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Volume 26, Number 11—November 2020
Dispatch

Multidrug-Resistant Candida auris Infections in Critically Ill Coronavirus Disease Patients, India, April–July 2020

Anuradha ChowdharyComments to Author , Bansidhar Tarai, Ashutosh Singh, and Amit Sharma
Author affiliations: Vallabhbhai Patel Chest Institute of the University of Delhi, New Delhi, India (A. Chowdhary, A. Singh); Max Health Care Institute, New Delhi (B. Tarai); International Centre for Genetic Engineering and Biotechnology, New Delhi (A. Sharma)

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Abstract

In New Delhi, India, candidemia affected 15 critically ill coronavirus disease patients admitted to an intensive care unit during April–July 2020. Candida auris accounted for two thirds of cases; case-fatality rate was high (60%). Hospital-acquired C. auris infections in coronavirus disease patients may lead to adverse outcomes and additional strain on healthcare resources.

The ongoing coronavirus disease (COVID-19) pandemic has overwhelmed healthcare systems worldwide. Reports from China and New York have highlighted the concern for nosocomial infections, primarily bacterial, in critically ill COVID-19 patients (13). Secondary Candida spp. bloodstream infections in COVID-19 patients with prolonged intensive care unit (ICU) stays have not been documented. However, a new concern coinciding with the brisk expansion of critical care facilities for COVID-19 patients is the potential for nosocomial spread of Candida auris infections (4). C. auris is a global health threat because of its ability to colonize skin, persist in environments, cause nosocomial outbreaks, and lead to severe disease with high mortality rates (5,6).

The Study

Following up on our prediction (4), we report bloodstream infections caused by multidrug resistant C. auris in 1 COVID-19 ICU in New Delhi, India. A total of 596 patients with confirmed COVID were admitted to the 65-bed ICU during April–July 2020. Of these, 420 patients required mechanical ventilation. Overall, candidemia was detected in 15 (2.5%) of the 596 ICU patients; the predominant agent was C. auris for 10 (67%) of those patients. For the remaining 5 patients, candidemia was caused by C. albicans (n = 3), C. tropicalis (n = 1), and C. krusei (n = 1).

We abstracted the following data for the candidemia patients: baseline demographics, medical history, laboratory parameters, microbiological findings, concomitant antimicrobial drug use, and treatments. Isolates were identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI Biotyper, https://www.bruker.com). In addition, species identification was conducted by amplification and sequencing of the internal transcribed spacer region of ribosomal DNA and of the D1/D2 domain of the large subunit ribosomal DNA. Antifungal susceptibility testing was performed by using the Clinical and Laboratory Standards Institute broth-microdilution method M27-A3/S4 (7). Antifungals tested were fluconazole, voriconazole, posaconazole, isavuconazole, 5-flucytosine, caspofungin, micafungin, anidulafungin, and amphotericin B.

Most of the 10 patients with C. auris infection were elderly (8 patients were 66–88 years of age) and male (7 patients) (Table 1, https://wwwnc.cdc.gov/EID/article/26/11/20-3504-T1.htm). C. auris was cultured from paired blood samples from all 10 patients and also from urine for 2 of these patients. All of the COVID-19 patients in whom C. auris infections developed had been hospitalized in the ICU for prolonged periods (20–60 days) and had underlying chronic conditions (e.g., hypertension, n = 7; diabetes mellitus, n = 6; and chronic kidney and liver disease, n = 2). Candidemia caused by C. auris developed 10–42 days after admission. Half (50%) of the patients with C. auris infections received mechanical ventilation as a result of severe COVID-19 pneumonia. Furthermore, all patients with candidemia had indwelling central lines and urinary catheters. Of the 15 patients, COVID-19 was hospital acquired for 2 (acquired 2 and 7 weeks after hospital admission). Severity parameters for COVID-19 were elevated for all patients with candidemia (Table 1). Among the 15 candidemia patients, 8 (53%) died; among those with C. auris infection, the fatality rate was 60%. Of note, 4 of the 6 patients who died experienced persistent fungemia, and despite micafungin therapy for 5 days, C. auris again grew in blood culture.

Antifungal susceptibility testing data for C. auris isolates from 10 patients showed that all isolates were resistant to fluconazole (MIC >32 mg/L) and 30% were nonsusceptible to voriconazole (MIC >2 mg/L). Furthermore, 40% were resistant to amphotericin B (MIC >2 mg/L) and 60% were resistant to 5-flucytosine (MIC >32 mg/L). Overall, 30% of C. auris isolates were multiazole (fluconazole + voriconazole) resistant; whereas, 70% were multidrug resistant, including 30% (n = 3) that were resistant to 3 classes of drugs (azoles + amphotericin B + 5-flucytosine) and 4 that were resistant to 2 classes of drugs (azoles + 5-flucytosine and azoles + amphotericin B). All isolates were susceptible to echinocandins (Table 2, https://wwwnc.cdc.gov/EID/article/26/11/20-3504-T2.htm).

Conclusions

Our findings highlight the role of hospital-acquired C. auris bloodstream infections; the patients were probably infected while hospitalized. C. auris can be transmitted in healthcare settings just like other multidrug-resistant organisms, such as carbapenem-resistant Enterobacteriaceae and methicillin-resistant Staphylococcus aureus (4). For 4 of 10 patients studied, bacteremia caused by Enterobacter cloacae and Staphylococcus haemolyticus was also noted. In patients with severe COVID-19, the rate of secondary infections was substantially higher, as has been reported by Goyal et al. (6% of cases of secondary bacterial infections in the United States) (3) and Zhou et al. (15% of cases of secondary bacterial infections in China) (8). Among fungal co-infections in France, the incidence of putative invasive pulmonary aspergillosis was high (30%) (9).

Several major outbreaks of bloodstream infections caused by C. auris have been reported in India, the United Kingdom, Colombia, South Africa, and the United States (5,1012). In our report, all patients in the ICU had indwelling invasive devices such as central venous and urinary catheters, which may be the source of C. auris infections (i.e., candidemia and urinary tract infection). We anticipate that transmission of C. auris to COVID-19 patients by healthcare personnel is unlikely because of the use of personal protective equipment. However, incorrect and extended use of personal protective equipment can lead to self-contamination and transmission.

Of note, 6 of the 10 patients died, possibly because of multiple underlying health conditions. However, 67% of those who died had persistent candidemia, which may have contributed to their death. Furthermore, multidrug-resistant C. auris affects the choice of antifungal therapy and treatment outcomes. Most C. auris isolates are resistant to fluconazole, and panresistant isolates have been described (13). All C. auris isolates in our study were resistant to fluconazole, and 40% were resistant to amphotericin B, both of which are commonly used in resource-limited countries; therefore, resistance to both classes of drug by C. auris is highly concerning because use of other antifungals such as echinocandins are limited in these countries.

Candidemia affected 2.5% of the COVID-19 patients in this cohort admitted to the ICU. In a tertiary care center in New Delhi, C. auris was reportedly the second most common Candida species that caused candidemia in non-COVID patients (14). Extensive contamination of the hospital environment has been detected in hospitals experiencing outbreaks of C. auris infection, warranting adherence to strict hospital infection prevention practices, such as enhanced cleaning of rooms with chlorine-based disinfectants at high concentrations (0.5%) for highly resistant pathogens such as C. auris. Critically ill COVID-19 patients with C. auris infection tend to have concurrent conditions (e.g., diabetes mellitus, chronic kidney disease) and risk factors (e.g., need for mechanical ventilation, receipt of steroids). To reduce complications, admission times in overburdened hospitals, and death rates among COVID-19 patients, identifying and treating C. auris infections is vital. A recent report that investigated changes in the fecal fungal microbiomes of COVID-19 patients has shown increasing prevalence of opportunistic fungal pathogens such as C. albicans, C. auris, and Aspergillus flavus (15). These data, along with our findings, provide evidence that the ongoing COVID-19 pandemic may provide ideal conditions for outbreaks of C. auris in hospital ICUs (4). Thus, during the COVID-19 pandemic, extra caution is warranted in hospitals, regions, cities, and countries where C. auris is prevalent.

Dr. Chowdhary is a clinical microbiologist and a professor at the Vallabhbhai Patel Chest Institute, New Delhi, India. Her main research interest includes fungal infections.

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Acknowledgment

A.C. and A. Sharma drafted the manuscript. A. Singh and B.T. collected the patient details and performed literature searches, identification, and susceptibility testing. All authors read and approved the manuscript.

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References

  1. Ruan  Q, Yang  K, Wang  W, Jiang  L, Song  J. Clinical predictors of mortality due to COVID-19 based on an analysis of data of 150 patients from Wuhan, China. Intensive Care Med. 2020;46:8468. DOIPubMed
  2. He  Y, Li  W, Wang  Z, Chen  H, Tian  L, Liu  D. Nosocomial infection among patients with COVID-19: a retrospective data analysis of 918 cases from a single center in Wuhan, China. Infect Control Hosp Epidemiol. 2020;41:9823.https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=32279676&dopt=Abstract DOI
  3. Goyal  P, Choi  JJ, Pinheiro  LC, Schenck  EJ, Chen  R, Jabri  A, et al. Clinical characteristics of Covid-19 in New York City. N Engl J Med. 2020;382:23724. DOIPubMed
  4. Chowdhary  A, Sharma  A. The lurking scourge of multidrug resistant Candida auris in times of COVID-19 pandemic. J Glob Antimicrob Resist. 2020;22:1756. DOIPubMed
  5. Cortegiani  A, Misseri  G, Fasciana  T, Giammanco  A, Giarratano  A, Chowdhary  A. Epidemiology, clinical characteristics, resistance, and treatment of infections by Candida auris. J Intensive Care. 2018;6:69. DOIPubMed
  6. Chowdhary  A, Sharma  C, Meis  JF. Candida auris: A rapidly emerging cause of hospital-acquired multidrug-resistant fungal infections globally. PLoS Pathog. 2017;13:e1006290. DOIPubMed
  7. Clinical and Laboratory Standards Institute. Reference method for broth dilution antifungal susceptibility testing of yeasts: 4th informational supplement (M27–S4). Wayne (PA): The Institute; 2012.
  8. Zhou  F, Yu  T, Du  R, Fan  G, Liu  Y, Liu  Z, et al. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Lancet. 2020;395:105462. DOIPubMed
  9. Alanio  A, Dellière  S, Fodil  S, Bretagne  S, Mégarbane  B. Prevalence of putative invasive pulmonary aspergillosis in critically ill patients with COVID-19. Lancet Respir Med. 2020;8:e489. DOIPubMed
  10. Chowdhary  A, Sharma  C, Duggal  S, Agarwal  K, Prakash  A, Singh  PK, et al. New clonal strain of Candida auris, Delhi, India. Emerg Infect Dis. 2013;19:16703. DOIPubMed
  11. Adams  E, Quinn  M, Tsay  S, Poirot  E, Chaturvedi  S, Southwick  K, et al.; Candida auris Investigation Workgroup. Candida auris Investigation Workgroup. Candida auris in healthcare facilities, New York, USA, 2013–2017. Emerg Infect Dis. 2018;24:181624. DOIPubMed
  12. Arensman  K, Miller  JL, Chiang  A, Mai  N, Levato  J, LaChance  E, et al. Clinical outcomes of patients treated for Candida auris infections in a multisite health system, Illinois, USA. Emerg Infect Dis. 2020;26:87680. DOIPubMed
  13. Chowdhary  A, Prakash  A, Sharma  C, Kordalewska  M, Kumar  A, Sarma  S, et al. A multicentre study of antifungal susceptibility patterns among 350 Candida auris isolates (2009-17) in India: role of the ERG11 and FKS1 genes in azole and echinocandin resistance. J Antimicrob Chemother. 2018;73:8919. DOIPubMed
  14. Mathur  P, Hasan  F, Singh  PK, Malhotra  R, Walia  K, Chowdhary  A. Five-year profile of candidaemia at an Indian trauma centre: High rates of Candida auris blood stream infections. Mycoses. 2018;61:67480. DOIPubMed
  15. Zuo  T, Zhan  H, Zhang  F, Liu  Q, Tso  EYK, Lui  GCY, et al. Alterations in fecal fungal microbiome of patients with COVID-19 during time of hospitalization until discharge. Gastroenterology. 2020;S0016-5085(20)34852-6; [Epub ahead of print].PubMed

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Tables

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Cite This Article

DOI: 10.3201/eid2611.203504

Original Publication Date: August 27, 2020

Table of Contents – Volume 26, Number 11—November 2020

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Pr. Anuradha Chowdhary, Department of Medical Mycology, VP Chest Institute, University of Delhi, New Delhi 110007, India

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Page created: August 18, 2020
Page updated: October 19, 2020 1:41 PM EDT
Page reviewed: October 19, 2020 1:41 PM EDT
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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