Translocation and effectiveness of foliar-fertilized boron in broccoli plants of varying boron status

The translocation and effectiveness of foliar-fertiilized boron (B) was investigated in broccoli plants supplied via the root system with luxury, sufficient or deficient levels of B. ¹⁰B-enriched boric acid was applied three times to lower leaves, beginning one week prior to inflorescence emergence, and the shoot and floret yields, as well as the ¹⁰B and ¹¹B contents or concentrations of xylem sap, phloem exudate and various plant parts, were determined three weeks after inflorescence emergence. The amount of ¹⁰B translocated in phloem from fed leaves to the remainder of the shoot did not exceed 0.5%, of that supplied, but it was inversely related to plant-B status. The partitioning of translocated ¹⁰B to florets (16–30%) and the degree of enhancement in floret yield (28–75%) was also inversely related to plant-B status. It is concluded that foliar-B fertilization may be more effective for preventing B deficiency than soil-derived B in leaves.Abbreviations ¹⁰B/¹¹B mass isotopes of boron - DM dry matter - FF foliar fertilization - RF root fertilization     

Xylem‐to‐phloem transfer of boron in broccoli and lupin during early reproductive growth

The aim of this study was to test the hypothesis that newly‐acquired boron (B) undergoes rapid xylem‐to‐phloem transfer in plants with restricted mobility. Analysis of the element accumulation and water usage by shoots of intact broccoli ( Brassica oleracea var. italica Plenck cv. Commander) and lupin ( Lupinus albus L. cv. Ultra) plants provided with a non‐deficient supply of B, revealed that the concentration of various mineral elements (K, P, Mg, Ca, B, Fe, Zn, Mo, Cu, Mn) in xylem sap of intact plants ranged from 0.3 µ M to 3.5 m M , with B being present at 2.9‐3.5 µ M . For each element assayed, the concentration was higher in phloem exudate (1.6 µ M to 91 m M ) than in xylem sap; B was present at about 0.4 m M . Intact broccoli and lupin plants or detached transpiring broccoli shoots were supplied simultaneously with enriched ¹⁰B, strontium (a xylem marker) and rubidium (a xylem/phloem marker) during early reproductive growth. The contents of these three compounds were determined in foliage and florets or fruits as a function of time (i.e. up to 12 h and 4 days for broccoli and lupin plants, respectively), and the content in florets or fruits was expressed as a percent of the total recovered. In general, the percent recovery of both ¹⁰B and rubidium in florets or fruits was similar and markedly greater than that for strontium, even at the earliest harvest times (within 2 h for broccoli and 1 day for lupin). The data indicate that in plants with restricted B mobility, B is supplied to sink tissues in the phloem, and the extent of B xylem‐to‐phloem transfer is closely determined by current uptake.     

Boron mobility in plants

Boron (B) is a micronutrient essential for the normal growth of monocots, dicots. conifers, ferns and several diatom species. Boron deficiency causes many anatomical, physiological and biochemical changes, making it difficult to identify a primary role for it: however, evidence does indicate that B is involved at the membrane level. Whatever the role(s). it likely involves the complexation of B with compounds containing cis -hydroxyl groups. Boron deficiency in crops is more widespread than deficiency of any other micronutrient. Nutritional disorders in vegetables include brown heart in rutabaga, turnip and radish roots, and hollow stem in cauliflower and broccoli. The occurrence of these disorders even when B is in ample supply suggests that they are physiological in nature and related to the mobility of B in the plant. The distribution of B is related to the loss of water from shoot organs, suggesting that it is primarily xylem-mobile with limited retranslocation in phloem. However, research has shown that B is present in the phloem, albeit at low concentration, and that it is generally retranslocated in the phloem to satisfy the demands of sink organs that do not readily transpire. Further progress into the mechanism(s) of B retranslocation will be facilitated by insights into the role and metabolism of B in plants.     

Antimicrobial resistance including Extended Spectrum Beta Lactamases (ESBL) among E. coli isolated from kenyan children at hospital discharge

BackgroundChildren who have been discharged from hospital in sub-Saharan Africa remain at substantial risk of mortality in the post-discharge period. Antimicrobial resistance (AMR) may be an important factor. We sought to determine the prevalence and risk factors associated with AMR in commensal Escherichia coli (E. coli) from Kenyan children at the time of discharge.Methodology/Principle findingsFecal samples were collected from 406 children aged 1–59 months in western Kenya at the time of discharge from hospital and cultured for E. coli. Susceptibility to ampicillin, ceftriaxone, cefotaxime, ceftazidime, cefoxitin, imipenem, ciprofloxacin, gentamicin, combined amoxicillin/clavulanic acid, trimethoprim-sulfamethoxazole, azithromycin, and chloramphenicol was determined by disc diffusion according to guidelines from the Clinical and Laboratory Standards Institute (CLSI). Poisson regression was used to determine associations between participant characteristics and the presence of extended-spectrum beta-lactamases (ESBL) producing E. coli. Non-susceptibility to ampicillin (95%), gentamicin (44%), ceftriaxone (46%), and the presence of ESBL (44%) was high. Receipt of antibiotics during the hospitalization was associated with the presence of ESBL (aPR = 2.23; 95% CI: 1.29–3.83) as was being hospitalized within the prior year (aPR = 1.32 [1.07–1.69]). Open defecation (aPR = 2.02; 95% CI: 1.39–2.94), having a toilet shared with other households (aPR = 1.49; 95% CI: 1.17–1.89), and being female (aPR = 1.42; 95% CI: 1.15–1.76) were associated with carriage of ESBL E. coliConclusions/SignificanceAMR is common among isolates of E. coli from children at hospital discharge in Kenya, including nearly half having detectable ESBL.