Bartonella spp. in Phlebotominae Sand Flies, Brazil.

Bartonella spp. are opportunistic, vectorborne bacteria that can cause disease in both animals and humans. We investigated the molecular occurrence of Bartonella spp. in 634 phlebotomine sand fly specimens, belonging to 44 different sand fly species, sampled during 2017-2021 in north and northeastern Brazil. We detected Bartonella sp. DNA in 8.7% (55/634) of the specimens by using a quantitative real-time PCR targeting the 16S-23S internal transcribed spacer intergenic region. Phylogenetic analysis positioned the Lutzomyia longipalpis sand fly-associated Bartonella gltA gene sequence in the same subclade as Bartonella ancashensis sequences and revealed a Bartonella sp. sequence in a Dampfomyia beltrani sand fly from Mexico. We amplified a bat-associated Bartonella nuoG sequence from a specimen of Nyssomyia antunesi sand fly. Our findings document the presence of Bartonella DNA in sand flies from Brazil, suggesting possible involvement of these insects in the epidemiologic cycle of Bartonella species.

Molecular detection and characterization of Bartonella spp. in rodents from central and southern Chile, with emphasis on introduced rats (Rattus spp.).

Bartonella spp. was screened in 155 rodents from Chile, mainly the invasive rats Rattus norvegicus and Rattus rattus. A total of 155 spleen and 50 blood samples were analyzed through real-time PCR for Bartonella spp. (nuoG gene). Positive samples were subjected to amplification of fragment of loci gltA, rpoB and ITS by conventional PCR (cPCR). Overall, 43 spleen samples (27.7%) and 6 rodent blood samples (12%) were positive for nuoG-Bartonella spp. Positive samples were found in R. norvegicus, R. rattus, Abrothrix olivacea and Oligoryzomys longicaudatus. Bartonella spp. DNA was amplified by cPCR in 16 samples, resulting in 21 sequences (6 gltA, 5 ITS and 10 rpoB). Sequencing and phylogenic analyses identified genotypes from Rattus spp., potentially belonging to Bartonella coopersplainsensis, Bartonella henselae, Bartonella tribocorum, and an undescribed Bartonella sp. From native rodents, one sequence was identified, being related B. machadoae. In conclusion, this work describes diverse and potentially zoonotic Bartonella spp. genotypes in Rattus spp. Additionally, this is the first report of Bartonella in O. longicaudatus, including a potentially novel Bartonella genotype or species.

Molecular analysis of Bartonella spp. in liver tissue of bats from the Atlantic Forest biome, Brazil / Análise molecular de Bartonella spp. em tecido hepático de morcegos do bioma Mata Atlântica, Brasil

The genus Bartonella comprises gram-negative bacilli that possess tropism for erythrocytes and endothelial cells in animals of the orders Rodentia, Lagomorpha, Carnivora, Artiodactyla, Eulipotyphla, and Chiroptera. Bacterial infection may be associated with lymphadenitis, endocarditis, bacillary angiomatosis, and peliosis hepatis. Thirteen species of Bartonella are recognized as zoonotic and bats are considered to be their potential reservoirs. This study aimed to analyze the occurrence of Bartonella spp. in livers of neotropical bats belonging to the families Molossidae, Phyllostomidae, and Vespertilionidae, classified into 21 genera from the Atlantic Forest biome in São Paulo. A total of 341 (n = 341) chiropterans samples were tested for the presence of citrate synthase (gltA) gene of Bartonella by partial amplification using polymerase chain reaction (PCR). Samples of two bats (0.6%) of the species Glossophaga soricina from the municipality of São Roque were tested positive for gltA gene. Phylogenetic analysis indicated that sequences clustered in a clade that was close to the Bartonella sp. detected in G. soricina, which was collected from the Cerrado biome in Tocantins, Brazil. Despite a low prevalence of the detected infection, results indicated that neotropical bats from the Atlantic Forest were potential hosts of Bartonella spp., which might be related to the maintenance of a wild enzootic cycle of the bacterium. Additional studies, particularly on bats of genus Glossophaga, are required to elucidate the dynamics of intraspecific relationships between etiologic agent-vector-hosts.

O gênero Bartonella compreende bacilos gram-negativos que possuem tropismo por eritrócitos e células endoteliais em animais das ordens Rodentia, Lagomorpha, Carnivora, Artiodactyla, Eulipotyphla e Chiroptera. A infecção bacteriana pode estar associada a linfadenite, endocardite, angiomatose bacilar e peliose hepática. Treze espécies de Bartonella são reconhecidas como zoonóticas e os morcegos são considerados seus potenciais reservatórios. Este estudo teve como objetivo analisar a ocorrência de Bartonella spp. em fígados de morcegos neotropicais pertencentes às famílias Molossidae, Phyllostomidae e Vespertilionidae, classificados em 21 gêneros do bioma Mata Atlântica em São Paulo. Um total de 341 (n = 341) amostras de quirópteros foram testados para a presença do gene da citrato sintase (gltA) de Bartonella por amplificação parcial usando reação em cadeia da polimerase (PCR). Amostras de dois morcegos (0,6%) da espécie Glossophaga soricina do município de São Roque foram testadas positivas para o gene gltA. A análise filogenética indicou que as sequências agrupadas em um clado próximo ao de Bartonella sp. detectada em G. soricina, que foi coletada no bioma Cerrado no Tocantins, Brasil. Apesar da baixa prevalência da infecção detectada, os resultados indicaram que os morcegos neotropicais da Mata Atlântica eram potenciais hospedeiros de Bartonella spp., o que pode estar relacionado à manutenção de um ciclo enzoótico selvagem da bactéria. Estudos adicionais, particularmente em morcegos do gênero Glossophaga, são necessários para elucidar a dinâmica das relações intraespecíficas entre agente etiológico-vetor-hospedeiro.

Molecular and serological detection of arthropod-borne pathogens in carnivorous birds from Brazil.

Rickettsiales, Haemosporida and Rhizobiales agents can cause diseases that affect various animal species, including humans. Due to predation behaviour, carnivorous birds may play an important role in spreading these etiological agentes across geographically distant areas, specially if they are migratory. The aim of this study was to investigate the occurrence and to access the phylogenetic relations among Anaplasmataceae (Ehrlichia, Anaplasma, Neorickettsia), Bartonellaceae (Bartonella spp.), and Haemosporida (Plasmodium, Haemoproteus and Leucocytozoon) agents in blood samples from 121 carnivorous birds sampled in the states of São Paulo and Rio de Janeiro, Brazil. Inclusions resembling hemoparasites were not observed in Giemsa-stained preparations. While three animals were seropositive for E. chaffeensis (3.41% [3/88]; 95% CI:1.17-9.55%), five showed antibodies to A. phagocytophilum (5.68% [5/88]; 95% CI: 2.45-12.62%). Despite the detection of rrs gene fragments closely related to E. chaffeensis (4.13% [5/121]; 95% CI: 1.78-9.31%), no positivity was observed in the qPCR based on the genes vlpt for the organism. Similarly, 12 (9.91% [12/121]; 95% CI: 5.76-16.74%) samples were positive in the qPCR for Anaplasma spp. based on groEL gene, but negative in the qPCR for A. phagocytophilum based on msp-2 gene. Three samples were positive in the nPCR for E. canis based on rrs gene. Three samples were positive for Haemoproteus spp. and one for Plasmodium spp. in the nPCR based on cytB gene. Four birds (3.3% [4/121]; 95% CI: 1.29-8.19%) presented co-positivity by Ehrlichia sp. and Anaplasma sp. in molecular assays. One (0.82% [1/121]; 95% CI:0.15-4.53%) bird showed to be seropositive for E. chaffeensis and and positive in PCR for Haemoproteus sp. All birds were negative in the qPCR assay for Bartonella spp. (nuoG). The present work showed the occurrence of Anaplasmataceae agents and hemosporidians in carnivorous birds from southeastern Brazil. The role of these animals in the dispersion of Anaplasmataceae agents should be further investigated.

Genetic Diversity of Bartonella spp. in Wild Mammals and Ectoparasites in Brazilian Pantanal.

The present work aimed to investigate the genetic diversity of Bartonella in mammals and ectoparasites in Pantanal wetland, Brazil. For this purpose, 31 Nasua nasua, 78 Cerdocyon thous, 7 Leopardus pardalis, 110 wild rodents, 30 marsupials, and 42 dogs were sampled. DNA samples were submitted to a quantitative real-time PCR assay (qPCR). Positive samples in qPCR were submitted to conventional PCR assays targeting other five protein-coding genes. Thirty-five wild rodents and three Polygenis (P.) bohlsi bohlsi flea pools showed positive results in qPCR for Bartonella spp. Thirty-seven out of 38 positive samples in qPCR were also positive in cPCR assays based on ftsZ gene, nine in nuoG-cPCR, and six in gltA-cPCR. Concatenated phylogenetic analyses showed that two main genotypes circulate in rodents and ectoparasites in the studied region. While one of them was closely related to Bartonella spp. previously detected in Cricetidae rodents from North America and Brazil, the other one was related to Bartonella alsatica, Bartonella pachyuromydis, Bartonella birtlesii, Bartonella acomydis, Bartonella silvatica, and Bartonella callosciuri. These results showed that at least two Bartonella genotypes circulate among wild rodents. Additionally, the present study suggests that Polygenis (P.) bohlsi bohlsi fleas could act as possible Bartonella vectors among rodents in Pantanal wetland, Brazil.

Evidence and molecular characterization of Bartonella spp. and hemoplasmas in neotropical bats in Brazil.

The order Chiroptera is considered the second largest group of mammals in the world, hosting important zoonotic virus and bacteria. Bartonella and hemotropic mycoplasmas are bacteria that parasite different mammals' species, including humans, causing different clinical manifestations. The present work aimed investigating the occurrence and assessing the phylogenetic positioning of Bartonella spp. and Mycoplasma spp. in neotropical bats sampled from Brazil. Between December 2015 and April 2016, 325 blood and/or tissues samples were collected from 162 bats comprising 19 different species sampled in five states of Brazil. Out of 322 bat samples collected, while 17 (5·28%) were positive to quantitative PCR for Bartonella spp. based on nuoG gene, 45 samples (13·97%) were positive to cPCR assays for hemoplasmas based on 16S rRNA gene. While seven sequences were obtained for Bartonella (nuoG) (n = 3), gltA (n = 2), rpoB (n = 1), ftsZ (n = 1), five 16S rRNA sequences were obtained for hemoplasmas. In the phylogenetic analysis, the Bartonella sequences clustered with Bartonella genotypes detected in bats sampled in Latin America countries. All five hemoplasmas sequences clustered together as a monophyletic group by Maximum Likelihood and Bayesian Inference analyses. The present work showed the first evidence of circulation of Bartonella spp. and hemoplasmas among bats in Brazil.