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1.
J Vet Diagn Invest ; 27(2): 206-10, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25776545

ABSTRACT

Coxiella burnetii and certain members of the Chlamydiales order are zoonotic, intracellular, Gram-negative bacteria, with abortigenic potential in ruminants. These pathogens have a broad host range and worldwide geographical distribution. The current study aimed to reveal the importance of C. burnetii and Chlamydiales spp. in abortions in domestic ruminants and their occurrence in wild ruminants with real-time polymerase chain reaction (qPCR) assays, histology, and immunohistochemical staining (IHC). From the 111 abortion cases of domestic ruminants examined, C. burnetii was detected in 33 placenta samples (cattle, n = 22; sheep, n = 10; goat, n = 1), and members of the Chlamydiales order were detected in 32 placenta samples (cattle, n = 14; sheep, n = 16; goat, n = 2) using qPCR. Coinfection with both C. burnetii and Chlamydiales spp. were identified in 12 cases (cattle, n = 3; sheep, n = 8; goat, n = 1) out of the qPCR-positive samples. The presence of the relevant antigen was confirmed by IHC in 20 cases (C. burnetii, n = 2, in sheep; Chlamydiaceae, n = 17, in sheep [n = 15] and goat [n = 2]; and both pathogens in 1 sheep). Coxiella burnetii was identified in 2.2% (2/91) of the wild ruminants, but the samples were negative by IHC. Uncultured Chlamydiales spp. were detected in 4.4% (4/91) of the placenta samples by qPCR. In conclusion, Q fever is widespread among domestic ruminants in Hungary, and, in several cases, C. burnetii was implicated as the primary cause of abortions. Waddlia chondrophila, Parachlamydia spp., and uncultured Chlamydiales spp. were present only sporadically in samples from cattle and wild ruminants.


Subject(s)
Chlamydiales/isolation & purification , Coxiella burnetii/isolation & purification , Q Fever/veterinary , Abortion, Veterinary/microbiology , Animals , Animals, Domestic , Animals, Wild , Cattle , Cattle Diseases/diagnosis , Cattle Diseases/epidemiology , Cattle Diseases/microbiology , Chlamydiaceae , Coinfection , DNA, Bacterial/analysis , Female , Goat Diseases/diagnosis , Goat Diseases/epidemiology , Goat Diseases/microbiology , Goats , Hungary/epidemiology , Immunohistochemistry/veterinary , Placenta/microbiology , Pregnancy , Q Fever/diagnosis , Q Fever/epidemiology , Real-Time Polymerase Chain Reaction/veterinary , Sheep , Sheep Diseases/diagnosis , Sheep Diseases/epidemiology , Sheep Diseases/microbiology
2.
Ticks Tick Borne Dis ; 5(6): 818-20, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25108781

ABSTRACT

The expanding family of Francisellaceae includes the genus Francisella, where several pathogen bacteria, e.g. the zoonotic F. tularensis, and different Francisella-like agents belong to. Francisella-like endosymbionts (FLEs) are widespread in hard and soft ticks and their pathogenicity is unknown. The examination of 296 ticks collected in Ethiopia was performed for the detection of F. tularensis and FLEs using polymerase chain reaction (PCR) assays based on the amplification of 16S rRNA, sdhA and tul4 gene fragments. FLE was described in one Hyalomma rufipes tick based on the 16S rRNA and sdhA gene sequences. The 16S rRNA gene fragment was identical with the ones detected previously in Rhipicephalus sanguineus and Hyalomma marginatum marginatum in Bulgaria. The presence of endosymbionts with identical 16S rRNA gene sequence in both Rhipicephalus and Hyalomma species further supports the hypotheses, that certain FLEs had independent evolution from their tick hosts.


Subject(s)
Arachnid Vectors/microbiology , Francisella tularensis/classification , Francisella/classification , Ixodidae/microbiology , Tularemia/microbiology , Animals , Base Sequence , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Ethiopia/epidemiology , Francisella/genetics , Francisella/isolation & purification , Francisella tularensis/genetics , Francisella tularensis/isolation & purification , Humans , Molecular Sequence Data , Phylogeny , Sequence Analysis, DNA , Symbiosis , Tularemia/epidemiology
3.
BMC Vet Res ; 10: 107, 2014 May 07.
Article in English | MEDLINE | ID: mdl-24885415

ABSTRACT

BACKGROUND: Information about the genotypic characteristic of Coxiella burnetii from Hungary is lacking. The aim of this study is to describe the genetic diversity of C. burnetii in Hungary and compare genotypes with those found elsewhere. A total of 12 samples: (cattle, n = 6, sheep, n = 5 and human, n = 1) collected from across Hungary were studied by a 10-loci multispacer sequence typing (MST) and 6-loci multiple-locus variable-number of tandem repeat analysis (MLVA). Phylogenetic relationships among MST genotypes show how these Hungarian samples are related to others collected around the world. RESULTS: Three MST genotypes were identified: sequence type (ST) 20 has also been identified in ruminants from other European countries and the USA, ST28 was previously identified in Kazakhstan, and the proposed ST37 is novel. All MST genotypes yielded different MLVA genotypes and three different MLVA genotypes were identified within ST20 samples alone. Two novel MLVA types 0-9-5-5-6-2 (AG) and 0-8-4-5-6-2 (AF) (Ms23-Ms24-Ms27-Ms28-Ms33-Ms34) were defined in the ovine materials correlated with ST28 and ST37. Samples from different parts of the phylogenetic tree were associated with different hosts, suggesting host-specific adaptations. CONCLUSIONS: Even with the limited number of samples analysed, this study revealed high genetic diversity among C. burnetii in Hungary. Understanding the background genetic diversity will be essential in identifying and controlling outbreaks.


Subject(s)
Cattle Diseases/microbiology , Coxiella burnetii/genetics , Genotype , Q Fever/veterinary , Sheep Diseases/microbiology , Animals , Cattle , Cattle Diseases/epidemiology , Coxiella burnetii/isolation & purification , Humans , Hungary/epidemiology , Phylogeny , Q Fever/epidemiology , Q Fever/microbiology , Sheep , Sheep Diseases/epidemiology , Species Specificity
4.
Acta Vet Hung ; 60(3): 361-70, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22903081

ABSTRACT

Smaller macropodid species (commonly referred to as wallabies) are extremely susceptible to toxoplasmosis: in most cases, infection with Toxoplasma gondii leads to death within a short time. Between June 2006 and July 2010, T. gondii was detected by immunohistochemical examination in six Tammar wallabies (Macropus eugenii) that died in the Budapest Zoo and Botanical Garden; in another four specimens histopathology revealed T. gondii-like organisms (which could not be differentiated from Neospora caninum solely by morphology), and in another 11 animals toxoplasmosis as the possible cause of death could not be excluded. The current zoo population of 12 Tammar wallabies was tested for T. gondii IgG antibodies by the modified agglutination test (MAT), with negative results. We suppose that most of the deaths were due to acute toxoplasmosis resulting from a recent infection.


Subject(s)
Macropodidae , Toxoplasmosis, Animal , Agglutination Tests , Agriculture , Animals , Animals, Zoo , Toxoplasma
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