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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Med.</journal-id>
<journal-title>Frontiers in Medicine</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Med.</abbrev-journal-title>
<issn pub-type="epub">2296-858X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fmed.2024.1500014</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Medicine</subject>
<subj-group>
<subject>Case Report</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Combination of metagenomic next-generation sequencing and morphology for identifying <italic>Coccidioides immitis</italic>: a case report</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name><surname>Liu</surname> <given-names>Hong</given-names></name>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Zhou</surname> <given-names>Kaixin</given-names></name>
<uri xlink:href="https://loop.frontiersin.org/people/717811/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Zhong</surname> <given-names>Chaoran</given-names></name>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
</contrib>
<contrib contrib-type="author" corresp="yes">
<name><surname>Guan</surname> <given-names>Ming</given-names></name>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1786710/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
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</contrib>
</contrib-group>
<aff><institution>Department of Laboratory Medicine, Huashan Hospital, Fudan University</institution>, <addr-line>Shanghai</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: Sam Donta, Falmouth Hospital, United States</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: Maria A. Islas-Osuna, National Council of Science and Technology (CONACYT), Mexico</p>
<p>Joshua Fierer, University of California, San Diego, United States</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Ming Guan, <email>guanming88@yahoo.com</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>22</day>
<month>01</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>11</volume>
<elocation-id>1500014</elocation-id>
<history>
<date date-type="received">
<day>26</day>
<month>09</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>30</day>
<month>12</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2025 Liu, Zhou, Zhong and Guan.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Liu, Zhou, Zhong and Guan</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Coccidioidomycosis is a systemic infection caused by the dimorphic fungus <italic>Coccidioides</italic> spp., endemic to the Southwestern United States and Central and South America. In this article, we report a case of <italic>Coccidioides immitis</italic>-induced meningitis in a 27-year-old man who was experiencing recurrent fever and headache. His cerebrospinal fluid (CSF) biochemical markers indicated an infection in the central nervous system. However, repeated routine cultures of the CSF for bacterial detection were all negative. Only metagenomic next-generation sequencing (mNGS) detected low reads of <italic>C. immitis</italic>. To verify the mNGS results, the Clinical Microbiology Laboratory in Huashan Hospital optimized its culture conditions. Ultimately, 12&#x202F;days after sampling, the fungal bottle containing the cerebrospinal fluid tested positive. Furthermore, the diagnosis of <italic>C. immitis</italic> was then confirmed by smear staining combined with morphological characteristics of the colony, which provided an important etiological basis for clinical diagnosis and treatment. As coccidioidomycosis is a rare disease in China, its pathogen-specific diagnostic methods are limited. In this case, we combined two universal methods, mNGS and traditional morphological observation, to confirm the diagnosis. This combined strategy is critical for quick and accurate diagnosis.</p>
</abstract>
<kwd-group>
<kwd><italic>Coccidioides immitis</italic></kwd>
<kwd>coccidioidomycosis</kwd>
<kwd>metagenomic next-generation sequencing (mNGS)</kwd>
<kwd>diagnosis strategy</kwd>
<kwd>meningitis</kwd>
</kwd-group>
<counts>
<fig-count count="4"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="16"/>
<page-count count="6"/>
<word-count count="2788"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Infectious Diseases: Pathogenesis and Therapy</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec1">
<title>Introduction</title>
<p><italic>Coccidioides</italic> is a type of dimorphic fungus that includes <italic>C. immitis</italic> and <italic>C. posadasii</italic>. Epidemiological data have shown that <italic>Coccidioides</italic> is mainly prevalent in central and southern California, the low-lying desert regions of Arizona, southeastern New Mexico, western Texas, the southwestern United States, Mexico, Central America, and South America, with strong geographical distribution patterns (<xref ref-type="bibr" rid="ref1">1</xref>). Inhalation of arthroconidia into the lungs is the primary exposure factor. Coccidioidomycosis commonly manifests as an asymptomatic infection or a mild respiratory infection in humans and other vertebrate hosts. Occasionally, approximately 4.7% of coccidioidomycosis cases are reported to spread from the lungs to other organs, such as the skin, bone, spine, and meninges. This condition is known as disseminated coccidioidomycosis (<xref ref-type="bibr" rid="ref2">2</xref>), which usually develops rapidly. Failure to diagnose and treat this condition in time can result in poor prognosis and even death (<xref ref-type="bibr" rid="ref2">2</xref>, <xref ref-type="bibr" rid="ref3">3</xref>). Therefore, early and accurate diagnosis is crucial for the treatment of disseminated coccidioidomycosis.</p>
<p>Coccidioidomycosis is rarely reported in China. From 1958 to 2021, only 47 cases were reported, and the majority of these cases have a history of travel to endemic areas (<xref ref-type="bibr" rid="ref4">4</xref>, <xref ref-type="bibr" rid="ref5">5</xref>). As it is rare in China, the majority of clinical laboratories do not carry out <italic>Coccidioides-</italic>specific routine detections. In addition, its clinical signs and imaging presentations are non-specific, making it easy to misdiagnosis as a tumor or another disease (<xref ref-type="bibr" rid="ref1">1</xref>, <xref ref-type="bibr" rid="ref6">6</xref>, <xref ref-type="bibr" rid="ref7">7</xref>). Therefore, diagnosing coccidioidomycosis is difficult in non-endemic areas (<xref ref-type="bibr" rid="ref8">8</xref>).</p>
<p>This article reports on a patient with unexplained recurrent fever and headache who was transferred to our hospital after receiving ineffective treatment at a local hospital. The cerebrospinal fluid (CSF) metagenomic next-generation sequencing (mNGS) analysis revealed low reads of <italic>C. immitis-</italic>specific gene sequences, but the repeated CSF bacterial cultures showed no pathogens. To confirm the diagnosis, the Clinical Microbiology Laboratory in Huashan Hospital extended the CSF culture duration, based on the growth characteristics of <italic>Coccidioides</italic> reported in the literature (<xref ref-type="bibr" rid="ref9">9</xref>, <xref ref-type="bibr" rid="ref10">10</xref>). Ultimately, 12&#x202F;days after sampling, the fungal bottle containing the cerebrospinal fluid tested positive. Furthermore, the diagnosis of <italic>C. immitis</italic> was then confirmed by smear staining and the morphological characteristics of the colony, providing an important etiological basis for clinical diagnosis and treatment. This article will describe and discuss this case along with relevant insights.</p>
</sec>
<sec id="sec2">
<title>Case presentation</title>
<p>A 27-year-old male patient was admitted to the emergency department of Huashan Hospital due to a headache and fever on 11 August 2022. Around 2&#x202F;months (25 June) earlier, he had been diagnosed with community-acquired pneumonia with symptoms including cough and irregular fever (up to 39.0&#x00B0;C) at the local hospital (Yangzhou, Jiangsu). After antibacterial treatment, the symptoms improved significantly. However, half a month earlier (31 July), the patient developed a persistent headache and fever, and the symptoms progressively worsened. For further diagnosis, he visited our hospital.</p>
<p>Upon admission, the chest CT scan showed scattered inflammation in the lower lobe of the left lung, but no abnormalities were observed in the head during the enhancement CT scan (<xref ref-type="fig" rid="fig1">Figure 1B</xref>). Except for the routine blood test showing increased leukocytosis and eosinophilia, all other laboratory exams, including urinalysis, blood routine, liver and kidney function, blood glucose, blood ketones, coagulation function, procalcitonin, and myocardial markers, showed no abnormalities. As headache was the most critical sign, lumbar puncture was performed on 13 August. The CSF analysis revealed positive Pandy test (protein 2,071&#x202F;mg/L), intracranial pressure greater than 300&#x202F;mmH<sub>2</sub>O, a white blood cell count (695&#x202F;&#x00D7;&#x202F;10<sup>6</sup>/L) higher than the normal range, and glucose (1.2&#x202F;mmol/L) and chloride(115&#x202F;mmol/L) levels lower than the normal range (<xref ref-type="fig" rid="fig2">Figure 2</xref>). All the above results indicated the possibility of an infection in the central nervous system. Empiric combinatory therapy (levofloxacin 0.5&#x202F;g ivgtt qd and ceftriaxone 2.0&#x202F;g ivgtt bid) for bacterial meningitis was administered. However, there was no relief from the symptoms.</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p><bold>(A)</bold> Chest CT scan shows increased pulmonary markings in both lungs, with scattered patchy shadows in the left lower lobe (Arrow indicated). The trachea and main bronchi were patent. No enlarged lymph nodes were seen in the mediastinum or hilum; <bold>(B)</bold> Enhanced CT of the head shows no apparent abnormalities.</p>
</caption>
<graphic xlink:href="fmed-11-1500014-g001.tif"/>
</fig>
<fig position="float" id="fig2">
<label>Figure 2</label>
<caption>
<p>CSF investigation and antimicrobial drugs. After adjusting the treatment, the CSF factors, including glucose content, protein content, WBC, and intracranial pressure, gradually returned to normal.</p>
</caption>
<graphic xlink:href="fmed-11-1500014-g002.tif"/>
</fig>
<p>As all etiological examinations showed negative results, CSF mNGS analysis was performed to further identify the pathogen. On 17 and 19 August, two CSF mNGS analyses suggested low reads of <italic>C. immitis</italic> (only four unique sequence reads matched). mNGS is a novel gene sequencing approach used to rapidly identify pathogens in clinical samples, but it cannot be used as a diagnosis method when only low reads of suspicious pathogens are detected (<xref ref-type="bibr" rid="ref11">11</xref>). Due to the detection of <italic>C. immitis</italic>, which is generally considered to be limited to the Western Hemisphere, the patient&#x2019;s travel history was further reviewed. The patient had lived in Los Angeles, USA, for approximately 3&#x202F;months (March 2018&#x202F;~&#x202F;June 2018) to support his wife with child-rearing. During this period, he grew scallions in his garden and had contact with the soil.</p>
<p>The subsequent second cerebrospinal fluid mNGS test also detected <italic>C. immitis</italic>. To verify the mNGS results, we improved the CSF culture condition according to references (<xref ref-type="bibr" rid="ref7">7</xref>). A cerebrospinal fluid fungal culture was then conducted. Fortunately, 12&#x202F;days after sampling (August 23), the fungus/mycobacteria culture flask showed positive results, and a cotton wool-like substance was produced in the flask (<xref ref-type="fig" rid="fig3">Figure 3A</xref>). Then, smear staining was performed, as shown in <xref ref-type="fig" rid="fig3">Figure 3</xref>, and thick-walled spheroids and segmented hyphae were observed using both Gram staining and Fluorescence staining. The culture material was stained with lactophenol cotton blue, revealing the characteristic microscopic features of <italic>Coccidioides</italic>, including barrel-shaped arthroconidia connected by thin-walled, empty-connected cells. The Gram staining and fluorescence staining revealed the presence of branching, septate hyphae, rather than thick-walled spherules, indicating a differential diagnosis of <italic>Malbranchea</italic> spp. At the same time, the products were transferred to Sabouraud dextrose agar (SDA) plates. The hyphal stage was observable on the SDA plates at 28&#x00B0;C, whereas the yeast phase appeared at 35&#x00B0;C, consistent with the traits of biphasic fungi (<xref ref-type="fig" rid="fig4">Figures 4A</xref>,<xref ref-type="fig" rid="fig4">B</xref>). Articular spores, a critical characteristic of <italic>C. immitis</italic>, were clearly identified through colony Medan staining (<xref ref-type="fig" rid="fig4">Figure 4C</xref>). Based on the growth and morphological characteristics of this fungus, we confirmed the mNGS results, identifying it as <italic>C. immitis</italic>. Subsequently, colony ITS sequencing and homology analysis were performed using BLASTp against the NCBI database to further confirm the species. Due to the lack of access to a laboratory capable of conducting serological testing, it was not performed in this study.</p>
<fig position="float" id="fig3">
<label>Figure 3</label>
<caption>
<p><bold>(A)</bold> Cerebrospinal fluid fungal culture flask annulation. After 12&#x202F;days of continuous monitoring, the flask reported positivity (with an increasing growth curve). Cotton wool-like precipitation (indicated by red arrow) was visible in the bottle; <bold>(B,C)</bold> The cottony material was extracted and subjected to Gram staining and fluorescent staining separately. At high magnification (10&#x00D7;40), thick-walled spheroids and segmented hyphae were visible.</p>
</caption>
<graphic xlink:href="fmed-11-1500014-g003.tif"/>
</fig>
<fig position="float" id="fig4">
<label>Figure 4</label>
<caption>
<p>Colony on SDA plates after incubation at different temperatures. <italic>Coccidioides</italic> is a temperature-dependent dimorphic fungus that exhibits different colony morphologies at different temperatures. <bold>(A)</bold> The colony grown at 28&#x00B0;C had suede to villi, gray-white, and tan to brown; <bold>(B)</bold> The colony grown at 35&#x00B0;C was in the white yeast phase. <bold>(C)</bold> Through lactophenol cotton blue staining, arthroconidia and a large number of rectangular, barrel-shaped arthroconidia with septa were observed. These are thin-walled, connected cells. The arthroconidia and thin-walled connected cells alternate to form chains (10&#x00D7;100).</p>
</caption>
<graphic xlink:href="fmed-11-1500014-g004.tif"/>
</fig>
<p>Therefore, the clinic changed his treatment from antibacterial to antifungal therapy. As the first-line drug for <italic>Coccidioides</italic>, Itraconazole was administered according to our identification results (<xref ref-type="bibr" rid="ref12">12</xref>, <xref ref-type="bibr" rid="ref13">13</xref>). The detailed treatments are shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>. With anti-coccidioidal treatment, the patient showed gradual improvement, which further corroborated that the patient&#x2019;s symptoms were indeed caused by disseminated <italic>Coccidioides</italic> infection. By 30 August, there was a notable improvement in the patient&#x2019;s CSF compared to the previous measurements and the symptoms also significantly improved. Subsequently, the patient was followed up at the infectious disease department of our hospital. After the diagnosis, the patient was treated with itraconazole, starting with a loading dose of 200&#x202F;mg IV q12h for 2&#x202F;days, followed by a maintenance dose of 200&#x202F;mg IV qd. After 6&#x202F;months, the treatment plan was changed from IV to oral administration: itraconazole oral solution 200&#x202F;mg po q12h and prednisone 5&#x202F;mg BID for treatment. The patient&#x2019;s condition remained stable, and he continued to be followed up in the infectious disease department. For patients with <italic>Coccidioides</italic> meningitis, lifelong treatment with triazole medications is recommended.</p>
</sec>
<sec sec-type="discussion" id="sec3">
<title>Discussion</title>
<p>As a result of population mobility, coccidioidomycosis cases are increasing in China (<xref ref-type="bibr" rid="ref14">14</xref>). In addition, coccidioidal meningitis has a high mortality rate (90% within 1&#x202F;year and 100% within 2&#x202F;years). Therefore, early identification of the pathogen and prompt antifungal treatment are critical for a favorable prognosis. However, the etiology examination of coccidioidal meningitis remains a clinical challenge in non-endemic areas.</p>
<p>The diagnosis of coccidioidomycosis is mainly based on clinical manifestations, exposure history, and laboratory tests (<xref ref-type="bibr" rid="ref15">15</xref>). In terms of laboratory tests, mNGS has emerged as one of the routine methods for detecting unknown pathogens in clinical microbiology laboratories, with the advantages of high sensitivity and specificity (<xref ref-type="bibr" rid="ref15">15</xref>). mNGS is particularly recommended for diagnosing infections caused by new, rare, difficult-to-culture, or mixed pathogens (<xref ref-type="bibr" rid="ref11">11</xref>). However, the cost of mNGS sequencing is high, and it cannot directly correlate suspected pathogens with clinical symptoms. Therefore, it is important to isolate pathogens using traditional cultural methods.</p>
<p>In this case, both the symptoms and the regular CSF analysis suggested an infection in the CNS; however, the standard CSF cultures showed negative results (no pathogen). This may be related to the fact that the culture was only observed for 3&#x202F;days at 35&#x00B0;C on common bacterial media, which are not suitable for the growth of <italic>Coccidioides</italic> (which requires 28&#x00B0;C, using SDA, and can take 2&#x2013;9&#x202F;days for growth) (<xref ref-type="bibr" rid="ref8">8</xref>). After adjusting the cultural conditions, we successfully observed the <italic>Coccidioides</italic> colony and its critical morphology. This finding highlights the need for microbiology laboratories to maintain close communication with clinics. When patients report a history of travel to endemic areas and exhibit symptoms such as headache, fever, and vomiting, along with CSF analysis revealing elevated opening pressure, increased protein levels, hypoglycorrhachia, and pleocytosis (<xref ref-type="bibr" rid="ref16">16</xref>), we should consider changing the standard culture conditions to those suitable for the growth of <italic>Coccidioides</italic>.</p>
<p>This case highlights the potential of combining mNGS with traditional cultural methods to diagnose unknown pathogens quickly and accurately.</p>
</sec>
</body>
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<title>Data availability statement</title>
<p>The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.</p>
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<title>Ethics statement</title>
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<sec sec-type="author-contributions" id="sec6">
<title>Author contributions</title>
<p>HL: Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. KZ: Writing &#x2013; review &#x0026; editing. CZ: Writing &#x2013; original draft. MG: Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing.</p>
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<title>Funding</title>
<p>The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.</p>
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