2011
DOI: 10.1590/s1517-83822011000200003
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Detection of Bartonella henselae in defibrinated sheep blood used for culture media supplementation

Abstract: Bartonella henselae was detected in defibrinated sheep blood employed in supplementing a selective bacteria culture medium by nested PCR. We recommended that highly sensitive technical tests be run to ensure a sterile culture medium for Bartonella spp. isolation, since infected blood samples used in preparation could lead to false-positive results.

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Cited by 6 publications
(4 citation statements)
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“…A negative control flask containing only BAPGM medium was added to each batch of samples tested and subjected to the same laboratory procedures and culture conditions. Subsequently, 1 mL of the blood-inoculated liquid culture was sub-inoculated onto agar enriched slant tubes containing 30% Bartonella spp.-negative sheep blood (confirmed by PCR and culture methods) [ 24 ] for additional 42 days. BAPGM-negative controls were also subcultured onto blood-agar.…”
Section: Methodsmentioning
confidence: 99%
“…A negative control flask containing only BAPGM medium was added to each batch of samples tested and subjected to the same laboratory procedures and culture conditions. Subsequently, 1 mL of the blood-inoculated liquid culture was sub-inoculated onto agar enriched slant tubes containing 30% Bartonella spp.-negative sheep blood (confirmed by PCR and culture methods) [ 24 ] for additional 42 days. BAPGM-negative controls were also subcultured onto blood-agar.…”
Section: Methodsmentioning
confidence: 99%
“…After a 14-day incubation period, a 1-ml aliquot of liquid culture medium was used for DNA extraction and another 1-ml aliquot was plated onto a blood agar plate and incubated for an additional 42 days. Blood agar plates were prepared with 30% of sheep blood confirmed to be free of Bartonella DNA by PCR (2). The liquid culture negative-control blood-agar plate was incubated under the same conditions.…”
mentioning
confidence: 99%
“…The pellets were then inoculated on BHI agar (Biolife, Ref. 4012352) containing 5% sheep blood that was confirmed to be Bartonella negative ( 20 , 21 ) and 2% Brucella growth supplement (HiMedia, FD005) and then incubated at 35°C in an atmosphere of 5% carbon dioxide (CO 2 ) for 4–8 weeks ( 18 , 22 ). Oral swabs and claw samples were enriched in 5 ml of BHI broth containing 5% sheep blood and Brucella growth supplement, before being incubated at 35°C in an atmosphere of 5% CO 2 for 10 days ( 21 , 23 , 24 ).…”
Section: Methodsmentioning
confidence: 99%