The family Leucospidae (Hymenoptera: Chalcidoidea) from the South of Saudi Arabia,with the first report of the genus Micrapion and description of Leucospis arabica sp. nov.

The family Leucospidae (Hymenoptera: Chalcidoidea) from Saudi Arabia is reviewed. Specimens were mainly collected from the south-western region of the country – Raydah (Abha, Asir), Sajid (Farasan Islands, Jazan) and Wadi Tourabah (Mandaq, Al Baha); and from Egypt – Wadi Khoshb (Sinai Peninsula), as well as a specimen (Leucospis elegans Klug) deposited in the Efflatoun Bey collection, Cairo University, Egypt. The genus Micrapion Kriechbaumer is here recorded for the first time from the fauna of the Arabian Peninsula, with a single species, M. clavaforme. Leucospis arabica Gadallah and Soliman sp. nov. (dorsigera group) is described. Leucospis africana (elegans group) is also newly recorded from the Saudi Arabian fauna, in addition to L. elegans which has been previously recorded. An illustrated key and a list of all leucospid species recorded and expected to occur in Saudi Arabia are provided.

www.zoobank.org/lsid:Zoobank.org:pub:40BEF37F-0D92-4AEF-9990-30C1CFC3A7A7     

Ant fauna (Hymenoptera: Formicidae) of the Socotra Archipelago (Yemen): zoogeography,distribution and description of a new species

The animal fauna of the Socotra Archipelago is influenced by three biogeographical regions, the Afrotropical, the Oriental and the Palaearctic. Consequently, the Archipelago shares faunal elements of these three regions in addition to unique endemic taxa. The ant fauna of Socotra Island was studied and is reviewed based on literature and newly collected material. In total, 28 species, belonging to 10 genera and four subfamilies, were collected from the main island. Eighteen of these (64%) are successful invasive species, seven are native (25%), and three are considered endemic (11%), Cardiocondyla longiceps Seifert, Monomorium elghazalyi sp. nov. and Monomorium nimihil Collingwood et al. Two genera are recorded for the first time from the island, Hypoponera Santschi, and Syllophopsis Santschi. Ten species are recorded for the first time, Cardiocondyla mauritanica Forel, Cardiocondyla minutior Forel, Monomorium atomum Forel, Monomorium dichroum Forel, Monomorium exiguum Forel, Pheidole pallidula (Nylander), Syllophopsis cryptobia (Santschi), Tetramorium pauper Forel, Tetramorium transformans Santschi and Hypoponera punctatissima (Roger). Ten invasive species are recorded from Socotra, reflecting human impacts on the Archipelago. These species are Tapinoma melanocephalum (Fabricius), Cardiocondyla emeryi Forel, Monomorium exiguum Forel, Pheidole indica Mayr, Syllophopsis cryptobia (Santschi), Tetramorium lanuginosum Mayr, Tetramorium simillimum (Smith), Tetramorium caldarium (Roger), Trichomyrmex destructor (Jerdon) and Trichomyrmex mayri (Forel). Our survey indicated a mixture of Afrotropical faunal elements (10 species, 36%), followed by cosmopolitan (nine species, 32%), Palaearctic (five species, 18%) and Oriental (four species, 14%) taxa. Two new synonyms of Monomorium exiguum Forel are proposed: Monomorium exiguum Forel = Monomorium baushare Collingwood & Agosti syn. nov. = Monomorium qarahe Collingwood & Agosti syn. nov. Tetramorium transformans Santschi is removed from synonymy with Tetramorium caldarium (Roger) and elevated to species rank. Ecological and biological notes for each species are given. Distribution maps for all species known from the Socotra Archipelago are provided.

http://zoobank/urn:lsid:zoobank.org:pub:89612083-9CE6-48E8-8975-1CE5334E098B     

Genome-wide association analysis identifies three new breast cancer susceptibility loci

Breast cancer is the most common cancer among women. To date, 22 common breast cancer susceptibility loci have been identified accounting for ～8% of the heritability of the disease. We attempted to replicate 72 promising associations from two independent genome-wide association studies (GWAS) in ～70,000 cases and ～68,000 controls from 41 case-control studies and 9 breast cancer GWAS. We identified three new breast cancer risk loci at 12p11 (rs10771399; P = 2.7 × 10(-35)), 12q24 (rs1292011; P = 4.3 × 10(-19)) and 21q21 (rs2823093; P = 1.1 × 10(-12)). rs10771399 was associated with similar relative risks for both estrogen receptor (ER)-negative and ER-positive breast cancer, whereas the other two loci were associated only with ER-positive disease. Two of the loci lie in regions that contain strong plausible candidate genes: PTHLH (12p11) has a crucial role in mammary gland development and the establishment of bone metastasis in breast cancer, and NRIP1 (21q21) encodes an ER cofactor and has a role in the regulation of breast cancer cell growth.     

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

Estrogen receptor (ER)-negative breast cancer shows a higher incidence in women of African ancestry compared to women of European ancestry. In search of common risk alleles for ER-negative breast cancer, we combined genome-wide association study (GWAS) data from women of African ancestry (1,004 ER-negative cases and 2,745 controls) and European ancestry (1,718 ER-negative cases and 3,670 controls), with replication testing conducted in an additional 2,292 ER-negative cases and 16,901 controls of European ancestry. We identified a common risk variant for ER-negative breast cancer at the TERT-CLPTM1L locus on chromosome 5p15 (rs10069690: per-allele odds ratio (OR) = 1.18 per allele, P = 1.0 × 10(-10)). The variant was also significantly associated with triple-negative (ER-negative, progesterone receptor (PR)-negative and human epidermal growth factor-2 (HER2)-negative) breast cancer (OR = 1.25, P = 1.1 × 10(-9)), particularly in younger women (<50 years of age) (OR = 1.48, P = 1.9 × 10(-9)). Our results identify a genetic locus associated with estrogen receptor negative breast cancer subtypes in multiple populations.     

Genome-wide association study identifies a common variant associated with risk of endometrial cancer

Endometrial cancer is the most common malignancy of the female genital tract in developed countries. To identify genetic variants associated with endometrial cancer risk, we performed a genome-wide association study involving 1,265 individuals with endometrial cancer (cases) from Australia and the UK and 5,190 controls from the Wellcome Trust Case Control Consortium. We compared genotype frequencies in cases and controls for 519,655 SNPs. Forty seven SNPs that showed evidence of association with endometrial cancer in stage 1 were genotyped in 3,957 additional cases and 6,886 controls. We identified an endometrial cancer susceptibility locus close to HNF1B at 17q12 (rs4430796, P = 7.1 × 10(-10)) that is also associated with risk of prostate cancer and is inversely associated with risk of type 2 diabetes.     

Unusual selection on the KIR3DL1/S1 natural killer cell receptor in Africans

Interactions of killer cell immunoglobulin-like receptors (KIRs) with major histocompatibility complex (MHC) class I ligands diversify natural killer cell responses to infection. By analyzing sequence variation in diverse human populations, we show that the KIR3DL1/S1 locus encodes two lineages of polymorphic inhibitory KIR3DL1 allotypes that recognize Bw4 epitopes of protein">HLA-A and HLA-B and one lineage of conserved activating KIR3DS1 allotypes, also implicated in Bw4 recognition. Balancing selection has maintained these three lineages for over 3 million years. Variation was selected at D1 and D2 domain residues that contact HLA class I and at two sites on D0, the domain that enhances the binding of KIR3D to HLA class I. HLA-B variants that gained Bw4 through interallelic microconversion are also products of selection. A worldwide comparison uncovers unusual KIR3DL1/S1 evolution in modern sub-Saharan Africans. Balancing selection is weak and confined to D0, KIR3DS1 is rare and KIR3DL1 allotypes with similar binding sites predominate. Natural killer cells express the dominant KIR3DL1 at a high frequency and with high surface density, providing strong responses to cells perturbed in Bw4 expression.     

一类分数阶随机发展方程非局部问题mild解的存在性

在非局部函数依赖于未知变量在整个定义区间上的值的情形下,应用随机分析理论、Schauder不动点定理及近似方法,假设非线性函数和非局部项是Carathéodory连续的并且满足较弱增长条件,获得了一类分数阶随机发展方程非局部问题mild解的存在性结果。此工作可以看作是对具有一般非局部初始条件的分数阶发展方程建立解的存在性理论的一种尝试。最后举例说明所得抽象结果在具有非局部积分条件的分数阶随机偏微分方程中的应用。     

Control of HIV infection by IFN-α: implications for latency and a cure

Viral infections, including HIV, trigger the production of type I interferons (IFNs), which in turn, activate a signalling cascade that ultimately culminates with the expression of anti-viral proteins. Mounting evidence suggests that type I IFNs, in particular IFN-α, play a pivotal role in limiting acute HIV infection. Highly active anti-retroviral treatment reduces viral load and increases life expectancy in HIV positive patients; however, it fails to fully eliminate latent HIV reservoirs. To revisit HIV as a curable disease, this article reviews a body of literature that highlights type I IFNs as mediators in the control of HIV infection, with particular focus on the anti-HIV restriction factors induced and/or activated by IFN-α. In addition, we discuss the relevance of type I IFN treatment in the context of HIV latency reversal, novel therapeutic intervention strategies and the potential for full HIV clearance.