Corticocortical connections within the primary somatosensory (SI) cortex of rat were investigated by using discrete injections of retro- and orthogradely transported neuroanatomical tracers (including HRP, WGA, PHA-L, and 3H-leucine). Tangential and vertical connections were defined with respect to the cytoarchitectonic divisions within the rat SI, specifically: (1) the "granular zones" (GZs), characterized by their dense layer IV granular aggregates, which receive the majority of direct ventroposterior (VP) thalamocortical terminations, (2) the "perigranular zones" (PGZs), the less-granular cortical matrix just surrounding the GZs, and (3) the "dysgranular zones" (DZs), the larger dysgranular regions lying centrally within and just lateral to the SI. Receptive fields recorded in the granular zones are small and discrete, whereas in the perigranular zones and especially in dysgranular zones they exhibit complex sensory convergence. A major aim of this study was to determine whether the pattern of intracortical connectivity within the SI is compatible with these observed physiological differences. In general, the perigranular and dysgranular zones contained more profuse systems of corticocortical connections than did the granular zones. For example, discrete tracer injections in the perigranular zones produced "walls" of labelling throughout the adjacent perigranular zones, while adjacent granular zones were relatively empty. Nevertheless, the granular zones were filled with dendritic branches of neurons in adjacent perigranular zones. Since these dendrites could presumably receive direct VP thalamocortical contacts, they represent one path through which this thalamic sensory information might be transmitted to the perigranular zones. Further transmission to the dysgranular zones might be subserved by a topographically organized system of reciprocal interconnections that was found between the perigranular zones and dysgranular zones. In coronal sections, labelling produced by relatively distant injections of either retro or orthograde tracers generally appeared in a columnar distribution, and was localized in perigranular zones and dysgranular zones. Within these zones, orthograde labelling consisted of vertically oriented axons emitting collateral sprays of terminals in all layers. Retrograde neuronal labelling (composed almost exclusively of pyramidal cells) was greatest in supragranular layers. Proximal to the injection site, labelling tended to spread out from these columns into supra- and infragranular layers in adjacent granular zones.(ABSTRACT TRUNCATED AT 400 WORDS)

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019 (COVID-19), which was first identified in Wuhan, China, in December 2019. With the global transmission of the virus, many SARS-CoV-2 variants have emerged due to the alterations of the spike glycoprotein. Therefore, the S glycoprotein encoding gene has widely been used for the molecular analysis of SARS-Co-2 due to its features affecting antigenicity and immunogenicity. We analyzed the S gene sequences of 35 SARS-CoV-2 isolates in Kuwait from March 2020 to February 2021 using the Sanger method and MinION nanopore technology to confirm novel nucleotide alterations. Our results show that the Kuwaiti strains from clade 19A and B were the dominant variants early in the pandemic, while clade 20I (Alpha, V1) was the dominant variant from February 2021 onward. Besides the known mutations, 21 nucleotide deletions in the S glycoprotein in one Kuwaiti strain were detected, which might reveal a recombinant SARS-CoV-2 with the defective viral genome (DVG). This study emphasizes the importance of closely perceiving the emerging clades with these mutations during this continuous pandemic as some may influence the specificity of diagnostic tests, such as RT-PCR and even vaccine design directing these positions.

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