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Ivermectin (IVM) is an anthelmintic compound commonly used off-label in mules due to its broad-spectrum of activity. Despite the general use of IVM in mules with the same dose and route of administration licensed for horses, significant pharmacokinetic differences might exist between horses and mules, as already observed for donkeys. The aim of the present study was to evaluate the pharmacokinetic profile and anthelmintic efficacy of an oral paste of IVM in mules naturally infected with cyathostomins. Fifteen adult mules with fecal egg counts (FEC) ≥200 eggs per gram (EPG), with exclusive presence of cyathostomins, were included in the study. All mules were orally treated with IVM according to the manufacturers recommended horse dosage (200 µg/kg body weight). FECs were performed before (day-10 and day-3) and after treatment at days 14 and 28 by using a modified McMaster method. The FEC reduction (FECR%) was also calculated. Blood samples were collected from five animals at various times between 0.5 h up to 30 days post treatment to determine pharmacokinetic parameters. The maximum IVM serum concentration (Cmax) was 42.31 ± 10.20 ng/mL and was achieved at 16.80 ± 9.96 hours post-treatment (Tmax), area under the curve (AUC) was 135.56 ± 43.71 ng × day/mL. FECR% remained high (>95%) until the 28th day.

Simple Summary: Dirofilaria immitis and Angiostrongylus vasorum are major parasitic nematodes affecting the pulmonary arteries of dogs. In Italy, these two parasites have recently changed their distribution patterns and have been detected in areas where their presence was previously unexpected. The present study has updated available data on the distribution and prevalence of D. immitis and A. vasorum in canine populations living in selected regions of Central and Southern Italy. The results indicate that both parasites occur stably in the investigated territories and that increased awareness and surveillance methods are of utmost importance. Dirofilaria immitis and Angiostrongylus vasorum are major parasitic nematodes of dogs. Many environmental and phenological changes have recently modified their geographic patterns in many countries; thus, this study has updated the distribution of D. immitis and A. vasorum in dog populations of selected regions of Central and Southern Italy. Also, collateral data on other endoparasites affecting the study population have been collected. Blood and fecal samples collected from 2000 dogs were tested using Knott's test and copromicroscopy (i.e., Baermann's and fecal flotation tests), respectively. Binomial logistic regression was performed to evaluate statistically significant associations between positivity for D. immitis and/or A. vasorum and potential risk factors. Overall, 35 (1.7%) and 62 (3.1%) dogs were positive for microfilariae of D. immitis and first stage larvae (L1) of A. vasorum, respectively, while 3 (0.1%) were co-infected by both nematodes. Microfilariae of Dirofilaria repens were found in 148 (7.4%) dogs, while at the flotation, eggs of Ancylostomatidae, Trichuris vulpis, and ascarids were found in the feces of 323 (16.5%), 249 (12.4%), and 172 (8.6%), dogs, respectively. Overall, 217 (10.8%) and 44 (2.2%) dogs were positive for eggs of Capillaria aerophila and Capillaria boehmi. The presence of cardiorespiratory clinical signs or non-specific signs, history of travel, and an age of >4 years old were significantly associated with positivity for D. immitis, while A. vasorum was significantly recorded in dogs with cardiorespiratory signs, or with a history of mollusk ingestion or permanent outdoor housing. These results confirm that D. immitis is enzootic in the investigated regions of Central and Southern Italy, even where it was rare/undetected until recently. Indeed, although some dogs positive for D. immitis had a history of travel in enzootic areas, the majority of them were never moved, indicating that they acquired the parasite in the region where they live. Additionally, A. vasorum is stably enzootic in the study areas, as also are other extraintestinal nematodes (i.e., D. repens and C. aerophila) that are more frequently detected today than in the past. A high level of vigilance and routine parasitological screening are necessary, considering the high prevalence of intestinal parasites in owned dogs that are also co-infected by respiratory parasites. The implementation of chemoprevention against D. immitis in dogs living in the examined area should be encouraged. [ABSTRACT FROM AUTHOR]

Feline pulmonary capillariosis is a significant disorder due to its distribution and clinical impact. This study evaluated the safety and efficacy of two administrations 28 days apart of a topical solution containing esafoxolaner, eprinomectin and praziquantel (NexGard® Combo) in treating Eucoleus aerophilus (syn. Capillaria aerophila) infection in naturally infected cats. Cats were allocated to two groups: G1 cats (n = 23) received two treatments at study days (SDs) 0 and 28 (±2) and were evaluated for 6 weeks, and G2 cats (n = 17) served as a negative control for 6 weeks and were then treated twice on SDs 42 (±2) and 70 (±2), allowing for an additional 6-week assessment of efficacy. Each cat was subjected to McMaster coproscopy at SDs −7/0, 28 (±2) and 42 (±2) for both groups, 70 (±2) and 84 (±2) only for G2. Clinical examination and chest radiographic images were performed at SDs 0, 28 (±2) and 42 (±2) for G1 and G2, 70 (±2) and 84 (±2) only for G2. The comparison of EPG (eggs per gram of feces), clinical (CS), and radiographic scores (RS) at each time-point was used as a criterion. The efficacy based on the EPG reduction was 99.5% (G1) and 100% (G2) after two administrations of NexGard® Combo 2 weeks apart. At SD 0, no significant differences for CS and RS were recorded between G1 and G2, while a significant reduction (p

Aims: Within the One Health paradigm, infectious disease surveillance have been developed for domestic and wild animals, leaving the role of captive non‐domestic populations, especially felids in zoos and circuses, less explored. This study addresses the proximity of these captive animals to urban areas, necessitating focused monitoring for potential zoonotic enteropathogens. The present work aimed to investigate the presence of such zoonotic enteropathogens in faecal samples from captive large felid populations. Methods and Results: A total of 108 faecal samples were collected in three circuses, five zoos and one rescue centre across Italy. Salmonella spp. isolation, serotyping and antimicrobial susceptibility testing were conducted on all samples. Additionally, 60 samples were also examined for gastrointestinal parasites using standard coprological techniques. Giardia spp. detection employed direct immunofluorescent staining and specific PCR, while Toxoplasma gondii was detected using PCR targeting B1 gene. A total of 51 Salmonella enterica subsp. enterica were isolated, with predominant serovariants including Infantis (43.1%), Coeln (11.8%) and Newport (11.8%). The captive felids likely act as asymptomatic carriers of foodborne Salmonella, with notable resistance ampicillin and trimethoprim‐sulfamethoxazole, no resistance to enrofloxacin was noted. Microscopic analysis revealed Toxascaris leonina eggs in 11 faecal samples (18.3%) and Giardia duodenalis cysts in one animal (1.7%). Conclusions: Captive animals in public settings may act as sources of Salmonella infection and enteroparasitosis for both occupational and general exposure. The study emphasizes the role of captive animals in antimicrobial resistance dynamics, highlighting the need for routine pathogen screening in the management practices of zoological structures. [ABSTRACT FROM AUTHOR]

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Copyright of Summa, Animali da Compagnia is the property of Point Veterinaire Italie s.r.l. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)