SREEVIDYA MEESALA

Dr. SREEVIDYA MEESALA


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 October 2013 in SpringerPlus
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Subramaniam GopalakrishnanSubramaniam Gopalakrishnan
Subramaniam Gopalakrishnan
VSVadlamudi Srinivas
Vadlamudi Srinivas
SMSREEVIDYA MEESALA
SREEVIDYA MEESALA
Abhishek RathoreAbhishek Rathore
Abhishek Rathore
Five strains of Streptomyces (CAI-24, CAI-121, CAI-127, KAI-32 and KAI-90) were earlier reported by us as biological control agents against Fusarium wilt of chickpea caused by Fusarium oxysporum f. sp. ciceri (FOC). In the present study, the Streptomyces were characterized for enzymatic activities, physiological traits and further evaluated in greenhouse and field for their plant growth promotion (PGP) of sorghum and rice. All the Streptomyces produced lipase, β-1-3-glucanase and chitinase (except CAI-121 and CAI-127), grew in NaCl concentrations of up to 6%, at pH values between 5 and 13 and temperatures between 20 and 40°C and were highly sensitive to Thiram, Benlate, Captan, Benomyl and Radonil at field application level. When the Streptomyces were evaluated in the greenhouse on sorghum all the isolates significantly enhanced all the agronomic traits over the control. In the field, on rice, the Streptomyces significantly enhanced stover yield (up to 25%; except CAI-24), grain yield (up to 10%), total dry matter (up to 18%; except CAI-24) and root length, volume and dry weight (up to 15%, 36% and 55%, respectively, except CAI-24) over the control. In the rhizosphere soil, the Streptomyces significantly enhanced microbial biomass carbon (except CAI-24), nitrogen, dehydrogenase (except CAI-24), total N, available P and organic carbon (up to 41%, 52%, 75%, 122%, 53% and 13%, respectively) over the control. This study demonstrates that the selected Streptomyces which were antagonistic to FOC also have PGP properties.

18 December 2012 in SpringerPlus
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Subramaniam GopalakrishnanSubramaniam Gopalakrishnan
Subramaniam Gopalakrishnan
HUHari D Upadhyaya
Hari D Upadhyaya
SVSrinivas Vadlamudi
Srinivas Vadlamudi
PHPagidi Humayun
Pagidi Humayun
SMSREEVIDYA MEESALA
SREEVIDYA MEESALA
OROm Rupela
Om Rupela
The amplitude of the acoustic startle response is increased when elicited in the presence of brief cues that predict shock (fear-potentiated startle) and also when elicited during sustained exposure to bright light (light-enhanced startle). Although both effects are thought to reflect fear or anxiety, their neuroanatomical substrates differ. Although fear-potentiated startle is disrupted by reversible inactivation of the central nucleus of the amygdala (CeA) but not the closely related bed nucleus of the stria terminalis (BNST), light-enhanced startle is disrupted by BNST inactivation but not by CeA inactivation. Intraventricular infusions of corticotropin-releasing factor (CRF) also increase startle (CRF-enhanced startle) and this effect is mediated by CRF receptors within the BNST, with no involvement of the CeA. Together, these observations suggest that CeA- and BNST-dependent fear and anxiety may be differentially sensitive to CRF receptor blockade. We tested this by orally administering the novel, potent, and selective CRF-R1 antagonist GSK876008 to rats before CRF-enhanced, light-enhanced, or fear-potentiated startle testing. GSK876008 disrupted CRF-enhanced startle with a linear dose–response curve, and light-enhanced startle with a U-shaped dose–response curve, but did not disrupt fear-potentiated startle to a visual stimulus at any dose tested, and even augmented the response in some animals. GSK876008 also disrupted shock-related ‘baseline’ startle increases, which may have reflected context conditioning (shown elsewhere to also be BNST-dependent). Overall, these results suggest that short-duration CeA-dependent threat responses can be pharmacologically dissociated from longer duration BNST-dependent responses in terms of their sensitivity to CRF1 receptor antagonists.


21 May 2016 in African Journal of Microbiology Research
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SMSREEVIDYA MEESALA
SREEVIDYA MEESALA
GSGopalakrishnan Subramaniam
Gopalakrishnan Subramaniam
In our earlier investigation, a fungal isolate Penicillium citrinum VFI-51 and its secondary metabolite was reported to have antagonistic potential against Botrytis cinerea, the causative agent of Botrytis gray mold disease in chickpea. In the present investigation, P. citrinum VFI-51 was further evaluated for its antagonistic potential against Macrophomina phaseolina, the causative agent of charcoal rot in sorghum. P. citrinum VFI-51 inhibited M. phaseolina in both dual culture as well as secondary metabolite production assays. In the in vivo blotter paper assay, under light chamber conditions, P. citrinum VFI-51 controlled 85% of the charcoal rot disease on the roots when compared to the positive control. Under greenhouse conditions, when M. phaseolina was inoculated by tooth pick method in to the stalk of sorghum plant, the charcoal rot disease was controlled by 75% in P. citrinum VFI-51 treatment over the positive control. This study demonstrates the biocontrol potential of P. citrinum VFI-51 against charcoal rot of sorghum. Key words: Macrophomina phaseolina, charcoal rot, sorghum, Penicillium citrinum VFI-51, biocontrol.