Evidence of West Nile virus circulation among humans in central northern Algeria.

West Nile Virus (WNV) is the most widely distributed flavivirus worldwide. It is a mosquito-borne virus, and birds constitute its natural reservoir. Humans and equines are considered accidental hosts. Human WNV infections are usually asymptomatic or express as a mild febrile syndrome; however, in around 1% of cases they are responsible for more serious neurological diseases with a potentially lethal outcome. In the Mediterranean basin the virus circulation is regarded as endemic. Outbreaks of WNV meningoencephalitis are regularly notified, especially during summer and autumn seasons. In Algeria, although some surveys have reported WNV activity in the Sahara, to date few data are available about virus circulation in the northern part of the country. We conducted this study to detect possible WNV activity in this part of Algeria. For this purpose, in 2010 a total of 164 human sera were collected from native patients of the Algiers district and surrounding areas, then tested retrospectively for IgG anti-WNV by ELISA. Plaque reduction neutralization technique (PRNT) was used for result confirmation. In this cohort, 9.8% of the 164 collected sera returned positive for anti-WNV IgG; after confirmation by PRNT; 6.7% had specific neutralizing antibodies. No statistically significant difference was observed according to the sex or transfusion status of the patients. In conclusion, these data show for the first time serological evidence of WNV circulation in Algiers and its surrounding areas. They also highlight the need for implementing an integrated surveillance programme covering all aspects of WNV disease in order to better understand the circulation dynamics of WNV in this region. Other flaviviruses antigenically related to WNV should be investigated, given the evidence of serological cross-reaction, as specific IgG antibodies decrease after PRNT confirmation.

Four Functionally Distinct Regions in the Left Supramarginal Gyrus Support Word Processing.

We used fMRI in 85 healthy participants to investigate whether different parts of the left supramarginal gyrus (SMG) are involved in processing phonological inputs and outputs. The experiment involved 2 tasks (speech production (SP) and one-back (OB) matching) on 8 different types of stimuli that systematically varied the demands on sensory processing (visual vs. auditory), sublexical phonological input (words and pseudowords vs. nonverbal stimuli), and semantic content (words and objects vs. pseudowords and meaningless baseline stimuli). In ventral SMG, we found an anterior subregion associated with articulatory sequencing (for SP > OB matching) and a posterior subregion associated with auditory short-term memory (for all auditory > visual stimuli and written words and pseudowords > objects). In dorsal SMG, a posterior subregion was most highly activated by words, indicating a role in the integration of sublexical and lexical cues. In anterior dorsal SMG, activation was higher for both pseudoword reading and object naming compared with word reading, which is more consistent with executive demands than phonological processing. The dissociation of these four "functionally-distinct" regions, all within left SMG, has implications for differentiating between different types of phonological processing, understanding the functional anatomy of language and predicting the effect of brain damage.

Predicting IQ change from brain structure: a cross-validation study.

Procedures that can predict cognitive abilities from brain imaging data are potentially relevant to educational assessments and studies of functional anatomy in the developing brain. Our aim in this work was to quantify the degree to which IQ change in the teenage years could be predicted from structural brain changes. Two well-known k-fold cross-validation analyses were applied to data acquired from 33 healthy teenagers - each tested at Time 1 and Time 2 with a 3.5 year interval. One approach, a Leave-One-Out procedure, predicted IQ change for each subject on the basis of structural change in a brain region that was identified from all other subjects (i.e., independent data). This approach predicted 53% of verbal IQ change and 14% of performance IQ change. The other approach used half the sample, to identify regions for predicting IQ change in the other half (i.e., a Split half approach); however--unlike the Leave-One-Out procedure--regions identified using half the sample were not significant. We discuss how these out-of-sample estimates compare to in-sample estimates; and draw some recommendations for k-fold cross-validation procedures when dealing with small datasets that are typical in the neuroimaging literature.

Data warehousing methods and processing infrastructure for brain recovery research.

In order to accelerate translational neuroscience with the goal of improving clinical care it has become important to support rapid accumulation and analysis of large, heterogeneous neuroimaging samples and their metadata from both normal control and patient groups. We propose a multi-centre, multinational approach to accelerate the data mining of large samples and facilitate data-led clinical translation of neuroimaging results in stroke. Such data-driven approaches are likely to have an early impact on clinically relevant brain recovery while we simultaneously pursue the much more challenging model-based approaches that depend on a deep understanding of the complex neural circuitry and physiological processes that support brain function and recovery. We present a brief overview of three (potentially converging) approaches to neuroimaging data warehousing and processing that aim to support these diverse methods for facilitating prediction of cognitive and behavioral recovery after stroke, or other types of brain injury or disease.

Lesion sites that predict the ability to gesture how an object is used.

We used a two stage procedure to predict which stroke patients would have chronic difficulties gesturing how to use an object when object recognition and hand movements were intact. First, we searched our PLORAS database by behavior and identified 5 patients who had chronic difficulty gesturing object use but no difficulty recognising objects, comprehending words or moving their hands. High definition lesion analyses showed that all 5 patients had damage to the white matter underlying the left ventral supramarginal gyrus, (A) close to the cortex, (B) deep towards the midline and (C) extending into the temporal lobe. In addition, 2 patients had damage to (D) the left posterior middle temporal cortex, and 3 patients had damage to (E) the left dorsal supramarginal gyrus and (F) the left premotor cortex. Second, we searched our database by lesion location for patients who had damage to any part of regions ABCDEF. The incidence of gesturing difficulties was higher in patients with damage to ABCD (7/9), ABCE (7/10) or ABCDE (10/13) than ABCF (7/13), ABC (8/16) or partial damage to ABCF (6/32). Thus behaviour was best predicted by the combination of regions that were damaged (a "network-lesion") rather than on the basis of each region alone or overall lesion size. Our results identify which parts of the temporal and parietal lobes impair the ability to gesture object use and which parts need to be intact to support it after damage. Our methods provide a framework for future studies aiming to predict the consequences of brain damage.

Multinomial inference on distributed responses in SPM.

In this work, we propose statistical methods to perform inference on the spatial distribution of topological features (e.g. maxima or clusters) in statistical parametric maps (SPMs). This contrasts with local inference on the features per se (e.g., height or extent), which is well-studied (e.g. Friston et al., 1991, 1994; Worsley et al., 1992, 2003, 2004). We present a Bayesian approach to detecting experimentally-induced patterns of distributed responses in SPMs with anisotropic, non-stationary noise and arbitrary geometry. We extend the framework to accommodate fixed- and random-effects analyses at the within and between-subject levels respectively. We illustrate the method by characterising the anatomy of language at different scales of functional segregation.

Inter-subject variability in the use of two different neuronal networks for reading aloud familiar words.

Cognitive models of reading predict that high frequency regular words can be read in more than one way. We investigated this hypothesis using functional MRI and covariance analysis in 43 healthy skilled readers. Our results dissociated two sets of regions that were differentially engaged across subjects who were reading the same familiar words. Some subjects showed more activation in left inferior frontal and anterior occipito-temporal regions while other subjects showed more activation in right inferior parietal and left posterior occipito-temporal regions. To explore the behavioural correlates of these systems, we measured the difference between reading speed for irregularly spelled words relative to pseudowords outside the scanner in fifteen of our subjects and correlated this measure with fMRI activation for reading familiar words. The faster the lexical reading the greater the activation in left posterior occipito-temporal and right inferior parietal regions. Conversely, the slower the lexical reading the greater the activation in left anterior occipito-temporal and left ventral inferior frontal regions. Thus, the double dissociation in irregular and pseudoword reading behaviour predicted the double dissociation in neuronal activation for reading familiar words. We discuss the implications of these results which may be important for understanding how reading is learnt in childhood or re-learnt following brain damage in adulthood.

Functional neuroimaging findings on the human perception of illusory contours.

Illusory contours (IC) have attracted a considerable interest in recent years to derive models of how sensory information is processed and integrated within the visual system. In addition to various findings from neuropsychology, neurophysiology, and psychophysics, several recent studies have used functional neuroimaging to identify the cerebral substrates underlying human perception of IC (in particular Kanizsa figures). In this paper, we review the results from more than 20 neuroimaging studies on IC perception and highlight the great diversity of findings across these studies. We then provide a detailed discussion about the localization ('where' debate) and the timing ('when' debate) of IC processing as suggested by functional neuroimaging. Cortical responses involving visual areas as early as V1/V2 and latencies as rapid as 100 ms have been reported in several studies. Particular issues concerning the role of the right hemisphere and the retinotopic encoding of IC are also discussed. These different findings are tentatively brought together to propose different hypothetical cortical mechanisms that might be responsible for the visual formation of IC. Several remaining questions on IC processing that could potentially be explored with functional neuroimaging techniques are finally emphasized.

Translational and Brownian motion in laser-Doppler flowmetry of large tissue volumes.

This study reports the derivation of a precise mathematical relationship existing between the different p-moments of the power spectrum of the photoelectric current, obtained from a laser-Doppler flowmeter (LDF), and the red blood cell speed. The main purpose is that both the Brownian (defining the 'biological zero') and the translational movements are taken into account, clarifying in this way what the exact contribution of each parameter is to the LDF derived signals. The derivation of the equations is based on the quasi-elastic scattering theory and holds for multiple scattering (i.e. measurements in large tissue volumes and/or very high red blood cell concentration). The paper also discusses why experimentally there exists a range in which the relationship between the first moment of the power spectrum and the average red blood cells speed may be considered as 'linear' and what are the physiological determinants that can result in nonlinearity. A correct way to subtract the biological zero from the LDF data is also proposed. The findings should help in the design of improved LDF instruments and in the interpretation of experimental data.

Mapping of the neuronal networks of human cortical brain functions.

OBJECTIVE: The principles and methodology of event-related fMRI, electromagnetic source imaging and intracranial evoked potentials will be described along with some examples of the mapping of the neuronal networks of human cortical brain functions with the use of these techniques. INTRODUCTION: Functional brain mapping using PET or fMRI has provided clues on the functioning brain and notably on the functional neuroanatomy of cognitive functions. These mapping possibilities can be used to delineate in an individual patient the brain areas subserving a cerebral function that might be compromised by a surgery in a nearby location, or to target a functional neurosurgical procedure. BACKGROUND: Brain functions and notably "higher brain functions" are served by a complex network of interrelating brain regions. Deeper insights into the functioning of a neuronal network can be gained by adding dynamic, i.e. temporal, information to the functional maps. This will demonstrate the orchestration of the activation of the different brain areas constituting the network, which gives clues to the information processing and therefore to the functioning of the different modules of the network. In order to track the flow of information and the sequential activation of the different brain regions constituting the network, brain activity has to be recorded at the speed of transfer of activation from one neuronal population to the other. The temporal resolution needed to achieve this is not in the range of traditional subtractive or comparative PET or fMRI techniques. NEW DEVELOPMENTS: Novel fMRI methods that record haemodynamic signal changes after single events (event-related fMRI) are now able to determine sequential neural processing by distinguishing the relative onset-time of activity between different areas. The temporal resolution of event-related (ER) fMRI is sufficient to detect changes of mental activity within the order of several hundreds of milliseconds. This allows the exploration of a broad range of cognitive functions. Nevertheless, this technique is currently not rapid enough to observe the transient coordinations and oscillations of neuronal activities occurring across certain cortical areas during the performance of cognitive tasks. The temporal resolution needed for that is within the order of tens or a few milliseconds and is only accessible by EEG or MEG that allow true real-time measurements of the neuronal activity elicited by a stimulus. Surface recordings of multichannel EEG or MEG combined with novel electromagnetic source localisation algorithms allow a relatively precise estimation of the activated areas. A more direct localisation of electric activity is achieved by intracranial recordings in patients having implanted electrodes for diagnostic reasons. In these cases, a high temporal and spatial resolution is achieved but with a limited sampling of brain regions. CONCLUSION: Although the temporal resolution of ER fMRI is due to improve, the temporal measures provided by EEG, MEG or intracranial event-related potentials (ERPs) are absolute, which remains a unique feature of these techniques. Therefore, ER fMRI and electromagnetic source imaging are complementary. The maps obtained with ER fMRI may be refined by electromagnetic ERPs that provide further insights into the temporal coordination or orchestration between the cortical areas already detected by ER fMRI and constituting a neuronal network, and ER fMRI can be used to precisely locate the areas coarsely situated and delineated by electromagnetic source imaging. Thus, the combination of ER fMRI and electromagnetic ERPs is essential in order to produce a mapping method with a millimetre spatial resolution and a millisecond temporal resolution. Future applications should combine these techniques to localise precisely and non-invasively relevant sensory, motor and cognitive processes in order to adequately tailor any brain surgery.

Language representation in a patient with a dominant right hemisphere: fMRI evidence for an intrahemispheric reorganisation.

Studies have suggested that congenital left hemispheric (LH) frontal arteriovenous malformations (AVMs) are associated with an early transfer of language to right hemisphere (RH) frontal regions. The question remains whether such anatomofunctional reorganisation is due to RH compensatory abilities or to a general principle of lateral shift. In this study, we used fMRI language paradigms to investigate the case of a patient presenting aphasic symptoms following an haemorrhage due to a right frontal AVM. Prior to surgery, fMRI showed that language processing was confined to the RH, suggesting that language had not shifted during childhood from this congenitally dominant RH to the LH. After surgery, the patient presented severe aphasia that recovered to presurgical level within 70 days. At this time, fMRI showed that language tasks were still not associated with activations in the LH. These results suggest that the principles of early cerebral reorganisation after congenital lesions may differ in the RH and the LH. In addition, they support the idea that efficient restoration of language is achieved if a sufficiently large neuronal network is preserved around the lesion.

Genomic features of intertypic recombinant sabin poliovirus strains excreted by primary vaccinees.

The trivalent oral poliomyelitis vaccine (OPV) contains three different poliovirus serotypes. It use therefore creates particularly favorable conditions for mixed infection of gut cells, and indeed intertypic vaccine-derived recombinants (VdRec) have been frequently found in patients with vaccine-associated paralytic poliomyelitis. Nevertheless, there have not been extensive searches for VdRec in healthy vaccinees following immunization with OPV. To determine the incidence of VdRec and their excretion kinetics in primary vaccinees, and to establish the general genomic features of the corresponding recombinant genomes, we characterized poliovirus isolates excreted by vaccinees following primary immunization with OPV. Isolates were collected from 67 children 2 to 60 days following vaccination. Recombinant strains were identified by multiple restriction fragment length polymorphism assays. The localization of junction sites in recombinant genomes was also determined. VdRec excreted by vaccinees were first detected 2 to 4 days after vaccination. The highest rate of recombinants was on day 14. The frequency of VdRec depends strongly on the serotype of the analyzed isolates (2, 53, and 79% of recombinant strains in the last-excreted type 1, 2, and 3 isolates, respectively). Particular associations of genomic segments were preferred in the recombinant genomes, and recombination junctions were found in the genomic region encoding the nonstructural proteins. Recombination junctions generally clustered in particular subgenomic regions that were dependent on the serotype of the isolate and/or on the associations of genomic segments in recombinants. Thus, VdRec are frequently excreted by vaccinees, and the poliovirus replication machinery requirements or selection factors appear to act in vivo to shape the features of the recombinant genomes.

Moving illusory contours activate primary visual cortex: an fMRI study.

Identifying the cortical areas activated by illusory contours provides valuable information on the mechanisms of object perception. We applied functional magnetic resonance imaging to identify the visual areas of the human brain involved in the perception of a moving Kanizsa-type illusory contour. Our results indicate that, in addition to other cortical regions, areas V5 and V1 are activated. Activity in area V1 was particularly prominent.

[Introduction to a study of specific antibodies (IgG and IgM) detection with ELISA in the diagnosis of poliomyelitis]. / Introduction à une étude sur la détection des anticorps spécifiques (IgG et IgM) par ELISA dans le diagnostic de la poliomyélite.

Samples of single sera collected from 38 patients with different clinical diagnosis were studied in order to perform ELISA techniques with the purpose of detecting poliomyelitis IgG and IgM antibodies. The résults were compared through antibody titration by neutralization test. 21 pairs of sera from infants suffering from acute flaccid paralysis were studied by ELISA-IgM, ELISA-IgG and neutralization test. Stool samples were collected from 20 of the latter patient. Wild poliovirus type 1 was isolated in 8 cases. ELISA-IgM technique was positive in 14 cases. The true positive poliomyelitis diagnosis was based on the persistence of flaccid paralysis 60 days after the onset and on wild poliovirus isolation with significant increase in antibody level. 16 cases were classified as poliomyelitis, 2 cases as non poliomyelitic paralysis and 3 cases as undetermined. 16 out of the 18 well established diagnosis were in agreement (88.8%) with the detection or not of IgM antibodies by ELISA. The specificity of these IgM ELISA antibodies was examined by studying 11 cases of lymphocytic meningitis. Cross reaction in serological responses between polioviruses and coxsackieviruses was observed. These cross reactions should be evaluated by studying a greater number of cases. The poliovirus ELISA-IgM is a sensitive, economical and rapid method to be used in poliomyelitis diagnosis to complete the neutralizing test and virus isolation.