AI Article Synopsis

  • The study analyzed the cases of 20 patients diagnosed with cystic echinococcosis (CE) in Sardinia, Italy, between 2017 and 2022, confirming CE in 18 patients and identifying other conditions in 2.
  • A total of 27 CE lesions were collected, from which DNA was extracted and amplified from 15 fertile cysts for genetic analysis using PCR techniques.
  • The findings revealed the presence of 10 G1 and 5 G3 genotypes, with the discovery of new haplotypes, including SAR17 and nd5SAR13, indicating significant genetic diversity among CE cases in the region.

Article Abstract

This study involved 20 patients affected by cystic echinococcosis (CE) who were referred to different hospitals of Sardinia (Italy) from 2017 to 2022. By means of a multidisciplinary approach, diagnosis was confirmed for CE in 18 patients and for different aetiologies in two subjects. Moreover, serology was positive for 15 subjects. Since multiple CE cysts were found in five patients, a total of 27 lesions were collected; however, only one for each patient was investigated for genetic characterization of DNA isolates. Our results included 15 fertile cysts that underwent DNA extraction and amplification by three different PCRs targeting nuclear () and mitochondrial genes (cox1 and nad5). DNA was sequenced, and by neighbour-joining phylogenetic trees we determined 10 G1 and five G3 genotypes previously reported in Sardinia. These sequences were used to construct a network, along with those circulating in Mediterranean areas. The haplotype network calculated on cox1 evidenced seven different haplotypes of the 15 isolates, with SAR2 the most represented, carried by seven cysts, and SAR17 never described in the Mediterranean area. Meanwhile, the nad5 sequences showed the most common haplotype as nd5SAR7, as well as two new haplotypes not previously described, nd5SAR13, isolated from a Sardinian patient, and nd5SAR14, isolated from a Romanian patient.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366878PMC
http://dx.doi.org/10.3390/diseases11030091DOI Listing

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