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1.
PLoS One ; 15(8): e0237655, 2020.
Article in English | MEDLINE | ID: mdl-32810167

ABSTRACT

BACKGROUND: Several tests are available for plague confirmation but bacteriological culture with Yersinia pestis strain isolation remains the gold standard according to the World Health Organization. However, this is a time consuming procedure; requiring specific devices and well-qualified staff. In addition, strain isolation is challenging if antibiotics have been administered prior to sampling. Here, we developed a loop-mediated isothermal amplification (LAMP) technique, a rapid, simple, sensitive and specific technique that would be able to detect Y. pestis in human biological samples. METHODS: LAMP primers were designed to target the caf1 gene which is specific to Y. pestis. The detection limit was determined by testing 10-fold serial dilution of Y. pestis DNA. Cross-reactivity was tested using DNA extracts from 14 pathogens and 47 residual samples from patients suffering from non-plague diseases. Specificity and sensitivity of the LAMP caf1 were assessed on DNA extracts of 160 human biological samples. Then, the performance of the LAMP caf1 assay was compared to conventional PCR and bacteriological culture. RESULTS: The detection limit of the developed Y. pestis LAMP assay was 3.79 pg/µl, similar to conventional PCR. The result could be read out within 45 min and as early as 35 minutes in presence of loop primer, using a simple water bath at 63°C. This is superior to culture with respect to time (requires up to 10 days) and simplicity of equipment compared to PCR. Furthermore, no cross-reactivity was found when tested on DNA extracts from other pathogens and human biological samples from patients with non-plague diseases. Compared to the gold standard, LAMP sensitivity and specificity were 97.9% (95% CI: 89.1%-99.9%) and 94.6% (95% CI: 88.6%-97.9%), respectively. CONCLUSION: LAMP detected Y. pestis effectively with high sensitivity and specificity in human plague biological samples. It can potentially be used in the field during outbreaks in resource limited countries such as Madagascar.


Subject(s)
Bacteriological Techniques/methods , DNA, Bacterial/isolation & purification , Nucleic Acid Amplification Techniques/methods , Plague/diagnosis , Yersinia pestis/isolation & purification , Bacteriological Techniques/economics , Feasibility Studies , Humans , Limit of Detection , Madagascar , Nucleic Acid Amplification Techniques/economics , Plague/microbiology , Time Factors , Yersinia pestis/genetics
3.
Proc Natl Acad Sci U S A ; 109(14): 5219-22, 2012 Apr 03.
Article in English | MEDLINE | ID: mdl-22431631

ABSTRACT

In an effort to deliver better outcomes for people and the ecosystems they depend on, many governments and civil society groups are engaging natural resource users in collaborative management arrangements (frequently called comanagement). However, there are few empirical studies demonstrating the social and institutional conditions conducive to successful comanagement outcomes, especially in small-scale fisheries. Here, we evaluate 42 comanagement arrangements across five countries and show that: (i) comanagement is largely successful at meeting social and ecological goals; (ii) comanagement tends to benefit wealthier resource users; (iii) resource overexploitation is most strongly influenced by market access and users' dependence on resources; and (iv) institutional characteristics strongly influence livelihood and compliance outcomes, yet have little effect on ecological conditions.


Subject(s)
Anthozoa , Conservation of Natural Resources , Ecosystem , Animals , Resource Allocation
4.
Rev Sci Instrum ; 83(2): 02B305, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22380284

ABSTRACT

Ge crystals were prepared by means of laser-induced ion implantation technique. A Nd:YAG pulsed laser (repetition rate: 10 Hz; pulse duration: 3.5 ns; pulse energy: ∼0.5 J) was used both as an ion source and to carry out the ablation processes. The optimization of the laser-generated ion beam parameters in a broad energy and current density range has been obtained controlling the electrostatic field parameters. Numerical simulations of the focusing system, performed adopting an OPERA 3D code, and an investigation of the ion characteristics, using the ion time-of-flight method, have allowed to optimize the preparation parameters. The structural properties of the samples were investigated by means of x-ray photoelectron, micro-Raman spectroscopies, and scanning electron microscopy techniques. Experimental results show that, by appropriately varying the ion implantation parameters and by a post-preparation annealing treatment, it is possible to achieve the development of a micrometer-sized crystalline Ge phase and∕or an amorphous one.

5.
Appl Radiat Isot ; 67(6): 1001-6, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19324559

ABSTRACT

Excitation functions were measured using the stacked foil irradiation technique from threshold energies to 28 MeV for (3)He- and to 21 MeV for alpha-particle induced nuclear reactions on natural antimony leading to the formation of (121,123,124)I radioisotopes. The measured excitation functions were compared with the contradicting results of the earlier investigations found in the literature and with the curves predicted by the ALICE-IPPE and EMPIRE-II codes. Integral yields were also calculated and compared with the experimental thick target yields reported in the literature.


Subject(s)
Iodine Radioisotopes/chemistry , Alpha Particles , Antimony , Helium
6.
Appl Radiat Isot ; 45(2): 239-49, 1994 Feb.
Article in English | MEDLINE | ID: mdl-8312883

ABSTRACT

Proton induced nuclear reactions on enriched 111Cd and 112Cd have been studied up to 30 MeV in the context of routine production of the medically used isotope 111In with low and medium energy cyclotrons. The excitation functions of 111Cd(p,n)111m,gIn and 112Cd(p,2n)111m,gIn as production reactions and 111Cd(p,2n)110mIn, 111Cd(p,2n)110In, 111Cd(p,3n)109ml,m2,In, 112Cd(p,3n)110mIn, 112Cd(p,3n)110gIn as competing processes have been measured using the activation method involving the stacked-foil technique. The deduced thick target yields are compared with those obtained experimentally.


Subject(s)
Cadmium , Indium Radioisotopes , Cyclotrons , Isotopes , Nuclear Medicine , Protons
8.
Int J Rad Appl Instrum A ; 41(8): 753-6, 1990.
Article in English | MEDLINE | ID: mdl-2172187

ABSTRACT

In order to understand the thermal processes occurring within a water target we carried out calculations of heat transfer of the beam energy absorbed from the target water to the target back wall, and compared them with the temperatures measured during irradiations. It was shown, by both the experimental results and the heat transfer calculations, that, at high beam currents, static small volume water targets have a working temperature at the boiling point of the target water. The heat transfer occurs only by movement of the water molecules generated by the boiling target water and not by heat conduction or free convection alone. There is no heat transfer arising from vaporization and reflux.


Subject(s)
Fluorine Radioisotopes , Nuclear Physics , Oxygen Isotopes , Particle Accelerators , Temperature , Water
9.
Biomedicine ; 33(1): 24-6, 1980 Feb.
Article in English | MEDLINE | ID: mdl-7370384

ABSTRACT

A rabbit immune serum against SSPE CSF reveals in these CSF, in addition to IgG, another protein with electrophoretic gamma-mobility which is never revealed by anti-normal human serum nor by anti-normal CSF. This protein, called B.T., has been found in 5 out of 8 CSF studied. The same immune serum against SSPE CSF reveals in normal brain extracts a specific protein sharing antigenic identity with the fraction B.T. from SSPE CSF. This brain protein is located in the white matter. It has not been found in the grey matter, nor in other tissue extracts. Due to its solubility and electrophoretic properties, this brain protein B.T. is not comparable with any of the brain specific proteins known at this time.


Subject(s)
Brain Chemistry , Cerebrospinal Fluid Proteins/analysis , Nerve Tissue Proteins/cerebrospinal fluid , Subacute Sclerosing Panencephalitis/cerebrospinal fluid , Cerebrospinal Fluid Proteins/immunology , Humans , Immunoelectrophoresis , Nerve Tissue Proteins/immunology
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