20 research outputs found
First insights into the phylogenetic diversity of Mycobacterium tuberculosis in Nepal
BACKGROUND: Tuberculosis (TB) is a major public health problem in Nepal. Strain variation in Mycobacterium tuberculosis may influence the outcome of TB infection and disease. To date, the phylogenetic diversity of M. tuberculosis in Nepal is unknown. METHODS AND FINDINGS: We analyzed 261 M. tuberculosis isolates recovered from pulmonary TB patients recruited between August 2009 and August 2010 in Nepal. M. tuberculosis lineages were determined by single nucleotide polymorphisms (SNP) typing and spoligotyping. Drug resistance was determined by sequencing the hot spot regions of the relevant target genes. Overall, 164 (62.8%) TB patients were new, and 97 (37.2%) were previously treated. Any drug resistance was detected in 50 (19.2%) isolates, and 16 (6.1%) were multidrug-resistant. The most frequent M. tuberculosis lineage was Lineage 3 (CAS/Delhi) with 106 isolates (40.6%), followed by Lineage 2 (East-Asian lineage, includes Beijing genotype) with 84 isolates (32.2%), Lineage 4 (Euro-American lineage) with 41 (15.7%) isolates, and Lineage 1 (Indo-Oceanic lineage) with 30 isolates (11.5%). Based on spoligotyping, we found 45 different spoligotyping patterns that were previously described. The Beijing (83 isolates, 31.8%) and CAS spoligotype (52, 19.9%) were the dominant spoligotypes. A total of 36 (13.8%) isolates could not be assigned to any known spoligotyping pattern. Lineage 2 was associated with female sex (adjusted odds ratio [aOR] 2.58, 95% confidence interval [95% CI] 1.42-4.67, p = 0.002), and any drug resistance (aOR 2.79; 95% CI 1.43-5.45; p = 0.002). We found no evidence for an association of Lineage 2 with age or BCG vaccination status. CONCLUSIONS: We found a large genetic diversity of M. tuberculosis in Nepal with representation of all four major lineages. Lineages 3 and 2 were dominating. Lineage 2 was associated with clinical characteristics. This study fills an important gap on the map of the M. tuberculosis genetic diversity in the Asian reg
Environmental footprint family to address local to planetary sustainability and deliver on the SDGs
The number of publications on environmental footprint indicators has been growing rapidly, but with limited efforts to integrate different footprints into a coherent framework. Such integration is important for comprehensive understanding of environmental issues, policy formulation and assessment of trade-offs between different environmental concerns. Here, we systematize published footprint studies and define a family of footprints that can be used for the assessment of environmental sustainability. We identify overlaps between different footprints and analyse how they relate to the nine planetary boundaries and visualize the crucial information they provide for local and planetary sustainability. In addition, we assess how the footprint family delivers on measuring progress towards Sustainable Development Goals (SDGs), considering its ability to quantify environmental pressures along the supply chain and relating them to the water-energy-food-ecosystem (WEFE) nexus and ecosystem services. We argue that the footprint family is a flexible framework where particular members can be included or excluded according to the context or area of concern. Our paper is based upon a recent workshop bringing together global leading experts on existing environmental footprint indicators
A framework to assess life cycle nitrogen use efficiency along livestock supply chains
to the significant contribution of the livestock sector to nitrogen (N) losses, improving N use efficiency (NUE-N) along the life cycle of livestock products is one of the important step towards increasing production performance and reduction of its environmental impacts. We developed a comprehensive framework and novel metrics to assess NUE-N along the livestock supply chain (i.e. -to-primary- ). Our framework was illustrated for the case study of mixed dairy production in Western Europe. Metrics developed included the life cycle NUE-N; total N losses to the environment per unit of N in the final co-products; and the N hotspot index (NHI-N), defined as the relative evenness of the N losses along the supply chain. Averaged across countries, the life cycle NUE-N was 36¿3.1%, N losses were 6.6¿1.8 g N per g N in the final animal co-products, and NHI-N of 1.0¿0.1. The N losses and NHI-N also revealed large differences in hotspots across supply chains, and allowed to identify priority areas where improvement actions are necessary to enhance the efficiency. We show that the combination of life cycle NUE-N, N losses and NHI-N gives valuable information to guide N management in livestock supply chain
Carbon stocks and dynamics at different successional stages in an Afromontane tropical forest
As a result of different types of disturbance, forests are a
mixture of stands at different stages of ecological succession. Successional
stage is likely to influence forest productivity and carbon storage, linking
the degree of forest disturbance to the global carbon cycle and climate.
Although tropical montane forests are an important part of tropical forest
ecosystems (ca. 8 %, elevation > 1000 m a.s.l.), there are still
significant knowledge gaps regarding the carbon dynamics and stocks of these
forests, and how these differ between early (ES) and late successional (LS)
stages. This study examines the carbon (C) stock, relative growth rate (RGR)
and net primary production (NPP) of ES and LS forest stands in an Afromontane
tropical rainforest using data from inventories of quantitatively important
ecosystem compartments in fifteen 0.5 ha plots in Nyungwe National Park in
Rwanda.
The total C stock was 35 % larger in LS compared to ES plots due to
significantly larger above-ground biomass (AGB; 185 and 76 Mg C ha−1
in LS and ES plots), while the soil and root C stock (down to
45 cm depth in the mineral soil) did not significantly differ between the
two successional stages (178 and 204 Mg C ha−1 in LS and ES plots). The main reasons for the difference in AGB were that ES trees
had significantly lower stature and wood density compared to LS trees.
However, ES and LS stands had similar total NPP (canopy, wood and roots of
all plots ∼ 9.4 Mg C ha−1) due to counterbalancing effects of
differences in AGB (higher in LS stands) and RGR (higher in ES stands). The
AGB in the LS plots was considerably higher than the average value reported
for old-growth tropical montane forest of south-east Asia and Central and
South America at similar elevations and temperatures, and of the same
magnitude as in tropical lowland forest of these regions.
The results of this study highlight the importance of accounting for
disturbance regimes and differences in wood density and allometry of tree
species dominating at different successional stages in an attempt to quantify
the C stock and sink strength of tropical montane forests and how they may
differ among continents
Fine-Needle Aspiration, an Efficient Sampling Technique for Bacteriological Diagnosis of Nonulcerative Buruli Ulcer ▿
Invasive punch or incisional skin biopsy specimens are currently employed for the bacteriological confirmation of the clinical diagnosis of Buruli ulcer (BU), a cutaneous infectious disease caused by Mycobacterium ulcerans. The efficacy of fine-needle aspirates (FNA) using fine-gauge needles (23G by 25 mm) for the laboratory confirmation of BU was compared with that of skin tissue fragments obtained in parallel by excision or punch biopsy. In three BU treatment centers in Benin, both types of diagnostic material were obtained from 33 clinically suspected cases of BU and subjected to the same laboratory analyses: i.e., direct smear examination, IS2404 PCR, and in vitro culture. Twenty-three patients, demonstrating 17 ulcerative and 6 nonulcerative lesions, were positive by at least two tests and were therefore confirmed to have active BU. A total of 68 aspirates and 68 parallel tissue specimens were available from these confirmed patients. When comparing the sensitivities of the three confirmation tests between FNA and tissue specimens, the latter yielded more positive results, but only for PCR was this significant. When only nonulcerative BU lesions were considered, however, the sensitivities of the confirmation tests using FNA and tissue specimens were not significantly different. Our results show that the minimally invasive FNA technique offers enough sensitivity to be used for the diagnosis of BU in nonulcerative lesions
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Multidrug-resistant tuberculosis control in Rwanda overcomes a successful clone that causes most disease over a quarter century
Summary background: Multidrug-resistant (MDR) tuberculosis (TB) poses an important challenge in TB management and control. Rifampicin resistance (RR) is a solid surrogate marker of MDR-TB. We investigated the RR-TB clustering rates, bacterial population dynamics to infer transmission dynamics, and the impact of changes to patient management on these dynamics over 27 years in Rwanda.
Methods: We analysed whole genome sequences of a longitudinal collection of nationwide RR-TB isolates. The collection covered three important periods: before programmatic management of MDR-TB (PMDT; 1991–2005), the early PMDT phase (2006–2013), in which rifampicin drug-susceptibility testing (DST) was offered to retreatment patients only, and the consolidated phase (2014–2018), in which all bacteriologically confirmed TB patients had rifampicin DST done mostly via Xpert MTB/RIF assay. We constructed clusters based on a 5 SNP cut-off and resistance conferring SNPs. We used Bayesian modelling for dating and population size estimations, TransPhylo to estimate the number of secondary cases infected by each patient, and multivariable logistic regression to assess predictors of being infected by the dominant clone.
Results: Of 308 baseline RR-TB isolates considered for transmission analysis, the clustering analysis grouped 259 (84.1%) isolates into 13 clusters. Within these clusters, a single dominant clone was discovered containing 213 isolates (82.2% of clustered and 69.1% of all RR-TB), which we named the “Rwanda Rifampicin-Resistant clone” (R3clone). R3clone isolates belonged to Ugandan sub-lineage 4.6.1.2 and its rifampicin and isoniazid resistance were conferred by the Ser450Leu mutation in rpoB and Ser315Thr in katG genes, respectively. All R3clone isolates had Pro481Thr, a putative compensatory mutation in the rpoC gene that likely restored its fitness. The R3clone was estimated to first arise in 1987 and its population size increased exponentially through the 1990s’, reaching maximum size (∼84%) in early 2000 s’, with a declining trend since 2014. Indeed, the highest proportion of R3clone (129/157; 82·2%, 95%CI: 75·3–87·8%) occurred between 2000 and 13, declining to 64·4% (95%CI: 55·1-73·0%) from 2014 onward. We showed that patients with R3clone detected after an unsuccessful category 2 treatment were more likely to generate secondary cases than patients with R3clone detected after an unsuccessful category 1 treatment regimen.
Conclusions: RR-TB in Rwanda is largely transmitted. Xpert MTB/RIF assay as first diagnostic test avoids unnecessary rounds of rifampicin-based TB treatment, thus preventing ongoing transmission of the dominant R3clone. As PMDT was intensified and all TB patients accessed rifampicin-resistance testing, the nationwide R3clone burden declined. To our knowledge, our findings provide the first evidence supporting the impact of universal DST on the transmission of RR-TB