SciELO - Scientific Electronic Library Online

 
vol.21 issue3Influence of subclinical infection by agents of tick fever in milking dairy cowsProductive performance of hair lambs, fed with fresh lemon pulp as an energy source author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Revista MVZ Córdoba

Print version ISSN 0122-0268

Rev.MVZ Cordoba vol.21 no.3 Córdoba Dec. 2016

https://doi.org/10.21897/rmvz.821 

EDITORIAL

Vector adaptation to microorganisms or adaptation of microorganisms to vectors?

Salim Mattar V

Marco González T


Forecasting the emergence of zoonotic infectious diseases and their geographical extent is a challenging task; this is despite recent technical advancements in the development of statistical and mathematical epidemiological tools for understanding disease distribution and dynamics. During the recent Ebola outbreak countries worldwide were concerned with transboundary transmission of infection fueled by enhanced human population mobility originating from infected countries in West Africa. Similarly, transboundary movement of live animals and their products can give rise to the introduction and spread of diseases of pandemic potential.

In the context of vector borne diseases, the mechanical translocation and subsequent adaptation of vectors between endemic and non-endemic areas is a common phenomenon that can lead to the introduction of infection; for example, it is well documented that the mosquito Aedes aegypti, vector of Yellow fever, Dengue, Chicungunya and Zika viruses was shipped by steamers along the Magdalena River from Cartagena in the 1880s 1. A century after the Yellow Fever epidemic in New Orleans and Alabama, the first outbreak of urban yellow fever arose in the state of Santander between 1906 and 1930; by the 1950's the mosquito had reached the south of the country.

In 2010 Aedes aegypti, had already been reported throughout the Colombian territory. This vector not only adapted and colonized rural environments where it originally emerged but also spread to sprawling urban landscapes; this is likely to contribute to the increase of urban transmission of diseases such as dengue hemorrhagic fever 2. In the past, infected mosquitoes traveled along rivers and canals but today their movement can be facilitated by road and airway networks. For this reason, the risk of vector borne diseases such as malaria, leishmaniasis or urban trypanosomiasis is becoming more of a concern in tropical countries like Colombia.

Recent evidence has demonstrated the presence of Zika and Chikungunya viruses in species of Culex mosquitoes 3. However, the detection of these viruses in Culex mosquitoes is not conclusive evidence of transmission in that their detection could be the result of recent bite of a transient viremic vertebrate. Whether Zika virus can effectively replicate in Culex requires further investigation. It is therefore important to conduct studies in Colombia and other Latin American countries to determine the role of wild and peridomestic vertebrates in the dynamics of viral transmission. While there is a greater frequency of Culex captures in peridomestic and rural areas of the Colombian Caribbean, preliminary entomological studies at our laboratory have shown the detection of dengue virus by PCR in Culex. However, neither Zika nor Chikungunya viruses were found in these investigations.

Not only arboviruses are changing their modes of transmission in association with vectors. The cat flea Ctenocephalides felis has traditionally been considered the only confirmed vector of Rickettsia felis; however, recent evidence has demonstrated that mosquitoes Anopheles gambiae -the main vector of malaria in sub-Saharan Africa- can be a competent vector for R. felis. Anopheles gambiae and Aedes albopictus mosquitoes are also a competent vector of R. felis4. In addition, R. felis has been detected in febrile patients in tropical areas where Aedes albopictus or Aedes aegypti readily bite humans. Therefore, it is very likely that Aedes spp mosquitoes might be able to transmit Rickettsia felis.

Recent evidence has also identified changing patterns of transmission of rodent borne diseases such as Leptospira, Hantavirus and Arenaviruses (including lymphocytic choriomeningitis virus). For example, while Leptospira and Lymphocytic choriomeningitis arenavirus are transmitted by urban rodents such as Rattus rattus and Mus muscullus, recent evidence suggests that wild rodents such as the New World Sigmodontins are chronic carriers of these roboviruses. Other mammals such as bats can act as reservoirs to groups of zoonotic bacteria, protozoa, viruses and fungi and are able to spread these pathogens over large distances, Including the Nipha, Hendra and Bat Lissa viruses, which are important zoonotic pathogens of bats in other parts of the world, especially in Australia and its neiborhoods countries. Little is known about the epidemiology of bat borne diseases in Colombia and other countries in Latin America and their role in the zoonotic transmission of viruses such as Ebola, coronavirus, influenza virus, dengue, and influenza among others 5.

The epidemiology and transmission dynamics of diseases transmitted by vectors, bats and rodents are currently a significant gap in knowledge in Latin America compared to other countries where diseases are endemic. The study of synanthropic and wild vectors is crucial in Latin America to better understand the adaptation and transmission of vector borne diseases, geographical boundaries, as well as the risk factors for their occurrence.

REFERENCES

1. Olano V. Aedes aegypti en el área rural: implicaciones en salud pública. Biomedica 2016; 36(2). [ Links ]

2. Kraemer MUG, Sinka ME, Duda KA, Mylne AQN, Shearer FM, Barker CM, et al. The global distribution of the arbovirus vectors Aedes aegypti and Ae. Albopictus. eLife 2015;4:e08347. DOI:10.7554/eLife.08347. [ Links ]

3. Huang YJ, Ayers VB, Lyons AC, Unlu I, Alto BW, Cohnstaedt LW, et al. Culex Species Mosquitoes and Zika Virus. Vector Borne Zoonotic Dis 2016; (10):673-6. DOI:10.1089/vbz.2016.2058 [ Links ]

4. Parola P, Musso D, Raoult D. Rickettsia felis: the next mosquito-borne outbreak?. Infection 2016; 116:1112-1113. DOI:10.1016/S1473-3099(16)30331-0 [ Links ]

5. Calderon A, Guzman C, Salazar-Bravo J, Figueiredo LT, Mattar S, Arrieta G. Viral Zoonoses That Fly with Bats: A Review. MANTER Journal of Parasite Biodiversity 2016; 6:1-13. DOI:10.13014/K2BG2KWF [ Links ]

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License