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      The Bacterium Pantoea ananatis Modifies Behavioral Responses to Sugar Solutions in Honeybees

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          Honeybees are important pollinators, and may contribute to the spread of plant bacteria during their foraging trips. Some of these bacteria, such as Pantoea ananatis, can become deleterious to crops, leading to leaf blotches, die-back, bulb rot, and fruit rot. It is unknown whether honeybees sense the bacteria in the nectar of flowers. We aimed to determine if bees can perceive these bacteria in sugar solutions and if they are deterred by them. Our results indicate that honeybees can perceive these plant bacteria only in high concentrations, which deters them from drinking the respective sugar solution. They may therefore spread P. ananatis bacteria between flowers in field-realistic densities during foraging.

          Abstract

          1. Honeybees, which are among the most important pollinators globally, do not only collect pollen and nectar during foraging but may also disperse diverse microbes. Some of these can be deleterious to agricultural crops and forest trees, such as the bacterium Pantoea ananatis, an emerging pathogen in some systems. P. ananatis infections can lead to leaf blotches, die-back, bulb rot, and fruit rot. 2. We isolated P. ananatis bacteria from flowers with the aim of determining whether honeybees can sense these bacteria and if the bacteria affect behavioral responses of the bees to sugar solutions. 3. Honeybees decreased their responsiveness to different sugar solutions when these contained high concentrations of P. ananatis but were not deterred by solutions from which bacteria had been removed. This suggests that their reduced responsiveness was due to the taste of bacteria and not to the depletion of sugar in the solution or bacteria metabolites. Intriguingly, the bees appeared not to taste ecologically relevant low concentrations of bacteria. 4. Synthesis and applications. Our data suggest that honeybees may introduce P. ananatis bacteria into nectar in field-realistic densities during foraging trips and may thus affect nectar quality and plant fitness.

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          Importance of pollinators in changing landscapes for world crops.

          The extent of our reliance on animal pollination for world crop production for human food has not previously been evaluated and the previous estimates for countries or continents have seldom used primary data. In this review, we expand the previous estimates using novel primary data from 200 countries and found that fruit, vegetable or seed production from 87 of the leading global food crops is dependent upon animal pollination, while 28 crops do not rely upon animal pollination. However, global production volumes give a contrasting perspective, since 60% of global production comes from crops that do not depend on animal pollination, 35% from crops that depend on pollinators, and 5% are unevaluated. Using all crops traded on the world market and setting aside crops that are solely passively self-pollinated, wind-pollinated or parthenocarpic, we then evaluated the level of dependence on animal-mediated pollination for crops that are directly consumed by humans. We found that pollinators are essential for 13 crops, production is highly pollinator dependent for 30, moderately for 27, slightly for 21, unimportant for 7, and is of unknown significance for the remaining 9. We further evaluated whether local and landscape-wide management for natural pollination services could help to sustain crop diversity and production. Case studies for nine crops on four continents revealed that agricultural intensification jeopardizes wild bee communities and their stabilizing effect on pollination services at the landscape scale.
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            How many flowering plants are pollinated by animals?

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              The Economic Value of Ecological Services Provided by Insects

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                Author and article information

                Journal
                Insects
                Insects
                insects
                Insects
                MDPI
                2075-4450
                12 October 2020
                October 2020
                : 11
                : 10
                : 692
                Affiliations
                [1 ]Behavioral Physiology & Sociobiology, Biocenter, Am Hubland, University of Würzburg, 97074 Würzburg, Germany; strauss.sina@ 123456web.de (S.S.); markus.thamm@ 123456uni-wuerzburg.de (M.T.)
                [2 ]Department of Biosciences, University of Salzburg, Hellbrunnerstraße 34, 5020 Salzburg, Austria; gerardfa1987@ 123456gmail.com (G.F.-A.); robert.junker@ 123456uni-marburg.de (R.R.J.)
                [3 ]Evolutionary Ecology of Plants, Department Biodiversity of Plants, Faculty of Biology, Philipps-University Marburg, Karl-von-Frisch-Str. 8, 35043 Marburg, Germany
                Author notes
                Article
                insects-11-00692
                10.3390/insects11100692
                7601739
                33053745
                7c02636e-c8e1-45d1-a0e6-b93dc4a9b4ad
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 30 August 2020
                : 07 October 2020
                Categories
                Article

                plant bacteria,bacterial spread,sucrose responsiveness,apis mellifera

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