Ísis Assis Braga

A novel Ehrlichia genotype strain distinguished by the TRP36 gene naturally infects cattle in Brazil and causes clinical manifestations associated with ehrlichiosis

A novel Ehrlichia genotype most closely related to E. canis was reported in North American cattle in 2010, and a similar agent was subsequently identified in the hemolymph of Brazilian Rhipicephalus (Boophilus) microplus ticks and isolated in 2012. The purpose of this study was to determine whether this or other novel ehrlichial agents naturally infect Brazilian cattle. Using PCR targeting the genus-conserved dsb gene, DNA from this novel ehrlichial agent in Brazilian cattle was detected. Attempts to isolate the organism in vitro were performed using DH82 cells, but morulae and ehrlichial DNA could only be detected for approximately one month. In order to further molecularly characterize the organism, PCR was performed using primers specific for multiple E. canis genes (dsb, rrs, and trp36). Sequence obtained from the conserved rrs and dsb genes demonstrated that the organism was 99-100% identical to the novel Ehrlichia genotypes previously reported in North American cattle (rrs gene) and Brazilian ticks (rrs and dsb genes). However, analysis of the trp36 gene revealed substantial strain diversity between these Ehrlichia genotypes strains, including divergent tandem repeat sequences. In order to obtain preliminary information on the potential pathogenicity of this ehrlichial agent and clinical course of infection, a calf was experimentally infected. The calf showed clinical signs of ehrlichiosis, including fever, depression, lethargy, thrombocytopenia, and morulae were observed in peripheral blood monocytes. This study reports a previously unrecognized disease-causing Ehrlichia sp. in Brazilian cattle that is consistent with the genotype previously described in North America cattle and ticks from Brazil. Hence, it is likely that this is the organism previously identified as Ehrlichia bovis in Brazil in 1982. Furthermore, we have concluded that strains of these Ehrlichia genotypes can be molecularly distinguished by the trp36 gene, which has been widely utilized to define E. canis strain diversity.

Novel Babesia and Hepatozoon agents infecting non-volant small mammals in the Brazilian Pantanal, with the first record of the tick Ornithodoros guaporensis in Brazil

Taking into account the diversity of small terrestrial mammals of the Pantanal, the present study aimed to verify the occurrence of infection by Ehrlichia spp., Anaplasma spp., Rickettsia spp., Hepatozoon spp., Babesia spp. and parasitism by ticks in non-volant small mammals collected in the Brazilian Pantanal. Samples of blood, liver and spleen were collected from 64 captured animals, 22 marsupials and 42 rodents. Pathogen detection was performed by the use of genus-specific Polymerase Chain Reaction (PCR) assays. Ticks collected from the animals consisted of Amblyomma sculptum and Amblyomma triste nymphs, and Ornithodoros guaporensis larvae. None of the vertebrate samples (blood, liver, or spleen) yielded detectable DNA of Rickettsia spp. or Ehrlichia spp. The blood of the rodent Hylaeamys megacephalus yielded an Anaplasma sp. genotype (partial 16S rRNA gene) 99% similar to multiple Anaplasma spp. genotypes around the world. The blood of three rodents of the species Calomys callosus were positive for a novel Hepatozoon sp. agent, phylogenetically related (18S rDNA gene) to distinct Hepatozoon genotypes that have been detected in rodents from different parts of the world. One marsupial (Monodelphis domestica) and three rodents (Thrichomys pachyurus) were positive to novel piroplasmid genotypes, phylogenetically (18S rDNA gene) related to Theileria bicornis, Cytauxzoon manul, and Cytauxzoon felis. The present study provides the first molecular detection of Hepatozoon sp. and piroplasmids in small mammals in Brazil. Additionally, we expanded the distribution of O. guaporensis to Brazil, since this tick species was previously known to occur only in Bolivia.

Detection of Ehrlichia canis in domestic cats in the central-western region of Brazil

Ehrlichiosis is a worldwide distributed disease caused by different bacteria of the Ehrlichia genus that are transmitted by arthropod vectors. Its occurrence in dogs is considered endemic in several regions of Brazil. Regarding cats, however, few studies have been done and, consequently, there is not enough data available. In order to detect Ehrlichia spp. in cats from the central-western region of Brazil, blood and serum samples were collected from a regional population of 212 individuals originated from the cities of Cuiabá and Várzea Grande. These animals were tested by the Immunofluorescence Assay (IFA) and the Polymerase Chain Reaction (PCR) designed to amplify a 409 bp fragment of the dsb gene. The results obtained show that 88 (41.5%) cats were seropositive by IFA and 20 (9.4%) cats were positive by PCR. The partial DNA sequence obtained from PCR products yielded twenty samples that were found to match perfectly the Ehrlichia canis sequences deposited on GenBank. The natural transmission of Ehrlichia in cats has not been fully established. Furthermore, tick infestation was not observed in the evaluated cats and was not observed any association between age, gender and positivity of cats in both tests. The present study reports the first serological and molecular detection of E. canis in domestic cats located in the endemic area previously mentioned.

Hematological values associated to the serological and molecular diagnostic in cats suspected of Ehrlichia canis infection

The literature contains several studies on feline ehrlichiosis. However, information about the characteristics of Ehrlichia infection in cats is still scanty. This study evaluated the association between Ehrlichia spp. infection and the hematologic data of 93 cats treated at the Federal University of Mato Grosso Veterinary Hospital in Cuiabá, state of Mato Grosso, Brazil. The presence of or exposure to Ehrlichia spp. infection was evaluated by Polymerase Chain Reaction (PCR) targeting the dsb and 16S rRNA gene of Ehrlichia, and by detection of anti-Ehrlichia canis IgG antibodies in Indirect Fluorescence Assay (IFA), respectively. Eight (8.6%) cats tested positive by PCR and the partial DNA sequence obtained from PCR products was a 100% match to E. canis. Forty-two (45.1%) cats showed antibody reactivity against Ehrlichia spp. Hematological alterations such as low erythrocyte count, thrombocytopenia, lymphopenia and monocytosis were observed in PCR positive cats. Among them, low erythrocyte counts were associated with IgG antibody titers of 40 to 640 and five cats also tested positive by PCR. Furthermore, PCR-positive cats showed a tendency to be lymphopenic. No correlation was found between age and sex, and no ticks were observed in any of the examined cats.

Molecular detection of Bartonella clarridgeiae in domestic cats from Midwest Brazil

Cat scratch disease (CSD) is caused by Bartonella henselae a hemotropic bacterium that infects human, domestic and wild mammals. Closely related to B. henselae, the B. clarridgeiae comprises approximately 10–30% of Bartonella isolates from clinically healthy cats and was found in cardiac and hepatic lesions in dogs.1 Moreover, B. clarridgeiae has been serologically associated with CSD-like illness in humans.2 Cats are considered the major reservoir and carriers of B. henselae, B. clarridgeiae and B. koehlerae. Bartonella spp. can be a vector transmitted by flea to susceptible cats. Few cats naturally infected have clinical signs. Medical problems of cats associated with Bartonella infections are variable, ranging from transient fever and lymphadenopathy to abscesses or microabscesses in different organs, endocarditis, and central nervous signs.1 Transmission from cats to humans and dogs mainly occurs through cat scratches or bites. In humans, this infection may be asymptomatic and can disappear spontaneously without any treatment; however, in some cases the disease may be fatal if left untreated.3 In order to identify arthropod-borne pathogens in domestic feline, 182 cats from different places of Cuiabá and Varzea Grande cities, both located in Mato Grosso State, Midwest Brazil, have been analyzed. Cats were seen at the Veterinary Hospital of the Federal University of Mato Grosso (HOVET-UFMT), Veterinary Hospital of the University of Cuiabá (UNIC-HV), and animal shelters and Zoonosis Control Centers (ZCC) of Cuiabá and Várzea Grande cities. Sample collection was conducted in agreement with the Ethical Principles for Animal Research under the institutional watch of the UFMT Committee for Ethics in Animal Research. Collected blood samples were subjected to a DNA extraction using the Axyprep Blood Genomic DNA Miniprep Kit (Axygen Biosciences, Hangzhou, China). Extracted DNA was then used as a template for Bartonella spp. PCR assay using the primer BARTON-1 (5-TAACCGATATTGGTTGTGTTGAAG3) and BARTON-2 (5-TAAAGCTAGAAAGTCTGGCAACATAACG3), which amplifies a segment of 585–588 bp of Riboflavin synthase C (ribC) gene of Bartonella genus.4 Three (1.6%) cats were positive to the presence of Bartonella DNA according to PCR targeting portions of the ribC gene. Partial DNA sequences of all PCR-positive samples were generated yielding a sequence (GenBank accession: KR092386) that was identical to KC331014 and HM588660 and 99% similarity to HQ012585, KC331017, KC331014, which corresponds to B. clarridgeiae sequences available in GenBank. The positive cats were found in the ZCC of Várzea Grande city. Usually, these animals are taken off the streets and kept until adoption. Boulouis et al. observed that stray cats present higher prevalence of Bartonella spp. infection than pet cats, mainly due to close contact between infected animals in large groups of cats, demonstrating that differences in the occurrence of the infection are associated with the type of feline population studied.5 Due to vigorous flea control among cat populations, the prevalence of Bartonella infection in cats have reduced and the risk of Bartonella-associated disease in pet owners decreased. However, cat owners and animal health professionals should be cautioned to avoid behaviors that increase the risk of animal bites or scratches, since the feline population acts as a source of zoonotic agents and represents a potential risk of infection.1 In Brazil, the occurrence of Bartonella infection in human was previously described. In the State of Rio de Janeiro, 41.6% of clinically asymptomatic HIV-positive patients were found seropositive for Bartonella species.3 In fact, veterinarians and medical doctors should consider the presence of these zoonotic pathogens in their diagnostic routine.

PREVALENCE OF ANTIBODIES AGAINST INFLUENZA VIRUS IN NON-VACCINATED EQUINES FROM THE BRAZILIAN PANTANAL

The prevalence of antibodies against Equine Influenza Virus (EIV) was determined in 529 equines living on ranches in the municipality of Poconé, Pantanal area of Brazil, by means of the hemagglutination inhibition test, using subtype H3N8 as antigen. The distribution and possible association among positive animal and ranches were evaluated by the chi-square test, spatial autoregressive and multiple linear regression models. The prevalence of antibodies against EIV was estimated at 45.2% (95% CI 30.2 - 61.1%) with titers ranging from 20 to 1,280 HAU. Seropositive equines were found on 92.0% of the surveyed ranches. Equine from non-flooded ranches (66.5%) and negativity in equine infectious anemia virus (EIAV) (61.7%) were associated with antibodies against EIV. No spatial correlation was found among the ranches, but the ones located in non-flooded areas were associated with antibodies against EIV. A negative correlation was found between the prevalence of antibodies against EIV and the presence of EIAV positive animals on the ranches. The high prevalence of antibodies against EIV detected in this study suggests that the virus is circulating among the animals, and this statistical analysis indicates that the movement and aggregation of animals are factors associated to the transmission of the virus in the region.

Detection of genotype-specific Ehrlichia canis exposure in Brazilian dogs by TRP36 peptide ELISA

We recently characterized a novel genotype of Ehrlichia canis based on the tandem repeat (TR) sequence of the TRP36 gene in Brazil. The TR amino acid sequence of the Brazilian (Br) genotype (ASVVPEAE) was divergent from the previously described US genotype (TEDSVSAPA) of E. canis. In this study, we developed an ELISA based on TRP36 TR synthetic peptides from both Br and US E. canis TRP36 genotypes to serologically detect and distinguish infections caused by these genotypes. Sera from 30 Brazilian dogs naturally infected with E. canis, sera from dogs experimentally infected E. canis (Jake and Cuiabá #1 strains) and E. chaffeensis (Arkansas strain) and 12 seronegative E. canis dogs were evaluated. Fifteen naturally infected Brazilian dogs had antibodies that reacted with the US TRP36 (n=9) or Br TRP36 (n=6) only, and 13 dogs had antibodies that reacted with both TPR36 peptides suggesting that these dogs were exposed to both genotypes. Most dogs (n=28) had antibodies that reacted with the highly conserved E. canis TRP19 peptide; however, two dogs had antibodies to E. canis TRP19, but did not have TRP36 antibodies, raising the possibility that another novel TRP36 genotype is circulating in Brazil. Our results demonstrate that synthetic peptides based on the TR region of E. canis TRP36 can be used to serologically distinguish infections or identify coinfections by different genotypes, and to determine the seroprevalence of various E. canis genotypes in Brazil.

Molecular assessment of the transplacental transmission of Toxoplasma gondii, Neospora caninum, Brucella canis and Ehrlichia canis in dogs

Given the fact that numerous microbial species can be detected in pregnant female dogs, the objective of this study was to assess the transplacental transmission of Brucella canis, Ehrlichia canis, Neospora caninum and Toxoplasma gondii in stillborn puppies. This study involved 41 stillborn puppies, 78.6% of which were positive for T. gondii, 52.4% for N. caninum and 59.5% for B. canis. E. canis was not detected in any of the analyzed puppies. Pregnancy is an important physiological condition for the transmission of infectious agents to puppies and transplacental transmission may be epidemiologically relevant in the spread of these opportunistic agents.

Detection of Theileria equi, Babesia caballi and anti-Ehrlichia spp antibodies in equides from the Pantanal of Mato Grosso State.

The present study evaluated 121 equids from 19 ranches in the Pantanal region of Mato Grosso State through Polimerase Chain Raction (PCR) to detect Babesia, Theileria, Anaplasma, Ehrlichia and Neorickettsia partial genes and the Imunofluorescent Antibody Test (IFAT) to evaluate anti-Ehrlichia spp. antibodies. From the total tested in PCR, 17 (14.0%) equids from 9 (47.3%) farms were positive, and 16 yielded amplicons 100% identical to Theileria equi and one presented 99% similarity to Babesia caballi available on GenBank. Forty eight (39.6%) equids were positive by IFAT and 40 showed titers of 40 (83.3%) and 8 showed titers of 320 (16.6%). All ranches (100%) presented seropositive equids. Our results showed that T. equi and B. caballi are infecting equids in the region and the presence of anti-Ehrlichia antibodies suggests that species closely related to the genera Ehrlichia and Anaplasma are circulating among the equid local population. Moreover, the negative results in PCR is possibly related to the chronic infection phase.

Molecular detection of tick-borne protozoan parasites in a population of domestic cats in midwestern Brazil.

Some tick-borne pathogens that infect domestic cats have been considered emergent in veterinary medicine. Occurrences of Hepatozoon spp., Babesia spp. and Cytauxzoon spp. have been described in several regions of Brazil. This paper offers a comprehensive analysis of the 18S rRNA gene of a Hepatozoon sp. strain detected in domestic cats in the metropolitan area of Cuiabá, in Midwestern Brazil. Based on a molecular analysis, we detected the presence of Hepatozoon species circulating among cats in this region. The aforementioned strain is closely related to other isolates of H. felis detected in wild felids. Moreover, a phylogenetic analysis indicates that this genotype is grouped into a clade of 18S rRNA sequences previously described for the genus Hepatozoon in wild felids around the world. Hepatozoon felis strains detected in cats from Spain and Israel showed, respectively, 98% and 97% identity to our sequence and are clustered on a separate branch of the phylogenetic tree. This finding suggests a high diversity of Hepatozoon genotypes occurring in cats in Europe and South America. None of the analyzed cats were positive for Babesia spp. or Cytauxzoon spp. by PCR analysis.