A Symbiotic Virus Facilitates Aphid Adaptation to Host Plants by Suppressing Jasmonic Acid Responses

Symbiotic viruses exist in many insects; however, their functions in host insects are not well understood. In this study, we explored the role of acyrthosiphon pisum virus (APV) in the interaction of its host aphid Acyrthosiphon pisum with plants. APV is primarily located in aphid salivary glands and gut and propagated in the insect. APV is horizontally transmitted to host plants during aphid feeding, but the virus does not replicate in the host plant. When the pea host race of aphids colonized two low-fitness plants, Medicago truncatula and Vicia villosa, the virus titers in both the aphids and plants significantly increased. Furthermore, APV infection strongly promoted the survival rate of the pea host race on V. villosa. Transcriptomic analysis showed that only 0.85% of aphid genes responded to APV infection when aphids fed on V. villosa, with a fold change in transcript levels of no more than fourfold. The improved survival due to APV infection was apparently related to the inhibitory effect of the virus on levels of phytohormone jasmonic acid (JA) and JA-isoleucine. Our data suggest a benefit of the symbiotic virus to its aphid host and demonstrate a novel case of symbiotic virus-mediated three-species interaction.

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Functional response of Harmonia axyridis preying on Acyrthosiphon pisum nymphs: the effect of temperature

Scientific Reports ◽

10.1038/s41598-021-92954-x ◽

2021 ◽

Vol 11 (1) ◽

Author(s):

Yasir Islam ◽

Farhan Mahmood Shah ◽

Xu Rubing ◽

Muhammad Razaq ◽

Miao Yabo ◽

...

Keyword(s):

Functional Response ◽

High Performance ◽

Acyrthosiphon Pisum ◽

Harmonia Axyridis ◽

Effect Of Temperature ◽

Functional Responses ◽

Aphid Control ◽

Host Aphid ◽

Predator Foraging

AbstractIn the current study, we investigated the functional response of Harmonia axyridis adults and larvae foraging on Acyrthosiphon pisum nymphs at temperatures between 15 and 35 °C. Logistic regression and Roger’s random predator models were employed to determine the type and parameters of the functional response. Harmonia axyridis larvae and adults exhibited Type II functional responses to A. pisum, and warming increased both the predation activity and host aphid control mortality. Female and 4th instar H. axyridis consumed the most aphids. For fourth instar larvae and female H. axyridis adults, the successful attack rates were 0.23 ± 0.014 h−1 and 0.25 ± 0.015 h−1; the handling times were 0.13 ± 0.005 h and 0.16 ± 0.004 h; and the estimated maximum predation rates were 181.28 ± 14.54 and 153.85 ± 4.06, respectively. These findings accentuate the high performance of 4th instar and female H. axyridis and the role of temperature in their efficiency. Further, we discussed such temperature-driven shifts in predation and prey mortality concerning prey-predator foraging interactions towards biological control.

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Temperature-Dependent Functional Response of Harmonia Axyridis Pallas (Coleoptera: Coccinellidae) Preying on Acyrthosiphon Pisum (Harris) (Hemiptera: Aphididae) Nymphs

10.21203/rs.3.rs-439244/v1 ◽

2021 ◽

Author(s):

Yasir Islam ◽

Farhan Mahmood Shah ◽

Xu Rubing ◽

Muhammad Razaq ◽

Miao Yabo ◽

...

Keyword(s):

Functional Response ◽

High Performance ◽

Acyrthosiphon Pisum ◽

Harmonia Axyridis ◽

Functional Responses ◽

Aphid Control ◽

Host Aphid ◽

Functional Response Models ◽

Biocontrol Potential

Abstract Functional response models are often used to understand the foraging interactions and determine the suitable biocontrol agents. We determined the functional response of Harmonia axyridis to nymph Acyrthosiphon pisum at different but constant temperatures (between 15 and 35 °C) and prey densities. Logistic regression and Roger’s random predator models were employed to determine the type and parameters of functional response. Harmonia axyridis larvae and adults exhibited Type II functional responses to different densities of A. pisum. Warming increased both the predation activity and host aphid control mortality. The 4th instar and female H. axyridis consumed the most aphids. Warming contributed markedly in accelerating the predator action. For fourth instar larvae and female H. axyridis adult, the successful attack rates were 0.234 ± 0.014 h−1 and 0.247 ± 0.015 h−1; the handling times were 0.132 ± 0.005 h and 0.156 ± 0.004 h; and the estimated maximum predation rates were 181.28 ± 14.54 and 153.85 ± 4.06, respectively. These findings accentuate the high performance of 4th instar and female H. axyridis and the role of temperature in their efficiency. Further studies exploring intraguild predation and mutual interference will be required to conclude the biocontrol potential of H. axyridis to A. pisum.

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Host recognition and acceptance behaviour in two aphid parasitoid species: Aphidius ervi and Aphidius microlophii (Hymenoptera: Braconidae)

Bulletin of Entomological Research ◽

10.1017/s0007485300032235 ◽

1994 ◽

Vol 84 (1) ◽

pp. 57-64 ◽

Cited By ~ 29

Author(s):

F. Pennacchio ◽

M.C. Digilio ◽

E. Tremblay ◽

A. Tranfaglia

Keyword(s):

Acyrthosiphon Pisum ◽

Selection Process ◽

Host Choice ◽

Aphid Species ◽

Host Recognition ◽

Aphidius Ervi ◽

Aphid Parasitoid ◽

Host Aphid ◽

Close Range

AbstractThe host preference and acceptance behaviour of populations of Aphidius ervi Haliday and A. microlophii Pennacchio & Tremblay from southern Italy was investigated. In no host-choice conditions, A. ervi females showed significantly higher attack and oviposition rates on the natural host Acyrthosiphon pisum (Harris) than on the non-host aphid Microlophium carnosum (Buckton)(Homoptera: Aphididae). In contrast, A. microlophii, which specifically parasitizes M. carnosum in the field, attacked both aphid species. However, dissections showed that oviposition of A. microlophii occurred only in a few of the attacked Acyrthosiphon pisum and was significantly less frequent than in M. carnosum. These results were confirmed in experimental host-choice conditions, suggesting that Aphidius microlophii oviposition is possibly regulated by a host haemolymphatic kairomone. Hybrids obtained by crossing A. ervi females with A. microlophii males attacked and oviposited in both aphid species, suggesting that these behavioural events have a strong genetic basis. The oviposition into host or non-host aphids did not elicit an immune defence reaction. The presence of the host's food-plant had no evident close-range effects on parasitoid attack and oviposition in non-host aphids. Aphidius microlophii reared on the non-host aphid Acyrthosiphon pisum produced a significant higher number of mummies after a few generations, suggesting a possible role of larval and early adult conditioning in the host selection process. These results, together with those from previous studies, suggest that Aphidius ervi is best considered as a complex of differentiated populations, characterized by a varying degree of genetic divergence.

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Effect of Dipyridamole on Spontaneous Platelet Aggregation in Whole Blood Decreases with the Time After Venepuncture: Evidence for the Role of ADP

Thrombosis and Haemostasis ◽

10.1055/s-0038-1645978 ◽

1987 ◽

Vol 58 (02) ◽

pp. 744-748 ◽

Cited By ~ 11

Author(s):

A R Saniabadi ◽

G D O Lowe ◽

J C Barbenel ◽

C D Forbes

Keyword(s):

Platelet Aggregation ◽

Correlation Coefficient ◽

Whole Blood ◽

Blood Platelet ◽

Inhibitory Effect ◽

Time Interval ◽

Adp Receptor ◽

Spontaneous Platelet Aggregation

SummarySpontaneous platelet aggregation (SPA) was studied in human whole blood at 3, 5, 10, 20, 30, 40 and 60 minutes after venepuncture. Using a whole blood platelet counter, SPA was quantified by measuring the fall in single platelet count upon rollermixing aliquots of citrated blood at 37° C. The extent of SPA increased with the time after venepuncture, with a correlation coefficient of 0.819. The inhibitory effect of dipyridamole (Dipy) on SPA was studied: (a) 10 μM at each time interval; (b) 0.5-100 μM at 3 and 30 minutes and (c) 15 μM in combination with 100 μM adenosine, 8 μM 2-chloroadenosine (2ClAd, an ADP receptor blocker) and 50 μM aspirin. There was a rapid decrease in the inhibitory effect of Dipy with the time after venepuncture; the correlation coefficient was -0.533. At all the concentrations studied, Dipy was more effective at 3 minutes than at 30 minutes after venepuncture. A combination of Dipy with adenosine, 2ClAd or aspirin was a more effective inhibitor of SPA than either drug alone. However, when 15 μM Dipy and 10 μM Ad were added together, the inhibitory effect of Dipy was not increased significantly, suggesting that Dipy inhibits platelet aggregation independent of Ad. The increase in SPA with the time after venepuncture was abolished when blood was taken directly into the anticoagulant containing 5 μM 2ClAd. It is suggested that ADP released from the red blood cells is responsible for the increased platelet aggregability with the time after venepuncture and makes a serious contribution to the artifacts of in vitro platelet function studies.

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Effect of human galanin on the response of circulating catecholamines to hypoglycemia in man

Acta Endocrinologica ◽

10.1530/eje.0.1330723 ◽

1995 ◽

Vol 133 (6) ◽

pp. 723-728 ◽

Cited By ~ 4

Author(s):

Ettore C degli Uberti ◽

Maria R Ambrosio ◽

Marta Bondanelli ◽

Giorgio Transforini ◽

Alberto Valentini ◽

...

Keyword(s):

Heart Rate ◽

Healthy Subjects ◽

Sympathetic Nerve Activity ◽

Heart Rate Response ◽

Statistical Significance ◽

Inhibitory Effect ◽

Amino Acid Residues ◽

Nerve Activity ◽

Receptor Stimulation

degli Uberti EC, Ambrosio MR, Bondanelli M, Trasforini G, Valentini A, Rossi R, Margutti A, Campo M. Effect of human galanin on the response of circulating catecholamines to hypoglycemia in man. Eur J Endocrinol 1995;133:723–8. ISSN 0804–4643 Human galanin (hGAL) is a neuropeptide with 30 amino acid residues that has been found in the peripheral and central nervous system, where it often co-exists with catecholamines. In order to clarify the possible role of hGAL in the regulation of sympathoadrenomedullary function, the effect of a 60 min infusion of hGAL (80 pmol·kg−1 · min−1) on plasma epinephrine and norepinephrine responses to insulin-induced hypoglycemia in nine healthy subjects was investigated. Human GAL administration significantly reduced both the release of basal norepinephrine and the response to insulin-induced hypoglycemia, whereas it attenuated the epinephrine response by 26%, with the hGAL-induced decrease in epinephrine release failing to achieve statistical significance. Human GAL significantly increased the heart rate in resting conditions and clearly exaggerated the heart rate response to insulin-induced hypoglycemia, whereas it had no effect on the blood pressure. We conclude that GAL receptor stimulation exerts an inhibitory effect on basal and insulin-induced hypoglycemia-stimulated release of norepinephrine. These findings provide further evidence that GAL may modulate sympathetic nerve activity in man but that it does not play an important role in the regulation of adrenal medullary function. Ettore C degli Uberti, Chair of Endocrinology, University of Ferrara, Via Savonarola 9, I-44100 Ferrara, Italy

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Biological role of AKT, and regulation of AKT signaling pathway by thymoquinone: perspectives in cancer therapeutics

Mini-Reviews in Medicinal Chemistry ◽

10.2174/1389557520666201005143818 ◽

2020 ◽

Vol 20 ◽

Author(s):

Md. Junaid ◽

Yeasmin Akter ◽

Syeda Samira Afrose ◽

Mousumi Tania ◽

Md. Asaduzzaman Khan

Keyword(s):

Clinical Trials ◽

Signaling Pathways ◽

Signaling Pathway ◽

Inhibitory Effect ◽

Akt Signaling ◽

Review Article ◽

Therapeutic Drug ◽

Akt Signaling Pathway ◽

Anti Cancer

Background: AKT/PKB is an important enzyme with numerous biological functions, and its overexpression is related to the carcinogenesis. AKT stimulates different signaling pathways that are downstream of activated tyrosine kinases and phosphatidylinositol 3-kinase, hence functions as an important target for anti-cancer drugs. Objective: In this review article, we have interpreted the role of AKT signaling pathways in cancer and natural inhibitory effect of Thymoquinone (TQ) in AKT and its possible mechanism. Method: We have collected the updated information and data on AKT, their role in cancer and inhibitory effect of TQ in AKT signaling pathway from google scholar, PubMed, Web of Science, Elsevier, Scopus and many more. Results: There are many drugs already developed, which can target AKT, but very few among them have passed clinical trials. TQ is a natural compound, mainly found in black cumin, which has been found to have potential anti-cancer activities. TQ targets numerous signaling pathways, including AKT, in different cancers. In fact, many studies revealed that AKT is one of the major targets of TQ. The preclinical success of TQ suggests its clinical studies on cancer. Conclusion: This review article summarizes the role of AKT in carcinogenesis, its potent inhibitors in clinical trials, and how TQ acts as an inhibitor of AKT and TQ’s future as a cancer therapeutic drug.

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The Immunomodulatory Role of G2013 (α-L-Guluronic Acid) on the Expression of TLR2 and TLR4 in HT29 cell line

Current Drug Discovery Technologies ◽

10.2174/1570163815666180226093711 ◽

2019 ◽

Vol 16 (1) ◽

pp. 91-95 ◽

Cited By ~ 4

Author(s):

Hamid Farhang ◽

Laleh Sharifi ◽

Mohammad Mehdi Soltan Dallal ◽

Mona Moshiri ◽

Zahra Norouzbabaie ◽

...

Keyword(s):

Inflammatory Responses ◽

Inflammatory Diseases ◽

Rna Extraction ◽

Cell Plate ◽

Inhibitory Effect ◽

Control Group ◽

Ht29 Cells ◽

Guluronic Acid ◽

Tlr4 Mrna

Background: The non-steroidal anti-inflammatory drugs (NSAIDs) play crucial role in the controlling of inflammatory diseases. Due to the vast side effects of NSAIDs, its use is limited. G2013 or &#945;-L-Guluronic Acid is a new NSAID with immunomodulatory features. Objectives: Considering the leading role of TLRs in inflammatory responses, in this study, we aimed to evaluate G2013 cytotoxicity and its effect on the expression of TLR2 and TLR4 molecules. Methods: HEK293-TLR2 and HEK293-TLR4 cells were cultured and seeded on 96-well cell plate, and MTT assay was performed for detecting the viability of the cells after treatment with different concentrations of G2013. HT29 cells were grown and treated with low and high doses of G2013. After total RNA extraction and cDNA synthesis, quantitative real-time PCR were performed to assess the TLR2 and TLR4 mRNA synthesis. Results: We found that concentrations of ≤125 &#181;g/ml of G2013 had no apparent cytotoxicity effect on the HEK293-TLR2 and -TLR4 cells. Our results indicated that after G2013 treatment (5 &#181;g/ml) in HT29 cells, TLR2 and TLR4 mRNA expression decreased significantly compared with the untreated control group (p=0.02 and p=0.001 respectively). Conclusion: The results of this study revealed that G2013 can down regulate the TLR2 and TLR4 gene expression and exerts its inhibitory effect. Our findings are parallel to our previous finding which showed G2013 ability to down regulate the signaling pathway of TLRs. However, further studies are needed to identify the molecular mechanism of G2013.<p>

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Albizia chinensis bark extract ameliorates the genotoxic effect of cyclophosphamide

Bulletin of the National Research Centre ◽

10.1186/s42269-020-00422-9 ◽

2020 ◽

Vol 44 (1) ◽

Author(s):

Marian Nabil ◽

Entesar E. Hassan ◽

Neven S. Ghaly ◽

Fawzia A. Aly ◽

Farouk R. Melek ◽

...

Keyword(s):

Folk Medicine ◽

Inhibitory Effect ◽

Protective Role ◽

Bark Extract ◽

Repeated Treatment ◽

Mouse Bone Marrow ◽

Sperm Abnormalities ◽

Wide Range ◽

Different Doses

Abstract Background The genus Albizia (Leguminoseae) is used in folk medicine for the treatment of a wide range of ailments. Recently, saponins from plant origin have attracted much attention. Saponins are recorded to have a broad range of biological and pharmacological activities. This study was performed to evaluate the protective role of Albizia chinensis bark methanolic extract (MEAC) against the genotoxicity induced by cyclophosphamide (CP) using different mutagenic parameters. Results The results showed that MEAC induced an inhibitory effect against chromosomal aberrations of CP in mouse bone marrow and spermatocytes. Such effect was found to be significant (p < 0.01) with a dose of 100 mg/kg treated once for 24 h and also after repeated treatment at a dose of 25 mg/kg for 7 days. In sperm abnormalities, the protective effect of Albizia extract showed a dose-related relationship. Different doses of MEAC (25, 50, and 100 mg/kg) significantly (p < 0.01) ameliorated sperm abnormalities induced by CP dose-dependently. The percentage of sperm abnormalities was decreased to 5.14 ± 0.72 in the group of animals treated with CP plus MEAC (100 mg/kg) indicating an inhibitory effect of about 50%. Conclusion MEAC at the doses examined was non-genotoxic compared to control (negative) and exhibited a protective role against CP genotoxicity.

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POSSIBLE ROLE OF 5α-ANDROSTANE-3α,17β-DIOL IN THE CONTROL OF FOLLICLE-STIMULATING HORMONE SECRETION IN THE IMMATURE FEMALE RAT

Journal of Endocrinology ◽

10.1677/joe.0.0920037 ◽

1982 ◽

Vol 92 (1) ◽

pp. 37-42 ◽

Cited By ~ 10

Author(s):

H. M. A. MEIJS-ROELOFS ◽

P. KRAMER ◽

L. GRIBLING-HEGGE

Keyword(s):

Inhibitory Action ◽

Combined Treatment ◽

Hormone Secretion ◽

Inhibitory Effect ◽

Ovariectomized Rats ◽

Female Rat ◽

Immature Rat ◽

Rat Strain ◽

Intact Rats

A possible role of 5α-androstane-3α,17β-diol (3α-androstanediol) in the control of FSH secretion was studied at various ages in ovariectomized rats. In the rat strain used, vaginal opening, coincident with first ovulation, generally occurs between 37 and 42 days of age. If 3α-androstanediol alone was given as an ovarian substitute, an inhibitory effect on FSH release was evident with all three doses tested (50, 100, 300 μg/100 g body wt) between 13 and 30 days of age; at 33–35 days of age only the 300 μg dose caused some inhibition of FSH release. Results were more complex if 3α-androstanediol was given in combined treatment with oestradiol and progesterone. Given with progesterone, 3α-androstanediol showed a synergistic inhibitory action on FSH release between 20 and 30 days of age. However, when 3α-androstanediol was combined with oestradiol a clear decrease in effect, as compared to the effect of oestradiol alone, was found between 20 and 30 days of age. Also the effect of combined oestradiol and progesterone treatment was greater than the effect of combined treatment with oestradiol, progesterone and 3α-androstanediol. At all ages after day 20 none of the steroid combinations tested was capable of maintaining FSH levels in ovariectomized rats similar to those in intact rats. It is concluded that 3α-androstanediol might play a role in the control of FSH secretion in the immature rat, but after day 20 the potentially inhibitory action of 3α-androstanediol on FSH secretion is limited in the presence of oestradiol.

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F4/80+ Kupffer Cell-Derived Oncostatin M Sustains the Progression Phase of Liver Regeneration through Inhibition of TGF-β2 Pathway

Molecules ◽

10.3390/molecules26082231 ◽

2021 ◽

Vol 26 (8) ◽

pp. 2231

Author(s):

Qingjun Lu ◽

Hao Shen ◽

Han Yu ◽

Jing Fu ◽

Hui Dong ◽

...

Keyword(s):

Liver Regeneration ◽

Serum Levels ◽

Inhibitory Effect ◽

Regenerative Process ◽

Oncostatin M ◽

Hepatocyte Proliferation ◽

Initiation Phase ◽

Distinct Role

The role of Kupffer cells (KCs) in liver regeneration is complicated and controversial. To investigate the distinct role of F4/80+ KCs at the different stages of the regeneration process, two-thirds partial hepatectomy (PHx) was performed in mice to induce physiological liver regeneration. In pre- or post-PHx, the clearance of KCs by intraperitoneal injection of the anti-F4/80 antibody (α-F4/80) was performed to study the distinct role of F4/80+ KCs during the regenerative process. In RNA sequencing of isolated F4/80+ KCs, the initiation phase was compared with the progression phase. Immunohistochemistry and immunofluorescence staining of Ki67, HNF-4α, CD-31, and F4/80 and Western blot of the TGF-β2 pathway were performed. Depletion of F4/80+ KCs in pre-PHx delayed the peak of hepatocyte proliferation from 48 h to 120 h, whereas depletion in post-PHx unexpectedly led to persistent inhibition of hepatocyte proliferation, indicating the distinct role of F4/80+ KCs in the initiation and progression phases of liver regeneration. F4/80+ KC depletion in post-PHx could significantly increase TGF-β2 serum levels, while TGF-βRI partially rescued the impaired proliferation of hepatocytes. Additionally, F4/80+ KC depletion in post-PHx significantly lowered the expression of oncostatin M (OSM), a key downstream mediator of interleukin-6, which is required for hepatocyte proliferation during liver regeneration. In vivo, recombinant OSM (r-OSM) treatment alleviated the inhibitory effect of α-F4/80 on the regenerative progression. Collectively, F4/80+ KCs release OSM to inhibit TGF-β2 activation, sustaining hepatocyte proliferation by releasing a proliferative brake.

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