Skip to main content
PLOS Neglected Tropical Diseases logoLink to PLOS Neglected Tropical Diseases
. 2020 Jul 23;14(7):e0008297. doi: 10.1371/journal.pntd.0008297

Marginalized mites: Neglected vectors of neglected diseases

Thomas Weitzel 1,2,*, Benjamin L Makepeace 3, Ivo Elliott 4,5, Kittipong Chaisiri 6, Allen L Richards 7, Paul N Newton 4,5
Editor: Andrew S Azman8
PMCID: PMC7377360  PMID: 32701946

Introduction

Trombiculid mites are tiny arthropods with a high species diversity and global distribution. The larvae (called “chiggers”) of some species are vectors of scrub typhus, a human febrile disease of potential lethality. Although scrub typhus threatens over a billion people within the Asia Pacific, its ecology is poorly understood compared to other vector-borne diseases. The recent discovery of scrub typhus in Chile and the Arabian Peninsula suggests a much wider distribution and highlights our profound knowledge gaps. How could scrub typhus be unrecognized outside Asia-Pacific region, where it has been known for more than 2,000 years? We hypothesize that the main reason is that scrub typhus is transmitted by mites, a vector group that has been overlooked by health organizations and scientists for decades. As a change of viewpoint, we suggest recognizing mites, these tiniest of all known arthropods transmitting infectious agents, as neglected vectors.

The expanding spectrum of chigger-borne rickettsioses

Since 2006, an unexpected endemic rickettsiosis, scrub typhus, was detected in various regions in southern Chile [13]. This ancient Asian-Pacific disease was unknown in the New World, and its discovery in South America raised many questions, including origin, distribution, and routes of transmission [4]. Speculations included an association with recent worldwide phenomena of globalization and climate change or the migration of animals such as rodents and birds [4,5]. The change of paradigm was supported by the isolation of a new species, Candidatus Orientia chuto, from a patient visiting the Arabian Peninsula and by additional serological and molecular data from countries in Africa, suggesting a much broader distribution of scrub typhus outside the traditional tsutsugamushi triangle [6].

Since trombiculid mites, the vector and reservoir of scrub typhus in the Asia Pacific, had never been documented in the Chilean region where scrub typhus was initially discovered, other vectors such as terrestrial leeches were suspected [1]. However, a recent study demonstrated that trombiculid mites are endemic in southern Chile and that they are infected with the Chilean Orientia strain [7]. Interestingly, the infected mites belong to the genus Herpetacarus, which has never been associated with scrub typhus elsewhere. Together with phylogenetic analyses, showing that the isolate from Chile is distinct to other Orientia species [8], these findings suggest an ancient origin rather than recent introduction of the pathogen. Thus, generations of medical doctors and scientists have missed this important rickettsial disease. As scrub typhus is effectively and inexpensively treated with tetracyclines, such disregard has key public health implications. How was this possible?

Chiggers: The neglected vector

The increasing awareness and research on vector-borne infections has led to tremendous advances in our knowledge of medically important arthropods. Similarly, the number of known rickettsial infections worldwide has more than tripled in the last three decades due to the use of new molecular diagnostic techniques [9]. How could this progress regarding arthropod-borne infections have spared scrub typhus, the rickettsial disease with the highest morbidity and mortality worldwide [10]?

We hypothesize that the principal cause is that scrub typhus is transmitted by trombiculid mites, a vector group that has been overlooked by health organizations and scientists for decades. Reasons behind this incomprehension might lay in the traditional association of these vectors with the (rather exotic) tsutsugamushi triangle, combined with methodological challenges related to their secluded life cycle and the minute size of larvae. The negligence also affects other mite-borne neglected diseases, such as rickettsial pox [11]. Therefore, mites, these smallest of all known arthropods transmitting infectious agents, should be recognized as neglected vectors. To underline this viewpoint, we assessed scientific interest in different arthropod vectors using PubMed entries (https://www.ncbi.nlm.nih.gov/pubmed) as a proxy. This surrogate analysis revealed that since 1950, the number of publications grew exponentially but only for mosquitos and ticks (Fig 1). In sharp contrast, the interest in mites as vectors was low during the past decades. It was not always so; there were reactive paroxysms of mite research during the medical emergency of scrub typhus in the Asia Pacific amongst combatants during World War II [5], but, even though the numbers affected must now be much greater, impetus declined dramatically. Following the logic of our analysis, the body of knowledge regarding mites as vectors in 2019 is at the same surrogate level it was for ticks and mosquitos in the years 1968 and 1973, respectively (1,100 to 1,200 cumulative publications). A similar “All Fields” search showed that the relationship between mites as vectors and climate change has almost been ignored up to now (11 publications), in comparison to mosquitos (513 publications) and ticks (245 publications). If the search was limited to “Title/Abstract,” the term “chigger OR trombiculid OR Leptotrombidium” scored 596 hits, compared to 15,798, 13,368, and 6,983 for Aedes, Anopheles, and Ixodes, respectively. A recent systematic review of Orientia ecology, the first since 1974 [12], also highlighted the limited knowledge on trombiculid mites; furthermore, many of the included studies were difficult to access and/or were published in Chinese, Japanese, Korean, or Russian [5].

Fig 1. PubMed results for “all fields” searches regarding certain arthropods as vector.

Fig 1

Numbers represent hits per decade (January 1, 1950 until December 31, 2019).

The scientific negligence of our understanding of mites as vectors seems pervasive. Although scrub typhus threatens more than 1 billion people worldwide [10], a recent “global brief on vector-borne diseases,” published by the World Health Organization (WHO), does not include mites as vectors [13]. Within the four conferences organized by the “European Network for Neglected Vectors and Vector-Borne Diseases (EurNegVec),” not a single presentation on mites can be found (https://www.eurnegvec.org/). Similarly, the main reviews on the impact of climate change on vector borne diseases published in 2019 do not mention trombiculid mites [14, 15], although climate is a key factor of their distribution [5].

A call for more mite research

There are no dedicated funding schemes, rare presentations at tropical medicine conferences, and very few acarologists worldwide able to morphologically distinguish trombiculid and other mites to species level. These experts are crucial, since genetic or proteomic identification techniques, which are available for mosquitos and ticks, are in their infancy for mites. Recognition of this data chasm might help to motivate more researchers and funding organizations to dedicate time and money to these tiny but important vectors. Indeed, it is highly likely that apart from chiggers, the blood-feeding gamasid mites are also involved in the transmission of a variety of known and unknown zoonotic infections. Both trombiculid and gamasid mites harbor a variety of potential bacterial pathogens and have been strongly implicated in the epidemiology of Korean hemorrhagic fever (Hantaan virus) [16,17]. Furthermore, they may have a role to play in vectoring Bartonella spp., Borrelia spp., and Rickettsia spp. [1820]. After decades of ignorance, there is an urgent need to catch up; trombiculid and other neglected mites might actually be more prolific and widespread vectors of zoonotic agents than is currently assumed.

Funding Statement

IE and PNN are supported by the Wellcome Trust and TW receives funding from by Fondo Nacional de Desarrollo Científico y Tecnológico FONDECYT (FONDECYT N° 1170810). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.Balcells ME, Rabagliati R, García P, Poggi H, Oddó D, Concha M, et al. Endemic scrub typhus-like illness, Chile. Emerg Infect Dis. 2011; 17: 1659–1663. 10.3201/eid1709.100960 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Weitzel T, Dittrich S, López J, Phuklia W, Martinez-Valdebenito C, Velásquez K, et al. Endemic scrub typhus in South America. N Engl J Med. 2016; 375: 954–961. 10.1056/NEJMoa1603657 [DOI] [PubMed] [Google Scholar]
  • 3.Weitzel T, Martínez-Valdebenito C, Acosta-Jamett G, Jiang J, Richards AL, Abarca K. Scrub typhus in continental Chile, 2016–2018. Emerg Infect Dis. 2019; 25: 1214–1217. 10.3201/eid2506.181860 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Walker DH. Scrub typhus—scientific neglect, ever-widening impact. N Engl J Med 2016; 375: 913–915. 10.1056/NEJMp1608499 [DOI] [PubMed] [Google Scholar]
  • 5.Elliott I, Pearson I, Dahal P, Thomas NV, Roberts T, Newton PN. Scrub typhus ecology: a systematic review of Orientia in vectors and hosts. Parasit Vectors. 2019; 12: 513 10.1186/s13071-019-3751-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Xu G, Walker DH, Jupiter D, Melby PC, Arcari CM. A review of the global epidemiology of scrub typhus. PLoS Negl Trop Dis. 2017; 11: e0006062 10.1371/journal.pntd.0006062 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Acosta-Jamett G, Martínez-Valdebenito C, Beltrami E, Silva-de la Fuente MC, Jiang J, Richards AL, et al. Identification of trombiculid mites (Acari: Trombiculidae) on rodents captured on Chiloé Island and molecular evidence of infection with Orientia species. PLoS Negl Trop Dis. 2020; 14: e0007619 10.1371/journal.pntd.0007619 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Abarca K, Martinez-Valdebenito C, Angulo J, Jiang J, Farris CM, Richards AL, et al. Molecular description of a novel Orientia species causing scrub typhus in South America. Emerg Infect Dis. 2020; 26 (9) (in press). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Parola P, Paddock CD, Socolovschi C, Labruna MB, Mediannikov O, Kernif T, et al. Update on tick-borne rickettsioses around the world: a geographic approach. Clin Microbiol Rev. 2013; 26: 657–702. 10.1128/CMR.00032-13 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Paris DH, Shelite TR, Day NP, Walker DH. Unresolved problems related to scrub typhus: a seriously neglected life-threatening disease. Am J Trop Med Hyg. 2013; 89: 301–307. 10.4269/ajtmh.13-0064 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Chikeka I, Dumler JS. Neglected bacterial zoonoses. Clin Microbiol Infect. 2015; 21: 404–415. 10.1016/j.cmi.2015.04.022 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Traub R, Wisseman CL Jr. The ecology of chigger-borne rickettsiosis (scrub typhus). J Med Entomol 1974; 11: 237–303. 10.1093/jmedent/11.3.237 [DOI] [PubMed] [Google Scholar]
  • 13.World Health Organization. A global brief on vector-borne diseases. Geneva: WHO Press, 2014. [cited 6 May 2020]. Available from: https://apps.who.int/iris/bitstream/handle/10665/111008/WHO_DCO_WHD_2014.1_eng.pdf. [Google Scholar]
  • 14.Caminade C, McIntyre KM, Jones AE. Impact of recent and future climate change on vector-borne diseases. Ann N Y Acad Sci. 2019; 1436: 157–173. 10.1111/nyas.13950 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Fouque F, Reeder JC. Impact of past and on-going changes on climate and weather on vector-borne diseases transmission: a look at the evidence. Infect Dis Poverty. 2019; 8: 51 10.1186/s40249-019-0565-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Chaisiri K, McGarry JW, Morand S, Makepeace BL. Symbiosis in an overlooked microcosm: a systematic review of the bacterial flora of mites. Parasitology. 2015; 142: 1152–1162. 10.1017/S0031182015000530 [DOI] [PubMed] [Google Scholar]
  • 17.Yu XJ, Tesh RB. The role of mites in the transmission and maintenance of Hantaan virus (Hantavirus: Bunyaviridae). J Infect Dis 2014; 210: 1693–1699. 10.1093/infdis/jiu336 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Kabeya H, Colborn JM, Bai Y, Lerdthusnee K, Richardson JH, Maruyama S, et al. Detection of Bartonella tamiae DNA in ectoparasites from rodents in Thailand and their sequence similarity with bacterial cultures from Thai patients. Vector Borne Zoonotic Dis. 2010; 10: 429–434. 10.1089/vbz.2009.0124 [DOI] [PubMed] [Google Scholar]
  • 19.Kampen H, Schöler A, Metzen M, Oehme R, Hartelt K, Kimmig P, et al. Neotrombicula autumnalis (Acari, Trombiculidae) as a vector for Borrelia burgdorferi sensu lato? Exp Appl Acarol. 2004; 33: 93–102. 10.1023/b:appa.0000029975.92510.90 [DOI] [PubMed] [Google Scholar]
  • 20.Linsuwanon P, Krairojananan P, Rodkvamtook W, Leepitakrat S, Davidson S, Wanja E. Surveillance for scrub typhus, rickettsial diseases, and leptospirosis in US and multinational military training exercise Cobra Gold sites in Thailand. US Army Med Dep J. 2018; 1–18: 29–39. [PubMed] [Google Scholar]

Articles from PLoS Neglected Tropical Diseases are provided here courtesy of PLOS

RESOURCES