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Use of a PCR assay to assess the prevalence and risk factors for Mycoplasma haemofelis and ‘Candidatus Mycoplasma haemominutum’ in cats in the United Kingdom

Citation
Tasker et al. (2003). Veterinary Record 152 (7)
Names
Ca. Mycoplasma haemominutum
Abstract
Blood samples from 426 healthy and sick cats in the UK were tested in a PCR assay for ‘Candidatus Mycoplasma haemominutum’ and Mycoplasma haemofelis (basonym Haemobartonella felis ). Seventy‐two of the cats (16·9 per cent) were positive for ‘Candidatus M haemominutum’ alone, six (1·4 per cent) were positive for
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Use of Real-Time PCR To Detect and QuantifyMycoplasma haemofelisand “CandidatusMycoplasma haemominutum” DNA

Citation
Tasker et al. (2003). Journal of Clinical Microbiology 41 (1)
Names
Ca. Mycoplasma haemominutum
Abstract
ABSTRACTA real-time PCR assay using Taqman probes was developed to detect and quantifyMycoplasma haemofelisand “CandidatusMycoplasma haemominutum” in feline blood samples. The assay was rapid and sensitive and was successfully used to monitor the in vivo kinetics of cats experimentally infected with each species.

Actinobaculum massiliae ,” a New Species Causing Chronic Urinary Tract Infection

Citation
Greub, Raoult (2002). Journal of Clinical Microbiology 40 (11)
Names
“Actinobaculum massiliense”
Abstract
ABSTRACT We report on a new Actinobaculum species, “ Actinobaculum massiliae ,” isolated from the urine of an elderly woman with recurrent cystitis. Its phenotypic pattern was similar to those of both of the other Actinobaculum species described to date. On 16S rRNA sequencing, the Marseille isolate shared 95% homology with Actinobaculum suis , 92 to 93% homology with
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