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. 2017 Jun:52:14-18.
doi: 10.1016/j.cimid.2017.05.003. Epub 2017 May 12.

Pathogenic Leptospira spp. in bats: Molecular investigation in Southern Brazil

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Pathogenic Leptospira spp. in bats: Molecular investigation in Southern Brazil

Fabiana Quoos Mayer et al. Comp Immunol Microbiol Infect Dis. 2017 Jun.

Abstract

The present study aimed to investigate the frequency of pathogenic Leptospira spp. in Brazilian bats and to determine possible risk factors associated to it. Ninety two bats of 12 species were evaluated. Whole genomic DNA from kidneys was extracted and real-time PCR specific to pathogenic Leptospira spp. was applied. Association between the frequency of specimens positive for Leptospira spp. and sex, age, bat species or family, season of collection, geographic localization and feeding habits was evaluated. The results showed that 39.13% of analyzed bats were found positive for Leptospira spp. Nine bat species had at least one positive result. There was no association among the evaluated variables and frequency of pathogenic Leptospira spp. Although the limitations due to lack of Leptospira spp. isolation, leptospiral carriage was demonstrated in bats of different species from southern Brazil, which reinforces the need for surveillance of infectious agents in wild animals.

Keywords: Emerging diseases; Leptospirosis; Molecular epidemiology; Public health; Zoonotic diseases.

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Figures

Fig. 1
Fig. 1
Geographical distribution of sampled bats. Rio Grande do Sul, the southern Brazilian state is shown. Municipalities in red (n = 20) had at least one bat with positive result for pathogenic Leptospira spp. Municipalities in green (n = 13) had at least one evaluated bat and the results were negative. Municipalities in white were not accessed. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 2
Fig. 2
Standard curve of real-time PCR to detect pathogenic Leptospira spp. Determination of the detection threshold by titration of plasmids contaning lipL32 sequence. The detection limit was 10 DNA molecules with 103.42% efficiency.

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