ABSTRACT:In total the samples of blood and kidneys of 379 small rodents and 154 wild swine were analysed. The antibodies to different serovars of leptospires were determined in 12.7% of small rodents, most o�en in the species Mus musculus (34.4%), A. agrestis (14.8%), A. flavicolis (10.8%), C. glareolus (9.4%) and A. sylvaticus (6.5%). Most frequent were the findings of antibodies to sv. pomona (27.1%), sv. sejroe (20.8%), and sv. australis (14.6%), and the antibodies to sv. hardjo, sv. saxkoebing, sv. tarassovi, sv. grippotyphosa, sv. bataviae and sv. icterohaemorrhagiae were also established. Seventeen (4.5%) isolates were identified, belonging to the serogroups sejroe (10 isolates), pomona (4 isolates) and australis (1 isolate) and one isolate was not identified. In wild swine positive reactions were established in 26% of the blood sera analysed. Most frequently the antibodies to sv. pomona (47.5%), sv. australis (40%), sv. grippotyphosa (10%) and sv. icterohaemorhagiae (2.5%) were established. Thirteen (8.4%) isolates belonging to the serogroups pomona (10 isolates), australis (2 isolates) and icterohaemorhagiae (1 isolate) were identified.
The circulation of SARS-CoV-2 in the environment has been confirmed numerous times, whilst research on the bioaccumulation in bivalve molluscan shellfish (BMS) has been rather scarce. The present study aimed to fulfil the knowledge gap on SARS-CoV-2 circulation in wastewaters and surface waters in this region and to extend the current knowledge on potential presence of SARS-CoV-2 contamination in BMS. The study included 13 archive wastewater and surface water samples from the start of epidemic and 17 influents and effluents from nine wastewater treatment plants (WWTP) of different capacity and treatment stage, sampled during the second epidemic wave. From that period are the most of 77 collected BMS samples, represented by mussels, oysters and warty venus clams harvested along the Dalmatian coast. All samples were processed according to EN ISO 15216-1 2017 using Mengovirus as a whole process control. SARS-CoV-2 detection was performed by real-time and conventional RT-PCR assays targeting E, N and nsp14 protein genes complemented with nsp14 partial sequencing. Rotavirus A (RVA) real-time RT-PCR assay was implemented as an additional evaluation criterion of virus concentration techniques. The results revealed the circulation of SARS-CoV-2 in nine influents and two secondary treatment effluents from eight WWTPs, while all samples from the start of epidemic (wastewaters, surface waters) were negative which was influenced by sampling strategy. All tertiary effluents and BMS were SARS-CoV-2 negative. The results of RVA amplification were beneficial in evaluating virus concentration techniques and provided insights into RVA dynamics within the environment and community. In conclusion, the results of the present study confirm SARS-CoV-2 circulation in Croatian wastewaters during the second epidemic wave while extending the knowledge on wastewater treatment potential in SARS-CoV-2 removal. Our findings represent a significant contribution to the current state of knowledge that considers BMS of a very low food safety risk regarding SARS-CoV-2.
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