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Research Articles

Function and insecticidal activity of bacteria associated with papaya mealybug, Paracoccus marginatus Williams & Granara de Willink (Hemiptera: Pseudococcidae)

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Pages 762-778 | Received 26 Nov 2019, Accepted 03 May 2020, Published online: 27 May 2020
 

ABSTRACT

This study isolated and determined the functional characteristics of bacterial flora associated with mealybug (Paracoccus marginatus) and their application as a bio-control agent. Second and fourth nymphal instars of the papaya mealybug were used for the isolation of the bacteria. These isolates were assessed for chitinolytic, protease, and glutathione S-transferase (GST) activities as well as mealybug wax degradation. An in vitro experiment was conducted with the most efficient isolates to control mealybugs reared on potato plants. A total of 102 bacterial isolates were obtained from the second (50 isolates) and fourth nymphal (52 isolates) stages of papaya mealybug. From these, 33 isolates were positive for chitinolytic activity, 25 isolates for protease, and 29 isolates showed glutathione S-transferase (GST) activity. In addition, 21 isolates were able to utilise mealybug wax as a carbon source. Regarding nutritional significance, the bacterial isolates exhibited nitrogen fixation, sulfur oxidation, as well as phosphate, zinc, and silica solubilisation. The application of bacterial isolates, Bacillus cereus PYP3, Bacillus sp. PLB1 and Serratia marcescens FLGB16 exhibited the highest mortality rates of 78.7%, 74.0%, and 69.3%, respectively on the second nymphal stage of papaya mealybug. Mealybug associated bacteria showed significantly higher mealybug mortality compared to antibiotics (kanamycin, carbenicillin, and spectinomycin) and commercial chemicals (profenophos and chlorpyrifos) used in this study. These efficient bacterial isolates may have the potential to control the mealybug under field conditions.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This study was supported by the Rapid Grant for Young Investigator (RGYI), Department of Biotechnology (DBT), Ministry of Science and Technology, Government of India grant number BT/PR6430/GBD/27/412/2012.

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