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Universidade Federal de Viçosa

EducationViçosa, Brazil
About: Universidade Federal de Viçosa is a education organization based out in Viçosa, Brazil. It is known for research contribution in the topics: Population & Biology. The organization has 16012 authors who have published 26711 publications receiving 353416 citations.


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Journal ArticleDOI
TL;DR: A comprehensive review of antimicrobial peptides, from synthesis procedures to mechanisms of action, with an emphasis on nisin is presented, and a historical outlook and the current perspectives of their potential applications in food packaging systems are addressed.
Abstract: Antimicrobial peptides are protein fragments present in the innate immune systems of invertebrates and vertebrates as host defense molecules. Due to their unique properties, these compounds have several useful appliances in human health by potentially playing antibacterial, antiviral, antifungal, and antitumor roles. The incorporation of antimicrobial peptides into polymer matrices as delivery systems has been studied recently with further interest towards the fields of medicine, pharmacy, personal care, and food packaging. The consumers' tendency to demand more natural products has paved the route for food industries to explore novel mechanisms as food preservation techniques. Antimicrobial peptide-containing active packaging materials emerge as a promising approach to retard food spoilage and increase food safety and shelf life. This text presents a comprehensive review of antimicrobial peptides, from synthesis procedures to mechanisms of action, with an emphasis on nisin. A historical outlook and the current perspectives of their potential applications in food packaging systems are also addressed.

138 citations

Journal ArticleDOI
TL;DR: The implementation of integrated control programmes and appropriate resistance management strategies as part of such programs is of utmost importance to keep tomato pinworm infestations under economic damage thresholds, thus guaranteeing sustainable yields.
Abstract: The South American tomato pinworm, Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae), is an invasive pest difficult to control. Insecticide application is quite common and remains the prevalent control method particularly in open-field cultivation systems. As a result, insecticide resistance to many chemical classes of insecticides has been described both in South America and in Europe. The development of insecticide resistance is relatively fast in this species, and the main mechanisms involved are altered target-site sensitivity and/or enhanced detoxification, depending on the chemical class. However, insecticide resistance mechanisms do not differ between South America and Europe and are mainly due to simple genotype variations leading to high levels of resistance. The presence of resistance alleles at low frequency, especially against newer chemistry, is of major concern, as they tend to spread with the invasions making tomato pinworm particularly difficult to control. The monitoring methods and management programmes developed for the species benefited from the pro-activity of the Insecticide Resistance Action Committee and its country groups, particularly in Brazil and Spain. Bioassay methods were developed, resistance monitoring activities initiated and resistance management guidance was provided. The implementation of integrated control programmes and appropriate resistance management strategies as part of such programs is of utmost importance to keep tomato pinworm infestations under economic damage thresholds, thus guaranteeing sustainable yields.

138 citations

Journal ArticleDOI
Pedro W. Crous1, J. Jennifer Luangsa-ard2, Michael J. Wingfield1, Angus J. Carnegie, Margarita Hernández-Restrepo, Lorenzo Lombard, Jolanda Roux1, Robert W. Barreto3, Iuri Goulart Baseia4, J. F. Cano-Lira5, María P. Martín6, O.V. Morozova7, Alberto M. Stchigel5, Brett A. Summerell8, Tor Erik Brandrud, Bálint Dima9, Dania García5, Alejandra Giraldo10, Josep Guarro5, Luís Fernando Pascholati Gusmão11, P. Khamsuntorn2, Machiel E. Noordeloos12, S. Nuankaew2, U. Pinruan2, E. Rodríguez-Andrade5, Cristina Maria de Souza-Motta13, R. Thangavel14, A. van Iperen, V.P. Abreu3, Thiago Accioly4, Janaina L. Alves3, J.P. Andrade11, Mohammad Bahram15, Mohammad Bahram16, Hans-Otto Baral, Eder Barbier13, C. W. Barnes, Egil Bendiksen, Enrico Bernard13, Jadson D. P. Bezerra13, José Jailson Lima Bezerra13, Enrico Bizio15, Jaime E. Blair17, T. M. Bulyonkova7, T.S. Cabral4, M.V. Caiafa18, T. Cantillo11, A.A. Colmán3, L.B. Conceição11, S. Cruz18, A.O.B. Cunha13, Blaise A. Darveaux, A.L. da Silva3, G. A. da Silva13, G.M. da Silva4, R. M. da Silva13, R.J.V. de Oliveira13, R.L. Oliveira4, J. T. De Souza, Margarita Dueñas6, Harry C. Evans19, Filomena Epifani, M.T.C. Felipe13, Javier Fernández-López6, B.W. Ferreira3, C.N. Figueiredo, Nina V. Filippova, J.A. Flores20, Josepa Gené5, G. Ghorbani21, Tatiana Baptista Gibertoni13, A. M. Glushakova22, Rosanne A. Healy18, Sabine M. Huhndorf, I. Iturrieta-González5, Mohammad Javan-Nikkhah21, R.F. Juciano13, Željko Jurjević, Aleksey V. Kachalkin22, K. Keochanpheng, Irmgard Krisai-Greilhuber23, Y.-C. Li24, AA Lima4, A. R. Machado13, Hugo Madrid25, Oliane Maria Correia Magalhães13, P.A.S. Marbach, Gislaine Cristina de Souza Melanda13, Andrew N. Miller26, Suchada Mongkolsamrit2, R.P. Nascimento, Thays Gabrielle Lins de Oliveira13, M.E. Ordoñez20, R. Orzes, M.A. Palma27, Cedric J. Pearce, Olinto Liparini Pereira3, Giancarlo Perrone, Stephen W. Peterson28, T.H.G. Pham, E. Piontelli27, Adel Pordel21, Luis Quijada29, Huzefa A. Raja30, E. Rosas de Paz5, Leif Ryvarden31, Alessandro Saitta32, S. S. Salcedo3, Marcelo Sandoval-Denis10, Tiago Santos11, Keith A. Seifert33, Bianca Denise Barbosa da Silva34, Matthew E. Smith18, Adriene Mayra Soares13, S. Sommai2, Julieth O. Sousa4, Satinee Suetrong2, Antonia Susca, Leho Tedersoo16, M.T. Telleria6, D. Thanakitpipattana2, N. Valenzuela-Lopez35, N. Valenzuela-Lopez5, Cobus M. Visagie, M. Zapata, Johannes Z. Groenewald 
TL;DR: Novel species of fungi described in this study include those from various countries as follows: Angola, Gnomoniopsis angolensis and Pseudopithomyces anglensis on unknown host plants.
Abstract: Novel species of fungi described in this study include those from various countries as follows: Angola, Gnomoniopsis angolensis and Pseudopithomyces angolensis on unknown host plants. Australia, Dothiora corymbiae on Corymbia citriodora, Neoeucasphaeria eucalypti (incl. Neoeucasphaeria gen. nov.) on Eucalyptus sp., Fumagopsis stellae on Eucalyptus sp., Fusculina eucalyptorum (incl. Fusculinaceae fam. nov.) on Eucalyptus socialis, Harknessia corymbiicola on Corymbia maculata, Neocelosporium eucalypti (incl. Neocelosporium gen. nov., Neocelosporiaceae fam. nov. and Neocelosporiales ord. nov.) on Eucalyptus cyanophylla, Neophaeomoniella corymbiae on Corymbia citriodora, Neophaeomoniella eucalyptigena on Eucalyptus pilularis, Pseudoplagiostoma corymbiicola on Corymbia citriodora, Teratosphaeria gracilis on Eucalyptus gracilis, Zasmidium corymbiae on Corymbia citriodora. Brazil, Calonectria hemileiae on pustules of Hemileia vastatrix formed on leaves of Coffea arabica, Calvatia caatinguensis on soil, Cercospora solani-betacei on Solanum betaceum, Clathrus natalensis on soil, Diaporthe poincianellae on Poincianella pyramidalis, Geastrum piquiriunense on soil, Geosmithia carolliae on wing of Carollia perspicillata, Henningsia resupinata on wood, Penicillium guaibinense from soil, Periconia caespitosa from leaf litter, Pseudocercospora styracina on Styrax sp., Simplicillium filiforme as endophyte from Citrullus lanatus, Thozetella pindobacuensis on leaf litter, Xenosonderhenia coussapoae on Coussapoa floccosa. Canary Islands (Spain), Orbilia amarilla on Euphorbia canariensis. Cape Verde Islands, Xylodon jacobaeus on Eucalyptus camaldulensis. Chile, Colletotrichum arboricola on Fuchsia magellanica. Costa Rica, Lasiosphaeria miniovina on tree branch. Ecuador, Ganoderma chocoense on tree trunk. France, Neofitzroyomyces nerii (incl. Neofitzroyomyces gen. nov.) on Nerium oleander. Ghana, Castanediella tereticornis on Eucalyptus tereticornis, Falcocladium africanum on Eucalyptus brassiana, Rachicladosporium corymbiae on Corymbia citriodora. Hungary, Entoloma silvae-frondosae in Carpinus betulus-Pinus sylvestris mixed forest. Iran, Pseudopyricularia persiana on Cyperus sp. Italy, Inocybe roseascens on soil in mixed forest. Laos, Ophiocordyceps houaynhangensis on Coleoptera larva. Malaysia, Monilochaetes melastomae on Melastoma sp. Mexico, Absidia terrestris from soil. Netherlands, Acaulium pannemaniae, Conioscypha boutwelliae, Fusicolla septimanifiniscientiae, Gibellulopsis simonii, Lasionectria hilhorstii, Lectera nordwiniana, Leptodiscella rintelii, Parasarocladium debruynii and Sarocladium dejongiae (incl. Sarocladiaceae fam. nov.) from soil. New Zealand, Gnomoniopsis rosae on Rosa sp. and Neodevriesia metrosideri on Metrosideros sp. Puerto Rico, Neodevriesia coccolobae on Coccoloba uvifera, Neodevriesia tabebuiae and Alfaria tabebuiae on Tabebuia chrysantha. Russia, Amanita paludosa on bogged soil in mixed deciduous forest, Entoloma tiliae in forest of Tilia × europaea, Kwoniella endophytica on Pyrus communis. South Africa, Coniella diospyri on Diospyros mespiliformis, Neomelanconiella combreti (incl. Neomelanconiellaceae fam. nov. and Neomelanconiella gen. nov.) on Combretum sp., Polyphialoseptoria natalensis on unidentified plant host, Pseudorobillarda bolusanthi on Bolusanthus speciosus, Thelonectria pelargonii on Pelargonium sp. Spain, Vermiculariopsiella lauracearum and Anungitopsis lauri on Laurus novocanariensis, Geosmithia xerotolerans from a darkened wall of a house, Pseudopenidiella gallaica on leaf litter. Thailand, Corynespora thailandica on wood, Lareunionomyces loeiensis on leaf litter, Neocochlearomyces chromolaenae (incl. Neocochlearomyces gen. nov.) on Chromolaena odorata, Neomyrmecridium septatum (incl. Neomyrmecridium gen. nov.), Pararamichloridium caricicola on Carex sp., Xenodactylaria thailandica (incl. Xenodactylariaceae fam. nov. and Xenodactylaria gen. nov.), Neomyrmecridium asiaticum and Cymostachys thailandica from unidentified vine. USA, Carolinigaster bonitoi (incl. Carolinigaster gen. nov.) from soil, Penicillium fortuitum from house dust, Phaeotheca shathenatiana (incl. Phaeothecaceae fam. nov.) from twig and cone litter, Pythium wohlseniorum from stream water, Superstratomyces tardicrescens from human eye, Talaromyces iowaense from office air. Vietnam, Fistulinella olivaceoalba on soil. Morphological and culture characteristics along with DNA barcodes are provided.

137 citations

Journal ArticleDOI
Pedro W. Crous, Michael J. Wingfield1, Treena I. Burgess2, G.E.St.J. Hardy2, Josepa Gené, Josep Guarro, Iuri Goulart Baseia3, Dania García, Luís Fernando Pascholati Gusmão4, Cristina Maria de Souza-Motta5, R. Thangavel6, Slavomír Adamčík7, A. Barili8, C. W. Barnes, Jadson D. P. Bezerra5, Juan-Julián Bordallo9, José F. Cano-Lira, R.J.V. de Oliveira5, Enrico Ercole10, Vit Hubka11, I. Iturrieta-González, Alena Kubátová11, María P. Martín12, Pierre-Arthur Moreau13, Asunción Morte9, M.E. Ordoñez8, A. Rodríguez9, Alberto M. Stchigel, Alfredo Vizzini10, Jafar Abdollahzadeh14, V.P. Abreu15, Katarína Adamčíková7, G.M.R. Albuquerque5, A. V. Alexandrova16, E. Alvarez Duarte17, C. Armstrong-Cho18, S. Banniza18, Renan do Nascimento Barbosa5, Jean-Michel Bellanger19, José Jailson Lima Bezerra5, T.S. Cabral3, M. Cabon7, E. Caicedo8, T. Cantillo4, Angus J. Carnegie, L.T. Carmo4, Rafael F. Castañeda-Ruiz, Charles R. Clement20, Adéla Čmoková, L.B. Conceição4, Rhudson Henrique Santos Ferreira da Cruz3, Ulrike Damm21, B.D.B. da Silva22, G. A. da Silva5, R. M. da Silva5, A. L. C. M. de A. Santiago5, L.F. De Oliveira23, C.A.F. De Souza5, Franck Déniel, Bálint Dima24, G. Dong25, Jacqueline Edwards26, Ciro R. Félix27, Jacques Fournier, Tatiana Baptista Gibertoni5, Kentaro Hosaka, Teresa Iturriaga28, M. Jadan, Jean-Luc Jany, Z. Jurjevic, Miroslav Kolarik11, I. Kusan, Melissa Fontes Landell27, T.R. Leite Cordeiro5, Diogo Xavier Lima5, Michael Loizides, S. Luo25, A. R. Machado5, Hugo Madrid29, Oliane Maria Correia Magalhães5, Paulo Marinho3, Neven Matočec, Armin Mešić, Andrew N. Miller30, O.V. Morozova31, R.P. Neves5, K. Nonaka32, Alena Nováková, Nicholas H. Oberlies33, José Ribamar C. Oliveira-Filho5, Thays Gabrielle Lins de Oliveira5, Viktor Papp34, Olinto Liparini Pereira15, Giancarlo Perrone, Stephen W. Peterson35, T.H.G. Pham, Huzefa A. Raja33, Daniel B. Raudabaugh28, J. Rehulka36, E. Rodríguez-Andrade, M. Saba37, A. Schauflerova, Roger G. Shivas38, G. Simonini, João Paulo Zen Siqueira, Julieth O. Sousa3, V. Stajsic39, T. Svetasheva40, T. Svetasheva31, Yu Pei Tan, Zdenko Tkalčec, S. Ullah41, Patricia Valente42, Nicomedes Valenzuela-Lopez43, Masoud Abrinbana44, D.A. Viana Marques23, P. T. W. Wong25, V. Xavier de Lima5, Johannes Z. Groenewald 
TL;DR: Novel species of fungi described in this study include those from various countries as follows: Australia, Chaetopsina eucalyPTi on Eucalyptus leaf litter, Colletotrichum cobbittiense from Cordyline stricta × C. australis hybrid.
Abstract: Novel species of fungi described in this study include those from various countries as follows: Australia, Chaetopsina eucalypti on Eucalyptus leaf litter, Colletotrichum cobbittiense from Cordyline stricta × C. australis hybrid, Cyanodermella banksiae on Banksia ericifolia subsp. macrantha, Discosia macrozamiae on Macrozamia miquelii, Elsinoe banksiigena on Banksia marginata, Elsinoe elaeocarpi on Elaeocarpus sp., Elsinoe leucopogonis on Leucopogon sp., Helminthosporium livistonae on Livistona australis, Idriellomyces eucalypti (incl. Idriellomyces gen. nov.) on Eucalyptus obliqua, Lareunionomyces eucalypti on Eucalyptus sp., Myrotheciomyces corymbiae (incl. Myrotheciomyces gen. nov., Myrotheciomycetaceae fam. nov.), Neolauriomyces eucalypti (incl. Neolauriomyces gen. nov., Neolauriomycetaceae fam. nov.) on Eucalyptus sp., Nullicamyces eucalypti (incl. Nullicamyces gen. nov.) on Eucalyptus leaf litter, Oidiodendron eucalypti on Eucalyptus maidenii, Paracladophialophora cyperacearum (incl. Paracladophialophoraceae fam. nov.) and Periconia cyperacearum on leaves of Cyperaceae, Porodiplodia livistonae (incl. Porodiplodia gen. nov., Porodiplodiaceae fam. nov.) on Livistona australis, Sporidesmium melaleucae (incl. Sporidesmiales ord. nov.) on Melaleuca sp., Teratosphaeria sieberi on Eucalyptus sieberi, Thecaphora australiensis in capsules of a variant of Oxalis exilis. Brazil, Aspergillus serratalhadensis from soil, Diaporthe pseudoinconspicua from Poincianella pyramidalis, Fomitiporella pertenuis on dead wood, Geastrum magnosporum on soil, Marquesius aquaticus (incl. Marquesius gen. nov.) from submerged decaying twig and leaves of unidentified plant, Mastigosporella pigmentata from leaves of Qualea parviflorae, Mucor souzae from soil, Mycocalia aquaphila on decaying wood from tidal detritus, Preussia citrullina as endophyte from leaves of Citrullus lanatus, Queiroziella brasiliensis (incl. Queiroziella gen. nov.) as epiphytic yeast on leaves of Portea leptantha, Quixadomyces cearensis (incl. Quixadomyces gen. nov.) on decaying bark, Xylophallus clavatus on rotten wood. Canada, Didymella cari on Carum carvi and Coriandrum sativum. Chile, Araucasphaeria foliorum (incl. Araucasphaeria gen. nov.) on Araucaria araucana, Aspergillus tumidus from soil, Lomentospora valparaisensis from soil. Colombia, Corynespora pseudocassiicola on Byrsonima sp., Eucalyptostroma eucalyptorum on Eucalyptus pellita, Neometulocladosporiella eucalypti (incl. Neometulocladosporiella gen. nov.) on Eucalyptus grandis × urophylla, Tracylla eucalypti (incl. Tracyllaceae fam. nov., Tracyllalales ord. nov.) on Eucalyptus urophylla. Cyprus, Gyromitra anthracobia (incl. Gyromitra subg. Pseudoverpa) on burned soil. Czech Republic, Lecanicillium restrictum from the surface of the wooden barrel, Lecanicillium testudineum from scales of Trachemys scripta elegans. Ecuador, Entoloma yanacolor and Saproamanita quitensis on soil. France, Lentithecium carbonneanum from submerged decorticated Populus branch. Hungary, Pleuromyces hungaricus (incl. Pleuromyces gen. nov.) from a large Fagus sylvatica log. Iran, Zymoseptoria crescenta on Aegilops triuncialis. Malaysia, Ochroconis musicola on Musa sp. Mexico, Cladosporium michoacanense from soil. New Zealand, Acrodontium metrosideri on Metrosideros excelsa, Polynema podocarpi on Podocarpus totara, Pseudoarthrographis phlogis (incl. Pseudoarthrographis gen. nov.) on Phlox subulata. Nigeria, Coprinopsis afrocinerea on soil. Pakistan, Russula mansehraensis on soil under Pinus roxburghii. Russia, Baorangia alexandri on soil in deciduous forests with Quercus mongolica. South Africa, Didymocyrtis brachylaenae on Brachylaena discolor. Spain, Alfaria dactylis from fruit of Phoenix dactylifera, Dothiora infuscans from a blackened wall, Exophiala nidicola from the nest of an unidentified bird, Matsushimaea monilioides from soil, Terfezia morenoi on soil. United Arab Emirates, Tirmania honrubiae on soil. USA, Arxotrichum wyomingense (incl. Arxotrichum gen. nov.) from soil, Hongkongmyces snookiorum from submerged detritus from a fresh water fen, Leratiomyces tesquorum from soil, Talaromyces tabacinus on leaves of Nicotiana tabacum. Vietnam, Afroboletus vietnamensis on soil in an evergreen tropical forest, Colletotrichum condaoense from Ipomoea pes-caprae. Morphological and culture characteristics along with DNA barcodes are provided.

137 citations

Journal ArticleDOI
TL;DR: Morphological examination of ticks in Brazil confirmed that A. cajennense (s.l.) is currently represented in Brazil by only one species, A. sculptum, while these species have distinct distribution areas in the country and are found in sympatry in some transition areas.
Abstract: Until recently, Amblyomma cajennense (Fabricius, 1787) was considered to represent a single tick species in the New World. Recent studies have split this taxon into six species. While the A. cajennense species complex or A. cajennense (sensu lato) (s.l.) is currently represented by two species in Brazil, A. cajennense (sensu stricto) (s.s.) and Amblyomma sculptum Berlese, 1888, their geographical distribution is poorly known. The distribution of the A. cajennense (s.l.) in Brazil was determined by morphological examination of all lots of A. cajennense (s.l.) in two large tick collections of Brazil, and by collecting new material during three field expeditions in the possible transition areas between the distribution ranges of A. cajennense (s.s.) and A. sculptum. Phylogenetic analysis inferred from the ITS2 rRNA gene was used to validate morphological results. Morphological description of the nymphal stage of A. cajennense (s.s.) is provided based on laboratory-reared specimens. From the tick collections, a total 12,512 adult ticks were examined and identified as 312 A. cajennense (s.s.), 6,252 A. sculptum and 5,948 A. cajennense (s.l.). A total of 1,746 ticks from 77 localities were collected during field expeditions, and were identified as 249 A. cajennense (s.s.), 443 A. sculptum, and 1,054 A. cajennense (s.l.) [these A. cajennense (s.l.) ticks were considered to be males of either A. cajennense (s.s.) or A. sculptum]. At least 23 localities contained the presence of both A. cajennense (s.s.) and A. sculptum in sympatry. DNA sequences of the ITS2 gene of 50 ticks from 30 localities confirmed the results of the morphological analyses. The nymph of A. cajennense (s.s.) is morphologically very similar to A. sculptum. Our results confirmed that A. cajennense (s.l.) is currently represented in Brazil by only two species, A. cajennense (s.s.) and A. sculptum. While these species have distinct distribution areas in the country, they are found in sympatry in some transition areas. The current distribution of A. cajennense (s.l.) has important implications to public health, since in Brazil A. sculptum is the most important vector of the bacterium Rickettsia rickettsii, the etiological agent of Brazilian spotted fever.

136 citations


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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202346
2022320
20212,074
20202,208
20191,941
20181,865