Evidence map›Paper›PMID 42087480›Full record

ArticleMicroscopy research and technique2026

Ultrastructural Insights Into the Reproductive Anatomy and Eggs of Cotton Pink Bollworm, Pectinophora gossypiella Saunders (Lepidoptera: Gelechiidae).

K Logeswaran, Suresh R Jambagi, Vinithashri Gautam, T Venkatesan, D Sagar, S N Sushil, M Mohan

Abstract read
In one paragraph

Article in Microscopy research and technique, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

K LogeswaranDivision of Genomic Resources, ICAR - National Bureau of Agricultural Insect Resources, Bengaluru, Karnataka, India.ORCID https://orcid.org/0009-0000-4529-8072
Suresh R JambagiDivision of Genomic Resources, ICAR - National Bureau of Agricultural Insect Resources, Bengaluru, Karnataka, India.ORCID https://orcid.org/0000-0002-4678-8396
Vinithashri GautamDivision of Genomic Resources, ICAR - National Bureau of Agricultural Insect Resources, Bengaluru, Karnataka, India.
T VenkatesanDivision of Genomic Resources, ICAR - National Bureau of Agricultural Insect Resources, Bengaluru, Karnataka, India.
D SagarDivision of Genomic Resources, ICAR - National Bureau of Agricultural Insect Resources, Bengaluru, Karnataka, India.
S N SushilDivision of Genomic Resources, ICAR - National Bureau of Agricultural Insect Resources, Bengaluru, Karnataka, India.
M MohanDivision of Genomic Resources, ICAR - National Bureau of Agricultural Insect Resources, Bengaluru, Karnataka, India.ORCID https://orcid.org/0000-0002-2327-6988

Funding

Indian Council of Agricultural Research
6 · The paper itself

Abstract

The pink bollworm, Pectinophora gossypiella Saunders is a major pest of cotton, notorious for its high reproductive potential and rapid evolution of resistance to Bacillus thuringiensis (Bt) toxins. Despite its economic significance, detailed knowledge of its reproductive anatomy and egg ultrastructure has remained limited, constraining the development of advanced molecular control strategies such as CRISPR/Cas9-based genome editing. The present study provides the first comprehensive characterization of the reproductive system and egg surface morphology of P. gossypiella using stereomicroscopy and scanning electron microscopy (SEM) techniques. The male reproductive system consists of fused, bean-shaped testes, seminal vesicles, duplex and simplex ejaculatory ducts, and paired accessory glands. The female reproductive system comprises paired ovaries with four polytrophic ovarioles per ovary, lateral and common oviducts, accessory glands, corpus bursae, and spermathecal glands. Eggs are oval, dorsoventrally flattened, exhibit a reticulated chorion with distinct micropylar and aeropylar regions. SEM images revealed 6-9 rosette cells encircling a circular micropylar plate, 14-19 first order and 17-23 s order ribs, and 250-291 polygonal surface cells. The structural features of P. gossypiella eggs reveal key sites for sperm entry, aeropylar respiration, and candidate zones for microinjection in gene editing applications. These findings establish a morphological baseline critical for optimizing embryo manipulation and ribonucleoprotein (RNP) delivery in lepidopteran genome editing. This study represents a pioneering effort to integrate classical egg morphology with molecular entomology, thereby advancing precision genetic interventions aimed at resistance management and population suppression in P. gossypiella.

Indexed as

MothsOvumAnimalsFemaleMaleMicroscopy, Electron, ScanningReproductionchorionic architecturemicropylar rosettemicroscopypink bollwormreproductive anatomy

Identifiers

PMID42087480
PMCPMC13535890

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.