Circulating miR-147b as a diagnostic marker for patients with bacterial sepsis and septic shock.

Background: Early diagnosis, precise antimicrobial treatment and subsequent patient stratification can improve sepsis outcomes. Circulating biomarkers such as plasma microRNAs (miRNAs) have proven to be surrogates for diagnosis, severity and case management of infections. The expression of four selected miRNAs (miR-146-3p, miR-147b, miR-155 and miR-223) was validated for their prognostic and diagnostic potential in a clinically defined cohort of patients with sepsis and septic shock.

, a new species of Gesneriaceae from Phu Quoc Island, South-western Vietnam.

A new species of Gesneriaceae, , is described and illustrated from Phu Quoc National Park, Kien Giang Province, South-western Vietnam. It is most similar to , and in having 3-verticillate petiolate leaves, morphologically similar calyx, corolla, stamens, pistil and fruit, but differs from all in the glandular-pubescent stems, petioles and leaf blades, 1(-2)-flowered cymes, longer corolla and fruit and longer and densely glandular-puberulent ovary. Data on distribution, ecology, phenology and provisional conservation assessment of the new species are given along with an illustration and a colour plate.

Clinical utility of an optimised multiplex real-time PCR assay for the identification of pathogens causing sepsis in Vietnamese patients.

Introduction: For the identification of bacterial pathogens, blood culture is still the gold standard diagnostic method. However, several disadvantages apply to blood cultures, such as time and rather large volumes of blood sample required. We have previously established an optimised multiplex real-time PCR method in order to diagnose bloodstream infections.

Enrichment of bacterial DNA for the diagnosis of blood stream infections.

Background: Blood cultures are commonly employed to identify bacterial pathogens causing sepsis. PCR assays to diagnose septicemia require extraction of bacterial DNA from blood samples and thus, delay the initiation of appropriate antimicrobial treatment. The presence of abundant human DNA may hamper the sensitivity of PCR in the detection of bacteria.