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- Chad (2)
- 16S amplicons (1)
- A. versicolor (1)
- Aeolian (1)
- Aspergillus sydowii (1)
- Bodélé Depression (1)
- Desert sand (1)
- Desert soil (1)
- Deserts (1)
- Eukaryota (1)
Ancient mariners knew that dust whipped up from deserts by strong winds travelled long distances, including over oceans. Satellite remote sensing revealed major dust sources across the Sahara. Indeed, the Bodélé Depression in the Republic of Chad has been called the dustiest place on earth. We analysed desert sand from various locations in Chad and dust that had blown to the Cape Verde Islands. High throughput sequencing techniques combined with classical microbiological methods showed that the samples contained a large variety of microbes well adapted to the harsh desert conditions. The most abundant bacterial groupings in four different phyla included: (a) Firmicutes—Bacillaceae, (b) Actinobacteria—Geodermatophilaceae, Nocardiodaceae and Solirubrobacteraceae, (c) Proteobacteria—Oxalobacteraceae, Rhizobiales and Sphingomonadaceae, and (d) Bacteroidetes—Cytophagaceae. Ascomycota was the overwhelmingly dominant fungal group followed by Basidiomycota and traces of Chytridiomycota, Microsporidia and Glomeromycota. Two freshwater algae (Trebouxiophyceae) were isolated. Most predominant taxa are widely distributed land inhabitants that are common in soil and on the surfaces of plants. Examples include Bradyrhizobium spp. that nodulate and fix nitrogen in Acacia species, the predominant trees of the Sahara as well as Herbaspirillum (Oxalobacteraceae), a group of chemoorganotrophic free-living soil inhabitants that fix nitrogen in association with Gramineae roots. Few pathogenic strains were found, suggesting that African dust is not a large threat to public health.
Desert dust seeds distant lands and waters
with minerals as well as micro-organisms raising the
question of whether this ancient phenomenon also
spreads pathogens across the globe. Severe dust
storms require strong winds blowing over land-masses
that are largely devoid of vegetation, effectively
limiting the scope for winds to raise pathogens into
the air. Nevertheless, changing patterns of land-use,
often driven by belligerency, result in refugees
spreading to areas that were previously deemed barely
habitable. With the help of the International Committee
of the Red Cross, a number of sand/dust samples
were collected from the Republic of Chad, some near
refugee camps, others further removed from human
influence. In parallel studies, we documented the
micro-organisms present in these samples and used a
number of the isolates here to test the effect of
environmental constraints on their ability to survive
intercontinental flight. We also added traditional
pathogens to the palette of microbes and tested the
effects of UV irradiation, desiccation and temperature
on survival of both bacteria and fungi. A clear trend
was obvious—those microbes that are coloured or able
to form conidia or spores (in other words, those that
are native to deserts) were well able to resist the
imposed stresses. On the other hand, most pathogens
were more sensitive to stresses than the environmental
isolates. Toxin production in two species of Aspergillus
was also investigated. Short-term desiccation
(simulating environmental conditions during intercontinental
travel) of sand amended with fungal spores
containing sterigmatocystin leads to increased mycotoxin
contents, but significant mycotoxin production
was only possible under growth-permissive conditions,
e.g. at higher humidity. It thus seems likely that an ever-decreasing fraction of the initial pathogen load
survives as the dust recedes from its desert source and
that those organisms that land on other continents are
highly enriched in desert dwellers.
Microbiological studies on the intercontinental transport of dust are confounded by the difficulty of obtaining sufficient material for analysis. Axenic samples of dust collected at high altitudes or historic specimens in museums are often so small and precious that the material can only be sacrificed when positive results are assured. With this in mind, we evaluated current methods and developed new ones in an attempt to catalogue all microbes present in small dust or sand samples. The methods used included classical microbiological approaches in which sand extracts were plated out on a variety of different media, polymerase chain reaction (PCR)-based amplification of 16S/18S rRNA sequences followed by construction of clone libraries, PCR amplification of 16S rRNA sequences followed by high-throughput sequencing (HtS) of the products and direct HtS of DNA extracted from the sand. A representative sand sample collected at Bahaï Wadi in the desert of the Republic of Chad was used. HtS with or without amplification showed the most promise and can be performed on ≤100 ng DNA. Since living microbes are often required, current best practices would involve geochemical and microscopic characterisation of the sample, followed by DNA isolation and direct HtS. Once the microbial content of the sample has been deciphered, growth conditions (including media) can be tailored to isolate the micro-organisms of interest.