reaction (PCR) and sequencing for the eight markers of the MLST scheme were performed on 31 human- and 21 animal-derived C. parvum samples. MLST data from 27 samples of animal origin previously sequenced at the genome level were also included. Sequence data for the glycoprotein 60 (gp60) gene were also generated. Phylogenetic and cluster analyses were conducted.

resultsFull genotyping data were obtained for 72 of 79 samples, and 39 different profiles were categorized, 28 of which were found in individual samples (singletons). A new allele was found at the marker on chromosome 2 in a human-derived sample. When compared with the 154 profiles previously described in Europe, 30 of the 39 profiles (76%) were found to be restricted to Italy, a result compatible with a model of isolation by distance, with geographically structured populations. Analysis of the gp60 sequences identified 19 different subtypes among the 55 samples belonging to family IIa, and 7 different subtypes among the 16 samples belonging to family IId. Phylogenetic and haplotype analyses did not identify clusters related to the host, the geographic origin (i.e., the Italian regions), or the time of collection of the samples but did identify two different populations, mirroring data obtained from whole genome comparative analyses.

conclusionsThe MLST scheme appears to be a promising method for genotyping C. parvum samples, as it provided higher discrimination compared with gp60 and enabled the recognition of the two major populations circulating in Europe and in Italy.

Indexed as

CryptosporidiosisCryptosporidium parvumMultilocus Sequence TypingZoonosesAnimalsCattleGenetic VariationGenotypeHumansItalyPhylogenyPolymerase Chain ReactionCryptosporidium parvumItalyMulti-locus genotypingPopulation structureZoonosis

Identifiers

PMID41580762
PMCPMC12911039

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