High prevalence of pathogenic Leptospira in alien American mink (Neovison vison) in Patagonia
© Barros et al.; licensee Springer. 2014
Received: 10 March 2014
Accepted: 22 September 2014
Published: 14 October 2014
Leptospirosis is an important zoonosis with worldwide distribution caused by pathogenic bacteria of the genus Leptospira. The North American mink (Neovison vison) has an important role in the environmental contamination with Leptospira, as minks live in aquatic environments and are the predators of rodents.
Blood and kidney samples were obtained from 57 minks in Southern Chile 39° S to 45° S. Pathogenic species of Leptospira were detected by PCR on 31/57 minks. To determine the species, we sequenced the 16S ribosomal RNA (rRNA) gene on nine of the positive samples. We predicted two pathogenic species: Leptospira interrogans (five samples) and Leptospira borgpetersenii (four samples).
This study showed that the American mink presents pathogenic species of Leptospira and confirm important environmental contamination of Patagonian rivers and lakes with pathogenic Leptospira.
Leptospirosis is the most widespread zoonosis in the world. Usually, it is transmitted between wild domestic mammals and humans through contaminated water or direct exposure to urine of infected animals. Leptospires can persist in natural environments for long periods of time; while this largely depends on the ability of the bacteria to adapt to a wide range of animals, the pathogen can also survive in water as well (Smith and Zochowski ).
Studies on leptospirosis in Chile have reported a high prevalence of infection: 37% in dogs, 88.7% in cattle, 24.9% in sheep, 7.1% in horses, and 69.9% in swine; see review by (Zunino and Pizarro ). However, only a few studies have investigated the prevalence of Leptospira spp. in wild animals. For example, only the prevalence of Leptospira spp. in wild rodents is currently known (47.2%); see reviews by (Zamora and Riedemann ; and Zunino and Pizarro ).
The North American mink (Neovison vison) is a semiaquatic mustelid that was introduced in Chile in the 1930s (Jaksic et al. ). Currently, the species has outgrowth considerably in number and distribution. The mink is now widely distributed throughout the riverine and marine habitats of the Patagonian lacustrine in both Argentina and the south of Chile (from 38° S latitude to Tierra del Fuego Island and adjacent archipelagos 55° S) (Medina ; Fasola et al. ). Mustelids are among the animals considered susceptible to infection with Leptospira; importantly, rodents are not only the primary reservoir of Leptospira, but also are an important part of the diet of minks. Additionally, the fact that minks often come into direct or indirect contact with different domestic animals suggests that inter-animal disease transmission events or potential human-transmission events are possible (Ullmann and Langoni 2011). While the role of minks as potential reservoir of Leptospira has not been determined yet, this role cannot been discarded as many emerging human, domestic animal, and wildlife diseases are usually maintained in specific reservoirs, many of which are rarely identified see reviews by (Adler and de la Peña. ; and by Smith and Zochowski , Lau et al. ). Furthermore, Leptospira transmission is very complex, in fact, this is a pathogen of multiple hosts, which often resides in one or more epidemiologically connected populations (Haydon et al. ). The complexity of Leptospira transmission along with the abundance of mink populations indicates that minks may be an important link in the ecology of leptospires, especially due to their wide distributions, semiaquatic live, and diet (Medina ; Millán et al. ; Moinet et al. ; Sepúlveda et al. ). In this study, we determined and characterized the presence of pathogenic Leptospira species in North American minks in Southern Chile.
2Materials and methods
2.1 Sample collection
2.2 Laboratory analysis
Total DNA from blood and kidney was extracted with the QIAamp DNA Mini Kit (Qiagen®, Germany). On three samples per individual (two blood and one kidney), we used PCR to screen for Leptospira spp. as previously described by Lester and LeFebvre, . To determine the species of Leptospira present in the positive samples, the amplified DNA (571 bp) of nine representative samples were sequenced at GenYtec (Santiago, Chile) using the ABI PRISM 310. To predict the species, sequences were compared with the GenBank database using the BLAST algorithm (http://www.ncbi.nlm.nih.gov/BLAST).
Number of positive samples and predicted Leptospira species in each study location
Number of positive minksa(sequenced samples)
Putative species ofLeptospirab(number of samples)
L. borgpetersenii (1)
L. borgpetersenii (1)
Todos los Santos
L. borgpetersenii (1)
L. interrogans (1)
Alto Rio Cisnes
L. interrogans (2), L. borgpetersenii (1)
L. interrogans (2)
Nine positive samples from different minks and from different locations were selected for sequencing of the 571 bp amplicon of the 16S ribosomal RNA (rRNA) (Table 1). The BLAST algorithm was used to (i) validate that the amplified PCR products correspond with Leptospira species and to (ii) predict the putative pathogenic species. We identified sequences closely related to two of the Leptospira pathogenic species. Leptospira interrogans was putatively predicted in five samples from three locations (i.e., Palena, Alto Rio Cisnes, and Islas Magdalena) and samples closely related to Leptospira borgpetersenii in four samples from four locations (i.e., Liquiñe, Neltume, Todos los Santos, and Alto Rio Cisnes) (Table 1). Our matches showed approximately 97% of nucleotide identity with the Leptospira species mentioned above. However, these findings need to be validated though the analysis of the complete 16 S rRNA gene.
We report for the first time evidence of pathogenic Leptospira in alien North American mink in South America. In this study, we used PCR to detect the pathogen; previous studies have used traditional detection methods (e.g., microscopic agglutination test [MAT]); while these methods are not easily compared, here we discuss the prevalence previously identified by other authors in comparison with our findings, regarding of the method used. Importantly, we identified a higher prevalence (55.6%, with 95% confidence interval = 24, 8–86, 4) compared with previous reports of 23.5% of Leptospira in wild animals in Spain (Millán et al., ), which used the MAT to detect the presence of Leptospira. Another study reported by Moinet et al. () identified a prevalence of 86% in wild American mink in France MAT detection. The same study detected by PCR a renal carriage of 26% on free-ranging American minks. The fact that we detected pathogenic species of Leptospira is relevant to both human and wild species health. Prevalence was high and transversal to almost all study sites, which are characterized by a mixture of natural forest and human activities. A previous study by Ghneim et al. () showed that dogs in rural areas were more likely to have been in contact with contaminated water with leptospires, as compared with dogs in urban areas. This may indicate that the complexity of animal species, along with environmental factors (e.g., rainfall and standing water) in rural areas, could facilitate the contact with the pathogen. Minks likely become infected after preying on rodents. In fact, studies carried out in the same region as our study demonstrate that mink preys heavily on rodents (Medina-Vogel et al. ), and that rodents may become infected by contact with garbage and contaminated water (Smith and Rochowski ). In the south of Chile, rodents present high rates of Leptospira infection (Zunino and Pizarro ). In fact Muñoz-Zanzi et al. () detected, by PCR, a 19.7% Leptospira prevalence in rodents associated with agricultural fields, 25.9% associated with rural villages, 21.1% associated with wild rodents, and 12.3% associated with slums.
In this study, we found L. interrogans in Palena, Alto Rio Cisnes, and Isla Magdalena, which is a Leptospira species largely associated to rodents (Himsworth et al. ). In addition, we found L. borgpetersenii in Liquiñe, Neltume, Lake Todos los Santos, and Alto Rio Cisnes, which is a Leptospira species associated with cattle farming. Importantly, in locations where we found L. borgpetersenii, livestock production systems are common. Thus, it is tempting to speculate that minks could be infected by predating on wild native and alien rodents in locations where livestock is rare, as well by contact with garbage and contaminated water from horse, cattle, sheep, and pig urine in locations where livestock is common.
In 13 individuals, samples from kidneys were positive; this not only demonstrates the presence of chronic disease in minks, but also that they present renal carrier status, which is the central point of the epidemiology of leptospirosis. Consequently, minks in the south of Chile may excrete leptospires though the urine to the environment (Ullmann and Langoni ). These initial data indicates that American mink can serve as hosts for leptospirosis, thus serving as a tool for measuring environmental contamination with this pathogen. This study represents a first insight of the mink’s role in the epidemiology of Leptospira in the south of Chile. This initial evidence suggests that mink abundance may pose a threat to human aquatic activities (e.g., canoeing, aquaculture, fisheries) and may as well affect the survival of aquatic species of conservation concern, such as the southern river otter (L. provocax) (Gaydos et al. ). Further investigation in order to identify source of infections, wild and domestic mammalian species involved, and the mechanism of transmission are necessary to provide evidence of the role of minks in the transmission of this important zoonotic pathogen.
Funding was provided by the Chilean Fund for Science and Technology (Fondecyt) project 1100139: ‘Presence of infectious diseases in wild species: the effect of alien invasive North American mink (Neovison vison) and the coexistence with stray dogs and cats.’ We also want to thank René Monsalve, Rodolfo Tardone, and Sergio Navarrete for field assistance. And we thank Drs. Nelly Lakestani and Andrea Moreno for English editing and comments.
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