<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Coyne, Robert S.</style></author><author><style face="normal" font="default" size="100%">Hannick, Linda</style></author><author><style face="normal" font="default" size="100%">Shanmugam, Dhanasekaran</style></author><author><style face="normal" font="default" size="100%">Hostetler, Jessica B.</style></author><author><style face="normal" font="default" size="100%">Brami, Daniel</style></author><author><style face="normal" font="default" size="100%">Joardar, Vinita S.</style></author><author><style face="normal" font="default" size="100%">Johnson, Justin</style></author><author><style face="normal" font="default" size="100%">Radune, Diana</style></author><author><style face="normal" font="default" size="100%">Singh, Irtisha</style></author><author><style face="normal" font="default" size="100%">Badger, Jonathan H.</style></author><author><style face="normal" font="default" size="100%">Kumar, Ujjwal</style></author><author><style face="normal" font="default" size="100%">Saier, Milton</style></author><author><style face="normal" font="default" size="100%">Wang, Yufeng</style></author><author><style face="normal" font="default" size="100%">Cai, Hong</style></author><author><style face="normal" font="default" size="100%">Gu, Jianying</style></author><author><style face="normal" font="default" size="100%">Mather, Michael W.</style></author><author><style face="normal" font="default" size="100%">Vaidya, Akhil B.</style></author><author><style face="normal" font="default" size="100%">Wilkes, David E.</style></author><author><style face="normal" font="default" size="100%">Rajagopalan, Vidyalakshmi</style></author><author><style face="normal" font="default" size="100%">Asai, David J.</style></author><author><style face="normal" font="default" size="100%">Pearson, Chad G.</style></author><author><style face="normal" font="default" size="100%">Findly, Robert C.</style></author><author><style face="normal" font="default" size="100%">Dickerson, Harry W.</style></author><author><style face="normal" font="default" size="100%">Wu, Martin</style></author><author><style face="normal" font="default" size="100%">Martens, Cindy</style></author><author><style face="normal" font="default" size="100%">Van de Peer, Yves</style></author><author><style face="normal" font="default" size="100%">Roos, David S.</style></author><author><style face="normal" font="default" size="100%">Cassidy-Hanley, Donna M.</style></author><author><style face="normal" font="default" size="100%">Clark, Theodore G.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative genomics of the pathogenic ciliate Ichthyophthirius multifiliis, its free-living relatives and a host species provide insights into adoption of a parasitic lifestyle and prospects for disease control</style></title><secondary-title><style face="normal" font="default" size="100%">Genome Biology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">OCT</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">Article Number: R100</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Background: Ichthyophthirius multifiliis, commonly known as Ich, is a highly pathogenic ciliate responsible for 'white spot', a disease causing significant economic losses to the global aquaculture industry. Options for disease control are extremely limited, and Ich's obligate parasitic lifestyle makes experimental studies challenging. Unlike most well-studied protozoan parasites, Ich belongs to a phylum composed primarily of free-living members. Indeed, it is closely related to the model organism Tetrahymena thermophila. Genomic studies represent a promising strategy to reduce the impact of this disease and to understand the evolutionary transition to parasitism. 
Results: We report the sequencing, assembly and annotation of the Ich macronuclear genome. Compared with its free-living relative T. thermophila, the Ich genome is reduced approximately two-fold in length and gene density and three-fold in gene content. We analyzed in detail several gene classes with diverse functions in behavior, cellular function and host immunogenicity, including protein kinases, membrane transporters, proteases, surface antigens and cytoskeletal components and regulators. We also mapped by orthology Ich's metabolic pathways in comparison with other ciliates and a potential host organism, the zebrafish Danio rerio. 
Conclusions: Knowledge of the complete protein-coding and metabolic potential of Ich opens avenues for rational testing of therapeutic drugs that target functions essential to this parasite but not to its fish hosts. Also, a catalog of surface protein-encoding genes will facilitate development of more effective vaccines. The potential to use T. thermophila as a surrogate model offers promise toward controlling 'white spot' disease and understanding the adaptation to a parasitic lifestyle.</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">11.313</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Reid, Adam James</style></author><author><style face="normal" font="default" size="100%">Vermont, Sarah J.</style></author><author><style face="normal" font="default" size="100%">Cotton, James A.</style></author><author><style face="normal" font="default" size="100%">Harris, David</style></author><author><style face="normal" font="default" size="100%">Hill-Cawthorne, Grant A.</style></author><author><style face="normal" font="default" size="100%">Koenen-Waisman, Stephanie</style></author><author><style face="normal" font="default" size="100%">Latham, Sophia M.</style></author><author><style face="normal" font="default" size="100%">Mourier, Tobias</style></author><author><style face="normal" font="default" size="100%">Norton, Rebecca</style></author><author><style face="normal" font="default" size="100%">Quail, Michael A.</style></author><author><style face="normal" font="default" size="100%">Sanders, Mandy</style></author><author><style face="normal" font="default" size="100%">Shanmugam, Dhanasekaran</style></author><author><style face="normal" font="default" size="100%">Sohal, Amandeep</style></author><author><style face="normal" font="default" size="100%">Wasmuth, James D.</style></author><author><style face="normal" font="default" size="100%">Brunk, Brian</style></author><author><style face="normal" font="default" size="100%">Grigg, Michael E.</style></author><author><style face="normal" font="default" size="100%">Howard, Jonathan C.</style></author><author><style face="normal" font="default" size="100%">Parkinson, John</style></author><author><style face="normal" font="default" size="100%">Roos, David S.</style></author><author><style face="normal" font="default" size="100%">Trees, Alexander J.</style></author><author><style face="normal" font="default" size="100%">Berriman, Matthew</style></author><author><style face="normal" font="default" size="100%">Pain, Arnab</style></author><author><style face="normal" font="default" size="100%">Wastling, Jonathan M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Comparative genomics of the apicomplexan parasites toxoplasma gondii and neospora caninum: coccidia differing in host range and transmission strategy</style></title><secondary-title><style face="normal" font="default" size="100%">Plos Pathogens</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAR</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Toxoplasma gondii is a zoonotic protozoan parasite which infects nearly one third of the human population and is found in an extraordinary range of vertebrate hosts. Its epidemiology depends heavily on horizontal transmission, especially between rodents and its definitive host, the cat. Neospora caninum is a recently discovered close relative of Toxoplasma, whose definitive host is the dog. Both species are tissue-dwelling Coccidia and members of the phylum Apicomplexa; they share many common features, but Neospora neither infects humans nor shares the same wide host range as Toxoplasma, rather it shows a striking preference for highly efficient vertical transmission in cattle. These species therefore provide a remarkable opportunity to investigate mechanisms of host restriction, transmission strategies, virulence and zoonotic potential. We sequenced the genome of N. caninum and transcriptomes of the invasive stage of both species, undertaking an extensive comparative genomics and transcriptomics analysis. We estimate that these organisms diverged from their common ancestor around 28 million years ago and find that both genomes and gene expression are remarkably conserved. However, in N. caninum we identified an unexpected expansion of surface antigen gene families and the divergence of secreted virulence factors, including rhoptry kinases. Specifically we show that the rhoptry kinase ROP18 is pseudogenised in N. caninum and that, as a possible consequence, Neospora is unable to phosphorylate host immunity-related GTPases, as Toxoplasma does. This defense strategy is thought to be key to virulence in Toxoplasma. We conclude that the ecological niches occupied by these species are influenced by a relatively small number of gene products which operate at the host-parasite interface and that the dominance of vertical transmission in N. caninum may be associated with the evolution of reduced virulence in this species.</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">7.003</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Magarinos, Maria P.</style></author><author><style face="normal" font="default" size="100%">Carmona, Santiago J.</style></author><author><style face="normal" font="default" size="100%">Crowther, Gregory J.</style></author><author><style face="normal" font="default" size="100%">Ralph, Stuart A.</style></author><author><style face="normal" font="default" size="100%">Roos, David S.</style></author><author><style face="normal" font="default" size="100%">Shanmugam, Dhanasekaran</style></author><author><style face="normal" font="default" size="100%">Van Voorhis, Wesley C.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">TDR Targets: a chemogenomics resource for neglected diseases</style></title><secondary-title><style face="normal" font="default" size="100%">Nucleic Acids Research</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2012</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JAN</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">40</style></volume><pages><style face="normal" font="default" size="100%">D1118-D1127</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">The TDR Targets Database (http://tdrtargets.org) has been designed and developed as an online resource to facilitate the rapid identification and prioritization of molecular targets for drug development, focusing on pathogens responsible for neglected human diseases. The database integrates pathogen specific genomic information with functional data (e.g. expression, phylogeny, essentiality) for genes collected from various sources, including literature curation. This information can be browsed and queried using an extensive web interface with functionalities for combining, saving, exporting and sharing the query results. Target genes can be ranked and prioritized using numerical weights assigned to the criteria used for querying. In this report we describe recent updates to the TDR Targets database, including the addition of new genomes (specifically helminths), and integration of chemical structure, property and bioactivity information for biological ligands, drugs and inhibitors and cheminformatic tools for querying and visualizing these chemical data. These changes greatly facilitate exploration of linkages (both known and predicted) between genes and small molecules, yielding insight into whether particular proteins may be druggable, effectively allowing the navigation of chemical space in a genomics context.</style></abstract><issue><style face="normal" font="default" size="100%">D1</style></issue><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">9.202</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Woo, Yong H.</style></author><author><style face="normal" font="default" size="100%">Ansari, Hifzur</style></author><author><style face="normal" font="default" size="100%">Otto, Thomas D.</style></author><author><style face="normal" font="default" size="100%">Klinger, Christen M.</style></author><author><style face="normal" font="default" size="100%">Kolisko, Martin</style></author><author><style face="normal" font="default" size="100%">Michalek, Jan</style></author><author><style face="normal" font="default" size="100%">Saxena, Alka</style></author><author><style face="normal" font="default" size="100%">Shanmugam, Dhanasekaran</style></author><author><style face="normal" font="default" size="100%">Tayyrov, Annageldi</style></author><author><style face="normal" font="default" size="100%">Veluchamy, Alaguraj</style></author><author><style face="normal" font="default" size="100%">Ali, Shahjahan</style></author><author><style face="normal" font="default" size="100%">Bernal, Axel</style></author><author><style face="normal" font="default" size="100%">del Campo, Javier</style></author><author><style face="normal" font="default" size="100%">Cihlar, Jaromir</style></author><author><style face="normal" font="default" size="100%">Flegontov, Pavel</style></author><author><style face="normal" font="default" size="100%">Gornik, Sebastian G.</style></author><author><style face="normal" font="default" size="100%">Hajduskova, Eva</style></author><author><style face="normal" font="default" size="100%">Horak, Ales</style></author><author><style face="normal" font="default" size="100%">Janouskovec, Jan</style></author><author><style face="normal" font="default" size="100%">Katris, Nicholas J.</style></author><author><style face="normal" font="default" size="100%">Mast, Fred D.</style></author><author><style face="normal" font="default" size="100%">Miranda-Saavedra, Diego</style></author><author><style face="normal" font="default" size="100%">Mourier, Tobias</style></author><author><style face="normal" font="default" size="100%">Naeem, Raeece</style></author><author><style face="normal" font="default" size="100%">Nair, Mridul</style></author><author><style face="normal" font="default" size="100%">Panigrahi, Aswini K.</style></author><author><style face="normal" font="default" size="100%">Rawlings, Neil D.</style></author><author><style face="normal" font="default" size="100%">Padron-Regalado, Eriko</style></author><author><style face="normal" font="default" size="100%">Ramaprasad, Abhinay</style></author><author><style face="normal" font="default" size="100%">Samad, Nadira</style></author><author><style face="normal" font="default" size="100%">Tomcala, Ales</style></author><author><style face="normal" font="default" size="100%">Wilkes, Jon</style></author><author><style face="normal" font="default" size="100%">Neafsey, Daniel E.</style></author><author><style face="normal" font="default" size="100%">Doerig, Christian</style></author><author><style face="normal" font="default" size="100%">Bowler, Chris</style></author><author><style face="normal" font="default" size="100%">Keeling, Patrick J.</style></author><author><style face="normal" font="default" size="100%">Roos, David S.</style></author><author><style face="normal" font="default" size="100%">Dacks, Joel B.</style></author><author><style face="normal" font="default" size="100%">Templeton, Thomas J.</style></author><author><style face="normal" font="default" size="100%">Waller, Ross F.</style></author><author><style face="normal" font="default" size="100%">Lukes, Julius</style></author><author><style face="normal" font="default" size="100%">Obornik, Miroslav</style></author><author><style face="normal" font="default" size="100%">Pain, Arnab</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chromerid genomes reveal the evolutionary path from photosynthetic algae to obligate intracellular parasites</style></title><secondary-title><style face="normal" font="default" size="100%">Elife</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JUL</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">ELIFE SCIENCES PUBLICATIONS LTD</style></publisher><pub-location><style face="normal" font="default" size="100%">SHERATON HOUSE, CASTLE PARK, CAMBRIDGE, CB3 0AX, ENGLAND</style></pub-location><volume><style face="normal" font="default" size="100%">4</style></volume><pages><style face="normal" font="default" size="100%">Article Number: e06974</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The eukaryotic phylum Apicomplexa encompasses thousands of obligate intracellular parasites of humans and animals with immense socio-economic and health impacts. We sequenced nuclear genomes of Chromera velia and Vitrella brassicaformis, free-living non-parasitic photosynthetic algae closely related to apicomplexans. Proteins from key metabolic pathways and from the endomembrane trafficking systems associated with a free-living lifestyle have been progressively and non-randomly lost during adaptation to parasitism. The free-living ancestor contained a broad repertoire of genes many of which were repurposed for parasitic processes, such as extracellular proteins, components of a motility apparatus, and DNA-and RNA-binding protein families. Based on transcriptome analyses across 36 environmental conditions, Chromera orthologs of apicomplexan invasion-related motility genes were co-regulated with genes encoding the flagellar apparatus, supporting the functional contribution of flagella to the evolution of invasion machinery. This study provides insights into how obligate parasites with diverse life strategies arose from a once free-living phototrophic marine alga.&lt;/p&gt;</style></abstract><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">8.303</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Lykins, Joseph D.</style></author><author><style face="normal" font="default" size="100%">Filippova, Ekaterina V</style></author><author><style face="normal" font="default" size="100%">Halavaty, Andrei S.</style></author><author><style face="normal" font="default" size="100%">Minasov, George</style></author><author><style face="normal" font="default" size="100%">Zhou, Ying</style></author><author><style face="normal" font="default" size="100%">Dubrovska, Ievgeniia</style></author><author><style face="normal" font="default" size="100%">Flores, Kristin J.</style></author><author><style face="normal" font="default" size="100%">Shuvalova, Ludmilla A.</style></author><author><style face="normal" font="default" size="100%">Ruan, Jiapeng</style></author><author><style face="normal" font="default" size="100%">El Bissati, Kamal</style></author><author><style face="normal" font="default" size="100%">Dovgin, Sarah</style></author><author><style face="normal" font="default" size="100%">Roberts, Craig W.</style></author><author><style face="normal" font="default" size="100%">Woods, Stuart</style></author><author><style face="normal" font="default" size="100%">Moulton, Jon D.</style></author><author><style face="normal" font="default" size="100%">Moulton, Hong</style></author><author><style face="normal" font="default" size="100%">Mcphillie, Martin J.</style></author><author><style face="normal" font="default" size="100%">Muench, Stephen P.</style></author><author><style face="normal" font="default" size="100%">Fishwick, Colin W. G.</style></author><author><style face="normal" font="default" size="100%">Sabini, Elisabetta</style></author><author><style face="normal" font="default" size="100%">Shanmugam, Dhanasekaran</style></author><author><style face="normal" font="default" size="100%">Roos, David S.</style></author><author><style face="normal" font="default" size="100%">Mcleod, Rima</style></author><author><style face="normal" font="default" size="100%">Anderson, Wayne F.</style></author><author><style face="normal" font="default" size="100%">Ngo, Huan M.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">CSGID solves structures and identifies phenotypes for five enzymes in toxoplasma gondii</style></title><secondary-title><style face="normal" font="default" size="100%">Frontiers in Cellular and Infection Microbiology</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">OCT</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">8</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Toxoplasma gondii, an Apicomplexan parasite, causes significant morbidity and mortality, including severe disease in immunocompromised hosts and devastating congenital disease, with no effective treatment for the bradyzoite stage. To address this, we used the Tropical Disease Research database, crystallography, molecular modeling, and antisense to identify and characterize a range of potential therapeutic targets for toxoplasmosis. Phosphoglycerate mutase II (PGMII), nucleoside diphosphate kinase (NDK), ribulose phosphate 3-epimerase (RPE), ribose-5-phosphate isomerase (RPI), and ornithine aminotransferase (OAT) were structurally characterized. Crystallography revealed insights into the overall structure, protein oligomeric states and molecular details of active sites important for ligand recognition. Literature and molecular modeling suggested potential inhibitors and druggability. The targets were further studied with vivoPMO to interrupt enzyme synthesis, identifying the targets as potentially important to parasitic replication and, therefore, of therapeutic interest. Targeted vivoPMO resulted in statistically significant perturbation of parasite replication without concomitant host cell toxicity, consistent with a previous CRISPR/Cas9 screen showing PGM, RPE, and RPI contribute to parasite fitness. PGM, RPE, and RPI have the greatest promise for affecting replication in tachyzoites. These targets are shared between other medically important parasites and may have wider therapeutic potential.&lt;/p&gt;</style></abstract><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;3.520&lt;/p&gt;</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Shukla, Anurag</style></author><author><style face="normal" font="default" size="100%">Olszewski, Kellen L.</style></author><author><style face="normal" font="default" size="100%">Llinas, Manuel</style></author><author><style face="normal" font="default" size="100%">Rommereim, Leah M.</style></author><author><style face="normal" font="default" size="100%">Fox, Barbara A.</style></author><author><style face="normal" font="default" size="100%">Bzik, David J.</style></author><author><style face="normal" font="default" size="100%">Xia, Dong</style></author><author><style face="normal" font="default" size="100%">Wastling, Jonathan</style></author><author><style face="normal" font="default" size="100%">Beiting, Daniel</style></author><author><style face="normal" font="default" size="100%">Roos, David S.</style></author><author><style face="normal" font="default" size="100%">Shanmugam, Dhanasekaran</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%"> Glycolysis is important for optimal asexual growth and formation of mature tissue cysts by Toxoplasma gondii</style></title><secondary-title><style face="normal" font="default" size="100%">International Journal for Parasitology </style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">OCT</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">48</style></volume><pages><style face="normal" font="default" size="100%">955-968</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Toxoplasma gondii can grow and replicate using either glucose or glutamine as the major carbon source. Here, we have studied the essentiality of glycolysis in the tachyzoite and bradyzoite stages of T. gondii, using transgenic parasites that lack a functional hexokinase gene (Delta hk) in RH (Type-1) and Prugniaud (Type-II) strain parasites. Tachyzoite stage 411k parasites exhibit a fitness defect similar to that reported previously for the major glucose transporter mutant, and remain virulent in mice. However, although Prugniaud strain Delta hk tachyzoites were capable of transforming into bradyzoites in vitro, they were severely compromised in their ability to make mature bradyzoite cysts in the brain tissue of mice. Isotopic labelling studies reveal that glucose-deprived tacyzoites utilise glutamine to replenish glycolytic and pentose phosphate pathway intermediates via gluconeogenesis. Interestingly, while glutaminedeprived intracellular Delta hk tachyzoites continued to replicate, extracellular parasites were unable to efficiently invade host cells. Further, studies on mutant tachyzoites lacking a functional phosphoenolpyruvate carboxykinase (Delta pepck1) revealed that glutaminolysis is the sole source of gluconeogenic flux in glucose-deprived parasites. In addition, glutaminolysis is essential for sustaining oxidative phosphorylation in zihk parasites, while wild type (wt) and Delta pepck1 parasites can obtain ATP from either glycolysis or oxidative phosphorylation. This study provides insights into the role of nutrient metabolism during asexual propagation and development of T. gondii, and validates the versatile nature of central carbon and energy metabolism in this parasite. (C) 2018 Australian Society for Parasitology. Published by Elsevier Ltd. All rights reserved.</style></abstract><issue><style face="normal" font="default" size="100%">12</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%"> Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">3.078</style></custom4></record></records></xml>