Vector-borne diseases result from the transmission of pathogens, including bacteria, parasites or viruses, by different hematophagous insects such as mosquitoes, phlebotomine sandflies, black flies, ticks, fleas, lice and triatomines, among others [1]. These vectors can transmit infectious pathogens between humans, animals, and vice versa throughout their lifetime with each bite or subsequent ingestion of blood [2].
These diseases account for over 17% of all global infectious diseases and cause more than 700,000 deaths per year [3]. Vector control is the primary method of combating these diseases, as there are often no alternative drug treatments or vaccines available [4]. Another approach is addressing the interactions between pathogens, hosts and the environment, which are crucial in understanding the emergence or re-emergence of these diseases [5].
Culicid mosquitoes are the most significant biological vectors in terms of morbidity and mortality associated with vector-borne diseases. Globally, there are an estimated 219 million cases of malaria transmitted by anopheline mosquitoes, causing more than 400,000 deaths per year. Aedes mosquitoes are responsible for the transmission of dengue, the most prevalent viral infection, along with other arboviruses such as Zika, Chikungunya and Mayaro, which have spread in recent years. The situation with West Nile virus (mainly linked to Culex mosquitoes) is similar, and this zoonosis is now considered endemic not only in the original foci in Africa, but also in other continents such as Europe and the Americas [3]. Also noteworthy is the presence of sandflies and ticks, both of which are implicated in the transmission of diseases that significantly impact humans. Among the most important diseases associated with them are leishmaniosis and phlebovirus infections, as well as Lyme encephalitis/disease and Crimean–Congo hemorrhagic fever, respectively.
The transmission of a wide range of vector-borne diseases is being influenced by climate change as vectors move to latitudes and altitudes higher than those that were previously reported [6].
The aim of this Special Issue was to bring together various studies about the presence of vectors, the spread and causes of vector-borne diseases, and vector–pathogen interactions including bionomic studies, surveillance projects and control experiences, among others. A study conducted by Wang et al. [7] found that high doses of X-rays could be used to reduce the sterility of Ae. albopictus males in a laboratory setting. However, they had no effect on egg numbers but did significantly reduce the survival time and hatching rate. Claver et al. [8] reported relatively modest vector competence for Aedes aegypti in Vientiane, Lao PDR, to transmit the Asian and ECSA-IOL lineages of chikungunya virus, which may be influenced by the longevity and density of female mosquitoes. Leandro et al. [9] evaluated the spatial and temporal association between vector infestation and the occurrence of dengue cases and reported a dynamic pattern indicating significant risks in certain areas of Foz do Iguaçu, Brazil, based on the entomological–virological index, while entomological indices were not effective in measuring dengue risk. Another study tested the efficacy of modifications to sewerage structures as an alternative to the use of biocides to prevent the breeding of Culex pipiens and Aedes albopictus in Barcelona, Spain [10]. Placing a concrete layer on the bottom of the sand sewers to prevent water accumulation completely eliminated mosquito breeding and, therefore, the need for biocides in the modified structures. Moreno-Gómez et al. [11] evaluated the effectiveness of the insecticide pyrethroid transfluthrin in providing protection against A. albopictus bites in humans, reporting high protection with mosquito mortality declining rapidly. In their comprehensive review, Morchón et al. [12] shed light on the epidemiological landscape of heartworm disease in Europe, uncovering its alarming spread and establishment as an endemic condition. The authors discuss a diverse array of dirofilariosis vectors and highlight key factors fueling this expansion, such as climate change, the emergence of new vectors, pet mobility, urbanization and the proliferation of irrigated crop regions. González et al. [13] providing new records for the Dominican catalogue of Diptera (Culex salinarius for the Greater Antilles, Culicoides jamaicensis for Hispaniola, and Culicoides haitiensis and Culicoides borinqueni for the Dominican Republic) consisting of the first COI DNA sequences available from different Diptera in GenBank. They discussed the spatial distribution, feeding preferences, and diagnostic features of closely related specimens in the Caribbean region. Guillot et al. [14] demonstrated that active sentinel surveillance of nymphal ticks provides a sustainable system for tracking enzootic risk for Lyme disease in southern Quebec. Lastly, Alevi et al. [15] presented the state-of-the-art taxonomy of the entire subfamily Triatominae, highlighting the transition from classical studies to the use of integrative taxonomy.
Acknowledgments
We are grateful to the contributing authors, to the anonymous referees, and to the Editorial Staff of Pathogens for their excellent and tireless work, which made this Special Issue possible.
Author Contributions
R.M. wrote the first draft of this editorial, and all authors edited the manuscript. All authors have read and agreed to the published version of the manuscript.
Conflicts of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
References
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