<?xml version="1.0" encoding="iso-8859-1" standalone="no"?>
<!DOCTYPE GmsArticle SYSTEM "http://www.egms.de/dtd/2.0.34/GmsArticle.dtd">
<GmsArticle xmlns:xlink="http://www.w3.org/1999/xlink">
  <MetaData>
    <Identifier>dgkh000370</Identifier>
    <IdentifierDoi>10.3205/dgkh000370</IdentifierDoi>
    <IdentifierUrn>urn:nbn:de:0183-dgkh0003701</IdentifierUrn>
    <ArticleType>Research Article</ArticleType>
    <TitleGroup>
      <Title language="en">Bacterial co-infections and antibiotic resistance in patients with COVID-19</Title>
      <TitleTranslated language="de">Bakterielle Co-Infektionen und Antibiotikaresistenz bei Patienten mit COVID-19</TitleTranslated>
    </TitleGroup>
    <CreatorList>
      <Creator>
        <PersonNames>
          <Lastname>Mahmoudi</Lastname>
          <LastnameHeading>Mahmoudi</LastnameHeading>
          <Firstname>Hassan</Firstname>
          <Initials>H</Initials>
          <AcademicTitle>Dr.</AcademicTitle>
        </PersonNames>
        <Address>Department of Microbiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran, Phone: &#43;989189539458<Affiliation>Department of Microbiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran</Affiliation><Affiliation>Department of Laboratory Medicine, Ayatollah Alimoradiyan Hospital, Nahavand, Hamadan, Iran</Affiliation></Address>
        <Email>Hassanmahmoudi24&#64;gmail.com</Email>
        <Creatorrole corresponding="yes" presenting="no">author</Creatorrole>
      </Creator>
    </CreatorList>
    <PublisherList>
      <Publisher>
        <Corporation>
          <Corporatename>German Medical Science GMS Publishing House</Corporatename>
        </Corporation>
        <Address>D&#252;sseldorf</Address>
      </Publisher>
    </PublisherList>
    <SubjectGroup>
      <SubjectheadingDDB>610</SubjectheadingDDB>
      <Keyword language="en">COVID-19</Keyword>
      <Keyword language="en">bacterial co-infections</Keyword>
      <Keyword language="en">antibiotic resistance</Keyword>
      <Keyword language="en">viral respiratory infections</Keyword>
      <Keyword language="en">SARS-CoV-2</Keyword>
      <Keyword language="de">COVID-19</Keyword>
      <Keyword language="de">bakterielle Co-Infektionen</Keyword>
      <Keyword language="de">Antibiotika-Resistenz</Keyword>
      <Keyword language="de">virale Atemwegsinfektionen</Keyword>
      <Keyword language="de">SARS-CoV-2</Keyword>
    </SubjectGroup>
    <DatePublishedList>
      
    <DatePublished>20201217</DatePublished></DatePublishedList>
    <Language>engl</Language>
    <License license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
      <AltText language="en">This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License.</AltText>
      <AltText language="de">Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung).</AltText>
    </License>
    <SourceGroup>
      <Journal>
        <ISSN>2196-5226</ISSN>
        <Volume>15</Volume>
        <JournalTitle>GMS Hygiene and Infection Control</JournalTitle>
        <JournalTitleAbbr>GMS Hyg Infect Control</JournalTitleAbbr>
      </Journal>
    </SourceGroup>
    <ArticleNo>35</ArticleNo>
  </MetaData>
  <OrigData>
    <Abstract language="de" linked="yes"><Pgraph><Mark1>Hintergrund:</Mark1> Bakterielle Co-Infektionen werden h&#228;ufig bei viralen Atemwegsinfektionen identifiziert und sind wesentliche Gr&#252;nde f&#252;r Morbidit&#228;t und Mortalit&#228;t. Es fehlen Informationen &#252;ber die Pr&#228;valenz bakterieller Co-Infektionen bei Patienten mit COVID-19.. Ziel dieser Studie war es, die Pr&#228;valenz von bakteriellen Infektionen und Antibiotikaresistenzen bei an COVID-19 erkrankten Patienten zu bestimmen.</Pgraph><Pgraph><Mark1>Methoden:</Mark1> In einer Querschnittsstudie wurden Blutkulturen (BC) und endotracheale Aspirate (ETA) von COVID-19-Patienten (RT-PCR positiv f&#252;r SARS-CoV-2) gewonnen. Die bakteriellen Isolate wurden mit den mikrobiologischen Standardmethoden best&#228;tigt. Die Antibiotikaresistenz wurde im Plattendiffusionstest bestimmt.</Pgraph><Pgraph><Mark1>Ergebnisse:</Mark1> Unter 340 Patienten mit COVID-19 hatten insgesamt 43 (12,46 &#37;) Patienten bakterielle Sekund&#228;rinfektionen. Die h&#228;ufigsten Bakterien, die durch ETA und BC isoliert wurden, waren Klebsiella-Spezies 11 (25,59&#37;), Methicillin-sensitiver <Mark2>Staphylococcus aureus</Mark2> (MSSA) 9 (20,93&#37;) und <Mark2>Escherichia coli</Mark2> 7 (16. 28&#37;), Methicillin-resistenter <Mark2>Staphylococcus aureus</Mark2> (MRSA) 6 (13,95&#37;), und Enterobacter-Arten 5 (11,63&#37;) sowie <Mark2>Streptococcus pneumoniae</Mark2> 1 (2,32&#37;) und <Mark2>Pseudomonas aeruginosa</Mark2> 4 (9,30&#37;). Die Ergebnisse zeigten, dass Enterobacteriaceae-Isolate von COVID-19-Patienten die h&#246;chste Resistenz gegen Cotrimoxazol (74&#37;), Piperacillin (67,5&#37;), Ceftazidim (47,5&#37;) und Cefepime (42,5&#37;) aufwiesen. Alle Isolate waren empfindlich gegen&#252;ber Amikacin (100&#37;). <Mark2>S. aureus</Mark2>-Isolate waren empfindlich gegen&#252;ber Vancomycin (100&#37;) und die Resistenzraten gegen&#252;ber Oxacillin, Erythromycin und Clindamycin waren &#252;ber 90&#37;. <Mark2>P. aeruginosa</Mark2> war empfindlich (90&#37;) gegen&#252;ber Imipenem.</Pgraph><Pgraph><Mark1>Schlussfolgerungen:</Mark1> Bakterielle Co-Infektionen sind bei hospitalisierten COVID-19-Patienten relativ selten. Nach den Ergebnissen k&#246;nnte eine der Todesursachen dieser Patienten eine Sekund&#228;rinfektion sein.</Pgraph></Abstract>
    <Abstract language="en" linked="yes"><Pgraph><Mark1>Background:</Mark1> Bacterial co-infections are frequently identified in viral respiratory infections and are significant reasons for morbidity and mortality. Information on the prevalence of bacterial co-infection in patients infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is lacking. The purpose of this study was to determine the prevalence of bacterial infections and antibiotic resistance in patients with coronavirus disease (COVID-19).</Pgraph><Pgraph><Mark1>Methods:</Mark1> In a cross-sectional study, blood culture (BC) and endotracheal aspirate (ETA) were obtained from COVID-19 patients (RT-PCR positive for SARS-CoV-2). The bacterial isolates were confirmed by the standard microbiological methods. Antibiotic resistance was determined using the disk diffusion method.</Pgraph><Pgraph><Mark1>Results:</Mark1> Among these 340 patients with COVID-19, a total of 43 (12.46&#37;) patients had secondary bacterial infections. The most common bacteria isolated through ETA and BC included Klebsiella species 11 (25.59&#37;), methicillin-sensitive <Mark2>Staphylococcus aureus</Mark2> (MSSA) 9 (20.93&#37;), <Mark2>Escherichia coli</Mark2> 7 (16.28&#37;), methicillin-resistant <Mark2>Staphylococcus aureus</Mark2> (MRSA) 6 (13.95&#37;), <Mark2>Enterobacter species</Mark2> 5 (11.63&#37;), <Mark2>Streptococcus pneumoniae</Mark2> 1 (2.32&#37;), and <Mark2>Pseudomonas aeruginosa</Mark2> 4 (9.30&#37;). The results showed that Enterobacteriaceae isolates from COVID-19 patients had the highest resistance to cotrimoxazole (74&#37;), piperacillin (67.5&#37;), ceftazidime (47.5&#37;), and cefepime (42.5&#37;). All isolates were susceptible to amikacin (100&#37;). <Mark2>S. aureus</Mark2> isolates were susceptible to vancomycin (100&#37;) and the rates of resistance to oxacillin, erythromycin and clindamycin were over (90&#37;). <Mark2>P. aeruginosa</Mark2> was susceptible (90&#37;) to imipenem.</Pgraph><Pgraph><Mark1>Conclusions:</Mark1> Bacterial co-infection is relatively infrequent in hospitalized COVID-19 patients. According to the results, one of the causes of death of these patients could be a secondary infections. </Pgraph></Abstract>
    <TextBlock linked="yes" name="Introduction">
      <MainHeadline>Introduction</MainHeadline><Pgraph>Bacterial co-infections are frequently determined in viral respiratory tract infections, such as influenza, and are a significant cause of morbidity and mortality. Thus, timely diagnosis and antibacterial treatment are necessary <TextLink reference="1"></TextLink>, <TextLink reference="2"></TextLink>, <TextLink reference="3"></TextLink> The frequency, incidence and features of bacterial co-infection in patients infected with (SARS-CoV-2) are not clear; in these critical circumstances, this is a crucial knowledge gap <TextLink reference="4"></TextLink>, <TextLink reference="5"></TextLink>, <TextLink reference="6"></TextLink>, <TextLink reference="7"></TextLink> Although antibiotics are ineffective treatment of COVID-19, physicians prescribed them for patients with suspected or documented COVID-19 for a variety of reasons <TextLink reference="8"></TextLink>. In terms of the mortality rate of patients with bacterial supra-infection during influenza pandemics, several guidelines support the usage of empirical antibiotic therapy for COVID-19 patients <TextLink reference="8"></TextLink>. It is difficult to rule out bacterial co-infection on presentation, but also the possibility of bacterial secondary infection during the course of the disease. Nevertheless, this approach increases concerns about antibiotic overuse and subsequent detrimental consequences related to bacterial resistance. Given a rise in mortality in patients with bacterial supra-infection during influenza pandemics, several guidelines supporting the application of empirical antibiotics for patients with severe COVID-19 have been developed <TextLink reference="8"></TextLink>. Given the fact that Covid-19 patients can have a bacterial co-infection and bearing in mind the action of the pathogens, it is critical to treat Covid-19 patients responsibly in terms of antibiotics in order to minimize the negative effects of overuse <TextLink reference="6"></TextLink>. Furthermore, the rate of bacterial co-infection in Covid-19 patients could have an important influence on refining empirical antibiotic management guidelines for patients with COVID-19. The purpose of this study was to identify the prevalence of bacterial co-infection in COVID-19 patients.</Pgraph></TextBlock>
    <TextBlock linked="yes" name="Methods">
      <MainHeadline>Methods</MainHeadline><SubHeadline>Study design</SubHeadline><Pgraph>Sampling for this cross-sectional study was done at Nahavand Hospitals, Hamedan, Iran. The study was performed from February 17, 2020 to October 20, 2020. Eligibility for participating in the study was determined by criteria itemized in a questionnaire completed by each patient. Initial laboratory investigations included complete blood count (CBC), erythrocyte sedimentation rate (ESR), arterial blood gas (ABG), lactate dehydrogenase (LDH), and C-reactive protein (CRP) tests. Serial monitoring of the laboratory profile was performed according to the clinical progress of the individual patient. All patients were laboratory-confirmed positive for SARS-CoV-2 by use of quantitative RT-PCR (qRT-PCR) on throat-swab samples. We reviewed the clinical laboratory findings for all the COVID-19 patients. All information was obtained and recorded in a customized data collection form. </Pgraph><SubHeadline>Culture and isolation of bacteria</SubHeadline><Pgraph>BC and ETA cultures were obtained from COVID-19 patients. In order to differentiate microorganisms, swabs and blood were cultured on blood agar and MacConkey agar plates and incubated at 37&#176;C for 18&#8211;24 hours. Identification of the isolated bacteria was performed using standard microbiological methods <TextLink reference="9"></TextLink>. </Pgraph><SubHeadline>Antibacterial susceptibility</SubHeadline><Pgraph>For all isolated strains, antibacterial susceptibility was tested using the standard Kirby-Bauer disk-diffusion method on Mueller Hinton agar (Merk Co., Germany) in accordance with the clinical and laboratory standards institute guidelines (CLSI; 2019, M100-S29) using gentamicin (10 &#181;g), vancomycin (30 &#181;g), trimethoprim&#47;sulfamethoxazole (25 &#181;g), amikacin (30 &#181;g), tobramycin (10 &#181;g), cephalotin (30 &#181;g), norfloxacin (5 &#181;g), and ceftizoxim (30 &#181;g) disks (Mast Co.UK) (<TextLink reference="10"></TextLink>, <TextLink reference="11"></TextLink>).</Pgraph></TextBlock>
    <TextBlock linked="yes" name="Results">
      <MainHeadline>Results</MainHeadline><Pgraph>A total of 43 positive cultures (12.46&#37;) of the blood and endotracheal aspirate samples were obtained. The most common bacteria isolated from endotracheal aspirate and blood cultures included Klebsiella species 11 (25.59&#37;), <Mark2>S. aureus</Mark2> (MSSA) 9 (20.93&#37;), <Mark2>E. coli</Mark2> 8 (18.6&#37;), <Mark2>S. aureus</Mark2> (MRSA), 6 (13.95&#37;), and Enterobacter species 5 (11.63&#37;), as well as confirmed presence of <Mark2>P. aeruginosa</Mark2> 4 (9.30&#37;) (Table 1 <ImgLink imgNo="1" imgType="table"/>). The sensitivity patterns to tested antibiotics are shown in Figure 1 <ImgLink imgNo="1" imgType="figure"/>.</Pgraph></TextBlock>
    <TextBlock linked="yes" name="Discussion">
      <MainHeadline>Discussion</MainHeadline><Pgraph>COVID-19, a viral pneumonia that is now a pandemic, is considered a novel public health concern. Recent studies show that 2019-nCoV originated from an animal source and later adapted to other variants as it crossed the species barrier to ultimately infect humans. It is well established that seasonal viral respiratory tract infections are related to increased risk of bacterial co-infection. In previous influenza pandemics, bacterial co-infections have been a major cause of mortality <TextLink reference="12"></TextLink>. We aimed to evaluate the burden of co-infections in patients with COVID-19. Among these 340 patients with COVID-19, secondary bacterial infections occurred in a total of 43 (12.46&#37;) patients. The most common bacteria isolated from endotracheal aspirate and blood cultures included <Mark2>Klebsiella</Mark2> species, <Mark2>S. aureus</Mark2> (MSSA), and <Mark2>E. coli</Mark2>, <Mark2>S. aureus</Mark2> (MRSA), and <Mark2>Enterobacter</Mark2> species, and the presence of <Mark2>S. pneumoniae</Mark2> and <Mark2>P. aeruginosa</Mark2>. Moreover, hospital admissions increase the risk of health-care related infections and the transmission of multidrug-resistant organisms, which in turn lead to increased use of antibiotics. A recent study in intensive care units (ICU) in 88 countries showed that although only 54&#37; of patients had suspected or confirmed bacterial co-infection, 70&#37; of them had received at least one antibiotic either as treatment or as antimicrobial prophylaxis <TextLink reference="13"></TextLink>. At Montefiore medical center (New York City), Amy Norton <TextLink reference="14"></TextLink> reported this earlier in the pandemic: Of more than 5,800 COVID-19 patients hospitalized from March through May, 2020, 71&#37; received at least one antibiotic drug dose <TextLink reference="14"></TextLink>. Two studies published on hospitalized COVID-19 patients determined that while 72&#37; of patients received antibiotics, only 8&#37; confirmed bacterial supra-infection or fungal co-infections <TextLink reference="13"></TextLink><TextLink reference="14"></TextLink>. Moreover, in the study by Sharifipour et al. <TextLink reference="10"></TextLink>, an evaluation of bacterial co-infections of the respiratory tract in COVID-19 patients admitted to the ICU also showed secondary infections with <Mark2>Acinetobacter baumannii</Mark2> and two <Mark2>S. aureus</Mark2> strains. Yang et al. <TextLink reference="15"></TextLink> reported that hospital-acquired infections were prominent in 13.5&#37; of patients, including one (2&#37;) patient who had pulmonary and blood-stream infection with <Mark2>K. pneumoniae</Mark2>. Other microorganisms recognized from respiratory tract secretions in five (10&#37;) patients included Aspergillus flavus, A fumigatus, extended spectrum &#946;-Lactamase (ESBL)-positive <Mark2>K. pneumonia</Mark2>, ESBL-positive <Mark2>P. aeruginosa</Mark2>, and ESBL-negative <Mark2>Serratia marcescens</Mark2>, with each microorganism found in one patient each. <Mark2>Candida albicans</Mark2> was detected in the urine culture of one (2&#37;) patient. In another study, Xavier Lescure et al. <TextLink reference="16"></TextLink> identified two pathogens: antibiotic-susceptible <Mark2>A. baumannii</Mark2> and <Mark2>A. flavus</Mark2>. Zhou et al. <TextLink reference="17"></TextLink> showed that half of the patients with COVID-19 developed sepsis. In the current study, we found that in 12.5&#37; patients, secondary bacterial infections occurred. Guo et al. <TextLink reference="18"></TextLink> reported that some patients, particularly severely ills ones, had co-infections with bacteria. The usual bacterial cultures from patients with secondary infections identified <Mark2>A. baumannii</Mark2> and <Mark2>K. pneumoniae</Mark2>. Compared with <Mark2>K. pneumoniae</Mark2>,<Mark2> A. baumannii</Mark2> was more highly resistant to antibiotics. Cucchiari <TextLink reference="19"></TextLink> and Xing <TextLink reference="20"></TextLink> in two separate studies reported various incidence rates of simultaneous bacterial infection in COVID-19. Xing et al. <TextLink reference="19"></TextLink> found the most common respiratory pathogens in COVID-19 patients to be <Mark2>Mycoplasma pneumoniae</Mark2> (23.33&#37;) and <Mark2>Legionella pneumophila</Mark2> (20&#37;). Xing et al. <TextLink reference="19"></TextLink> in two separate studies reported 1 to 10&#37; of COVID-19 patients to contract secondary bacterial infections. In a systematic review, Lansbury et al. <TextLink reference="12"></TextLink> reported that 7&#37; of hospitalized COVID-19 patients had a bacterial co-infection. The most common bacteria were <Mark2>M. pneumonia</Mark2>, <Mark2>P. aeruginosa,</Mark2> and <Mark2>Haemophilus influenza</Mark2>. Toombs et al. <TextLink reference="21"></TextLink> found that two COVID-19 patients (0.4&#37;) were co-infected with <Mark2>S. pneumoniae</Mark2>, as determined by blood culture positivity upon hospitalization in the United Kingdom. These results support the hypothesis of secondary infection in COVID 19 patients. According to information from studies of antibiotic usage in treating COVID-19 patients, an average 70&#37; of patients receive antibiotics. Nevertheless, extreme caution should be used, given that inappropriate usage or overuse of antibiotics is known to be an important driver of the emergence of antimicrobial resistance. This is why significant efforts against antimicrobial resistance revolve around reducing inappropriate or overuse of antibiotics <TextLink reference="22"></TextLink>. Excessive use of antimicrobial soaps and disinfectants by hospital staff will have become more common over the last few months. If these products based on chlorhexidine digluconate or quaternary ammonium compounds, this too can lead to antibiotic resistance. The present study found that COVID-19 patients with secondary bacterial infections were highly resistant to common antibiotics in the isolated bacteria. The results showed that <Mark2>Enterobacteriaceae</Mark2> isolates from COVID-19 patients had the highest resistance to cotrimoxazole (74&#37;), piperacillin (67.5&#37;), ceftazidime (47.5&#37;), and cefepime (42.5&#37;); all isolates were susceptible to amikacin (100&#37;). <Mark2>S. aureus</Mark2> isolates were susceptible to vancomycin (100&#37;), but the rates of resistance to oxacillin, erythromycin and clindamycin were over (90&#37;); furthermore, <Mark2>P. aeruginosa</Mark2> spp. was susceptible (90&#37;) to imipenem. Another possible threat is the extensive application of biocidal agents for personal and environmental disinfection in non-healthcare settings. A low level of exposure to biocidal agents can select for drug resistant strains and increase the risk of cross-resistance to different antibiotics, mainly those that treat Gram-negative bacteria <TextLink reference="13"></TextLink>. In recent months, less attention has been paid to nosocomial infections and opportunistic microorganisms, which could be due to the outbreak of COVID-19, its consequent long-term hospitalization of patients, and high workload on the healthcare personnel. </Pgraph><Pgraph>Nevertheless, our findings were based on a limited number of observational studies. Further well-designed studies with larger sample sizes are necessary to increase our knowledge of the prevalence and risk of COVID-19 bacterial co-infection, as well as the influence of co-infection on the clinical outcomes of COVID-19 patients.</Pgraph></TextBlock>
    <TextBlock linked="yes" name="Conclusions">
      <MainHeadline>Conclusions</MainHeadline><Pgraph>The current report highlights the need to consider co-infection of SARS-CoV-2 with other pathogens to optimize treatment. After obtaining more data regarding co-infection with SARS-CoV-2, empirical antimicrobial agents in suspected COVID-19 cases can be suggested.</Pgraph></TextBlock>
    <TextBlock linked="yes" name="Abbreviation">
      <MainHeadline>Abbreviation</MainHeadline><Pgraph><Mark1>SARS-CoV-2:</Mark1> Severe acute respiratory syndrome coronavirus 2</Pgraph><Pgraph><Mark1>COVID-19:</Mark1> coronavirus  disease</Pgraph><Pgraph><Mark1>BC:</Mark1> Blood culture</Pgraph><Pgraph><Mark1>ETA:</Mark1> Endotracheal aspirate</Pgraph><Pgraph><Mark1>MSSA:</Mark1> Methicillin sensitive <Mark2>Staphylococcus aureus</Mark2></Pgraph><Pgraph><Mark1>MRSA:</Mark1> Methicillin resistance <Mark2>Staphylococcus aureus</Mark2></Pgraph><Pgraph><Mark1>ESBL:</Mark1> Extended spectrum &#946;-Lactamase </Pgraph><Pgraph><Mark1>CBC:</Mark1> Complete blood count </Pgraph><Pgraph><Mark1>ESR:</Mark1> Erythrocyte sedimentation rate </Pgraph><Pgraph><Mark1>ABG:</Mark1> Arterial blood gas </Pgraph><Pgraph><Mark1>LDH:</Mark1> lactate dehydrogenase </Pgraph><Pgraph><Mark1>CRP:</Mark1> C-reactive protein</Pgraph><Pgraph><Mark1>QRT-PCR:</Mark1> Quantitative RT-PCR</Pgraph></TextBlock>
    <TextBlock linked="yes" name="Notes">
      <MainHeadline>Notes</MainHeadline><SubHeadline>Competing interests</SubHeadline><Pgraph>The author declares that he has no competing interests.</Pgraph><SubHeadline>Acknowledgements</SubHeadline><Pgraph>I would like to thank all members of laboratory medicine of Ayatollah Alimoradiyan Hospital, Nahavand, Hamadan, Iran. </Pgraph><SubHeadline>Funding</SubHeadline><Pgraph>This research was supported by Vice Chancellor for Research &#38; Technology of Hamadan University of Medical Sciences, Hamadan, Iran.  </Pgraph><SubHeadline>Authors&#8217; contributions</SubHeadline><Pgraph>All stages of this study were performed by HM.</Pgraph><SubHeadline>Ethics approval and consent to participate</SubHeadline><Pgraph>This study has been approved by the Hamadan University of Medical Sciences, Iran, ethics code IR.UMSHA.REC.1399.095.</Pgraph></TextBlock>
    <References linked="yes">
      <Reference refNo="1">
        <RefAuthor>Clancy CJ</RefAuthor>
        <RefAuthor>Nguyen MH</RefAuthor>
        <RefTitle>COVID-19, superinfections and antimicrobial development: What can we expect&#63; Clin Infect Dis</RefTitle>
        <RefYear>2020</RefYear>
        <RefTotal>Clancy CJ, Nguyen MH. COVID-19, superinfections and antimicrobial development: What can we expect&#63; Clin Infect Dis. 2020 May. DOI: 10.1093&#47;cid&#47;ciaa524</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1093&#47;cid&#47;ciaa524</RefLink>
      </Reference>
      <Reference refNo="2">
        <RefAuthor>Morens DM</RefAuthor>
        <RefAuthor>Taubenberger JK</RefAuthor>
        <RefAuthor>Fauci AS</RefAuthor>
        <RefTitle>Predominant role of bacterial pneumonia as a cause of death in pandemic influenza: implications for pandemic influenza preparedness</RefTitle>
        <RefYear>2008</RefYear>
        <RefJournal>J Infect Dis</RefJournal>
        <RefPage>962-70</RefPage>
        <RefTotal>Morens DM, Taubenberger JK, Fauci AS. Predominant role of bacterial pneumonia as a cause of death in pandemic influenza: implications for pandemic influenza preparedness. J Infect Dis. 2008 Oct;198(7):962-70. DOI: 10.1086&#47;591708</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1086&#47;591708</RefLink>
      </Reference>
      <Reference refNo="3">
        <RefAuthor>Esper FP</RefAuthor>
        <RefAuthor>Spahlinger T</RefAuthor>
        <RefAuthor>Zhou L</RefAuthor>
        <RefTitle>Rate and influence of respiratory virus co-infection on pandemic (H1N1) influenza disease</RefTitle>
        <RefYear>2011</RefYear>
        <RefJournal>J Infect</RefJournal>
        <RefPage>260-6</RefPage>
        <RefTotal>Esper FP, Spahlinger T, Zhou L. Rate and influence of respiratory virus co-infection on pandemic (H1N1) influenza disease. J Infect. 2011 Oct;63(4):260-6. DOI: 10.1016&#47;j.jinf.2011.04.004</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;j.jinf.2011.04.004</RefLink>
      </Reference>
      <Reference refNo="4">
        <RefAuthor>Langford BJ</RefAuthor>
        <RefAuthor>So M</RefAuthor>
        <RefAuthor>Raybardhan S</RefAuthor>
        <RefAuthor>Leung V</RefAuthor>
        <RefAuthor>Westwood D</RefAuthor>
        <RefAuthor>MacFadden DR</RefAuthor>
        <RefAuthor>Soucy JR</RefAuthor>
        <RefAuthor>Daneman N</RefAuthor>
        <RefTitle>Bacterial co-infection and secondary infection in patients with COVID-19: a living rapid review and meta-analysis</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Clin Microbiol Infect</RefJournal>
        <RefPage>1622-9</RefPage>
        <RefTotal>Langford BJ, So M, Raybardhan S, Leung V, Westwood D, MacFadden DR, Soucy JR, Daneman N. Bacterial co-infection and secondary infection in patients with COVID-19: a living rapid review and meta-analysis. Clin Microbiol Infect. 2020 Dec;26(12):1622-9. DOI: 10.1016&#47;j.cmi.2020.07.016</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;j.cmi.2020.07.016</RefLink>
      </Reference>
      <Reference refNo="5">
        <RefAuthor>Adeiza SS</RefAuthor>
        <RefAuthor>Shuaibu AB</RefAuthor>
        <RefAuthor>Shuaibu GM</RefAuthor>
        <RefTitle>Random effects meta-analysis of COVID-19&#47;S. aureus partnership in co-infection</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>GMS Hyg Infect Control</RefJournal>
        <RefPage>Doc29</RefPage>
        <RefTotal>Adeiza SS, Shuaibu AB, Shuaibu GM. Random effects meta-analysis of COVID-19&#47;S. aureus partnership in co-infection. GMS Hyg Infect Control. 2020 Nov 27;15:Doc29. DOI: 10.3205&#47;dgkh000364</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.3205&#47;dgkh000364</RefLink>
      </Reference>
      <Reference refNo="6">
        <RefAuthor>Huttner BD</RefAuthor>
        <RefAuthor>Catho G</RefAuthor>
        <RefAuthor>Pano-Pardo JR</RefAuthor>
        <RefAuthor>Pulcini C</RefAuthor>
        <RefAuthor>Schouten J</RefAuthor>
        <RefTitle>COVID-19: don&#39;t neglect antimicrobial stewardship principles&#33;</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Clin Microbiol Infect</RefJournal>
        <RefPage>808-10</RefPage>
        <RefTotal>Huttner BD, Catho G, Pano-Pardo JR, Pulcini C, Schouten J. COVID-19: don&#39;t neglect antimicrobial stewardship principles&#33;. Clin Microbiol Infect. 2020 07;26(7):808-10. DOI: 10.1016&#47;j.cmi.2020.04.024</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;j.cmi.2020.04.024</RefLink>
      </Reference>
      <Reference refNo="7">
        <RefAuthor>Cox MJ</RefAuthor>
        <RefAuthor>Loman N</RefAuthor>
        <RefAuthor>Bogaert D</RefAuthor>
        <RefAuthor>O&#39;grady J</RefAuthor>
        <RefTitle>Co-infections: potentially lethal and unexplored in COVID-19</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Lancet Microbe</RefJournal>
        <RefPage>e11</RefPage>
        <RefTotal>Cox MJ, Loman N, Bogaert D, O&#39;grady J. Co-infections: potentially lethal and unexplored in COVID-19. Lancet Microbe. 2020;1(1):e11. DOI: 10.1016&#47;S2666-5247(20)30009-4</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;S2666-5247(20)30009-4</RefLink>
      </Reference>
      <Reference refNo="8">
        <RefAuthor>Alhazzani W</RefAuthor>
        <RefAuthor>M&#248;ller MH</RefAuthor>
        <RefAuthor>Arabi YM</RefAuthor>
        <RefAuthor>Loeb M</RefAuthor>
        <RefAuthor>Gong MN</RefAuthor>
        <RefAuthor>Fan E</RefAuthor>
        <RefAuthor>Oczkowski S</RefAuthor>
        <RefAuthor>Levy MM</RefAuthor>
        <RefAuthor>Derde L</RefAuthor>
        <RefAuthor>Dzierba A</RefAuthor>
        <RefAuthor>Du B</RefAuthor>
        <RefAuthor>Aboodi M</RefAuthor>
        <RefAuthor>Wunsch H</RefAuthor>
        <RefAuthor>Cecconi M</RefAuthor>
        <RefAuthor>Koh Y</RefAuthor>
        <RefAuthor>Chertow DS</RefAuthor>
        <RefAuthor>Maitland K</RefAuthor>
        <RefAuthor>Alshamsi F</RefAuthor>
        <RefAuthor>Belley-Cote E</RefAuthor>
        <RefAuthor>Greco M</RefAuthor>
        <RefAuthor>Laundy M</RefAuthor>
        <RefAuthor>Morgan JS</RefAuthor>
        <RefAuthor>Kesecioglu J</RefAuthor>
        <RefAuthor>McGeer A</RefAuthor>
        <RefAuthor>Mermel L</RefAuthor>
        <RefAuthor>Mammen MJ</RefAuthor>
        <RefAuthor>Alexander PE</RefAuthor>
        <RefAuthor>Arrington A</RefAuthor>
        <RefAuthor>Centofanti JE</RefAuthor>
        <RefAuthor>Citerio G</RefAuthor>
        <RefAuthor>Baw B</RefAuthor>
        <RefAuthor>Memish ZA</RefAuthor>
        <RefAuthor>Hammond N</RefAuthor>
        <RefAuthor>Hayden FG</RefAuthor>
        <RefAuthor>Evans L</RefAuthor>
        <RefAuthor>Rhodes A</RefAuthor>
        <RefTitle>Surviving Sepsis Campaign: Guidelines on the Management of Critically Ill Adults with Coronavirus Disease 2019 (COVID-19)</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Crit Care Med</RefJournal>
        <RefPage>e440-e469</RefPage>
        <RefTotal>Alhazzani W, M&#248;ller MH, Arabi YM, Loeb M, Gong MN, Fan E, Oczkowski S, Levy MM, Derde L, Dzierba A, Du B, Aboodi M, Wunsch H, Cecconi M, Koh Y, Chertow DS, Maitland K, Alshamsi F, Belley-Cote E, Greco M, Laundy M, Morgan JS, Kesecioglu J, McGeer A, Mermel L, Mammen MJ, Alexander PE, Arrington A, Centofanti JE, Citerio G, Baw B, Memish ZA, Hammond N, Hayden FG, Evans L, Rhodes A. Surviving Sepsis Campaign: Guidelines on the Management of Critically Ill Adults with Coronavirus Disease 2019 (COVID-19). Crit Care Med. 2020 06;48(6):e440-e469. DOI: 10.1097&#47;CCM.0000000000004363</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1097&#47;CCM.0000000000004363</RefLink>
      </Reference>
      <Reference refNo="9">
        <RefAuthor>Hall GS</RefAuthor>
        <RefTitle>Bailey &#38; Scott&#39;s Diagnostic Microbiology, 13th edition</RefTitle>
        <RefYear>2013</RefYear>
        <RefJournal>Lab Med</RefJournal>
        <RefPage>e138-e139</RefPage>
        <RefTotal>Hall GS. Bailey &#38; Scott&#39;s Diagnostic Microbiology, 13th edition. Lab Med. 2013;44(4):e138-e139. DOI: 10.1309&#47;LM5JC0PH0OGGBSZZ</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1309&#47;LM5JC0PH0OGGBSZZ</RefLink>
      </Reference>
      <Reference refNo="10">
        <RefAuthor>Sharifipour E</RefAuthor>
        <RefAuthor>Shams S</RefAuthor>
        <RefAuthor>Esmkhani M</RefAuthor>
        <RefAuthor>Khodadadi J</RefAuthor>
        <RefAuthor>Fotouhi-Ardakani R</RefAuthor>
        <RefAuthor>Koohpaei A</RefAuthor>
        <RefAuthor>Doosti Z</RefAuthor>
        <RefAuthor>Ej Golzari S</RefAuthor>
        <RefTitle>Evaluation of bacterial co-infections of the respiratory tract in COVID-19 patients admitted to ICU</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>BMC Infect Dis</RefJournal>
        <RefPage>646</RefPage>
        <RefTotal>Sharifipour E, Shams S, Esmkhani M, Khodadadi J, Fotouhi-Ardakani R, Koohpaei A, Doosti Z, Ej Golzari S. Evaluation of bacterial co-infections of the respiratory tract in COVID-19 patients admitted to ICU. BMC Infect Dis. 2020 Sep;20(1):646. DOI: 10.1186&#47;s12879-020-05374-z</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1186&#47;s12879-020-05374-z</RefLink>
      </Reference>
      <Reference refNo="11">
        <RefAuthor>CLSI MEE</RefAuthor>
        <RefTitle></RefTitle>
        <RefYear>2019</RefYear>
        <RefBookTitle>Performance Standards for Antimicrobial Susceptibility Testing: 29th Informational Supplement</RefBookTitle>
        <RefPage></RefPage>
        <RefTotal>CLSI MEE. Performance Standards for Antimicrobial Susceptibility Testing: 29th Informational Supplement. Wayne, PA: Clinical and Laboratory Standards Institute; 2019.</RefTotal>
      </Reference>
      <Reference refNo="12">
        <RefAuthor>Lansbury L</RefAuthor>
        <RefAuthor>Lim B</RefAuthor>
        <RefAuthor>Baskaran V</RefAuthor>
        <RefAuthor>Lim WS</RefAuthor>
        <RefTitle>Co-infections in people with COVID-19: a systematic review and meta-analysis</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>J Infect</RefJournal>
        <RefPage>266-75</RefPage>
        <RefTotal>Lansbury L, Lim B, Baskaran V, Lim WS. Co-infections in people with COVID-19: a systematic review and meta-analysis. J Infect. 2020 Aug;81(2):266-75. DOI: 10.1016&#47;j.jinf.2020.05.046</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;j.jinf.2020.05.046</RefLink>
      </Reference>
      <Reference refNo="13">
        <RefAuthor>Getahun H</RefAuthor>
        <RefAuthor>Smith I</RefAuthor>
        <RefAuthor>Trivedi K</RefAuthor>
        <RefAuthor>Paulin S</RefAuthor>
        <RefAuthor>Balkhy HH</RefAuthor>
        <RefTitle>Tackling antimicrobial resistance in the COVID-19 pandemic</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Bull World Health Organ</RefJournal>
        <RefPage>442-442A</RefPage>
        <RefTotal>Getahun H, Smith I, Trivedi K, Paulin S, Balkhy HH. Tackling antimicrobial resistance in the COVID-19 pandemic. Bull World Health Organ. 2020 07;98(7):442-442A. DOI: 10.2471&#47;BLT.20.268573</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.2471&#47;BLT.20.268573</RefLink>
      </Reference>
      <Reference refNo="14">
        <RefAuthor>Norton A</RefAuthor>
        <RefTitle></RefTitle>
        <RefYear>2020</RefYear>
        <RefBookTitle>Many COVID-19 patients given useless antibiotics, study finds</RefBookTitle>
        <RefPage></RefPage>
        <RefTotal>Norton A. Many COVID-19 patients given useless antibiotics, study finds. Isle of Man, UK: Medical Xpress; Aug 4 2020. Available from: https:&#47;&#47;medicalxpress.com&#47;news&#47;2020-08-covid-patients-useless-antibiotics.html</RefTotal>
        <RefLink>https:&#47;&#47;medicalxpress.com&#47;news&#47;2020-08-covid-patients-useless-antibiotics.html</RefLink>
      </Reference>
      <Reference refNo="15">
        <RefAuthor>Yang X</RefAuthor>
        <RefAuthor>Yu Y</RefAuthor>
        <RefAuthor>Xu J</RefAuthor>
        <RefAuthor>Shu H</RefAuthor>
        <RefAuthor>Xia J</RefAuthor>
        <RefAuthor>Liu H</RefAuthor>
        <RefAuthor>Wu Y</RefAuthor>
        <RefAuthor>Zhang L</RefAuthor>
        <RefAuthor>Yu Z</RefAuthor>
        <RefAuthor>Fang M</RefAuthor>
        <RefAuthor>Yu T</RefAuthor>
        <RefAuthor>Wang Y</RefAuthor>
        <RefAuthor>Pan S</RefAuthor>
        <RefAuthor>Zou X</RefAuthor>
        <RefAuthor>Yuan S</RefAuthor>
        <RefAuthor>Shang Y</RefAuthor>
        <RefTitle>Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Lancet Respir Med</RefJournal>
        <RefPage>475-81</RefPage>
        <RefTotal>Yang X, Yu Y, Xu J, Shu H, Xia J, Liu H, Wu Y, Zhang L, Yu Z, Fang M, Yu T, Wang Y, Pan S, Zou X, Yuan S, Shang Y. Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study. Lancet Respir Med. 2020 May;8(5):475-81. DOI: 10.1016&#47;S2213-2600(20)30079-5</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;S2213-2600(20)30079-5</RefLink>
      </Reference>
      <Reference refNo="16">
        <RefAuthor>Lescure FX</RefAuthor>
        <RefAuthor>Bouadma L</RefAuthor>
        <RefAuthor>Nguyen D</RefAuthor>
        <RefAuthor>Parisey M</RefAuthor>
        <RefAuthor>Wicky PH</RefAuthor>
        <RefAuthor>Behillil S</RefAuthor>
        <RefAuthor>Gaymard A</RefAuthor>
        <RefAuthor>Bouscambert-Duchamp M</RefAuthor>
        <RefAuthor>Donati F</RefAuthor>
        <RefAuthor>Le Hingrat Q</RefAuthor>
        <RefAuthor>Enouf V</RefAuthor>
        <RefAuthor>Houhou-Fidouh N</RefAuthor>
        <RefAuthor>Valette M</RefAuthor>
        <RefAuthor>Mailles A</RefAuthor>
        <RefAuthor>Lucet JC</RefAuthor>
        <RefAuthor>Mentre F</RefAuthor>
        <RefAuthor>Duval X</RefAuthor>
        <RefAuthor>Descamps D</RefAuthor>
        <RefAuthor>Malvy D</RefAuthor>
        <RefAuthor>Timsit JF</RefAuthor>
        <RefAuthor>Lina B</RefAuthor>
        <RefAuthor>van-der-Werf S</RefAuthor>
        <RefAuthor>Yazdanpanah Y</RefAuthor>
        <RefTitle>Clinical and virological data of the first cases of COVID-19 in Europe: a case series</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Lancet Infect Dis</RefJournal>
        <RefPage>697-706</RefPage>
        <RefTotal>Lescure FX, Bouadma L, Nguyen D, Parisey M, Wicky PH, Behillil S, Gaymard A, Bouscambert-Duchamp M, Donati F, Le Hingrat Q, Enouf V, Houhou-Fidouh N, Valette M, Mailles A, Lucet JC, Mentre F, Duval X, Descamps D, Malvy D, Timsit JF, Lina B, van-der-Werf S, Yazdanpanah Y. Clinical and virological data of the first cases of COVID-19 in Europe: a case series. Lancet Infect Dis. 2020 Jun;20(6):697-706. DOI: 10.1016&#47;S1473-3099(20)30200-0</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;S1473-3099(20)30200-0</RefLink>
      </Reference>
      <Reference refNo="17">
        <RefAuthor>Zhou F</RefAuthor>
        <RefAuthor>Yu T</RefAuthor>
        <RefAuthor>Du R</RefAuthor>
        <RefAuthor>Fan G</RefAuthor>
        <RefAuthor>Liu Y</RefAuthor>
        <RefAuthor>Liu Z</RefAuthor>
        <RefAuthor>Xiang J</RefAuthor>
        <RefAuthor>Wang Y</RefAuthor>
        <RefAuthor>Song B</RefAuthor>
        <RefAuthor>Gu X</RefAuthor>
        <RefAuthor>Guan L</RefAuthor>
        <RefAuthor>Wei Y</RefAuthor>
        <RefAuthor>Li H</RefAuthor>
        <RefAuthor>Wu X</RefAuthor>
        <RefAuthor>Xu J</RefAuthor>
        <RefAuthor>Tu S</RefAuthor>
        <RefAuthor>Zhang Y</RefAuthor>
        <RefAuthor>Chen H</RefAuthor>
        <RefAuthor>Cao B</RefAuthor>
        <RefTitle>Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Lancet</RefJournal>
        <RefPage>1054-62</RefPage>
        <RefTotal>Zhou F, Yu T, Du R, Fan G, Liu Y, Liu Z, Xiang J, Wang Y, Song B, Gu X, Guan L, Wei Y, Li H, Wu X, Xu J, Tu S, Zhang Y, Chen H, Cao B. Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Lancet. 2020 Mar 28;395(10229):1054-62. DOI: 10.1016&#47;S0140-6736(20)30566-3</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;S0140-6736(20)30566-3</RefLink>
      </Reference>
      <Reference refNo="18">
        <RefAuthor>Chen N</RefAuthor>
        <RefAuthor>Zhou M</RefAuthor>
        <RefAuthor>Dong X</RefAuthor>
        <RefAuthor>Qu J</RefAuthor>
        <RefAuthor>Gong F</RefAuthor>
        <RefAuthor>Han Y</RefAuthor>
        <RefAuthor>Qiu Y</RefAuthor>
        <RefAuthor>Wang J</RefAuthor>
        <RefAuthor>Liu Y</RefAuthor>
        <RefAuthor>Wei Y</RefAuthor>
        <RefAuthor>Xia J</RefAuthor>
        <RefAuthor>Yu T</RefAuthor>
        <RefAuthor>Zhang X</RefAuthor>
        <RefAuthor>Zhang L</RefAuthor>
        <RefTitle>Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Lancet</RefJournal>
        <RefPage>507-13</RefPage>
        <RefTotal>Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y, Qiu Y, Wang J, Liu Y, Wei Y, Xia J, Yu T, Zhang X, Zhang L. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020 Feb 15;395(10223):507-13. DOI: 10.1016&#47;S0140-6736(20)30211-7</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;S0140-6736(20)30211-7</RefLink>
      </Reference>
      <Reference refNo="19">
        <RefAuthor>Xing Q</RefAuthor>
        <RefAuthor>Li GJ</RefAuthor>
        <RefAuthor>Xing YH</RefAuthor>
        <RefAuthor>Chen T</RefAuthor>
        <RefAuthor>Li WJ</RefAuthor>
        <RefAuthor>Ni W</RefAuthor>
        <RefAuthor></RefAuthor>
        <RefTitle>Precautions are needed for COVID-19 patients with coinfection of common respiratory pathogens &#91;Preprint&#93;</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Lancet SSRN</RefJournal>
        <RefPage></RefPage>
        <RefTotal>Xing Q, Li GJ, Xing YH, Chen T, Li WJ, Ni W, et al. Precautions are needed for COVID-19 patients with coinfection of common respiratory pathogens &#91;Preprint&#93;. Lancet SSRN. 2020. DOI: 10.2139&#47;ssrn.3550013</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.2139&#47;ssrn.3550013</RefLink>
      </Reference>
      <Reference refNo="20">
        <RefAuthor>Cucchiari D</RefAuthor>
        <RefAuthor>Peric&#224;s JM</RefAuthor>
        <RefAuthor>Riera J</RefAuthor>
        <RefAuthor>Gumucio R</RefAuthor>
        <RefAuthor>Md EC</RefAuthor>
        <RefAuthor>Nicol&#225;s D</RefAuthor>
        <RefAuthor> Hospital Cl&#237;nic 4H Team</RefAuthor>
        <RefTitle>Pneumococcal superinfection in COVID-19 patients: A series of 5 cases</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Med Clin (Barc)</RefJournal>
        <RefPage></RefPage>
        <RefTotal>Cucchiari D, Peric&#224;s JM, Riera J, Gumucio R, Md EC, Nicol&#225;s D; Hospital Cl&#237;nic 4H Team. Pneumococcal superinfection in COVID-19 patients: A series of 5 cases. Med Clin (Barc). 2020 Jun. DOI: 10.1016&#47;j.medcli.2020.05.022</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1016&#47;j.medcli.2020.05.022</RefLink>
      </Reference>
      <Reference refNo="21">
        <RefAuthor>Toombs JM</RefAuthor>
        <RefAuthor>Van den Abbeele K</RefAuthor>
        <RefAuthor>Democratis J</RefAuthor>
        <RefAuthor>Mandal AKJ</RefAuthor>
        <RefAuthor>Missouris CG</RefAuthor>
        <RefTitle>Pneumococcal coinfection in COVID-19 patients</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>J Med Virol</RefJournal>
        <RefPage></RefPage>
        <RefTotal>Toombs JM, Van den Abbeele K, Democratis J, Mandal AKJ, Missouris CG. Pneumococcal coinfection in COVID-19 patients. J Med Virol. 2020 Jul. DOI: 10.1002&#47;jmv.26278</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.1002&#47;jmv.26278</RefLink>
      </Reference>
      <Reference refNo="22">
        <RefAuthor>Murray AK</RefAuthor>
        <RefTitle>The Novel Coronavirus COVID-19 Outbreak: Global Implications for Antimicrobial Resistance</RefTitle>
        <RefYear>2020</RefYear>
        <RefJournal>Front Microbiol</RefJournal>
        <RefPage>1020</RefPage>
        <RefTotal>Murray AK. The Novel Coronavirus COVID-19 Outbreak: Global Implications for Antimicrobial Resistance. Front Microbiol. 2020;11:1020. DOI: 10.3389&#47;fmicb.2020.01020</RefTotal>
        <RefLink>https:&#47;&#47;doi.org&#47;10.3389&#47;fmicb.2020.01020</RefLink>
      </Reference>
    </References>
    <Media>
      <Tables>
        <Table format="png">
          <MediaNo>1</MediaNo>
          <MediaID>1</MediaID>
          <Caption><Pgraph><Mark1>Table 1: Occurrence and frequency of bacterial species isolated from COVID-19 patients</Mark1></Pgraph></Caption>
        </Table>
        <NoOfTables>1</NoOfTables>
      </Tables>
      <Figures>
        <Figure format="png" height="831" width="794">
          <MediaNo>1</MediaNo>
          <MediaID>1</MediaID>
          <Caption><Pgraph><Mark1>Figure 1: Antimicrobial susceptibility patterns of bacterial strains isolated from COVID-19   patients</Mark1></Pgraph></Caption>
        </Figure>
        <NoOfPictures>1</NoOfPictures>
      </Figures>
      <InlineFigures>
        <NoOfPictures>0</NoOfPictures>
      </InlineFigures>
      <Attachments>
        <NoOfAttachments>0</NoOfAttachments>
      </Attachments>
    </Media>
  </OrigData>
</GmsArticle>