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Prevalence of spp. Infection in Patients with Sickle Cell Disease. | LitMetric

AI Article Synopsis

  • Sickle Cell Disease (SCD) increases the likelihood of infections, and this study focused on the prevalence of Bartonella bacteria in SCD patients, a group that may face severe health risks due to infections.
  • The research involved analyzing blood samples from 107 SCD patients using molecular methods to detect Bartonella DNA, and 10 of these patients tested positive for the infection.
  • The study concluded that positive infections were not linked to factors like animal contact or blood transfusions, and affected patients were informed and offered treatment.

Article Abstract

The inherent characteristics of the sickle cell disease (SCD), the most common genetic hematological disorder, increase the propensity of infections. spp. are emerging and neglected bacteria. A large spectrum of clinical manifestations has been linked to bartonella bloodstream infection in the last two decades that can cause fatal outcomes, especially in immunodeficient patients. The goal of this study was to evaluate the prevalence of bartonella infection in SCD patients. We evaluated spp. prevalence in 107 SCD patients. Blood samples and enrichment blood cultures were analyzed by molecular detection of spp. DNA. Bartonella DNA was amplified using conventional genus-specific PCR which amplifies the Intergenic Transcribed Spacer region and specific nested PCR which amplifies the gene. Positive patient DNAs were tested with ssrA conventional PCR. All amplicons were sequenced. Ten of 107 patients tested positive for infection in at least one molecular test. All obtained amplicons were sequenced and similar to sequences deposited in GenBank (accession number BX897699). Based on statistical results, bloodstream infection with was not associated with animal contact or blood transfusions. We detected DNA in 10 (9.3%) SCD studied patients. These patients were notified and treatment was offered to them.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336878PMC
http://dx.doi.org/10.1089/vbz.2019.2545DOI Listing

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