84 research outputs found

    Tap water access and its relationship with cholera and other diarrhoeal diseases in an urban, cholera-endemic setting in the Democratic Republic of the Congo

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    Globally 1.3 billion people are at risk of cholera in endemic countries, where nearly 3 million cases occur annually, of which 3 % are fatal. The burden is highest in South-Asia and Sub-Saharan Africa, where diarrhoeal diseases in general are also a leading cause of mortality and morbidity, especially for children under 5. Uvira, the second largest city of South-Kivu province in the eastern part of the Democratic Re-public of the Congo, has been affected by cholera since it reached the region in the late 1970s. Suspected cholera cases have been reported nearly every week since 2004 by the Uvira cholera treatment centre (CTC). This thesis first shows that about 40% of the patients admitted to the CTC test positive for cholera with rapid diagnostic tests, and that infections with other common enteric pathogens are highly prevalent. Two surveys of water-related practices in more than 500 households indicate that tap water is sometimes used by nearly 80% of households for drinking purposes but only systematically by less than 50%, whilst surface water is the main source of domestic water for nearly 40% of households. Tap water access is a predictor of the quality and quantity of domestic water used in households. Time-series regression reveals a 2.5-fold increase in CTC admissions within the 12 days following a 24h interruption in tap water supply. Finally, a multivariable time-series model high-lights the influence of tap water supply variability in time and space on suspected chol-era incidence, especially that attributed to epidemic transmission. By demonstrating the influence of coverage disparities and intermittency of the current tap water supply network on households’ water-related practices and suspected cholera incidence in Uvira, this research establishes a solid base for a much-needed impact evaluation of on-going improvements on suspected cholera in an endemic area

    Multi-parallel qPCR provides increased sensitivity and diagnostic breadth for gastrointestinal parasites of humans: field-based inferences on the impact of mass deworming

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    BACKGROUND: Although chronic morbidity in humans from soil transmitted helminth (STH) infections can be reduced by anthelmintic treatment, inconsistent diagnostic tools make it difficult to reliably measure the impact of deworming programs and often miss light helminth infections. METHODS: Cryopreserved stool samples from 796 people (aged 2-81 years) in four villages in Bungoma County, western Kenya, were assessed using multi-parallel qPCR for 8 parasites and compared to point-of-contact assessments of the same stools by the 2-stool 2-slide Kato-Katz (KK) method. All subjects were treated with albendazole and all Ascaris lumbricoides expelled post-treatment were collected. Three months later, samples from 633 of these people were re-assessed by both qPCR and KK, re-treated with albendazole and the expelled worms collected. RESULTS: Baseline prevalence by qPCR (n = 796) was 17 % for A. lumbricoides, 18 % for Necator americanus, 41 % for Giardia lamblia and 15% for Entamoeba histolytica. The prevalence was <1% for Trichuris trichiura, Ancylostoma duodenale, Strongyloides stercoralis and Cryptosporidium parvum. The sensitivity of qPCR was 98% for A. lumbricoides and N. americanus, whereas KK sensitivity was 70% and 32%, respectively. Furthermore, qPCR detected infections with T. trichiura and S. stercoralis that were missed by KK, and infections with G. lamblia and E. histolytica that cannot be detected by KK. Infection intensities measured by qPCR and by KK were correlated for A. lumbricoides (r = 0.83, p < 0.0001) and N. americanus (r = 0.55, p < 0.0001). The number of A. lumbricoides worms expelled was correlated (p < 0.0001) with both the KK (r = 0.63) and qPCR intensity measurements (r = 0.60). CONCLUSIONS: KK may be an inadequate tool for stool-based surveillance in areas where hookworm or Strongyloides are common or where intensity of helminth infection is low after repeated rounds of chemotherapy. Because deworming programs need to distinguish between populations where parasitic infection is controlled and those where further treatment is required, multi-parallel qPCR (or similar high throughput molecular diagnostics) may provide new and important diagnostic information

    Prevalence and risk factors of helminths and intestinal protozoa infections among children from primary schools in western Tajikistan

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    BACKGROUND: Intestinal parasitic infections represent a public health problem in Tajikistan, but epidemiological evidence is scarce. The present study aimed at assessing the extent of helminths and intestinal protozoa infections among children of 10 schools in four districts of Tajikistan, and to make recommendations for control. METHODS: A cross-sectional survey was carried out in early 2009. All children attending grades 2 and 3 (aged 7-11 years) from 10 randomly selected schools were invited to provide a stool sample and interviewed about sanitary situation and hygiene behaviour. A questionnaire pertaining to demographic and socioeconomic characteristics was addressed to the heads of households. On the spot, stool samples were subjected to duplicate Kato-Katz thick smear examination for helminth diagnosis. Additionally, 1-2 g of stool was fixed in sodium acetate-acetic acid formalin, transferred to a specialized laboratory in Europe and examined for helminths and intestinal protozoa. The results from both methods combined served as diagnostic 'gold' standard. RESULTS: Out of 623 registered children, 602 participated in our survey. The overall prevalence of infection with helminths and pathogenic intestinal protozoa was 32.0% and 47.1%, respectively. There was pronounced spatial heterogeneity. The most common helminth species was Hymenolepis nana (25.8%), whereas the prevalences of Ascaris lumbricoides, hookworm and Enterobius vermicularis were below 5%. The prevalence of pathogenic intestinal protozoa, namely Giardia intestinalis and Entamoeba histolytica/E. dispar was 26.4% and 25.9%, respectively. Almost half of the households draw drinking water from unimproved sources, such as irrigation canals, rivers and unprotected wells. Sanitary facilities were pit latrines, mostly private, and a few shared with neighbours. The use of public tap/standpipe as a source of drinking water emerged as a protective factor for G. intestinalis infection. Protecte spring water reduced the risk of infection with E. histolytica/E. dispar and H. nana. CONCLUSIONS: Our data obtained from the ecological 'lowland' areas in western Tajikistan call for school-based deworming (recommended drugs: albendazole and metronidazole), combined with hygiene promotion and improved sanitation. Further investigations are needed to determine whether H. nana represents a public health problem

    Measurements of the branching fractions for BKγB \to K^{*}\gamma decays at Belle II

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    This paper reports a study of BKγB \to K^{*}\gamma decays using 62.8±0.662.8\pm 0.6 fb1^{-1} of data collected during 2019--2020 by the Belle II experiment at the SuperKEKB e+ee^{+}e^{-} asymmetric-energy collider, corresponding to (68.2±0.8)×106(68.2 \pm 0.8) \times 10^6 BBB\overline{B} events. We find 454±28454 \pm 28, 50±1050 \pm 10, 169±18169 \pm 18, and 160±17160 \pm 17 signal events in the decay modes B0K0[K+π]γB^{0} \to K^{*0}[K^{+}\pi^{-}]\gamma, B0K0[KS0π0]γB^{0} \to K^{*0}[K^0_{\rm S}\pi^{0}]\gamma, B+K+[K+π0]γB^{+} \to K^{*+}[K^{+}\pi^{0}]\gamma, and B+K+[K+π0]γB^{+} \to K^{*+}[K^{+}\pi^{0}]\gamma, respectively. The uncertainties quoted for the signal yield are statistical only. We report the branching fractions of these decays: B[B0K0[K+π]γ]=(4.5±0.3±0.2)×105,\mathcal{B} [B^{0} \to K^{*0}[K^{+}\pi^{-}]\gamma] = (4.5 \pm 0.3 \pm 0.2) \times 10^{-5}, B[B0K0[KS0π0]γ]=(4.4±0.9±0.6)×105,\mathcal{B} [B^{0} \to K^{*0}[K^0_{\rm S}\pi^{0}]\gamma] = (4.4 \pm 0.9 \pm 0.6) \times 10^{-5}, B[B+K+[K+π0]γ]=(5.0±0.5±0.4)×105, and\mathcal{B} [B^{+} \to K^{*+}[K^{+}\pi^{0}]\gamma] = (5.0 \pm 0.5 \pm 0.4)\times 10^{-5},\text{ and} B[B+K+[KS0π+]γ]=(5.4±0.6±0.4)×105,\mathcal{B} [B^{+} \to K^{*+}[K^0_{\rm S}\pi^{+}]\gamma] = (5.4 \pm 0.6 \pm 0.4) \times 10^{-5}, where the first uncertainty is statistical, and the second is systematic. The results are consistent with world-average values

    Determination of Vub|V_{ub}| from untagged B0π+νB^0\to\pi^- \ell^+ \nu_{\ell} decays using 2019-2021 Belle II data

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    We present an analysis of the charmless semileptonic decay B0π+νB^0\to\pi^- \ell^+ \nu_{\ell}, where =e,μ\ell = e, \mu, from 198.0 million pairs of BBˉB\bar{B} mesons recorded by the Belle II detector at the SuperKEKB electron-positron collider. The decay is reconstructed without identifying the partner BB meson. The partial branching fractions are measured independently for B0πe+νeB^0\to\pi^- e^+ \nu_{e} and B0πμ+νμB^0\to\pi^- \mu^+ \nu_{\mu} as functions of q2q^{2} (momentum transfer squared), using 3896 B0πe+νeB^0\to\pi^- e^+ \nu_{e} and 5466 B0πμ+νμB^0\to\pi^- \mu^+ \nu_{\mu} decays. The total branching fraction is found to be (1.426±0.056±0.125)×104(1.426 \pm 0.056 \pm 0.125) \times 10^{-4} for B0π+νB^0\to\pi^- \ell^+ \nu_{\ell} decays, where the uncertainties are statistical and systematic, respectively. By fitting the measured partial branching fractions as functions of q2q^{2}, together with constraints on the nonperturbative hadronic contribution from lattice QCD calculations, the magnitude of the Cabibbo-Kobayashi-Maskawa matrix element VubV_{ub}, (3.55±0.12±0.13±0.17)×103(3.55 \pm 0.12 \pm 0.13 \pm 0.17) \times 10^{-3}, is extracted. Here, the first uncertainty is statistical, the second is systematic and the third is theoretical

    Angular analysis of B+ρ+ρ0B^+ \to \rho^+\rho^0 decays reconstructed in 2019, 2020, and 2021 Belle II data

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    We report on a Belle II measurement of the branching fraction (B\mathcal{B}), longitudinal polarization fraction (fLf_L), and CP asymmetry (ACP\mathcal{A}_{CP}) of B+ρ+ρ0B^+\to \rho^+\rho^0 decays. We reconstruct B+ρ+(π+π0(γγ))ρ0(π+π)B^+\to \rho^+(\to \pi^+\pi^0(\to \gamma\gamma))\rho^0(\to \pi^+\pi^-) decays in a sample of SuperKEKB electron-positron collisions collected by the Belle II experiment in 2019, 2020, and 2021 at the Υ\Upsilon(4S) resonance and corresponding to 190 fb1^{-1} of integrated luminosity. We fit the distributions of the difference between expected and observed BB candidate energy, continuum-suppression discriminant, dipion masses, and decay angles of the selected samples, to determine a signal yield of 345±31345 \pm 31 events. The signal yields are corrected for efficiencies determined from simulation and control data samples to obtain $\mathcal{B}(B^+ \to \rho^+\rho^0) = [23.2^{+\ 2.2}_{-\ 2.1} (\rm stat) \pm 2.7 (\rm syst)]\times 10^{-6},, f_L = 0.943 ^{+\ 0.035}_{-\ 0.033} (\rm stat)\pm 0.027(\rm syst),and, and \mathcal{A}_{CP}=-0.069 \pm 0.068(\rm stat) \pm 0.060 (\rm syst).Theresultsagreewithpreviousmeasurements.Thisisthefirstmeasurementof. The results agree with previous measurements. This is the first measurement of \mathcal{A}_{CP}in in B^+\to \rho^+\rho^0$ decays reported by Belle II

    Measurement of the branching fractions and CPCP asymmetries of B+π+π0B^+ \rightarrow \pi^+ \pi^0 and B+K+π0B^+ \rightarrow K^+ \pi^0 decays in 2019-2021 Belle II data

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    We determine the branching fractions B{\mathcal{B}} and CPCP asymmetries ACP{\mathcal{A}_{{\it CP}}} of the decays B+π+π0B^+ \rightarrow \pi^+ \pi^0 and B+K+π0B^+ \rightarrow K^+ \pi^0. The results are based on a data set containing 198 million bottom-antibottom meson pairs corresponding to an integrated luminosity of 190  fb1190\;\text{fb}^{-1} recorded by the Belle II detector in energy-asymmetric electron-positron collisions at the Υ(4S)\Upsilon (4S) resonance. We measure B(B+π+π0)=(6.12±0.53±0.53)×106{\mathcal{B}(B^+ \rightarrow \pi^+ \pi^0) = (6.12 \pm 0.53 \pm 0.53)\times 10^{-6}}, B(B+K+π0)=(14.30±0.69±0.79)×106{\mathcal{B}(B^+ \rightarrow K^+ \pi^0) = (14.30 \pm 0.69 \pm 0.79)\times 10^{-6}}, ACP(B+π+π0)=0.085±0.085±0.019{\mathcal{A}_{{\it CP}}(B^+ \rightarrow \pi^+ \pi^0) = -0.085 \pm 0.085 \pm 0.019}, and ACP(B+K+π0)=0.014±0.047±0.010{\mathcal{A}_{{\it CP}}(B^+ \rightarrow K^+ \pi^0) = 0.014 \pm 0.047 \pm 0.010}, where the first uncertainties are statistical and the second are systematic. These results improve a previous Belle II measurement and agree with the world averages

    Measurement of the branching fraction for the decay BK(892)+B \to K^{\ast}(892)\ell^+\ell^- at Belle II

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    We report a measurement of the branching fraction of BK(892)+B \to K^{\ast}(892)\ell^+\ell^- decays, where +=μ+μ\ell^+\ell^- = \mu^+\mu^- or e+ee^+e^-, using electron-positron collisions recorded at an energy at or near the Υ(4S)\Upsilon(4S) mass and corresponding to an integrated luminosity of 189189 fb1^{-1}. The data was collected during 2019--2021 by the Belle II experiment at the SuperKEKB e+ee^{+}e^{-} asymmetric-energy collider. We reconstruct K(892)K^{\ast}(892) candidates in the K+πK^+\pi^-, KS0π+K_{S}^{0}\pi^+, and K+π0K^+\pi^0 final states. The signal yields with statistical uncertainties are 22±622\pm 6, 18±618 \pm 6, and 38±938 \pm 9 for the decays BK(892)μ+μB \to K^{\ast}(892)\mu^+\mu^-, BK(892)e+eB \to K^{\ast}(892)e^+e^-, and BK(892)+B \to K^{\ast}(892)\ell^+\ell^-, respectively. We measure the branching fractions of these decays for the entire range of the dilepton mass, excluding the very low mass region to suppress the BK(892)γ(e+e)B \to K^{\ast}(892)\gamma(\to e^+e^-) background and regions compatible with decays of charmonium resonances, to be \begin{equation} {\cal B}(B \to K^{\ast}(892)\mu^+\mu^-) = (1.19 \pm 0.31 ^{+0.08}_{-0.07}) \times 10^{-6}, {\cal B}(B \to K^{\ast}(892)e^+e^-) = (1.42 \pm 0.48 \pm 0.09)\times 10^{-6}, {\cal B}(B \to K^{\ast}(892)\ell^+\ell^-) = (1.25 \pm 0.30 ^{+0.08}_{-0.07}) \times 10^{-6}, \end{equation} where the first and second uncertainties are statistical and systematic, respectively. These results, limited by sample size, are the first measurements of BK(892)+B \to K^{\ast}(892)\ell^+\ell^- branching fractions from the Belle II experiment
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