Abstract
Background:
Infectious Keratitis (Ik) Is A Potential Vision-Threatening Ocular Infection Caused By A Variety Of Microorganisms.
Aim:
To Explore Risk Factors And Etiological Agents Associated With Ik.
Design:
A Prospective Cross-Sectional Study In Which Corneal Scrapings From 120 Suspected Cases Were Evaluated At A Tertiary Health Care Institute From January To December 2019.
Methods:
Scrapings Were Subjected To Direct Microscopy, Culture, And Identification By Both Conventional Methods And Maldi-Tof-Ms. The Patient's Demographic Data And Predisposing Factors, If Any Were Recorded.
Results:
The Mean Age Of Patients Was 48.9 Years And Predisposing Factors Were Documented In 46% (55/120) Of Cases. Overall, Infective Etiology Could Be Established In 51% (N = 61/120) Of Cases. Fungal Growth In 26% (N = 31/120) Of Cases And Bacterial Growth In 22% (N = 27/120) Of Cases Was Obtained. Growth Of More Than One Species Of Fungi Or Growth Of Bacteria Along With Fungus Were Observed In 2% (N = 3/120) Of Cases. Of All The Fungal Isolates Obtained (N = 34), The Most Common Isolate Was Fusarium (18/34) Followed By Aspergillus (8/34), Curvularia (4/34), Pseudallescheria Boydii (3/34), And Geotrichum (1/34). Among The Gram-Positive Bacterial Isolates (N = 16), Staphyloccus Species (15/16) Were Isolated In Maximum Number Followed By Streptococcus Pneumoniae (1/16). Among The Gram-Negative Isolates (N = 13), Pseudomonas Species (8/13) Were Isolated In Maximum Number Of Cases, Followed By Acinetobacter (3/13), Klebsiella Pneumoniae (1/13), And Escherichia Coli (1/13).
Conclusion:
For Initiating Appropriate Empirical Therapy, The Knowledge Of The Epidemiological Pattern Of Infectious Keratitis Of A Particular Geographical Region Is Crucial.
Keywords: Corneal Ulcer, Fusarium Keratitis, Infectious Keratitis
Introduction
Infectious keratitis (IK) can have a major impact on the quality of life of individuals leading to significant visual impairment or even loss of vision.[1] Corneal infections are known to be one of the most significant causes of monocular blindness in some developing countries, especially in tropics. It may be caused by a variety of microorganisms like bacteria, fungi, viruses, or parasites.[2]
Proper diagnosis of the causative organism is critical and culture is the most utilized diagnostic tool to delineate aetiology.[3] After culture growth, microbial identification by matrix-assisted laser desorption/ionization time of flight–mass spectrometry (MALDI-TOF MS) is a steadfast technique being utilized in many clinical microbiology laboratories. Implementation of this method enables conclusive organism identifications in minutes that was previously unimaginable.[4]
Several studies have established the etiological profile of IK from various parts of India. Knowledge of etiology in a specific region is crucial for the optimal management of these infections. However, meagre data is available from the foothills of the Himalayas in particular. As it varies geographically, the purpose of the study is to determine the aetiology of IK using conventional techniques and MALDITOF-MS at a tertiary healthcare institute and to explore epidemiological risk factors.
Material and Methods
Study design, setting, duration, and population
The prospective cross-sectional study was carried out in a tertiary healthcare institute from January 2019 to December 2019. The ethical clearance was taken from the Institute Ethics Committee. The patients were clinically examined by experienced clinicians and after taking informed consent, corneal scraping samples were collected from 120 clinically suspected IK cases. Inclusion criteria were the presence of signs of IK in slit-lamp examination (i.e., epithelial defect, underlying stromal infiltrate with signs of acute inflammation, e.g., circumcorneal congestion, stromal infiltrates, hypopyon, scarring, or perforation).
Collection of samples
Corneal scrapes were obtained under topical anesthesia by scraping the leading edges and base of the ulcer under the magnification of a slit lamp, using a sterile Bard-Parker blade. The patient's age, gender, occupation, history of any predisposing factor like trauma, systemic illness, past and current use of topical medicines, and use of contact lens use were entered in the Microsoft Excel sheets. Samples were sent to the ocular microbiology section and were processed by standard procedures for the diagnosis of causative pathogens.
Direct microscopy and inoculation on culture media
For each patient, a portion of the corneal scrape material obtained had been used for direct microscopy (Potassium hydroxide mount/KOH mount, Gram staining or calcofluor white staining). Another portion was inoculated directly onto the following media that support the growth of bacteria and fungi: Blood agar, Chocolate agar, Sabouraud dextrose agar (SDA) (HiMedia, Mumbai). Inoculated media were incubated at temperatures of 37°C and 25°C and were examined daily for 7 days. SDA was examined twice a week for the next three weeks.
The cultures were considered positive if the growth of the same organism was demonstrated in more than one solid media, or growth on one medium was consistent with direct microscopy findings, or confluent growth was obtained on inoculated single solid medium, or direct microscopy was suggestive of non-cultivable microorganism like Microsporidia. The bacteria isolated had been identified by standard biochemical test methods and MALDITOF-MS (Bruker Biotyper Microflex, MA, USA). Antibiotic susceptibility was put for bacterial isolates by Kirby Bauer's disc diffusion method. Fungi isolated had been identified by its cultural characteristics on media and sporulation patterns on lactophenol cotton blue mount and slide culture.
Results
The study was conducted in the Department of Microbiology and Ophthalmology in a tertiary healthcare teaching institute in the foothills of Himalayas for 1 year. A total of 120 samples from clinically suspected IK cases were submitted. There was a male preponderance in the study, with a male to female ratio of 2:1. The mean age of patients was 48.9 years and a maximum number of patients, that is, 53% (64/120) belonged to 41–60 years’ age group. Among the participants, 72% (n = 86/120) belonged to the rural background and 52% (n = 63/120) had an agricultural occupation. Table 1 shows the demographic parameters of the patients enrolled in the study and associated predisposing factors, if present.
Table 1.
Demographic parameters of the patients (n=120) enrolled in study and predisposing factors associated
| Demographics | Particulars | Number (%) |
|---|---|---|
| Gender | Male | 80 (67) |
| Female | 40(33) | |
| Age in years | <20 | 6(5) |
| 21-40 | 35 (29) | |
| 41-60 | 64 (53) | |
| 61 onwards | 15(13) | |
| Residence | Rural | 86(72) |
| Urban | 34(28) | |
| Occupation | Agricultural | 63(52.5) |
| Non-agricultural | 57(47.5) | |
| Predisposing factors (documented in 55/120 i.e. 46%) cases | Corneal trauma | 47 (39) |
| Pre-existing illness | 5(4.2) | |
| Structural abnormality | 2(1.7) | |
| Use Topical steroids | 1(0.8) | |
| Contact lens | 0 (0) | |
| Traumatic agents (documented in 47/120 i.e. 39%) cases | Vegetative matter/wooden stick | 32(27) |
| Stone/particle | 5(4) | |
| Chemical | 2(2) | |
| Rubbing of eye lid | 2 (2) | |
| NAil | 2(2) | |
| Hair | 2(2) | |
| Occupational hazard | 1(1) | |
| Trauma by insect | 1 (1) |
Predisposing factors were documented in 46% (55/120) of cases. Corneal trauma was the chief predisposing factor documented in 39% (n = 47/120) of cases, followed by pre-existing illness like Diabetes mellitus type II and carcinoma with brain metastasis in 4% (n = 5/120) of cases, structural lid abnormalities in 2% (n = 2/120) of cases and use of topical steroids in 1% (n = 1/120) of cases. None of the participants gave history of contact lens use. History of trauma with a wooden stick or vegetative matter was most common followed by injury from stone or particle, injury from chemical exposure, rubbing of eyelashes, hair, nail, insect, and injury while doing welding. Two cases of chemical exposure were noticed. One because of occupational exposure of cement and another because of a copper oxychloride containing based commercially available broad fungicide.
Clinical features
The most common complaint was pain followed by a diminution of vision, redness, and lacrimation. Clinical signs included stromal infiltrates (n = 65) in maximum number of cases, followed by circumcorneal congestion (n = 53), hypopyon (n = 38), Descemet's membrane folds (n = 13), scar (n = 8), perforation (n = 5), and impending perforation (n = 4).
Microbiological analysis
KOH mount/calcofluor white staining was positive for fungal elements in 40% of cases (n = 48/120) [Figures 1 and 2]. On gram staining, gram-variable hyphae in 19% (n = 23/120) cases, gram-positive cocci in 7% (n = 8/120) of cases and gram-negative bacilli in 2.5% (n = 3/120) of cases were seen. In one patient, on gram stain, a cluster of ovoid spore-like structures was also seen resembling Microsporidia species [Figure 3]. Growth on culture was obtained in 50% of cases (n = 60/120). Fungal growth in 26% (n = 31/120) of cases and bacterial growth in 22% (n = 27/120) of cases was obtained. In 2% (n = 2/120) of cases, scraping yielded significant growth of more than one species of fungi or growth of bacteria along with fungus like Fusarium and Geotrichum, Fusarium and Escherichia coli, Aspergillus flavus and Klebsiella. Overall, infective aetiology could be established in 51% (n = 61/120) of cases according to the predefined criteria. Table 2. summarizes identified causative micro-organisms responsible for the infection.
Figure 1.

Direct Potassium hydroxide mount showing hyaline septate hyphae. (magnification 400×)
Figure 2.

Calcofluor white staining mount showing fluorescing hyphae. (magnification 400×)
Figure 3.

Gram staining smear showing cluster of ovoid spore like structures resembling Microsporidia species. (magnification 1000×)
Table 2.
Causative micro-organism responsible for infectious keratitis
| Aetiology | Number (%) |
|---|---|
| Total culture positive cases | 60 (50) |
| Fungal growth | 31 (26) |
| Bacterial growth | 27 (22) |
| Mixed fungal and bacterial growth | 02 (2) |
| Microsporidia (identified in direct microscopy) | 01 (1) |
| Cases in which no organism identified | 59 (49) |
Table 3 illustrates the distribution of pathogens identified in the study using traditional techniques as well as MALDI-TOF. MALDI-TOF is an exemplar and rapid method for precise identification of microorganism. Of all the fungal isolates obtained (n = 34), the most common fungal isolate was Fusarium (18/34) followed by Aspergillus (8/34), Curvularia (4/34), Pseudallescheria boydii (3/34), and Geotrichum (1/34). Among the gram-positive bacterial isolates (n = 16), Coagulase negative Staphyloccus species (13/16) were isolated in maximum number followed by Staphlyococcus aureus (2/16) and Streptococcus pneumoniae (1/16). Among the gram-negative isolates (n = 13), Pseudomonas species (8/13) were isolated in a maximum number of cases, followed by Acinetobacter (3/13), Klebsiella pneumoniae (1/13), and Escherichia coli (1/13).
Table 3.
Distribution of identified pathogens from infectious keratitis cases in 1-year study period (n=64)
| Pathogens | Identification by Conventional Method | Identification by MALDI-TOF-MS | Pure isolate in culture (number) | Mixed with other species in culture (number) |
|---|---|---|---|---|
| Fungal isolates (n=34) | ||||
| Fusarium species | 18 | Fusarium proliferatum (10) | 16 | 2 |
| Fusarium oxysporum (04) | ||||
| Fusarium solani (04) | ||||
| Aspergillus flavus | 5 | Aspergillus flavus (05) | 4 | 1 |
| Aspergillus fumigatus | 3 | Aspergillus fumigatus (03) | 3 | - |
| Pseudallescheria boydii | 3 | Scedosporium apiospermum (03) | 3 | - |
| Curvularia geniculata | 3 | Not identified | 3 | - |
| Curvularia lunata | 1 | Not identified | 1 | - |
| Geotrichum | 1 | Not identified ( Not in database) | - | 1 |
| Gram positive bacterial isolates (n-=16) | ||||
| Coagulase negative | 13 | Staphylococcus epidermidis (13) | 13 | - |
| Staphylococcus species | ||||
| Staphylococcus aureus | 2 | Staphylococcus aureus (2) | 2 | - |
| Streptococcus pneumoniae | 1 | Streptococcus pneumoniae (1) | 1 | - |
| Gram negative bacterial isolates (n=13) | ||||
| Pseudomonas species | 8 | Pseudomonas aeruginosa (8) | 8 | - |
| Acinetobacter baumannii complex | 3 |
Acinetobacter lwofii (02) Acinetobacter junii (1) |
3 | - |
| Klebsiella pneumoniae | 1 | Klebsiella pneumoniae (1) | - | 1 |
| Escherichia coli | 1 | Escherichia coli (1) | - | 1 |
| Non-cultivable microorganism (identified on basis of direct microscopy) | ||||
| Microsporidia | 1 | NA | - | - |
Fusarium forms reproductive ovoid structures in vivo, this phenomenon is known as adventitious sporulation.[5] This phenomena was also observed in few cases and a rapid presumptive diagnosis of Fusarium infection can be made while awaiting the results of the culture.
Management and Outcome
The standard protocol for the empirical treatment of cases was the topical instillation of antibiotics, antiviral and antifungals drugs, in combination with oral antifungals. Table 4 shows the antimicrobial treatment of the patients (n = 120) enrolled and their clinical outcomes. Table 5 illustrates organisms identified in culture-proven cases (n = 63) and clinical outcomes associated with them.
Table 4.
Antimicrobial treatment of the patients (n=120) enrolled and their clinical outcome
| Treatment | Natamycin, Voriconazole, oral ketoconazole | Natamycin, Voriconazole, Moxifloxacin | Acyclovir | Antiviral, Cefuroxime, Moxifloxacin | Cefuroxime, Moxifloxacin | Moxifloxacin, Acyclovir | Moxifloxacin, Tobramycin | Azithromycin | Voriconazole, Natamycin | Natamycin, Gatifloxacin, Gancyclovir, Itraconazole | Moxifloxacin |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Worse (n=19) | 10 | 1 | 1 | - | 6 | - | 1 | - | - | - | - |
| Symptomatically better (n=24) | 10 | 3 | 1 | - | 7 | - | 2 | - | - | 1 | - |
| Healed (n=61) | 32 | 5 | 1 | 2 | 14 | 1 | 3 | 1 | 1 | - | 1 |
| Lost to follow up (n=16) | 7 | - | 3 | 1 | 4 | - | - | - | 1 | - | - |
Table 5.
Pathogens identified in culture (n=63) and associated clinical outcome
| Worse n=9 (14%) | Symptomatically better n=13 (21%) | Healed n=31 (49%) | Lost to follow up n=10 (16%) | |
|---|---|---|---|---|
| Fungal | ||||
| Fusarium species (18) | 2 | 8 | 7 | 1 |
| Aspergillus flavus (5) | 2 | 1 | 1 | 1 |
| Aspergillus fumigatus (3) | 1 | -- | 2 | -- |
| Pseudallescheria boydii (3) | -- | -- | 1 | 2 |
| Curvularia geniculate (3) | 1 | 1 | -- | 1 |
| Curvularia lunata (1) | -- | -- | 1 | -- |
| Geotrichum (1) | -- | -- | 1 | -- |
| Bacterial | ||||
| Staphylococcus epidermidis (13) | -- | -- | 12 | 1 |
| Staphylococcus aureus (2) | -- | -- | 1 | 1 |
| Streptococcus pneumoniae (1) | -- | -- | 1 | -- |
| Pseudomonas species (8) | 2 | -- | 4 | 2 |
| Acinetobacter baumannii complex (3) | - | 2 | -- | 1 |
| Klebsiella pneumoniae (1) | 1 | -- | -- | -- |
| Escherichia coli (1) | -- | 1 | -- | -- |
Discussion
IK is a potentially damaging ocular infection when the corneal epithelial barrier is breached owing to injury or trauma. Immediate diagnosis and treatment are required if vision threating outcomes are to be avoided.[6] We have explored epidemiological risk factors, clinical features, etiological agents associated with IK and described clinical outcomes.
In the study, 41–60 was the age group in which most of the keratitis cases were recorded. This is in contrast to the findings of an epidemiological study from North India which states 31–40 years as the age group with the highest number of cases. A study from Delhi for over 16 years, that is, 2010–2016 and a study from Nagpur state also states 31–40 as the most affected age group. A study from Tamil Nadu states 21–50 as the commonest age group affected and studies from Ahmedabad and Bengal describes 21–40 as the age group with highest number of cases.[2,7,8,9,10,11] There was a male predominance which can be attributed to outdoor work done by them. Similar findings were reported by many authors as Manikandan et al. and Deorukhkar S et al.[12,13] The majority of them belonged to the rural background, had an agricultural occupation and trauma was the most significant risk factor observed. Agricultural practices in rural areas and humid environments as in the state of Uttarakhand is favorable for the development of IK from minor trauma.[7]
Corneal trauma has always been identified as the chief risk factor behind IK.[8,9,11,14] Trauma with the vegetative matter, leaves, wood, some particle or stone was the leading predisposing factor. Interestingly, two cases of chemical injury have also been documented: one with cement fall and another with a fungicide. The patient was exposed to a commercially available copper-based broad fungicide while spraying it in fields. To the best of our knowledge, no case of keratitis has been reported after ocular exposure with copper oxychloride.
IK can be caused by a variety of microorganisms like bacteria, viruses, fungi, or parasites. In this study, of all the cases with established infective aetiology, 26% of cases were attributed to fungal, 22% to bacterial, and 2% to mixed bacterial and fungal etiology. Similarly, other studies regarding the microbiological profile of IK from Gujarat, Tamil Nadu, and Delhi, state fungal etiology as leading cause followed by bacterial aetiology. Whereas a study from Mysore, Karnataka reports bacterial aetiology as the commonest.[1,15,16,17]
Compared to other infective corneal ulcers, fungal corneal ulcers are difficult to diagnose as well as treat. Also, these are more likely to get perforated and the patient presents with increased ocular morbidity like scarring. Hence, rapid communication between microbiologist and ophthalmologist is of utmost significance. Fusarium was the most frequently isolated fungus. that is, 53% (18/34) of all fungal isolates in the study. A similar finding has been observed in many studies from the west and south India and neighbor countries with similar climate, where Fusarium was the commonest fungal isolate.[8,12,15,18,19] While few studies from North India have reported Aspergillus to be the commonest causative agent. Fusarium and Aspergillus are said to be the frequently reported agents of IK in tropical areas. Poor response to medical treatment in fungal keratitis has been documented.[10,11,14,16,20] In our study also, among all culture positive cases, poor outcome in the form of enlarged infiltrate size and perforation has been observed in 9.5% (6/63) of fungal, 3% of (2/63) gram-positive bacterial and 1.5% of (1/63) gram-negative bacterial keratitis cases.
As there are no CLSI (The Clinical and Laboratory Standards Institute)/EUCAST (The European Committee on Antimicrobial Susceptibility Testing) guidelines yet for topical ocular antimicrobial agents, sensitivity pattern coupled with clinical improvement is needed to assess the efficacy of a particular antimicrobial agent. Knowledge of causative microorganism in a particular region and judicious use of s ocular antibiotics or antifungal agent can be a pivotal step in resource limited primary health centres in the management of corneal ulcer, thereby decreasing ocular morbidities. To summarize, infective aetiology (fungal more than bacterial) could be established using conventional as well as MALDI-TOF technique in 51% cases and mixed infections can only be diagnosed using culture. Ocular trauma with vegetative material stays the most common predisposing factor for corneal ulcers.
Conclusion
For initiating appropriate empirical therapy, the knowledge of the epidemiological pattern of IK of a particular geographical region is crucial. Early and accurate diagnosis allows timely specific treatment and is the corner-stone of vision-saving management. However, relevant empirical treatment needs to be started until the time a microbiological diagnosis is made. For initiating the most appropriate empirical therapy, the knowledge of the epidemiological pattern of IK of a particular geographical region is crucial. Comprehensive analysis of results obtained over a period of time from different geographical areas can enhance the knowledge and understanding of such patterns.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
References
- 1.Chidambaram JD, Prajna NV, Srikanthi P, Lanjewar S, Shah M, Elakkiya S, et al. Epidemiology, risk factors, and clinical outcomes in severe microbial keratitis in South India. Ophthalmic Epidemiol. 2018;25:297–305. doi: 10.1080/09286586.2018.1454964. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Tewari A, Sood N, Vegad MM, Mehta DC. Epidemiological and microbiological profile of infective keratitis in Ahmedabad. Indian J Ophthalmol. 2012;60:267–72. doi: 10.4103/0301-4738.98702. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Austin A, Lietman T, Rose-Nussbaumer J. Update on the management of infectious keratitis. Ophthalmology. 2017;124:1678–89. doi: 10.1016/j.ophtha.2017.05.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Dingle TC, Butler-Wu SM. MALDI-TOF mass spectrometry for microorganism identification. Clin Lab Med. 2013;33:589–609. doi: 10.1016/j.cll.2013.03.001. [DOI] [PubMed] [Google Scholar]
- 5.Nucci M, Anaissie E. Fusarium infections in immunocompromised patients. Clin Microbiol Rev. 2007;20:695–704. doi: 10.1128/CMR.00014-07. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Kaliamurthy J, Kalavathy CM, Parmar P, Jesudasan CA N, Thomas PA. Spectrum of bacterial keratitis at a tertiary eye care centre in India? BioMed Res Int. 2013;2013:181564. doi: 10.1155/2013/181564. doi: 10.1155/2013/ [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Chowdhary A, Singh K. Spectrum of fungal keratitis in North India. Cornea. 2005;24:8–15. doi: 10.1097/01.ico.0000126435.25751.20. [DOI] [PubMed] [Google Scholar]
- 8.Bharathi MJ, Ramakrishnan R, Vasu S, Meenakshi R, Palaniappan R. Epidemiological characteristics and laboratory diagnosis of fungal keratitis. a three-year study. Indian J Ophthalmol. 2003;51:315–21. [PubMed] [Google Scholar]
- 9.Basak SK, Basak S, Mohanta A, Bhowmick A. Epidemiological and microbiological diagnosis of suppurative keratitis in gangetic West Bengal, Eastern India. Indian J Opthalmol. 2005;53:17–22. doi: 10.4103/0301-4738.15280. [DOI] [PubMed] [Google Scholar]
- 10.Satpathy G, Ahmed NH, Nayak N, Tandon R, Sharma N, Agarwal T, et al. Spectrum of mycotic keratitis in north India: Sixteen years study from a tertiary care ophthalmic centre. J Infect Public Health. 2019;12:367–71. doi: 10.1016/j.jiph.2018.12.005. [DOI] [PubMed] [Google Scholar]
- 11.Raut S, Chavan S, Shweta, Khadse R, Tore RP. Mycological profile of corneal ulcer at tertiary care centre in central India. Indian J Appl Res. 2019;9:21–3. [Google Scholar]
- 12.Manikandan P, Abdel-hadi A, Babu Singh YR, Revathi R, Anita R, Banawas S, et al. Fungal keratitis: Epidemiology, rapid detection, and antifungal susceptibilities of Fusarium and Aspergillus isolates from corneal scrapings? BioMed Res Int. 2019;2019:6395840. doi: 10.1155/2019/6395840. doi: 10.1155/2019/ [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Deorukhkar S, Katiyar R, Saini S. Epidemiological features and laboratory results of bacterial and fungal keratitis: A five-year study at a rural tertiary -care hospital in western Maharashtra, India. Singapore Med J. 2012;53:264–7. [PubMed] [Google Scholar]
- 14.Das S, Sharma S, Mahapatra S, Sahu SK. Fusarium keratitis at a tertiary eye care centre in India. Int Ophthalmol. 2014;35:387–89. doi: 10.1007/s10792-014-9961-5. [DOI] [PubMed] [Google Scholar]
- 15.Katara RS, Patel ND, Sinha M. A Clinical microbiological study of corneal ulcer patients at Western Gujarat, India. Acta Med Iran. 2013;51:399–403. [PubMed] [Google Scholar]
- 16.Gupta A, Capoor M R, Gupta S, Kochhar S, Tomer A, Gupta V. Clinico-demographical profile of keratomycosis in Delhi, North India. Indian J Med Microbiol. 2014;32:310–14. doi: 10.4103/0255-0857.136582. [DOI] [PubMed] [Google Scholar]
- 17.Amrutha KB, Venkatesha D. Microbiological profile of ulcerative keratitis in a tertiary care hospital. Int J Res Health Sci. 2014;30:599–603. [Google Scholar]
- 18.Ranjini CY, Waddepally VV. Microbial profile of corneal ulcers in a tertiary care hospital in South India. J Ophthalmic Vis Res. 2016;11:363–7. doi: 10.4103/2008-322X.194071. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Suwal S, Bhandari D, Thapa P, Shrestha MK, Amatya J. Microbiological profile of corneal ulcer cases diagnosed in a tertiary care ophthalmological institute in Nepal. BMC Ophthalmol. 2016;16:209. doi: 10.1186/s12886-016-0388-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Gupta IK, Chandra A, Prakash P, Banerjee T, Maurya OPS, Tilak R. Fungal keratitis in north India; Spectrum and diagnosis by Calcofluor white stain. Indian J Med Microbiol. 2015;33:462–3. doi: 10.4103/0255-0857.158609. [DOI] [PubMed] [Google Scholar]
