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Chagas disease is a leading cause of non-ischemic cardiomyopathy in endemic regions of Central and South America. In Belize, Triatoma dimidiata sensu lato has been identified as the predominate taxon but vectorial transmission of Chagas disease is considered to be rare in the country. We recently identified an acute case of vector-borne Chagas disease in the northern region of Belize. Here we present a subsequent investigation of triatomines collected around the case-patient's home. We identified yet undescribed species, closely related to Triatoma huehuetenanguensis vector by molecular systematics methods occurring in the peridomestic environment. The identification of a T. cruzi-positive, novel species of Triatoma in Belize indicates an increased risk of transmission to humans in the region and warrants expanded surveillance and further investigation. [ABSTRACT FROM AUTHOR]

Soft ticks from the Ornithodoros genus are vectors of relapsing fever (RF) spirochetes around the world. In Mexico, they were originally described in the 19th century. However, few recent surveillance studies have been conducted in Mexico, and regions where RF spirochetes circulate remain vague. Here, the presence of soft ticks in populated areas was assessed in two sites from the Mexican states of Aguascalientes and Zacatecas. Argasidae ticks were collected, identified by morphology and mitochondrial 16S rDNA gene sequencing, and tested for RF borreliae. The specimens in both sites were identified as Ornithodoros turicata but no RF spirochetes were detected. These findings emphasize the need to update the distribution of these ticks in multiple regions of Mexico and to determine the circulation of RF borreliosis in humans and domestic animals. [ABSTRACT FROM AUTHOR]

This work is a comparative genomics investigation of the aromatic and xenobiotic compound degradation capabilities and heavy metal resistance of environmental bacterial isolates previously identified by our lab, Achromobacter xylosoxidans ADAF13, Exiguobacterium sp. KKBO11, Ochrobactrum anthropi FRAF13, Pseudomonas putida CBF10-2, Pseudomonas stutzeri ODKF13, Rhizobium radiobacter GHKF11, and Stenotrophomonas maltophilia CBF10-1. This work sought to assess the potential of these isolates as bioremediation tools. We found a variety of aromatic degradation pathways though none directly acts on industrial compounds such as polycyclic aromatic compounds, benzene, phthalate, or xylene. Achromobacter xylosoxidans ADAF13, P. putida CBF10-2, and P. stutzeri ODKF13 showed the most complete pathways for aromatic compound degradation and halobenzoate degradation. All isolates contained heavy metal resistance genes for arsenic, cadmium, copper, chromium, lead, mercury, and zinc. Arsenic resistance genes were the most common among isolates and were organized into structurally diverse ars operons. Collectively, our data indicated that A. xylosoxidans ADAF13, P. putida CBF10-2, and P. stutzeri ODKF13 are strong candidates for further enhancement and development as bioremediation tools. [ABSTRACT FROM AUTHOR]

The mitochondrial genome (mitogenome) has proven to be important for the taxonomy, systematics, and population genetics of ticks. However, current methods to generate mitogenomes can be cost-prohibitive at scale. To address this issue, we developed a cost-effective approach to amplify and sequence the whole mitogenome of individual tick specimens. Using two different primer sites, this approach generated two full-length mitogenome amplicons that were sequenced using the Oxford Nanopore Technologies' Mk1B sequencer. We used this approach to generate 85 individual tick mitogenomes from samples comprised of the three tick families, 11 genera, and 57 species. Twenty-six of these species did not have a complete mitogenome available on GenBank prior to this work. We benchmarked the accuracy of this approach using a subset of samples that had been previously sequenced by low-coverage Illumina genome skimming. We found our assemblies were comparable or exceeded the Illumina method, achieving a median sequence concordance of 99.98%. We further analyzed our mitogenome dataset in a mitophylogenomic analysis in the context of all three tick families. We were able to sequence 72 samples in one run and achieved a cost/sample of ~ $10 USD. This cost-effective strategy is applicable for sample identification, taxonomy, systematics, and population genetics for not only ticks but likely other metazoans; thus, making mitogenome sequencing equitable for the wider scientific community. [ABSTRACT FROM AUTHOR]