Assessment of habitat suitability for the cattle tick Rhipicephalus (Boophilus) microplus in temperate areas.

The aim of this research was to analyze and model the aptitude of temperate areas to support permanent populations of the cattle tick Rhipicephalus microplus, which is principally distributed in tropical and subtropical areas. This work integrated field-derived data of tick development with temperature and land-based models of tick spread in Argentina. The integrated analysis of the results suggest that approximately 31°S is the southern limit where R. microplus finds appropriate climatic conditions to be established permanently. The establishment of permanent populations of R. microplus south of this latitudinal threshold is currently restricted because the low temperatures in autumn and winter inhibit the development of its eggs, but the introduction of cattle infested with R. microplus from early spring to late summer in temperate areas could produce engorged females laying eggs that would originate viable larvae from late spring to winter. The comparison of the temperature-based maps of habitat suitability with those obtained considering the lands suitable for livestock grazing, clearly shows that the models based only on climatic variables overestimate the potential dispersal of the cattle tick. The outcomes of this study suggest that an increase of temperature in the months of autumn and winter around 2°-2.75 °C should be necessary for the establishment of permanent populations of R. micoplus in the region belonging to temperate areas. This would allow that a tick generation emerged in early spring due to the overwintering of eggs and larvae originated from females detached from cattle during autumn or early winter.

New host species for Leptospira borgpetersenii and Leptospira interrogans serovar Copenhageni.

We investigated the presence of infection by Leptospira spp. in an assembly of Sigmodontinae rodents from the Paraná Delta, Argentina. Rodents were captured in places with natural grassland, implanted forest, with and without raising cattle and in sites prone and not prone to flooding. The DNA was amplified from cultured isolates by PCR and Leptospira spp. strains were genotyped using Multiple - Locus Variable Number Tandem Repeat Analysis (MLVA). We isolated Leptospira interrogans serovar Copenhageni from Oligoryzomys nigripes, Leptospira borgpetersenii from Scapteromys aquaticus and Leptospira interrogans serovar Icterohaemorrhagiae from Akodon azarae. The zoonotic Leptospira isolated and genotyped from O. nigripes and S. aquaticus are the first reports from these species. The geographic range of these rodent species include, in addition to Argentina, the countries of Paraguay, Uruguay and Brazil, suggesting that these rodents might be involved in the transmission of spirochetes in other regions. Human and animal health care professionals should be alert to the potential occurrence of leptospirosis in areas where these rodent species are present.

Evaluation of cocktails with recombinant proteins of Mycobacterium bovis for a specific diagnosis of bovine tuberculosis.

The Delayed type hypersensitivity skin test (DTH) and interferon-gamma assay are used for the diagnosis of bovine tuberculosis (TBB). The specificity of these diagnoses, however, is compromised because both are based on the response against purified protein derivative of Mycobacterium bovis (PPD-B). In this study, we assessed the potential of two cocktails containing M. bovis recombinant proteins: cocktail 1 (C1): ESAT-6, CFP-10 and MPB83 and cocktail 2 (C2): ESAT-6, CFP-10, MPB83, HspX, TB10.3, and MPB70. C1, C2, and PPD-B showed similar response by DTH in M. bovis-sensitized guinea pigs. Importantly, C1 induced a lower response than PPD-B in M. avium-sensitized guinea pigs. In cattle, C1 displayed better performance than PPD-B and C2; indeed, C1 showed the least detection of animals either vaccinated or Map-infected. To optimize the composition of the cocktails, we obtained protein fractions from PPD-B and tested their immunogenicity in experimentally M. bovis-infected cattle. In one highly reactive fraction, seven proteins were identified. The inclusion of FixB in C1 enhanced the recognition of M. bovis-infected cattle without compromising specificity. Our data provide a promising basis for the future development of a cocktail for TBB detection without interference by the presence of sensitized or infected animals with other mycobacteria.