» Articles » PMID: 38188968

Identification of and Subtype ST3 in Cholga Mussel and Treated Sewage: Preliminary Evidence of Fecal Contamination in Harvesting Area

Overview
Date 2024 Jan 8
PMID 38188968
Authors
Affiliations
Soon will be listed here.
Abstract

and are foodborne parasites known for causing diarrhea. They accumulate in mussels grown on contaminated water bodies, due to the discharge of treated sewage from sewage treatment plants (STP). Despite this, some countries like Chile do not include these parasites in the control or monitoring of sewage water. The objective of this research was to evaluate the contamination of . and from treated sewage (disinfected by chlorination) and Cholga mussels in a touristic rural cove from the bay of Concepción. Cholga mussels from commercial stores and a treated sewage sample were analyzed. spp. was identified by Ziehl-Neelsen-Staining (ZNS) and by direct-immunofluorescence assay (IFA) from ZNS-positive samples. was identified by PCR using locus SSU rDNA. and subtype ST3 were found in 40% and 45% of Cholga mussel samples, respectively, and both parasites were identified in the treated sewage. SSU rDNA gene alignment from Cholga mussels and treated sewage showed 89% of similarity, indicating that could be the same parasite in both samples. We describe the first evidence of possible contamination with these parasites from treated sewage to Cholga mussel suggesting an environmental contamination with high human risk. Based on these results, further studies will consider all the rural coves and STP from the bay to prevent possible contamination of these parasites.

Citing Articles

Genetic diversity of single-celled microorganism sp. and its associated gut microbiome in free-ranging marine mammals from North-Western Mediterranean Sea.

Marangi M, Boughattas S Curr Res Microb Sci. 2025; 8:100349.

PMID: 39926158 PMC: 11803257. DOI: 10.1016/j.crmicr.2025.100349.


Foodborne concerns of spp. in marine animals (fish, bivalves, and sponges): A systematic review and meta-analysis of global prevalence and subtypes distribution.

Ghafari-Cherati M, Karampour A, Nazem-Sadati S, Asghari A Food Waterborne Parasitol. 2024; 36:e00242.

PMID: 39282659 PMC: 11399649. DOI: 10.1016/j.fawpar.2024.e00242.


Molecular detection of in wild rodents () inhabiting protected and rural transitional areas in north-central Chile.

Carrera-Jativa P, Acosta-Jamett G, Munoz P Int J Parasitol Parasites Wildl. 2024; 24:100971.

PMID: 39210974 PMC: 11359768. DOI: 10.1016/j.ijppaw.2024.100971.


Molecular Identification and Subtype Analysis of sp. Isolates from Wild Mussels () in Northern France.

Ryckman M, Gantois N, Dominguez R, Desramaut J, Li L, Even G Microorganisms. 2024; 12(4).

PMID: 38674653 PMC: 11051716. DOI: 10.3390/microorganisms12040710.

References
1.
Daraei H, Oliveri Conti G, Sahlabadi F, Thai V, Gholipour S, Turki H . Prevalence of Cryptosporidium spp. in water: a global systematic review and meta-analysis. Environ Sci Pollut Res Int. 2020; 28(8):9498-9507. DOI: 10.1007/s11356-020-11261-6. View

2.
King B, Fanok S, Phillips R, Lau M, van den Akker B, Monis P . Cryptosporidium Attenuation across the Wastewater Treatment Train: Recycled Water Fit for Purpose. Appl Environ Microbiol. 2017; 83(5). PMC: 5311398. DOI: 10.1128/AEM.03068-16. View

3.
Srisuphanunt M, Wilairatana P, Kooltheat N, Damrongwatanapokin T, Karanis P . Occurrence of oocysts in commercial oysters in southern Thailand. Food Waterborne Parasitol. 2023; 32:e00205. PMC: 10412772. DOI: 10.1016/j.fawpar.2023.e00205. View

4.
Nasser A . Removal of Cryptosporidium by wastewater treatment processes: a review. J Water Health. 2016; 14(1):1-13. DOI: 10.2166/wh.2015.131. View

5.
Cazeaux C, Lalle M, Durand L, Aubert D, Favennec L, Dubey J . Evaluation of real-time qPCR-based methods to detect the DNA of the three protozoan parasites Cryptosporidium parvum, Giardia duodenalis and Toxoplasma gondii in the tissue and hemolymph of blue mussels (M. edulis). Food Microbiol. 2021; 102:103870. DOI: 10.1016/j.fm.2021.103870. View