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Purpose <p><i>Anopheles stephensi</i>, a malaria vector in South Asia and parts of the Middle East, has been detected as an invasive species in numerous African countries in recent years. It threatens to increase malaria disease burden and reverse gains made in malaria control and elimination. To halt further expansion, it is critical to understand the biological characteristics that may have facilitated <i>An. stephensi</i> range expansion. In its invasive range, <i>An. stephensi</i> larvae have been found to colonize artificial containers, many of which are shared with <i>Aedes aegypti</i>. The success of <i>Ae. aegypti</i> as an invasive vector is often attributed to the use of artificial containers and the ability of <i>Ae. aegypti</i> eggs to remain viable in the absence of water for months. While <i>An. stephensi</i> is found in artificial containers, it is unclear whether the eggs can remain viable without water for extended periods.</p> Methods <p>In this study, we used two laboratory strains of <i>An. stephensi</i> (SDA500 and STE2) and one <i>Ae. aegypti</i> strain (LVP-IB12) to evaluate 1) whether <i>An. stephensi</i> eggs can remain viable like <i>Ae. aegypti</i> when egg substrates are completely dried and 2) assess egg viability duration at varying temperatures when eggs are held on a moistened substrate in a high humidity environment.</p> Results <p><i>An. stephensi</i> egg viability and subsequent larval survival was observed consistently when moistened egg sheets were held at 15&#xa0;˚C in a high humidity environment for up to 14 days in both strains. <i>An. stephensi</i> eggs were not viable when completely dried, except when the protocol was amended to include a 15&#xa0;°C storage temperature. Though egg viability and larval survival was observed in the amended protocol for SDA500 and STE2 (16% and 21% respectively), it was significantly less than that of LVP-IB12 (83%) and was only observed in the eggs stored for the shortest time point.</p> Conclusions <p>These findings suggest that <i>An. stephensi</i> may remain viable if eggs are transported under ideal conditions (15&#xa0;˚C and &gt;75% RH) through trade routes. Thus, the persistence of <i>An. stephensi</i> eggs in the absence of water should be considered in programs that engage in surveillance and control of <i>An. stephensi</i> in Africa.</p> Graphical Abstract <p></p>

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An evaluation of longitudinal Anopheles stephensi egg viability and resistance to desiccation at different thermal conditions over time

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年1月24日

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  • Laura Leite,
  • Jeanne N. Samake,
  • Fitsum G. Tadesse,
  • Seth R. Irish,
  • Ellen M. Dotson,
  • Sarah Zohdy

摘要

Purpose

Anopheles stephensi, a malaria vector in South Asia and parts of the Middle East, has been detected as an invasive species in numerous African countries in recent years. It threatens to increase malaria disease burden and reverse gains made in malaria control and elimination. To halt further expansion, it is critical to understand the biological characteristics that may have facilitated An. stephensi range expansion. In its invasive range, An. stephensi larvae have been found to colonize artificial containers, many of which are shared with Aedes aegypti. The success of Ae. aegypti as an invasive vector is often attributed to the use of artificial containers and the ability of Ae. aegypti eggs to remain viable in the absence of water for months. While An. stephensi is found in artificial containers, it is unclear whether the eggs can remain viable without water for extended periods.

Methods

In this study, we used two laboratory strains of An. stephensi (SDA500 and STE2) and one Ae. aegypti strain (LVP-IB12) to evaluate 1) whether An. stephensi eggs can remain viable like Ae. aegypti when egg substrates are completely dried and 2) assess egg viability duration at varying temperatures when eggs are held on a moistened substrate in a high humidity environment.

Results

An. stephensi egg viability and subsequent larval survival was observed consistently when moistened egg sheets were held at 15 ˚C in a high humidity environment for up to 14 days in both strains. An. stephensi eggs were not viable when completely dried, except when the protocol was amended to include a 15 °C storage temperature. Though egg viability and larval survival was observed in the amended protocol for SDA500 and STE2 (16% and 21% respectively), it was significantly less than that of LVP-IB12 (83%) and was only observed in the eggs stored for the shortest time point.

Conclusions

These findings suggest that An. stephensi may remain viable if eggs are transported under ideal conditions (15 ˚C and >75% RH) through trade routes. Thus, the persistence of An. stephensi eggs in the absence of water should be considered in programs that engage in surveillance and control of An. stephensi in Africa.

Graphical Abstract