Accession Number : AD1012080


Title :   Culture, Polymerase Chain Reaction and Restriction Fragment Length Polymorphism Studies in Bartonella bacilliformis


Descriptive Note : Technical Report


Corporate Author : UNIFORMED SERVICES UNIV OF THE HEALTH SCIENCES BETHESDA MD BETHESDA United States


Personal Author(s) : Zentrich,Eve C


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/1012080.pdf


Report Date : 22 Sep 1998


Pagination or Media Count : 40


Abstract : Bartonella ssp. have gained importance as etiologic agents of human disease, both in temperate and tropical regions. Reports of increasing numbers of clinical cases of Bartonellosis in Peru (B. bacilli/ormis), documentation of chronic bacteremia in domestic cats with cat scratch fever (B. henselae), and the association of bacillary angiomatosis and parenchymal peliosis (R. henselae and B. quintana) in AIDS patients demand improved laboratory diagnostic detection and isolation techniques for this fastidious organism. We report successful culture and polymerase chain reaction (PCR) techniques applicable for this purpose. Lyophilized B. bacilli/armis was suspended in PBS and cultured on blood and chocolate agar plates to verify survival. Characteristic colonies were used to seed an 8% suspension of human red blood cells in RPMI 1640 media with 10% FBS and 0.7% NaHC03. Aliquots incubated at 280C in a candle jar for3-7 days showed numerous, pleomorphic intraerythrocytic bacteria when thin smears were stained with Giemsa. Ethidium bromide staining and visualization using ultraviolet light of fixed smears of washed red cells showed numerous fluorescent organisms within the cells. B. henselae was similarly cultivated and detected after incubation at 370C. This culture system allows for early presumptive detection of Bartonella ssp., taking advantage of the organism's predeliction for intraerythrocytic habitation and the ability to stain fixed RBCs. For PCR, primers were designed to amplify regions between the16S and 23SrRNA genes of Bartonella, or the entire spacer region. In each case, the primers represented sequences conserved among Bartonella species, and the procedures amplified variable regions 40-1700 bp in length that should be useful for distinguishing species of Bartonella and for molecular epidemiology in restriction length polymorphism analysis.


Descriptors :   Bartonella bacilliformis , bacterial infections , DNA SEQUENCE ANALYSIS


Subject Categories : Microbiology
      Medicine and Medical Research


Distribution Statement : APPROVED FOR PUBLIC RELEASE