Utility of Whole-Genome Sequencing to Ascertain Locally Acquired Cases of Coccidioidomycosis, Washington, USA.
Coccidioides spp. are endemic to warm, arid regions of the Western Hemisphere that have low rainfall (1,8). The 2 species have colonized different geographic locations: C. posadasii is largely found in Arizona, Texas, Mexico, and Central and South America; and C. immitis is primarily found in central and southern California. Coccidioidomycosis causes a major burden of disease in many of these areas; the annual incidence in Arizona is >75 cases/100,000 population (9). Case counts have recently increased in California; >5,300 cases were reported in 2016 (13.7 cases/100,000 population (10). Climate suitability projections predict expansion of the suitable environment for coccidioidomycosis and increasing incidence in areas that already sustain Coccidioides growth (11).
During 2010-2011, three cases of coccidioidomycosis were identified and reported in southeastern Washington (7). Subsequently, Coccidioides DNA and viable propagules were isolated from soil at a location of suspected exposure for 1 of these cases (12,13). Whole-genome sequencing (WGS) analysis of the recovered isolates demonstrated near identical genetic identity between soil and clinical isolates, further confirming endemic presence of infectious C. immitis in Washington (13).
Public health surveillance for coccidioidomycosis was implemented statewide in Washington in April 2014. Before 2014, cases of coccidioidomycosis were reported sporadically, but no standard reporting procedure existed. Since 2014, the number of reported cases of coccidioidomycosis has increased each year; reported cases in Washington suspected to be locally acquired have higher rates of hospitalization and death compared with cases from other disease-endemic regions (14).
Because most persons infected with Coccidioides spp. are asymptomatic or have only mild illness, and most illness self-resolves, we believe that only the most severe cases of coccidioidomycosis with exposure in Washington are being identified and reported to public health authorities. In addition, Coccidioides spp. infections might be asymptomatic or only manifest as subclinical disease until a reactivation or complication develops later. Also, most residents of Washington have some travel history to historically disease-endemic areas, such as Arizona, California, or Mexico. These findings create a challenge in differentiating between autochthonous and imported cases of coccidioidomycosis, which is a useful distinction for public health surveillance in Washington.
To better determine the nature of exposure for reported cases of coccidioidomycosis in Washington, the Washington Department of Health, in collaboration with the Centers for Disease Control and Prevention (CDC; Atlanta, GA, USA) and the Translational Genomics Research Institute (Flagstaff, AZ, USA), initiated enhanced surveillance by incorporating WGS of clinical isolates aimed at determining the geographic origins of Coccidioides spp. strains. This approach is based on previous population structure studies providing evidence that C. immitis and C. posadasii have well-defined geographic structures (15-19). Subsequently, Engelthaler et al. demonstrated that isolates can generally be assigned to the specific geographic populations on the basis of WGS analysis (20). This approach is consistent with a general trend in molecular epidemiology that uses WGS and a One Health approach to ascertain clusters or outbreaks of bacterial, fungal, viral, and parasitic diseases (21-23).
We report WGS analyses of isolates from 17 recent coccidioidomycosis cases in Washington, and demonstrate that 13 (76%) cases involved coccidioidomycosis most likely acquired outside Washington; 4 cases (24%) likely involved local acquisition. We discuss the utility of the WGS method to enhance epidemiologic surveillance.
Materials and Methods
Cases and Isolates
We identified coccidioidomycosis cases through passive reporting to local health jurisdictions from healthcare providers in Washington and laboratories performing testing for residents of Washington. Confirmed cases, as classified according to the Council of State and Territorial Epidemiologists case definition (24), reported during 2014-2017 were included in the analysis. Reported case-patients were interviewed by local health jurisdictions to determine clinical course, travel history, and any potential soil or dust exposures. Medical records were requested when possible for complete data abstraction to case reporting forms. When the exposure was suspected to have occurred in the disease-endemic area of Washington or exposure history was unknown, available clinical isolates were sent to CDC for confirmation.
At CDC, all isolates were grown on brain heart infusion (BHI) agar at 25[degrees]C for 10 days. Genomic DNA was extracted by using the DNeasy Blood and Tissue kit (QIAGEN, https://www.qiagen.com/us) according to the manufacturer's recommendations. Genomic DNA was stored at -20[degrees]C until further use. The Washington State and CDC Institutional Review Boards determined this project to be enhancing surveillance for a notifiable condition and did not require human subjects review.
Genome Sequencing, Assembly, and Analyses
We sequenced genomes of 18 isolates from 17 patients using Illumina (https://www.illumina.com) HiSeq and MiSeq sequencing platforms, as described (20,25). We prepared DNA samples for paired-end sequencing by using the Kapa Biosystems (https://www.kapabiosystems.com) Library Preparation Kit protocol with an 8-bp index modification and sequenced to a read length of 250 bp on the Illumina HiSeq or 250 bp on the Illumina MiSeq. All WGS data files have been deposited in the National Center for Biotechnology Information Sequence Read Archive under BioProject PRJNA472461.
We performed genome assembly and analyses as described (20). In brief, the Washington-1(B10637) strain was used as the reference for C. immitis single-nucleotide polymorphism (SNP) matrices, and the B10813_Tx strain was used as a reference in the C. posadasii SNP matrix. We aligned Illumina read data against the respective reference assemblies by using Burrow-Wheeler Aligner version 0.7.7 (http://bio-bwa.sourceforge.net) and identified SNP variants by using SamTools version 0.1.19 (http://samtools.sourceforge.net). We filtered SNP calls by using a publicly available SNP analysis pipeline (26) (http://tgennorth.github.io/ NASP), as described, to remove positions with <10 times coverage with <90% variant allele calls, or identified by using Nucmer (http://nebc.nox.ac.uk/bioinformatics/docs/nucmer.html) as being within duplicated regions in the reference (20,25). We constructed a maximum-parsimony phylogeny on the basis of SNP matrices by using MEGA7 (http://www. megasoftware.net), including 17 described strains from various geographic areas for comparison; we determined bootstrap support for the tree by using 1,000 reiterations (20).
We extracted candidate SNPs that distinguish Washington strains from non-Washington strains (Appendix Table, https://wwwnc.cdc.gov/EID/article/25/3/18-1155-App1.pdf) from whole-genome assemblies by using Samtools version 1.8, EMBOSS version 6.5.7, and NCBI-toolkit version 7.0.0 (27-29). We chose SNPs if their positions were consecutive or no more than 1 nt apart and had [greater than or equal to]10 times coverage. In brief, we extracted an ~1-kb region surrounding candidate SNP positions from all draft assemblies, aligned it to Washington-1(B10637) reference, and designed degenerate primers by using Primer3 version 3.0 (30). We compared regions with those of C. immitis strain H538-4 to determine genomic loci annotation.
During 2014-2017, a total of 167 confirmed cases of coccidioidomycosis were reported in Washington. For these cases, 18 isolates (Table) from 17 cases were available. Travel and exposure histories suggested local acquisition in Washington (9 case-patients) or were unknown at the time of specimen collection (8 case-patients).
We speciated 14 isolates as C. immitis and 4 as C. posadasii and subjected these isolates to WGS with 25160 times sequencing coverage. A total of 68,717 SNPs were identified by comparison with the reference isolate. Phylogenetic analysis and comparison with sequenced isolates of C. immitis demonstrated that 5 isolates from 4 patients in Washington were highly genetically related to each other and to isolates from the identified Washington clade that contained human and soil isolates (13). No more than 354 SNPs differentiated any 2 isolates within the Washington cluster, which was also supported by 100% bootstrap values (Figure). In contrast, >10,000 SNPs differentiated the Washington cluster from its nearest neighbor, an isolate from another case-patient in Washington. This case-patient (B12496) reported travel history to disease-endemic regions in California and Mexico. Tens of thousands of SNPs differentiated Washington cluster isolates from those from other states. No more than 3 SNPs were identified among multiple soil isolates collected 4 years apart from a single sampling site, and 4 SNPs were identified between isolates collected 2 years apart from 1 patient in Washington who had a chronic infection. However, 234-324 SNPs were identified in pairwise comparisons between isolates from different patients in the Washington clade (Figure, panel B).
Three of the 4 case-patients infected with Washington clade strains reported no travel history outside Washington. Conversely, 8 of 9 C. immitis isolates that did not cluster with the Washington clade were isolated from patients who reported travel to California.
Washington strains can be distinguished from non-Washington strains in 3 genomic regions on the basis of annotations from C. immitis strain H538-4; locus DS016982: adipocyte-derived leucine aminopeptidase; locus DS01702: hypothetical protein; and locus DS016985: glyoxal oxidase (Appendix). The DNA fragment from locus DS016982 contains SNP GG at positions 94460-94461 for Washington strains and SNP CA for non-Washington strains and can be amplified by using forward primer 5'-GGTACGTCACAAGTCCCCAG-3' and reverse primer 3'-AAGAGTACTCGCGAAGGAAGC-5'. For locus DS017021, the DNA fragment amplified with forward primer 5'-CTTGACTGTGCAGGGCCTTA-3' and reverse primer 3'-ACCGGCCTAACTCCATGGTA-5' encompasses SNPs GGT for Washington strains and TGC for non-Washington strains at positions 105566-105568) The fragment of locus DS016985 can be amplified by using primer pairs 5'-TTCCGCTTGATGGCTGAAGT3'/3'-TGTGGCCCTCCTATTGCTTG-5' and contains consecutive SNP CC for Washington strains and SNP GA for non-Washington strains (positions 232442-232443).
We identified 4 case-patients who had C. posadasii infections by using internal transcribed spacer sequencing and confirmed by WGS. Isolates from the 4 case-patients clustered with described C. posadasii populations from Arizona (data not shown). Three of those case-patients had traveled to Arizona, and 1 case-patient had an unknown travel history.
Determining the potential sources of exposure and geographic distribution of Coccidioides in areas where coccidioidomycosis is uncommon is a surveillance challenge because patients often report travel histories to other disease-endemic areas. To address this problem, we implemented WGS to better determine the likely geographic origin of isolates obtained from patients in Washington who had suspected local acquisition or unknown exposure histories. This method is based on the observation that Coccidioides populations have well defined geographic structure, and most isolates can be assigned to specific geographic areas on the basis of their WGS genotypes, such as Arizona, Texas, Mexico, central California, or Washington (20). We demonstrated the utility of this tool for investigating the epidemiology of coccidioidomycosis in Washington.
Of 18 isolates from 17 patients included in this study, 5 (28%) clustered with strains isolated from soil in Washington, which was consistent with local exposure. The remaining 13 (72%) isolates clustered with populations from other areas, such as Arizona, California, or Mexico, which was generally consistent with reported travel histories of patients. The only discordance between WGS and epidemiologic data was observed for isolate B11863, which clustered with C. immitis isolates from California. The patient from whom this isolate originated reported travel out of state but also reported extensive soil exposure in a county in Washington that had previously reported autochthonous cases. Specifically, the only reported travel was to Hawaii 2 months before disease onset and to Costa Rica 1 year before disease onset, with a layover in California during which the patient did not leave the airport. In addition, the patient reported 1 trip to southern California 6 years before disease onset. This discordance was an unexpected finding and might represent more diversity among Coccidioides spp. in Washington than previously understood, reactivated infection because of previous travel, or infection from a fomite or other carrier source of C. immitis. Further investigation and surveillance data are needed to determine which hypothesis is most plausible.
Of the 4 patients infected with the local strains from Washington, 3 patients reported no travel history outside Washington. The fourth patient reported travel to Arizona 1 year before the onset of coccidioidomycosis but also reported extensive exposure to local soils in Washington and dust during hiking and gardening. This result indicates that compatible travel history alone does not exclude the possibility of local exposure and demonstrates the added value of genomic approaches to determining exposure location. Although isolates in the Washington clade were genetically related (Figure, panel A), considerably higher genetic diversity was observed for new strains compared with that detected for the original isolates from Washington identified in 2013 (13). Specifically, 245-299 pairwise SNPs were identified among the newly identified strains from Washington, compared with <5 SNPs detected among previously described isolates from Washington from the same exposure site (Figure, panel B). This small but apparent genetic divergence of the new isolates indicates that new infections were acquired from different local C. immitis populations, likely at different sites, and suggests the presence of multiple environmental loci for Coccidioides spp. in Washington. The divergent isolates were collected from soil in a location ~70 miles from the suspected exposure location of 1 of the patients. However, in sharp contrast to the populations of Coccidioides spp. in Arizona or California, where isolates are differentiated by thousands of SNPs, the overall low genetic variability in the Washington population is consistent with a relatively small population size, strongly suggesting a recent common ancestry of Washington strains and a relatively recent expansion of C. immitis to Washington, (Figure).
Our study has 2 main limitations. First, there might be additional genetically diverse populations of Coccidioides in Washington that have not yet been discovered or proven; therefore, some genotypes that have been deemed as acquired outside Washington might have been acquired locally. For example, 1 isolate from a patient who was highly suspected of having local acquisition clustered with isolates from California. Likewise, there might be genetically similar populations of Coccidioides spp. in Oregon, California, or other nearby states that have not yet been documented. These genetically similar populations might add complexity to determination of location of exposure. However, to date, no clinical or environmental isolates with strong epidemiologic links to locations outside Washington that cluster with isolates from Washington have been identified. This finding is consistent with those of previous studies that demonstrated that C. immitis and C. posadasii have well-defined geographic structures (15-19).
Second, all patients in our study were given diagnoses of rather atypical cases of coccidioidomycosis that were either asymptomatic (diagnosed during biopsy), cutaneous, chronic, or unusually severe. In general, the acute primary pulmonary form of coccidioidomycosis constitutes the most common manifestation in highly endemic areas and often represents the earliest manifestation of the disease. Conversely, reactivation of latent infections can occur months to years after initial exposure, typically in immunosuppressed persons. Many complicated infections might follow a subacute or chronic disease progression. This lack of acute respiratory cases and preponderance of atypical disease in Washington indicates the likely gap between early identification and delayed diagnosis because of lack of awareness and might also explain the high prevalence of the out-of-state strains of C. immitis in our study. However, even in highly endemic regions, acute pulmonary disease is often missed or delayed in diagnosis for months (31,32), supporting the possibility that an underlying background of typical acute disease might remain unidentified in Washington (33).
Our results indicate that WGS is a useful tool to assist in determining exposure location in surveillance situations in which exposure histories are unclear or unknown. For patients in this study, coccidioidomycosis was more commonly associated with travel to other disease-endemic areas compared with local exposure; however, travel to endemic regions does not preclude local acquisition of the disease. Our results also indicate that coccidioidomycosis is likely to be underdiagnosed and underreported in Washington on the basis of atypical disease manifestations for locally acquired cases. More research is needed to determine the true prevalence of locally acquired coccidioidomycosis in Washington.
We thank Denny Flodin-Hursh, Jill Stiffler, Cindy Ralston, Heather Hill, and all other local health jurisdiction and healthcare facility staff who supported this study by obtaining isolates and interviewing patients, and Joyce Peterson and Ngoc Le for assistance with processing and identification of isolates.
This study was supported by an Advanced Molecular Detection Initiative and Epidemiology and Laboratory Capacity grant from CDC.
Ms. Oltean is a zoonotic and vectorborne disease epidemiologist in the Office of Communicable Disease Epidemiology, Washington State Department of Health, Shoreline, WA. Her primary research interests are zoonotic disease surveillance system design, implementation, and evaluation.
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Address for correspondence: Hanna N. Oltean, Washington State Department of Health, 1610 NE 150th St, Mailstop K17-9, Shoreline, WA 98155, USA; email: firstname.lastname@example.org
Author affiliations: Washington State Department of Health, Shoreline, Washington, USA (H.N. Oltean); Centers for Disease Control and Prevention, Atlanta, Georgia, USA (K.A. Etienne, L. Gade, O.Z. McCotter, A.P. Litvintseva); Translational Genomics Research Institute, Flagstaff, Arizona, USA (C.C. Roe, D.M. Engelthaler)
Caption: Figure. Genetic relationships among Coccidioides immitis isolates. A) Isolates from patients in Washington, USA, compared with isolates from other locations. B) Genetic relationships among C. immitis isolates from the Washington clade; single-nucleotide polymorphism numbers are shown above the branches. Dark blue indicates previously described environmental and human isolates (13) from Washington, light blue indicates isolates from new cases that were likely acquired in Washington, and orange indicates isolates from cases that were likely acquired outside Washington. Isolates from patients with the documented travel histories are indicated as Traveler. Travel history is detailed in the Table. Isolates with SJV names are from the San Joaquin Valley, California, as described (20). Bootstrap values shown in green circle indicate 100% support. Scale bars indicate nucleotide substitutions per site. CDC, Centers for Disease Control and Prevention; Env, environment.
Table. Characteristics of 18 clinical isolates subjected to whole- genome sequencing analysis from patients with coccidioidomycosis, Washington, USA, 2014-2017 * Travel history CDC-ID of patient Coccidioides species Collection date B10917 Unknown C. posadasii 2014 B10918 AZ, MT, SD, OR C. posadasii 2014 B11036 AZ C. posadasii 2015 B11034 AZ C. immitis 2014 B11019 None C. immitis 2014 B11035 CA C. immitis 2015 B11080 Mexico, CA C. immitis 2015 B11198 Mexico, CA C. immitis 2015 B11299 AZ C. posadasii 2015 B11517 CA C. immitis 2016 B11518 None C. immitis 2016 B11587 CA C. immitis 2016 B11863 HI, Costa Rica C. immitis 2016 B11873 CA C. immitis 2016 B12398 None C. immitis 2016 B12495 CA C. immitis 2016 B12496 Mexico, CA C. immitis 2016 B13956 None C. immitis 2017 CDC-ID Specimen source site Phylogenetic population B10917 Sputum Non-Washington B10918 Sputum Non-Washington B11036 Lung Non-Washington B11034 Lung Washington B11019 BAL Washington ([dagger]) B11035 Cerebrospinal fluid Non-Washington B11080 Neck Non-Washington B11198 Tissue Non-Washington B11299 Bronchial washings Non-Washington B11517 Throat Non-Washington B11518 Testicle Washington ([dagger]) B11587 Tissue Non-Washington B11863 Sputum Non-Washington B11873 Bronchial washings Non-Washington B12398 Blood Washington B12495 Cerebrospinal fluid Non-Washington B12496 Knee wound Non-Washington B13956 BAL Washington * BAL, bronchoalveolar lavage; CDC, Centers for Disease Control and Prevention; ID, identification. ([dagger]) These isolates were from the same patient.
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|Author:||Oltean, Hanna N.; Etienne, Kizee A.; Roe, Chandler C.; Gade, Lalitha; McCotter, Orion Z.; Engelthale|
|Publication:||Emerging Infectious Diseases|
|Date:||Mar 1, 2019|
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