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1 December 2013 First isolation of Leptospira interrogans from the arboreal squirrel Callosciurus erythraeus introduced in Argentina
Ana Cecilia Gozzi, M. Laura Guichón, Verónica Victoria Benitez, Graciela Noemi Romero, Carmelo Auteri, Bibiana Brihuega
Author Affiliations +
Abstract

We isolated Leptospira strains from renal tissue samples of Asiatic red-bellied squirrels Callosciurus erythraeus, captured in Argentina. In December 2008, we captured 34 squirrels in the province of Santa Fe during a short control campaign, which were screened for Leptospira spp. by direct immunofluorescence assays and isolation attempts in renal tissue samples. A prevalence of 38% of Leptospira spp. was obtained by direct immunofluorescence. The isolates, genotyped by the MLVA, were identified as L. interrogans Canicola (N = 2) and L. interrogans Icterohaemorraghiae (N = 1), showing an identical genetic profile to the reference strains Hond Utrech IV (serovar Canicola, serogroup Canicola) and M20 (serovar Copenhageni, serogroup Icterohaemorrhagiae), respectively. Our study shows for the first time that the red-bellied squirrel is a renal carrier of Leptospira interrogans and might act as a reservoir of leptospirosis both in native range and areas of introduction within several European countries, Japan and Argentina. The close association of this introduced squirrel species with humans and domestic animals may increase the probability of disease transmission, particularly in favourable environments.

Approximately 60% of human pathogens are zoonotic (Woolhouse 2002), and wildlife is the source of approximately 75% of the diseases that have emerged over the past two decades (Taylor et al. 2001). The increase in wildlife translocation plays an important role in the transmission of zoonotic diseases and in the maintenance of worldwide pathogens, thus, increasing the risk of zoonotic disease outbreaks (Daszak et al. 2000, Bengis et al. 2004, Kruse et al. 2004, Reed et al. 2004) particularly from synanthropic species (McFarlane et al. 2012). Reemerging infectious diseases can be broadly defined as infectious diseases whose geographical range, host range or prevalence has increased in recent years (Bengis et al. 2004). Leptospirosis is a worldwide zoonotic disease caused by the infection of a pathogenic spiroquete of the genus Leptospira (Levett 2001, Bharti et al. 2003, Vijayachari et al. 2008) and is considered a reemergent disease given its increase in prevalence and the occurrence of new pathogenic strains (Bengis et al. 2004, Mahajan & Daljeet 2008, Pappas et al. 2008, Vijayachari et al. 2008). A wide variety of animals such as mammals, reptiles and amphibians may serve as reservoir of the pathogenic Leptospira interrogans (Seijo et al. 2002, Rossetti et al. 2003, Brihuega & Tealdo 2011) and may be a source of infection to humans and other domestic and wild animals (Michel et al. 2001, 2002, Bharti et al. 2003, Masuzawa et al. 2006). The existence of periodic epizootics may cause significant die-offs in mammals, as reported for example in marine mammals (Cameron et al. 2008). Humans are exposed to leptospirosis infection by commensal and peridomestic wild mammals such as rats and mice Mus domesticus that are worldwide carriers of Leptospira interrogans (Vijayachari et al. 2008). However, some squirrel species, such as the white neck squirrel Sciurus stramineus and the fox squirrel Sciurus niger, may also act as carriers of Leptospira interrogans (Diesch et al. 1967, Montes Aliaga et al. 2011) and others, such as the southern flying squirrel Glaucomys volans and the fox squirrel may transmit leptospirosis to humans (Diesch et al. 1967, Masuzawa et al. 2006).

The red-bellied squirrel Callosciurus erythraeus is a sciurid rodent native to southeastern Asia (Corbet & Hill 1992) which was intentionally introduced into Argentina (Aprile & Chicco 1999), Belgium (Dozières et al. 2010), France (Gerriet 2009), Italy (LIFE09 NAT/IT/095 EC-Square Project 2012), Japan (Miyamoto et al. 2004) and The Netherlands (Dijkstra et al. 2009). In 1970, 10 red-bellied squirrels were introduced for ornamental purposes into the Buenos Aires province, Argentina (Aprile & Chicco 1999), where an expanding, large wild population is now established, and further intentional releases have created new invasion foci within the country (Benitez et al. 2013). This introduced rodent can now be found in three Argentinean provinces, two of which have environmental characteristics that favour leptospirosis infection (Martin et al. 2002, Seijo et al. 2002, Musacchio et al. 2010); it inhabits rural and urban areas in close association with humans and domestic animals, and is also illegally traded as pet (Guichón et al. 2005, Benitez et al. 2013). Red-bellied squirrels serve as an occasional host of local parasites acquired mainly from sympatric wild mammals (Gozzi et al. 2013), cause economic damages in cables and irrigation systems, and in fruit and timber plantations (Guichón et al. 2005), and were therefore declared a harmful species in various districts where numerous local producers and residents demand control actions (CDL 2011, DFF 2012).

To our knowledge, no studies have evaluated the role that red-bellied squirrels may play in the maintenance and transmission of leptospirosis either in their native or introduced ranges. The aim of our study was to evaluate if red-bellied squirrels are renal carriers of Leptospira interrogans in Argentina and may constitute a health risk.

Material and methods

Our study site is located in Cañada de Gómez (32°48‘S, 61°23‘W), southern Santa Fe province, Argentina, belonging to the Rolling Pampa region, which is the main agricultural area of the country. Mean annual temperature is 17.5°C and annual rainfall is 1,019 mm, with a relatively high mean annual humidity of 74% (EEAO INTA 2008). In Cañada de Gómez, red-bellied squirrels were released in ca 1999 within a private ranch mainly used for agriculture, tourism and equine activities. Bark stripping by these squirrels was the major damage recorded 10 years after liberation of the species when the ranch owner conducted a short control campaign for five consecutive days in a 7-ha grid to reduce damage caused by squirrels. Within this context, 34 squirrels were live-trapped in December 2008 using baited cage traps (30 x 13 x 13 cm) on tree branches, and were euthanised following animal handling procedures approved by international guidelines (American Veterinary Medical Association 2007, Animal Care and Use Committee 1998). Captured squirrels looked healthy and had no evident lesions. Kidneys were obtained aseptically by necropsy in the field, frozen and then analysed in the Leptospirosis Laboratory, OIE Reference, INTA. Logistical limitations prevented obtaining other kind of samples (e.g. urine, blood and serum) and the immediate inoculation of the kidneys into the culture medium when extracted in the field. Direct immunofluorescence (DI) assays were used to test for the presence of leptospires in kidney tissue smears (N = 68), using a conjugate polyvalent USDA (USA). For isolation attempts, aliquots of squirrel renal tissue were plated in modified Ellinghausen McCullough-Johnson-Harris (EMJH) liquid medium and the Fletcher semi-solid medium, under a biosafety cabin of the Leptospirosis Laboratory. Isolation is the best confirmatory method to evaluate whether an animal is a renal carrier of leptospires, while DI was used as a complementary test. Cultures were incubated at 30°C and weekly assessed under dark field microscopy. Isolations were made within 20-60 days postculture. Molecular characterisation of the strains isolated was carried out by Multiple-Locus Variable-number tandem repeat Analysis (MLVA), using the loci VNTR4, VNTR7, VNTR9, VNTR10, VNTR19, VNTR23 and VNTR31, as described by Majed et al. (2005).

Results

A total of 13 individuals out of 34 captured squirrels were positive for Leptospira with direct immunofluorescence assays, resulting in a prevalence of 38% (95% CI = 22-54; Table 1). Leptospira strains were isolated in Fletcher medium, but no isolations were obtained with the modified (EMJH) liquid medium. The three isolates (corresponding to three different individuals) were genotyped by the MLVA and identified as L. interrogans Canicola (N = 2) and L. interrogans Icterohaemorraghiae (N = 1), showing an identical genetic profile to the reference strains Hond Utrech IV (serovar Canicola, serogroup Canicola) and M20 (serovar Copenhageni, serogroup Icterohaemorrhagiae), respectively.

Discussion

Studies assessing the potential role of squirrels as maintenance hosts of L. interrogans all over the world are scarce and no reports of dead squirrels or individuals showing clinical symptoms of leptospirosis have been found. Squirrels of the genus Sciurus are known to be seropositive or carriers of eight serogroups of Leptospira sp. (see Table 1). Leptospira kirschneri was re-ported for the southern flying squirrel Glaucomys volans, while five other serogroups, which are different from the two serogroups identified in our study, were detected in Callosciurus squirrels (see Table 1). The prevalence of Leptospira spp. obtained in the red-bellied squirrel with direct immunofluorescence assays was amongst the highest reported values (see Table 1), even if fieldwork was conducted during a particularly drought period and other studies used laboratory techniques more sensible, such as a Microscopic Agglutination Test (MAT). The serogroups Icterohaemorrhagiae and Canicola found in our study have only been previously reported for the grey squirrel Sciurus carolinensis and the white neck squirrel S. stramineus (see Table 1). Both serogroups have a universal distribution (Levett 2001, Bharti et al. 2003) being frequently found in domestic and wild mammals such as rats, mice, marsupials, deer, cattle and dogs (Bharti et al. 2003, Brihuega et al. 2007). The susceptibility of humans and cattle to these serogroups reinforces their sanitary and economic importance (Szyfres 1976, Vanasco et al. 2000, Acha & Szyfres 2001).

Several wild and domestic mammals in Argentina are found to be seropositive or carriers of L. interrogans Canicola and Icterohaemorrhagiae serogroups (Table 2). The red-bellied squirrel co-inhabit with many of these wild (e.g. rats Rattus spp., sigmodontine rodents Akodon azarae and Oligoryzomys spp. and opossums Didelphis albiventris) and domestic mammals given their rural-urban habits, which could explain the isolation of these two serogroups from the squirrels captured in the Santa Fe province. This region of Argentina is considered to have high risk of leptospirosis infection (Vanasco et al. 2000, Seijo et al. 2002, Vanasco et al. 2008, Musacchio et al. 2010), where reported cases of human leptospirosis have been associated to urban and suburban areas exposed to floods and the high number of residents close to backwaters and landfills, together with abundant pigs, dogs and rodents nearby (Vanasco et al. 2000, 2008). The two serogroups identified in the red-bellied squirrel in our study are within the four serogroups potentially associated with cases of human leptospirosis in this region (Vanasco et al. 2000).

Our study shows that the red-bellied squirrel introduced into Argentina is a renal carrier of L. interrogans. Our study is the first to evaluate the role of the red-bellied squirrel in leptospira infection worldwide (see Table 1) and suggests that this species may act as a reservoir of L. interrogans playing a role in the epidemiology of leptospirosis. Further studies are needed to be able to make conclusions about the status of the red-bellied squirrel as a reservoir of leptospirosis both in native and introduced ranges. Squirrels have been reported to transmit leptospirosis to humans, as occurred with the fox squirrel in the United States (Diesch et al. 1967) and the introduced southern flying squirrel in Japan (Masuzawa et al. 2006). The introduction of wild fauna may result in an increased prevalence of L. interrogans in the en-vironment, increasing the risk of leptospirosis transmission. It must be noted that the introduced red-bellied squirrel lives in close association with humans and domestic animals as they inhabit urbanised and agricultural areas not only in Argentina, but also in Japan and European countries. Moreover, these squirrels are illegally translocated and traded as a pet, increasing the risk of disease transmission particularly in favourable environments. The outcome of our study will inform new regulations for preventing the capture, possession, trade and translocation of the red-bellied squirrel to minimise the associated sanitary risks.

Acknowledgements

We thank Sylvia Grune for her assistance in the laboratory work, the owner and personnel of the ranch Del Sel for assistance in the field and A. Valeria Bussetti, who helped with the extensive bibliography search. Our study was supported by the Universidad Nacional de Luján and the ANPCYT-PICT 32195.

References

1.

P.N Acha& B Szyfres 2001: Zoonosis y enfermedades transmisibles comunes al hombre y a los animales. Bacteriosis y Micosis. - Publicación Científica y Técnica No. 580. Organización Panamericana de la Salud, pp. (In Spanish). Google Scholar

2.

American Veterinary Medical Association (AVMA) 2007: Guidelines on Euthanasia, - Available at:  http://www.avma.org/issues/animal_welfare/euthanasia.pdf (Last accessed on 10 november 2011). Google Scholar

3.

Animal Care and Use Committee 1998: Guidelines for the capture, handling, and care of mammals as approved by the American Society of Mammalogists. - Journal of Mammalogy 79: 1416–1431. Google Scholar

4.

G Aprile& D Chicco 1999: Nueva especie exótica de mamífero en la Argentina: la ardilla de vientre rojo (Callosciurus erythraeus). - Mastozoología Neotropical 6: 7–14. (In Spanish). Google Scholar

5.

J Arango E Cittadino A Agostini G Dorta de Mazzonelli C Alvarez M Colusi A Koval Cabrera A Britos& F Kravetz 2001: Prevalencia de leptospiras en Rattus rattus y Rattus norvegicus en el Gran Buenos Aires, Argentina. (In Spanish with an English summary:Leptospires prevalence in Rattus rattus and Rattus norvegicus in Buenos Aires Province, Argentina).- Ecología Austral 11: 25–30. Google Scholar

6.

R.G Bengis F.A Leighton J.R Fischer M Artois T Mörner& C.M Tate 2004: The role of wildlife in emerging and re-emerging zoonoses. - Revue Scientifique et Technique-Office International des Epizooties 23: 497–511. Google Scholar

7.

V.V Benitez Almada S Chavez A.C Gozzi M.L Messetta& M.L Guichón 2013: Invasion status of Asiatic red-bellied squirrels in Argentina. - Mammalian Biology 78: 143–153. Google Scholar

8.

A.R Bharti J.E Nally J.N Ricaldi M.A Matthias M.M Diaz M.A Lovett P.N Levett R.H Gilman M.R Willig E Gotuzzo& J.M Vinetz 2003: Leptospirosis: a zoonotic disease of global importance. - The Lancet Infectious Diseases 3: 757–771. Google Scholar

9.

B Brihuega M Paván F Cairó A Venzano C Auteri D Funes G Romero& L Samartino 2007: Leptospira patógena en riñón de Didelphys albiventris (comadreja). - Revista Argentina de Microbiología 39: 1–19. (In Spanish). Google Scholar

10.

B Brihuega& M Tealdo 2011: Importancia de los animales silvestres en la leptospirosis. In: J Basualdo R Cacchione R Durlach P Martino& A Seijo (Eds.); Tema de Zoonosis V. Asociación Argentina de Zoonosis, Buenos Aires, Argentina, pp. 169–174. (In Spanish). Google Scholar

11.

C.E Cameron R.L Zuerner S Raverty K.A Colegrove S.A Norman D.M Lamboum S.J Jeffiies& F.M Gulland 2008: Detection of pathogenic Leptospira bacteria in pinniped populations via PCR and identification of a source of transmission for zoonotic leptospirosis in the marine environment. - Journal of Clinical Microbiology 46: 1728–1733. Google Scholar

12.

CDL 2011: Ordenanza 5696/2011. Concejo Deliberante del Municipio de Luján, Provincia de Buenos Aires, Argentina, pp. Google Scholar

13.

G.B Corbet& J.E Hill 1992: The mammals of the Indomalayan Region: A Systematic Review. Oxford University Press, Oxford, UK, pp. Google Scholar

14.

P Daszak A.A Cunningham& A.D Hyatt 2000: Emerging infectious diseases of wildlife threats to biodiversity and human health. - Science 287: 443–449. Google Scholar

15.

DFF 2012: Modificatorio del Decreto 110/81 “Especies susceptibles de caza” y de su decreto modificatorio 8996/86. - Dirección de Flora y Fauna. Ministerio de Asuntos Agrarios, Provincia de Buenos Aires, Argentina. Google Scholar

16.

S.L Diesch R.P Crawford W.F McCulloch& F.H Top 1967: Human leptospirosis acquired from squirrels. - The New England Journal of Medicine276: 838-842. Google Scholar

17.

V Dijkstra W Overman& G Verbeylen 2009: Inventarisatie Pallas' eekhoorn bij Weert. - Zoogdiervereniging rapport 2009 21, Zoogdiervereniging, Arnhem, Nederland, pp. (In Dutch with an English summary). Google Scholar

18.

A Dozières B Pisanu O Gerriet C Lapeyre J Stuyck& J-L Chapuis 2010: Macroparasites of Pallas's squirrels, Callosciurus erythraeus, introduced into Europe. - Veterinary Parasitology 172: 172–176. Google Scholar

19.

EEAO-INTA 2008: Agencia de Extensión Rural Cañada de Gómez. Estación Experimental Agropecuaria Oliveros, La Información metereológica. - Available at:  http://www.inta.gov.ar/oliveros/ins/unidades/cgomez.htm (Last accessed on 15 september 2011). Google Scholar

20.

O Gerriet 2009: Répartition de l'écureuil à ventre rouge Callosciurus eryhtraeus (Pallas, 1779) (Rodentia, Sciuridae) dans les Alpes-Maritimes (France). - Biocosme Mésogéen (Nice) 26: 139–148. (In French with an English summary). Google Scholar

21.

C.E Gordon Smith L.H Turner J.L Harrison& J.C Broom 1961: Animal leptospirosis in Malaya. Methods, Zoogeographical Background, and Broad Analysis of results. - Bulletin de L'Organisation Mondale de la Santé. Bulletin of the World Health Organization 24: 5–21. Google Scholar

22.

A.C Gozzi M.L Guichón V.V Benitez& M Lareschi 2013: Arthropod parasites of the red-bellied squirrel Callosciurus erythraeus (Rodentia: Sciuridae) introduced into Argentina. - Medical and Veterinary Entomology 27: 203–208. Google Scholar

23.

M.L Guichón L Fasola& M Bello 2005: Expansión poblacional de una especie introducida en la Argentina: la ardilla de vientre rojo Callosciurus erythraeus. (In Spanish with an English summary:Population expansion of an exotic mammal in Argentina: the Red-Bellied Squirrel Callosciurus erythraeus) - Mastozoolología Neotropical 12: 189–197. Google Scholar

24.

H Kruse A-M Kirkemo& K Handeland 2004: Wildlife as Source of Zoonotic Infections. - Emerging Infectious Diseases 10: 2067–2072. Google Scholar

25.

P.N Levett 2001: Leptospirosis. - Clinical Microbiology Reviews 14: 296–326. Google Scholar

26.

LIFE09 NAT/IT/095 EC-Square Project 2012: Guida al riconoscimento degli scoiattoli presenti in Italia. - Available at:  http://www.rossoscoiattolo.eu/ (Last accessed on 12 July 2012). (In Italian). Google Scholar

27.

S Mahajan& C Daljeet 2008: Leptospirosis: A Re-emerging Disease. - Veterinary World 1: 182–185. Google Scholar

28.

Z Majed E Bellenger D Postic C Pourcel G Baranton& M Picardeau 2005: Identification of variable-number tandem repeat loci in Leptospira interrogans sensu stricto. - Journal of Clinical Microbiology 43: 539–545. Google Scholar

29.

U.O Martin A Sensevy J Colombo& V Tramontin 2002: Leptospirosis en la provincia de Santa Fe. Descripción epidemiológica, clínica y socioeconómica. (In Spanish with an English summary: Leptospirosis in the Province of Santa Fe, Argentina). - Medicina (Buenos Aires) 62: 164–168. Google Scholar

30.

P.E Martino J.L Montenegro J.A Preziosi C Venturini D Bacigalupe N.O Stanchi& E.L Bautista 2004: Serological survey of selected pathogens of free-ranging foxes in southern Argentina, 1998-2001. - Revue Scientifique et Technique 23: 801–806. Google Scholar

31.

T Masuzawa Y Okamoto Y Une T Takeuchi K Tsukagoshi N Koizumi H Kawabata S Ohta& Y Yoshikawa 2006: Leptospirosis in squirrels imported from United States to Japan. - Emerging Infectious Dis-eases 12: 1153–1155. Google Scholar

32.

R McFarlane A Sleigh& T McMichael 2012: Synanthropy of Wild Mammals as a Determinant of Emerging Infectious Diseases in the Asian-Australasian Region. - Ecohealth 9: 24–35. Google Scholar

33.

V Michel C Branger& G Andre-Fontaine 2002: Epidemiology of leptospirosis. - Revista Cubana de Me-dicina Tropical 54: 7–10. Google Scholar

34.

V Michel N Ruvoen-Clouet A Menard C Sonrier C Fillonneau F Rakotovao J.P Ganière& G André-Fontaine 2001: Role of the coypu (Myocastor coypus) in the epidemiology of leptospirosis in domestic animals and humans in France. - European Journal of Epidemiology 17: 111–121. Google Scholar

35.

A Miyamoto N Tamura K Sugimura& F.A Yamada 2004: Predicting habitat distribution of the alien Formosan squirrel using logistic regression model. - Global Environmental Research 8: 13–21. Google Scholar

36.

D Montes Aliaga G.H Rivera V.M Ramirez M.P Ríos J.C Angulo& D.K Muñoz 2011: Frecuencia de infección por Leptospira sp. en ardillas nuca blanca (Sciurus stramineus) en un zoológico de la ciudad de Lima. (In Spanish with an English summary:Frequency of infection by Leptospira sp. in White Neck squirrel (Sciurus stramineus) in a Zoo of Lima city). - Revistas de In-vestigaciones Veterinarias del Perú 22: 66–71. Google Scholar

37.

H.M Musacchio C Dorigo V Volpato& M.H Vicco 2010: Características clínicas y epidemiológicas de leptospirosis: 10 años de experiencia en Santa Fe, Argentina. (In Spanish with an English summary: Clinical and epidemiological characteristics of leptospirosis: 10 years of experience in Santa Fe, Argentina). - Revista Panamericana de Infectología 12: 43–46. Google Scholar

38.

D.M Myers A Cuba Caparo& J.P Moreno 1977: Aislamiento del seroptipo Hardjo y otras Leptospiras de armadillos de Argentina. (In Spanish with an English summary: Isolation of serotype hardjo and other leptospirae from armadillos in Argentina). - Boletín de la Oficina Sanitaria Panamericana 83: 56–65. Google Scholar

39.

G Pappas P Papadimitriou V Siozopoulou L Christou& N Akritidis 2008: The globalization of leptospirosis: worldwide incidence trends. - International Journal of Infectious Diseases 12: 351–357. Google Scholar

40.

M.E Pavan F Cairó M.J Pettinari L Samartino& B Brihuega 2010: Genotyping of Leptospira interrogans strains from Argentina by Multiple-Locus Variable-number tandem repeat Analysis (MLVA). - Comparative Immunology, Microbiology and Infectious Diseases 34: 135–141. Google Scholar

41.

L.C Perez Carusi M.I Farace M.M Ribicich& I.E. Gómez Villafañe 2009: Reproduction and parasitology of Didelphis albiventris (Didelphimorphia) in an agroecosystem landscape in central Argentina. - Mammalia 73: 89–97. Google Scholar

42.

K.D Reed J.W Melski M.B Graham R.L Regnery M.J Sotir M.V Wegner J.J Kazmierczak E.J Stratman Y Li J.A Fairley G.R Swain V.A Olson E.K Sargent S.C Kehl M.A Frace R Kline S.L Foldy J.P Davis& I.K Damon 2004: The detection of monkeypox in humans in the Western Hemisphere. - The New England Journal of Medicine 350: 342–50. Google Scholar

43.

D.J Richardson& J.L Gauthier 2003. A serosurvey of leptospirosis in Connecticut peridomestic wildlife. - Vector Borne and Zoonotic Diseases 3: 187–193. Google Scholar

44.

C.A Rossetti M Uhart G.N Romero& W Prado 2003: Detection of leptospiral antibodies in caimans from the Argentinian Chaco. - Veterinary Record15: 632-633. Google Scholar

45.

A Seijo G Draghi G Dorta de Mazzonelli J Mazzonelli C Stiebel E Argento R Caminoa& B Deodato colaboradores de CCLA 2002: Comisión Científica sobre Leptospirosis de la República Argentina (CCLA-AAVLD). - Informe sobre Leptospirosis en la República Argentina. Serie Enfermedades Transmisibles. Publicación Monográfica N° 3. Fundación Mundo Sano, Buenos Aires, Argentina, pp. (In Spanish). Google Scholar

46.

E.B Shotts Jr C.L Andrews& T.W Harvey 1975: Leptospirosis in selected wild mammals of the Florida panhandle and southwestern Georgia. - Journal of the American Veterinary Medical Association 167: 587–589. Google Scholar

47.

B Szyfres 1976: Leptospirosis as an animal and public health problem in Latin America and the Caribbean area. VIII Inter-American Meeting on Foot-and-Mouth Disease and Zoonoses Control, PAHO Scientific Publication 316, Washington, USA, pp. 115–130. Google Scholar

48.

L.H Taylor S.M Lathman& M.E Woolhouse 2001: Risks factors for human disease emergence. - Philosophical Transactions of the Royal Society of London B 356: 983–989. Google Scholar

49.

S Thayaparan I Robertson F Amraan L Su‘ut& M.T Abdullah 2013: Serological prevalence of Leptospiral infection in wildlife in Sarawak, Malaysia. - Borneo Journal of Resource Science and Technology 2: 79–82. Google Scholar

50.

C-C Tsai& W.D Kundin 1970: Isolation of Leptospira javanica from wild rat and squirrel in Chi-Ian Mountain, I-Ian Taiwan. - Chinese Journal of Microbiology 3: 56–57. Google Scholar

51.

B Vanasco M.F Schmeling J Lottersberger F Costac A.I Koc& H.D Tarabla 2008: Clinical characteristics and risk factors of human leptospirosis in Argentina (1999-2005). - Acta Tropica 107: 255–258. Google Scholar

52.

N.B Vanasco G Sequeira M.L Fontana S Fusco M.D Sequeira& D Enría 2000: Descripción de un brote de leptospirosis en la ciudad de Santa Fe, Argentina, marzo-abril de 1998. (In Spanish with an English summary:Description of a leptospirosis outbreak in the city of Santa Fe, Argentina, March-April 1998) - Revista Pa-namericana de Salud Pública 7: 35–40. Google Scholar

53.

N.B Vanasco M.D Sequeira G Sequeira& H.D Tarabla 2003: Associations between leptospiral infection and seropositivity in rodents and environmental characteristics in Argentina. - Preventive Veterinary Medicine 60: 227–235. Google Scholar

54.

P Vijayachari A.P Sugunan& A.N Shiriram 2008: Leptospirosis: an emerging global public health problem. - Journal of Biosciences 33: 557–569. Google Scholar

55.

M.E Woolhouse 2002: Population biology of emerging and re-emerging pathogens. - Trends in Microbiology 10: S3–7. Google Scholar

Notes

[1] Edited by Associate Editor: Christian Sonne

Table 1.

Squirrel species as reservoirs of Leptospira, indicating collection site, laboratory tests (MAT: microagglutination test, DI: direct inmunofluorescence or Isolation), Leptospira species or serogroup, number of positive squirrels of the total number of squirrels analysed and references. The abbreviations are: Ictero = Icterohaemorragiae; Can = Canicola; Geor = Georgia; Aus = Australis; Pom = Pomona; Hard = Hardjo; Grippo = Grippotyphosa. a Corresponds to Callosciurus erythraeus taiwanensis (Corbet & Hill 1992) Ascribes to: b L. interrogans (Bharti et al. 2003); c L. santarosai (Bharti et al. 2003); d L. kirschneri (Bharti et al. 2003); e L. borgpetersenii (Bharti et al. 2003); f Lepto 175 (Sarawak) is a poorly known strain endemic to Malaysia, but its pathogenic potential is still unknown (Thayaparan et al. 2013).

i0909-6396-19-4-483-t01.eps

Table 2.

Wild and domestic mammals reported to be seropositive or carriers of L. interrogans Canicola and Icterohaemorragiae serogroups in Argentina, indicating laboratory tests, serogroup and references. The abbreviations are: Can = Canicola; Ictero = Icterohaemorragiae.

i0909-6396-19-4-483-t02.eps
Ana Cecilia Gozzi, M. Laura Guichón, Verónica Victoria Benitez, Graciela Noemi Romero, Carmelo Auteri, and Bibiana Brihuega "First isolation of Leptospira interrogans from the arboreal squirrel Callosciurus erythraeus introduced in Argentina," Wildlife Biology 19(4), 483-489, (1 December 2013). https://doi.org/10.2981/13-051
Received: 13 April 2013; Accepted: 1 June 2013; Published: 1 December 2013
KEYWORDS
Asiatic red-bellied squirrel
Callosciurus erythraeus
Leptospira interrogans
leptospirosis
renal carrier
Rolling Pampas
squirrels
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