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49 results for “Bacterial symbiont”
Dataset 'Yeast facilitates the multiplication of Drosophila bacterial symbionts but has no effect on the form or parameters of Taylor's law'
<p>Dataset from the manuscript 'Yeast facilitates the multiplication of <em>Drosophila </em>bacterial symbionts but has no effect on the form or parameters of Taylor’s law' (2020)</p> <p>Each line corresponds to a single experimental unit.</p>
Figure 5 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 5. Phylogenetic tree based on 16S rRNA sequences of Cardinium, constructed by a neighbor-joining procedure. Cardinium strains are depicted by the host name. The accession numbers are shown after the host name. Numbers on the nodes indicate bootstrap percent confidence values.
Figure 2 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 2. Neighbor-joining tree of COI sequences of the Erythraeidae mites of the present study and the Genbank sequence data. Numbers above/below nodes represent bootstrap values.
Figure 1 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 1. Erythraeus (Erythraeus) pistacicus Haitlinger, Mehrnejad & Šundić, 2016 larva (Black arrow)inside the gall, feeding on the aphid, Forda hirsuta Mordvilko, 1928, on pistachio trees. June 2022, Mashhad, Northeast of Iran.
Figure 7 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 7. Phylogenetic relationship of Planomicrobium symbiont identified from Erythraeus (Erythraeus) pistacicus with related sequences retrieved from GenBank. The tree was constructed using neighbor-joining procedure. The sequence obtained from E. (E.) pistacicus in this study is in red box. Sequence from Bacillus subtilis was used as an
Figure 7 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 7. Scanning electron microscopy images of Steinernema beitlechemi infective juvenile and female. A–D: Infective juvenile. A: Head region with four papillae, amphid openings (a) and excretory pore (ep); B: Lateral field in mid-body (ridges numbered 1–6); C: Lateral field in tail region with anus and phasmid opening (arrow); D: Tail region with anus and phasmid openings (arrows), ventral view. E, F: First generation female. E: Vulva; F: Tail with mucron (m), ventro-lateral.
Figure 6 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 6. Storage of entomopathogenic nematodes in clear tissue culture flasks on the left and Tetrapak containers on the right.
Figure 3 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 3. White trap system with entomopathogenic nematode-infected Galleria mellonella and Tenebrio molitor cadavers. Color change of infected cadavers is observed a few days after death. Heterorhabdid- infected cadaver generally turns red (A and C); steinernematids- infected are brown, tan or even black (C and D).
Data from: How do host age and nutrition affect density regulation of obligate versus facultative bacterial symbionts? Insights from the tsetse fly
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Core symbionts, age at inoculation, and diet affect colonization of the bumble bee gut by a common bacterial pathogen
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No evidence of bacterial symbionts influencing host specificity in Aphis gossypii Glover (Hemiptera: Aphididae)
<p class="MDPI17abstract"><span>The cotton-melon aphid, <em>Aphis gossypii</em> Glover, is a polyphagous insect pest with many host-specialized biotypes, such as Cucurbitaceae- and Malvaceae-specialized (CU and MA) biotype. Bacterial symbionts were reported to determine host range in some aphids. Whether this is the case in<em> A. gossypii</em> remains unknown. Here, we tested host specificity of CU and MA biotype and compared host specificity between wingless and winged morph within the same biotype, and analyzed the composition of bacterial symbionts. The reproduction of CU and MA biotype reduced by 66.67% and 82.79% </span><span>res</span><span>pectively on non-native hosts, compared with that on native hosts. The composition of bacterial symbionts was not significantly different between CU and MA biotype, with <em>Buchnera</em> abundance >95% in both biotypes. While, winged morph produced significantly more nymphs than wingless morph on non-native hosts, and<a name="OLE_LINK1"></a> <em>Buchnera</em> abundance in winged morph was only about 10% of that in wingless morph. There seemed to be a relationship between <em>Buchnera</em> abundance and host specificity. We regulated <em>Buchnera</em> abundance by temperature and antibiotics, but did not find that low <em>Buchnera</em> abundance resulted in high reproduction on non-native hosts. We conclude that host specificity of <em>A. gossypii</em> is not controlled by specific bacterial symbionts or by <em>Buchnera</em> abundance.</span></p>
Figure 6 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 6. Haplotype network of Cardinium endosymbionts based on 16S rDNA sequences.
Figure 4 in New host detection of the parasitic mite, Erythraeus pistacicus (Trombidiformes: Erythraeidae) from Iran and indication of possible infection with bacterial symbionts
Figure 4. Haplotype network of Wolbachia endosymbionts based on wsp gene.
Figure 13 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 13. Sponge types which can be used for nematode storage and formulation.
Figure 2 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 2. Endotokia matricida stage of an entomopathogenic nematode.
Figure 12 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 12. Setup of infectivity bioassay in 24-well plates with tape to prevent escape of insects.
Figure 1 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 1. Life cycle of entomopathogenic nematode/bacteria complex in a lepidopteran insect.
Figure 10 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 10. Isolation of Xenorhabdus and Photorhabdus from Galleria mellonella hemolymph.
Figure 4 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 4. Steps in isolating entomopathogenic nematodes from soil.
Transmission of yeast and bacterial symbionts between sexual partners in Drosophila suzukii and Drosophila melanogaster
<p>Data from "Transmission of yeast and bacterial symbionts between sexual partners in Drosophila suzukii and Drosophila melanogaster"</p>
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