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Journal articles on the topic 'Tropilaelaps mites'

Author: Grafiati

Published: 7 June 2025

Last updated: 16 July 2025

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1

Gill, Maggie C., Bajaree Chuttong, Paul Davies, et al. "Assessment of the efficacy of field and laboratory methods for the detection of Tropilaelaps spp." PLOS ONE 19, no. 9 (2024): e0301880. http://dx.doi.org/10.1371/journal.pone.0301880.

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Tropilaelaps spp. are invasive mites that cause severe disease in Apis mellifera colonies. The UK has deployed an elaborate surveillance system that seeks to detect these mites early in any invasion to allow the best opportunity to eradicate any incursion. Effective field and laboratory protocols, capable of reliably detecting low numbers of mites, are key to the success of any intervention. Here we compared the efficacy of established field monitoring using brood removal with an uncapping fork, and brood ‘bump’ methods with novel methods for Tropilaelaps detection modified from Varroa monitor

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2

Shrestha, Monica, Jakob Wegener, Ishan Gautam, Madhusudan Singh, Christoph Schwekendiek, and Kaspar Bienefeld. "Individual-Level Comparisons of Honey Bee (Hymenoptera: Apoidea) Hygienic Behavior Towards Brood Infested with Varroa destructor (Parasitiformes: Varroidae) or Tropilaelaps mercedesae (Mesostigmata: Laelapidae)." Insects 11, no. 8 (2020): 510. http://dx.doi.org/10.3390/insects11080510.

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The mites Varroa destructor Anderson and Trueman and Tropilaelaps mercedesae Anderson and Morgan are both serious threats to the Apis mellifera beekeeping industry. A trait frequently used in selection programs for V. destructor resistance is hygienic behavior, the selective removal of diseased/damaged brood. Here, we measured the level of association of the expression of hygienic behavior against both mites in A. mellifera, by observing whether the same individual bees would carry out the opening and removal of brood infested by the two parasites. The groups of bees showing these behaviors on

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3

Khongphinitbunjong, Kitiphong, Panuwan Chantawannakul, Orlando Yañez, and Peter Neumann. "Survival of Ectoparasitic Mites Tropilaelaps mercedesae in Association with Honeybee Hive Products." Insects 10, no. 2 (2019): 36. http://dx.doi.org/10.3390/insects10020036.

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The global trade of honeybee hive products imposes the risk of the introduction of exotic pests. However, data on the potential of specific products enabling pest survival are often lacking. This holds especially true for ectoparasitic mites Tropilaelaps spp., which are mandatory pests of honeybees in many countries. Here, we evaluated the longevity of Tropilaelaps mercedesae mites associated with empty honeycomb and dry pollen as two possible global import routes. Mites were able to survive up to three days in dry pollen and up to six days in empty honeycomb, thereby suggesting a sufficient t

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4

Anderson, Denis L., and John M. K. Roberts. "Standard methods for Tropilaelaps mites research." Journal of Apicultural Research 52, no. 4 (2013): 1–16. http://dx.doi.org/10.3896/ibra.1.52.4.21.

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5

Manic, Marija, Bosiljka Djuricic, and Z. Raicevic. "Tropilaelaps of bees - epizootiological picture with special emphasis on the first description of the parasite in bumblebees and bees in Serbia." Veterinarski glasnik 68, no. 5-6 (2014): 371–78. http://dx.doi.org/10.2298/vetgl1406371m.

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Honey bees are the most significant pollinators of plants worlwide. Importance of plant pollination widely exceeds all other economic benefits of modern beekeeping such as production of honey, Royal jelly, propolis, beeswax, honeybee venom etc. The issues concerning bees diseases are of extreme importance in modern commercial beekeeping. That especially regards to the fact that the number of disease agents in bees has considerably increased in recent decades. Using international transport, export or import of bees and their products, the possibility of entering various agents (parasites, bacte

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6

de Guzman, Lilia I., Geoffrey R. Williams, Kitiphong Khongphinitbunjong, and Panuwan Chantawannakul. "Ecology, Life History, and Management of Tropilaelaps Mites." Journal of Economic Entomology 110, no. 2 (2017): 319–32. http://dx.doi.org/10.1093/jee/tow304.

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7

Luo, Qi Hua, Ting Zhou, Qiang Wang, Ping Li Dai, Yan Yan Wu, and Huai Lei Song. "Identification of Tropilaelaps mites (Acari, Laelapidae) infesting Apis mellifera in China." Apidologie 42, no. 4 (2011): 485–98. http://dx.doi.org/10.1007/s13592-011-0028-6.

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8

de Guzman, Lilia I., Michael Simone-Finstrom, Cleofas Cervancia, Philip Tokarz, and Amanda M. Frake. "Tropilaelaps species identification and viral load evaluation of Tropilaelaps and Varroa mites and their Apis mellifera hosts in Palawan, Philippines." Journal of Invertebrate Pathology 170 (February 2020): 107324. http://dx.doi.org/10.1016/j.jip.2020.107324.

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9

Waghchoure-Camphor, Elizabeth S., and Stephen J. Martin. "Population changes of Tropilaelaps clareae mites in Apis mellifera colonies in Pakistan." Journal of Apicultural Research 48, no. 1 (2009): 46–49. http://dx.doi.org/10.3896/ibra.1.48.1.10.

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10

Chernik, M., and О. Prishchepchik. "Tropilelapsosis of bees as a potential threat to Belarusian beekeeping." Science and Innovations, no. 10 (November 13, 2024): 79–83. http://dx.doi.org/10.29235/18189857-2024-10-79-83.

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Tropilelapsosis of bees is a contagious disease of the brood of hon- ey bees caused by mites of the genus Tropilaelaps. The tense epizootic situation regarding this disease in the Russian Federation and a number of other countries is considered as a potential threat of the introduction of this parasite into the territory of the Republic of Belarus. This article provides an overview of scientific research on the biology and morphology of the pathogen, its distribution, the clinical manifestation of the disease, pathogenesis and diagnostic methods. Requirements are given to prevent the spread of

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11

MinOo, Hlaing, Parawee Kanjanaprachoat, Tipwan Suppasat, and Siriwat Wongsiri. "Honey Bee Virus Detection on Tropilaelaps and Varroa Mites in Chiang Mai Thailand." Journal of Apiculture 33, no. 2 (2018): 77–81. http://dx.doi.org/10.17519/apiculture.2018.06.33.2.77.

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12

Dong, Xiaofeng, Makiko Kashio, Guangda Peng, Xinyue Wang, Makoto Tominaga, and Tatsuhiko Kadowaki. "Isoform-specific modulation of the chemical sensitivity of conserved TRPA1 channel in the major honeybee ectoparasitic mite, Tropilaelaps mercedesae." Open Biology 6, no. 6 (2016): 160042. http://dx.doi.org/10.1098/rsob.160042.

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We identified and characterized the TRPA1 channel of Tropilaelaps mercedesae (TmTRPA1), one of two major species of honeybee ectoparasitic mite. Three TmTRPA1 isoforms with unique N-terminal sequences were activated by heat, and the isoform highly expressed in the mite's front legs, TmTRPA1b, was also activated by 27 plant-derived compounds including electrophiles. This suggests that the heat- and electrophile-dependent gating mechanisms as nocisensitive TRPA1 channel are well conserved between arthropod species. Intriguingly, one TmTRPA1 isoform, TmTRPA1a, was activated by only six compounds

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13

Nikanorova, Anna M., and Nadezhda D. Moskovskaya. "Tropilelapsosis and varroatosis are common bee infestations." Veterinariya, Zootekhniya i Biotekhnologiya 12/2, no. 132 (2024): 148–55. https://doi.org/10.36871/vet.zoo.bio.202412215.

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The spread of infestations in beekeeping is a serious problem that can cause significant damage to the ecosystem and agriculture. The two most common invasive bee diseases, tropilelapsosis and varroa, are widespread throughout the world and lead to significant losses in hive populations. The article is of a review nature. The common diseases tropilelapsosis and varroatosis are analyzed. Domestic and foreign literature sources were analyzed using the method of structuring and abstracting. Hemolymph-sucking mites weaken the health of bees and make them more vulnerable to other diseases and stres

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14

Suppasat, Tipwan, and Siriwat Wongsiri. "Morphometric and Genetic Variation of Tropilaelaps Mites Infesting Apis dorsata and A. mellifera in Thailand." Journal of Apiculture 33, no. 4 (2018): 227–37. http://dx.doi.org/10.17519/apiculture.2018.11.33.4.227.

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15

Boonmee, Thummanoon, Laedlugkana Wongthaveethong, Chainarong Sinpoo, Terd Disayathanoowat, Jeffery S. Pettis, and Veeranan Chaimanee. "Surface Modification of Materials by Atmospheric-Pressure Plasma to Improve Impregnation with Essential Oils for the Control of Tropilaelaps Mites in Honeybees (Apis mellifera)." Applied Sciences 12, no. 12 (2022): 5800. http://dx.doi.org/10.3390/app12125800.

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In this research, the absorption and release rate of the essential oil, Amomum krervanh, by seven different materials were evaluated. Cardboard showed the highest EO absorption capacity (0.93 ± 0.0052 μL of oil/mg of dry cardboard) followed by balsa wood and drawing board with the EO absorption of 0.77 ± 0.043 and 0.62 ± 0.010 μL of oil/mg of dry material, respectively. The results also demonstrated that cardboard had the highest EO retention (52.84 ± 0.687% after 20 min of analysis). Additionally, the essential oil was released from the drawing board and cardboard at the same rate during the

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16

Bertola, Michela, and Franco Mutinelli. "Sensitivity and Resistance of Parasitic Mites (Varroa destructor, Tropilaelaps spp. and Acarapis woodi) Against Amitraz and Amitraz-Based Product Treatment: A Systematic Review." Insects 16, no. 3 (2025): 234. https://doi.org/10.3390/insects16030234.

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Resistance to amitraz in Varroa destructor mites poses a significant challenge to global beekeeping, leading to the declining efficacy of treatments and increased colony losses. This study aims to comprehensively map, characterize, and analyze the status of amitraz efficacy and resistance in Varroa and other parasitic mites such as Tropilaelaps spp. and Acarapis woodi. A systematic review, following PRISMA 2020 guidelines, examined 74 studies, revealing substantial variability in experimental protocols, mite origins, and environmental factors, all of which impacted toxicity assessments. These

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17

FAN, QING-HAI, MARGOT CAMOIN, OLIVER QUINN, and RICHARD HALL. "Parasitic and phoretic mites of honeybees (Apis mellifera) from Wallis and Futuna." Zoosymposia 22 (November 30, 2022): 304. http://dx.doi.org/10.11646/zoosymposia.22.1.187.

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This is the first report of parasitic and phoretic mites on honeybee (Apis mellifera) from the south Pacific islands, Wallis and Futuna which have 12 registered beekeepers, 27 apiaries and 178 hives. Seventy eight samples were collected from 20 apiaries belonging to 11 beekeepers of the two main islands during a honeybee multi-pathogen survey in the framework of PROTEGE project implemented by SPC (South Pacific Community). A total of 8415 bees (including 7973 workers and 442 drones) were washed for external mites and thirty worker bees from each sample were examined for internal mites using th

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18

Pettis, Jeffery S., Robyn Rose, and Veeranan Chaimanee. "Chemical and cultural control of Tropilaelaps mercedesae mites in honeybee (Apis mellifera) colonies in Northern Thailand." PLOS ONE 12, no. 11 (2017): e0188063. http://dx.doi.org/10.1371/journal.pone.0188063.

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19

Anderson, Denis L., and Mathew J. Morgan. "Genetic and morphological variation of bee-parasitic Tropilaelaps mites (Acari: Laelapidae): new and re-defined species." Experimental and Applied Acarology 43, no. 1 (2007): 1–24. http://dx.doi.org/10.1007/s10493-007-9103-0.

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20

Ling, Tial C., Patcharin Phokasem, Chainarong Sinpoo, Panuwan Chantawannakul, Kitiphong Khongphinitbunjong, and Terd Disayathanoowat. "Tropilaelaps mercedesae Infestation Is Correlated with Injury Numbers on the Brood and the Population Size of Honey Bee Apis mellifera." Animals 13, no. 8 (2023): 1318. http://dx.doi.org/10.3390/ani13081318.

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Tropilaelaps mercedesae, one of the most devastating parasitic mites of honey bee Apis mellifera hosts, is a major threat to honey products by causing severe damage to honey bee colonies. Here, we recorded injury numbers caused by T. mercedesae to different body parts of the larval, pupal, and crippled adult stages of honey bee A. mellifera. We evaluated the relationship between infestation rate and injury numbers per bee for both larvae and pupae. We also noted the total bee numbers per beehive and examined the relationship between the infestation rate and population size. T. mercedesae infes

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21

Chaimanee, Veeranan, Natapot Warrit, Thummanoon Boonmee, and Jeffery S. Pettis. "Acaricidal activity of essential oils for the control of honeybee (Apis mellifera) mites Tropilaelaps mercedesae under laboratory and colony conditions." Apidologie 52, no. 3 (2021): 561–75. http://dx.doi.org/10.1007/s13592-021-00843-z.

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22

Khongphinitbunjong, Kitiphong, Lilia I. de Guzman, Ninat Buawangpong, Thomas E. Rinderer, Amanda M. Frake, and Panuwan Chantawannakul. "Observations on the removal of brood inoculated with Tropilaelaps mercedesae (Acari: Laelapidae) and the mite’s reproductive success in Apis mellifera colonies." Experimental and Applied Acarology 62, no. 1 (2013): 47–55. http://dx.doi.org/10.1007/s10493-013-9728-0.

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23

Mahmudov, S., F. Dunyamaliyev, M. Mammadov, and R. Najafov. "TROPİLAELAPS MİTES İN HONEYBEE COLONİES AND CONTROL MEASURES." Norwegian Journal of development of the International Science 147 (December 26, 2024). https://doi.org/10.5281/zenodo.14577652.

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<strong>Abstract</strong> Tropilaelaps mites are ectoparasitic organisms that feed on the hemolymph of honeybee pupae, leading to substantial damage to bee colonies. This infestation results in physical deformities in both pupae and adults, viral transmission, and a decline in colony productivity. The reproductive cycle of these mites is rapid and occurs exclusively within capped brood cells, which complicates effective control. Mitigation strategies include the application of formic acid, thymol, and queen bee caging. Research has demonstrated that appropriate intervention can halt mite proli

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24

Phokasem, Patcharin, Lilia I. de Guzman, Kitiphong Khongphinitbunjong, Amanda M. Frake, and Panuwan Chantawannakul. "Feeding by Tropilaelaps mercedesae on pre- and post-capped brood increases damage to Apis mellifera colonies." Scientific Reports 9, no. 1 (2019). http://dx.doi.org/10.1038/s41598-019-49662-4.

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Abstract Tropilaelaps mercedesae parasitism can cause Apis mellifera colony mortality in Asia. Here, we report for the first time that tropilaelaps mites feed on both pre- and post-capped stages of honey bees. Feeding on pre-capped brood may extend their survival outside capped brood cells, especially in areas where brood production is year-round. In this study, we examined the types of injury inflicted by tropilaelaps mites on different stages of honey bees, the survival of adult honey bees, and level of honey bee viruses in 4th instar larvae and prepupae. The injuries inflicted on different

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25

Naveen, Ashok S. Yadav, and Neeraj Kumar. "Seasonal Incidence of Ectoparasitic mites and Greater Wax Moth in Apis mellifera L. Colonies." Indian Journal of Entomology, February 18, 2022, 1–5. http://dx.doi.org/10.55446/ije.2021.145.

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The incidence of ectoparasitic mites Varroa destructor (Anderson and Trueman), Tropilaelaps clareae (Delfinado and Baker) and wax moth Galleria mellonella (L.) on the honey bee Apis mellifera L. was assessed during 2019-20 at the Krishi Vigyan Kendra, Morena, Madhya Pradesh. The results revealed that V. destructor infestation was at minimum (4%) in the first fortnight of July 2019 and maximum (14%) in the first fortnight of September 2019 with the visual examination method. There existed a negative correlation with the brood area. Tropilaelaps clareae infestation was minimum (6 mites/colony) i

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26

Han, Bin, Jiangli Wu, Qiaohong Wei, et al. "Life-history stage determines the diet of ectoparasitic mites on their honey bee hosts." Nature Communications 15, no. 1 (2024). http://dx.doi.org/10.1038/s41467-024-44915-x.

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AbstractEctoparasitic mites of the genera Varroa and Tropilaelaps have evolved to exclusively exploit honey bees as food sources during alternating dispersal and reproductive life history stages. Here we show that the primary food source utilized by Varroa destructor depends on the host life history stage. While feeding on adult bees, dispersing V. destructor feed on the abdominal membranes to access to the fat body as reported previously. However, when V. destructor feed on honey bee pupae during their reproductive stage, they primarily consume hemolymph, indicated by wound analysis, preferen

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27

Mohamadzade Namin, Saeed, Omid Joharchi, Sunil Aryal, et al. "Exploring genetic variation and phylogenetic patterns of Tropilaelaps mercedesae (Mesostigmata: Laelapidae) populations in Asia." Frontiers in Ecology and Evolution 12 (February 22, 2024). http://dx.doi.org/10.3389/fevo.2024.1275995.

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IntroductionThe mites belonging to the genus Tropilaelaps are ectoparasites of honey bees, primarily infesting the larval and pupal stages. Originating from subtropical regions, these mites can cause brood malformation, bee mortality, and subsequent decline or absconding of colonies.Material and methodsDuring field surveys conducted in Nepal, South Korea, and Uzbekistan to investigate honey bee pests, several populations of T. mercedesae were collected. This is the first record of T. mercedesae from Uzbekistan. The morphological characteristics of the collected populations were analyzed, and t

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28

Wei, Qiaohong, Jiangli Wu, Fengying Liu, et al. "Proteomics profiling of the honeybee parasite Tropilaelaps mercedesae across post-embryonic development." Scientific Data 11, no. 1 (2024). http://dx.doi.org/10.1038/s41597-024-03355-4.

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AbstractTropilaelaps mercedesae, an ectoparasitic mite of honeybees, is currently a severe health risk to Apis mellifera colonies in Asia and a potential threat to the global apiculture industry. However, our understanding of the physiological and developmental regulation of this pest remains significantly insufficient. Using ultra-high resolution mass spectrometry, we provide the first comprehensive proteomic profile of T. mercedesae spanning its entire post-embryonic ontogeny, including protonymphs, deutonymphs, mature adults, and reproductive mites. Consequently, a total of 4,422 T. mercede

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29

Pakwan, Chonthicha, Martin Kaltenpoth, Benjamin Weiss, Panuwan Chantawannakul, Guo Jun, and Terd Disayathanoowat. "Bacterial communities associated with the ectoparasitic mites Varroa destructor and Tropilaelaps mercedesae of the honey bee (Apis mellifera)." FEMS Microbiology Ecology 94, no. 1 (2017). http://dx.doi.org/10.1093/femsec/fix160.

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30

Truong, A.-Tai, Mi-Sun Yoo, Bo-Ram Yun, et al. "Prevalence and pathogen detection of Varroa and Tropilaelaps mites in Apis mellifera (Hymenoptera, Apidae) apiaries in South Korea." Journal of Apicultural Research, January 6, 2022, 1–9. http://dx.doi.org/10.1080/00218839.2021.2013425.

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31

Choi, Yong-Soo. "Molphological Analysis and Determination of Interference Competition between Two Honeybee Mites: Varroa destructor and Tropilaelaps clareae (Acari: Varroidae and Laelapidae)." Journal of Apiculture 29, no. 4 (2014). http://dx.doi.org/10.17519/apiculture.2014.11.29.4.327.

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32

Sankovitz, Madison, Nathalie Steinhauer, Tanawat Yemor, Steven C. Cook, Jay D. Evans, and Samuel D. Ramsey. "Evaluation of efficacy of formic acid and thermal remediation for management of Tropilaelaps and Varroa mites in central Thailand." Journal of Apicultural Research, May 16, 2025, 1–10. https://doi.org/10.1080/00218839.2025.2495393.

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