Increased number of intestinal villous M cells in levamisole -pretreated weaned pigs experimentally infected with F4ac+ enterotoxigenic Escherichia coli strain

Immunoprophylaxis of porcine postweaning colibacillosis (PWC) caused by enterotoxigenic Escherichia coli (ETEC) expressing F4 fimbriae is an unsolved problem. Just as ETEC strains can exploit intestinal microfold (M) cells as the entry portal for infection, their high transcytotic ability make them an attractive target for mucosally delivered vaccines, adjuvants and therapeutics. We have developed a model of parenteral/oral immunization of 4-weeks-old pigs with either levamisole or vaccine candidate F4ac+ non-ETEC strain to study their effects on de novo differentiation of antigen-sampling M cells. Identification, localization and morphometric quantification of cytokeratin 18 positive M cells in the ileal mucosa of 6-weeks-old pigs revealed that they were: 1) exclusively located within villous epithelial layer, 2) significantly numerous (P< 0.01) in levamisole pretreated/challenged pigs, and 3) only slightly, but not significantly numerous in vaccinated/challenged pigs compared with non-pretreated/challenged control pigs. The fact that levamisole may affect the M cells frequency by increasing their numbers, makes it an interesting adjuvant to study development of an effective M cell-targeted vaccine against porcine PWC

Effect of levamisole on the number of intestinal goblet cells in weaned pigs experimentally vaccinated against colibacillosis

VALPOTIĆ: Effect of levamisole on the number of intestinal goblet cells in weaned pigs experimentally vaccinated against colibacillosis. Vet. arhiv 79, 543-553, 2009. Postweaning colibacillosis (PWC) is an etiologically complex disease commonly induced by porcine F4ac + enterotoxigenic Escherichia coli (ETEC) for which no effective vaccine is available. The objective of this study was to determine the nonspecific immunomodulatory effect of levamisole in combination with specific intragastric immunization of weaned pigs with a candidate F4ac + non-ETEC oral vaccine on the population of intestinal goblet cells (GC). The pigs were immunized with F4ac + non-ETEC strain, in combination with or without levamisole. Seven days after immunization the pigs were challenged with F4ac + ETEC strain and 14 days following immunization they were euthanatized for sampling of specimens of the small intestine for immunohistochemistry and morphometric analyses. Samples of the ileum were tested for the presence of acidic and neutral carbohydrates, components of mucus produced and secreted by the intestinal goblet cells (GC). The volume density (V) of the PAS V + and AB +/PAS+ GC was determined using the stereological point-counting method. The Vv of the ileal PAS + GC was lowest (0.130 ± 0.075 mm3) in the pigs that were immunized wit

Worldwide diversity of endophytic fungi and insects associated with dormant tree twigs

International trade in plants and climate change are two of the main factors causing damaging tree pests (i.e. fungi and insects) to spread into new areas. To mitigate these risks, a large-scale assessment of tree-associated fungi and insects is needed. We present records of endophytic fungi and insects in twigs of 17 angiosperm and gymnosperm genera, from 51 locations in 32 countries worldwide. Endophytic fungi were characterized by high-throughput sequencing of 352 samples from 145 tree species in 28 countries. Insects were reared from 227 samples of 109 tree species in 18 countries and sorted into taxonomic orders and feeding guilds. Herbivorous insects were grouped into morphospecies and were identified using molecular and morphological approaches. This dataset reveals the diversity of tree-associated taxa, as it contains 12,721 fungal Amplicon Sequence Variants and 208 herbivorous insect morphospecies, sampled across broad geographic and climatic gradients and for many tree species. This dataset will facilitate applied and fundamental studies on the distribution of fungal endophytes and insects in trees

Climate, host and geography shape insect and fungal communities of trees

13 Pág.Non-native pests, climate change, and their interactions are likely to alter relationships between trees and tree-associated organisms with consequences for forest health. To understand and predict such changes, factors structuring tree-associated communities need to be determined. Here, we analysed the data consisting of records of insects and fungi collected from dormant twigs from 155 tree species at 51 botanical gardens or arboreta in 32 countries. Generalized dissimilarity models revealed similar relative importance of studied climatic, host-related and geographic factors on differences in tree-associated communities. Mean annual temperature, phylogenetic distance between hosts and geographic distance between locations were the major drivers of dissimilarities. The increasing importance of high temperatures on differences in studied communities indicate that climate change could affect tree-associated organisms directly and indirectly through host range shifts. Insect and fungal communities were more similar between closely related vs. distant hosts suggesting that host range shifts may facilitate the emergence of new pests. Moreover, dissimilarities among tree-associated communities increased with geographic distance indicating that human-mediated transport may serve as a pathway of the introductions of new pests. The results of this study highlight the need to limit the establishment of tree pests and increase the resilience of forest ecosystems to changes in climate.We gratefully acknowledge the financial support of the Swiss National Science Foundation (Project C15.0081) Grant 174644 and the Swiss Federal Office for the Environment Grant 00.0418.PZ/P193-1077. This work was supported by COST Action “Global Warning” (FP1401). CABI is an international intergovernmental organisation, and R.E., M.K., H.L. and I.F. gratefully acknowledge the core financial support from our member countries (and lead agencies) including the United Kingdom (Foreign, Commonwealth and Development Office), China (Chinese Ministry of Agriculture and Rural Affairs), Australia (Australian Centre for International Agricultural Research), Canada (Agriculture and Agri-Food Canada), Netherlands (Directorate General for International Cooperation), and Switzerland (Swiss Agency for Development and Cooperation). See https://www.cabi.org/aboutcabi/who-we-work-with/key-donors/ for full details. M.B. and M.K.H. were financially supported by the Slovak Research and Development Agency (Project APVV-19-0116). H.B. would like to thank the botanist Jorge Capelo who helped with Myrtaceae identification and INIAV IP for supporting her contribution to this study. Contributions of M. de G. and B.P. were financed through Slovenian Research Agency (P4-0107) and by the Slovenian Ministry of Agriculture, Forestry and Food (Public Forestry Service). G.C, C.B.E. and A.F.M. were supported by OTKA 128008 research grant provided by the National Research, Development and Innovation Office. Contributions of K.A. and R.D. were supported by the Estonian Research Council grants PSG136 and PRG1615. M.J.J., C.L.M. and H.P.R. were financially supported by the 15. Juni Fonden (Grant 2017-N-123). P.B., B.G. and M.Ka. were financially supported by the Ministry of Science and Higher Education of the Republic of Poland for the University of Agriculture in Krakow (SUB/040013-D019). C.N. was financially supported by the Slovak Research and Development Agency (Grant APVV-15-0531). N.K. was partially supported by the Russian Science Foundation (grant № 22-16-00075) [species identification] and the basic project of Sukachev Institute of Forest SB RAS (№ FWES-2021-0011) [data analysis]. R.OH. was supported by funding from DAERA, and assistance from David Craig, AFBI. T.P. thanks the South African Department of Forestry, Fisheries and the Environment (DFFE) for funding noting that this publication does not necessarily represent the views or opinions of DFFE or its employees. In preparing the publication, materials of the bioresource scientific collection of the CSBG SB RAS “Collections of living plants indoors and outdoors” USU_440534 (Novosibirsk, Russia) were used. M.Z. was financially supported by Ministry of Science, Technological Development and Innovation of the Republic of Serbia (contract no. 451-03-47/2023-01/200197). We acknowledge the Genetic Diversity Centre (GDC) at ETH Zurich for providing computational infrastructure and acknowledge the contribution of McGill University and Génome Québec Innovation Center (Montréal, Quebec, Canada) for pair-end sequencing on Illumina MiSeq. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Peer reviewe

MORPHOLOGICAL CHANGES IN ASTACUS ASTACUS GONADS DURING THE REPRODUCTIVE CYCLE

The reproductive cycle of Astacus astacus was described by the external observation of the gonads, recording changes in the gonadosomatic index (GSI) and by the histological analysis of the reproductive organs. A total of 37 males and 13 females of Astacus astacus were collected from the Vukovina gravel pit located at northwest Croatia from May 2003 until January 2004. All crayfish were mature with total body lengths between 7.84 and 13.7 cm and weights between 16 and 125 g. There was a pronounced difference between the GSI values of the sexes. GSI fluctuated within a very small range (between 0.2 and 1.5%) in males while in females it increased up to 12.3% during the mating season. The external appearance of the testes and ovaries during the reproductive cycle was compared with the histological sections of germ cells in the testes, the vas deferens and ovaries. Besides the germinative cells, the morphological changes in testis and vasa deferentia of A. astacus extended also to the connective tissue and secretory epithelium. The maturation of germinative cells was synchronized, both in testes and ovaries

MORPHOLOGICAL CHANGES IN ASTACUS ASTACUS GONADS DURING THE REPRODUCTIVE CYCLE

The reproductive cycle of Astacus astacus was described by the external observation of the gonads, recording changes in the gonadosomatic index (GSI) and by the histological analysis of the reproductive organs. A total of 37 males and 13 females of Astacus astacus were collected from the Vukovina gravel pit located at northwest Croatia from May 2003 until January 2004. All crayfish were mature with total body lengths between 7.84 and 13.7 cm and weights between 16 and 125 g. There was a pronounced difference between the GSI values of the sexes. GSI fluctuated within a very small range (between 0.2 and 1.5%) in males while in females it increased up to 12.3% during the mating season. The external appearance of the testes and ovaries during the reproductive cycle was compared with the histological sections of germ cells in the testes, the vas deferens and ovaries. Besides the germinative cells, the morphological changes in testis and vasa deferentia of A. astacus extended also to the connective tissue and secretory epithelium. The maturation of germinative cells was synchronized, both in testes and ovaries